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{
"caption": "Intraoperative: incision through extended lip split (left), surgical defect after tumor resection with a display of lingual nerve",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272209-4-CCR3-10-e6047-g009.jpg"
} | 009200 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Bending the plate with the aid of the stereographic created 3D model of the mandible (L) and the titanium plate placed in the surgical defect",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272209-5-CCR3-10-e6047-g004.jpg"
} | 009201 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Superimposition of 3D bio‐printed model on the tumor surface(R) and with the reproduced mirror image of the normal side(R)",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272209-6-CCR3-10-e6047-g003.jpg"
} | 009202 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Histopathological picture showing peripheral tall columnar cells with hyperchromatic nuclei surrounding a central mass of stellate reticulum‐like cells features of ameloblastoma",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272209-7-CCR3-10-e6047-g002.jpg"
} | 009203 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "10 weeks post‐operative appearance (left) and satisfactory occlusal relationship of the spared teeth",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272209-8-CCR3-10-e6047-g005.jpg"
} | 009204 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Postoperative view of the patient",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272213-1-CCR3-10-e6029-g002.jpg"
} | 009205 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Chest radiograph at initial presentation showing bilateral consolidation and pleural effusion",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272214-0-CCR3-10-e5973-g003.jpg"
} | 009206 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "(A) Chest radiograph 4 days prior to initiation of extracorporeal membrane oxygenation (ECMO) showing bilateral consolidation, a left pneumothorax with chest drain in‐situ (open arrow) and left‐sided subcutaneous emphysema (solid arrow). (B) Chest radiograph taken on Day 6 of ECMO showing bilateral consolidation, ECMO cannula (open arrow), a coop‐loop chest drain within the left pneumothorax (solid arrow) and 2 left chest drains",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272214-1-CCR3-10-e5973-g004.jpg"
} | 009207 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "(A) CT Thorax done on Day 7 of extracorporeal membrane oxygenation (ECMO) shows bilateral collapse and consolidation (arrows). (B) CT Thorax on Day 37 of ECMO shows bilateral collapse and consolidation (arrows). (C and D) CT Thorax 2 months and 7 months post‐ECMO, respectively, showing significant improvement with minimal residual parenchymal changes",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272214-2-CCR3-10-e5973-g005.jpg"
} | 009208 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Chest radiograph performed post‐decannulation of tracheostomy 3 months post‐discharge",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272214-3-CCR3-10-e5973-g002.jpg"
} | 009209 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Clinical characteristics of the patient. (A) Flat face; round face; wide‐set eyes; the red arrows indicates both palms have a single transverse palmar crease",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272217-3-CCR3-10-e5990-g003.jpg"
} | 009210 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "MRI scan of the patient's brain showed abnormal signal changes in the deep white matter area near the lateral ventricle and a mild delay of myelination compared with a healthy child at the age of 7 months",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272217-5-CCR3-10-e5990-g001.jpg"
} | 009211 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "(A + B): F + profile view of the left foot, 3 weeks after limping. The dotted arrows show proximal callus formation of the cuboid bone, thus revealing the cause of limping (cuboid fracture)",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272219-1-CCR3-10-e6021-g002.jpg"
} | 009212 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "(A) Radiograph of the hand shows absence/short middle phalanges of fingers. (B) Radiograph of the foot shows absence/short middle phalanges of toes",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272223-2-CCR3-10-e6000-g002.jpg"
} | 009213 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "(A and B) Note transposition of the penis and prominent median raphe",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272223-4-CCR3-10-e6000-g004.jpg"
} | 009214 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Parasagittal intra‐axial right rolandic mass lesion (white asterisk in “A–C”) presenting with T1, T2 (image A) and FLAIR (image B) isosignal and showing intense gadolinium enhancement (image C). Extensive fronto‐parietal vasogenic edema is seen around the lesion (black arrows in “A–C”). Images “D” and “E” show a normal hypophyse with no supra‐sellar lesion. Note the subtentorial metastatic lesions in the right cerebellum and the vermis (white arrows in “F”) presenting as round lesions with intense gadolinium enhancement",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272224-0-CCR3-10-e6025-g001.jpg"
} | 009215 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "First operation. (A) Operative findings. A thin, dilated, brachial artery with the aberrant branched vessel and a small aneurysm (arrow). (B) Elastica van Gieson stain of the abnormal branch, magnification ×4. The aberrant vessels were composed of collagen fibers and smooth muscle that lack elastic fibers, suggesting arteriovenous malformation",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272232-0-CCR3-10-e6026-g004.jpg"
} | 009216 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Second operation. (A) Operative findings. The brachial artery (arrow) is thin, dilated, and twisted around the mass. The mass is 3 × 3 cm (triangle), involving the median nerve (dotted arrow). The aberrant branch of the brachial artery was ligated and resected. After resection of the mass, revascularization of the brachial artery was performed via direct anastomosis. (B) Elastica van Gieson stain of the mass, magnification ×10. The wall of the mass lacked a vascular structure accompanied by elastic lamina and was composed of fibrillar connective tissues with tiny vessels, which is a characteristic histological picture of a pseudoaneurysm. (C) Elastica van Gieson stain of the brachial artery, magnification ×4. The wall of the brachial artery was composed of a fragmented internal elastic layer and fibrillated tunica media of the brachial artery, which had histological properties comparable to a vein",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272232-1-CCR3-10-e6026-g003.jpg"
} | 009217 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Perioperative status. Blue arrow = Mitrofanoff appendicovesicostomy. White arrow = sutured ileum. Green arrow = enterocystoplasty. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272336-0-gr2.jpg"
} | 009218 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Assessment of five TILs variables including eTILs, etTILs, esTILs, eaTILs and easTILs. (a) Schematic diagram illustrating the variables (created with BioRender.com). (b) Forest plot of DSS in stage I and II combined discovery set. The optimal cut-points defined in the TCGA cohort as a training set for each variable, the p-values (log-rank) and HRs with 95% CI derived for measurement of the cohorts from assessing the optimal cut-points were shown.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272337-2-gr3.jpg"
} | 009219 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Images of the adenoma during surgery.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272338-1-gr2.jpg"
} | 009220 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "MRI shows intravesical protrusion of giant median prostatic lobe.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272338-2-gr1.jpg"
} | 009221 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Moderate to severe hydronephrosis with displacement of DJ down to upper ureter with no evidence of encrustation.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272339-0-gr1.jpg"
} | 009222 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Antegrade pyelogram showed around 3 cm upper ureteric strictures.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272339-1-gr2.jpg"
} | 009223 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Microscopic examination of tumor showed back to back cords and few tubular structures of bland looking cells with eosinophilic cytoplasm, H&E ×100 (A) and H&E ×400 (B). Immunohistochemical examination. Calretinin (C), WT1 (D), Inhibin (E) and Ki67 index (F).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272340-0-gr3.jpg"
} | 009224 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Macroscopic manifestation of the mass during surgery (multiple intratesticular cysts).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272340-1-gr2.jpg"
} | 009225 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Ultrasound images of the patient. Right Testis (A) and Left Testis (B).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272340-2-gr1.jpg"
} | 009226 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
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{
"caption": "(A) Fundus fluorescein angiography of the right eye. (B) Fundus fluorescein angiography of the left eye (arrows show blocked fluorescence and capillary non-perfusion).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272389-0-cureus-0014-00000025842-i02.jpg"
} | 009227 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Optical coherence tomography scan of the left eye (arrows show disorganized retinal inner layers and disruption of inner segment-outer segment junction). (B) Optical coherence tomography angiography scan of the left eye (arrows show enlarged foveal avascular zone and capillary non-perfusion).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272389-1-cureus-0014-00000025842-i01.jpg"
} | 009228 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
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{
"caption": "Side-chain-hydroxycholesterols protect endometrial cells against Staphylococcus aureus α-hemolysin. Leakage of LDH and viability of epithelial (A) and stromal (B) cells treated with vehicle or 25 ng/ml 27-hydroxycholesterol (27HC) for 24 h, and then challenged for 24 h with control medium () or 8 μg α-hemolysin (). Data are presented as mean (SEM) using cells from 4 independent animals; statistical significance is determined using ANOVA and Dunnett’s multiple comparison post hoc test, *p < .05; **p < .01. Potassium in supernatants from epithelial (C) and stromal cells (D) treated with vehicle or 25 ng/ml 27-hydroxycholesterol for 24 h, and then challenged for 15 min with control medium () or 8 μg α-hemolysin (). Data are presented as mean (SEM) using cells from 4 independent animals; statistical significance is determined using ANOVA and Dunnett’s post hoc test. Fluorescent microscope images of epithelial (E) and stromal cells (F) treated with vehicle or 25 ng/ml 27-hydroxycholesterol (27HC) for 24 h, challenged for 24 h with control medium or 8 μg α-hemolysin, and then stained with Alexa Fluor 555-conjugated phalloidin to visualize actin (white; nuclei are red; scale bars are 20 μm). Images are representative of cells from 3 animals",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272411-34-nihms-1817176-f0007.jpg"
} | 009229 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Trajectory plots of Li and Na in (a) Li2NaOCl, (b) Na2LiOCl, (c) Li2NaOBr and (d) Na2LiOBr compounds after 2 ns. Blue and green lines represent the Li and Na trajectory lines, respectively.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272413-5-d2ra03370d-f8.jpg"
} | 009230 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
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{
"caption": "Fluoro-angiographic and real-time 3D TEE procedural steps showing the crossing of the residual leakage in close proximity of the already implanted 14 × 6 mm rectangular waist PLD (A–C), the distal disc opening of the 7 mm square twist PLD (D) still anchored to the delivery cable and the inference with the tilting disc of the mechanical aortic valve (E,F). RW, rectangular waist; ST, square twist.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272523-0-fcvm-09-839159-g0003.jpg"
} | 009231 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
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{
"caption": "Intraprocedural fluoro-angiographic and real-time 3D TEE procedural steps showing the guide wire (A) (black arrowhead) across the leakage with the distal soft tip in the left ventricle; the 5- Fr multipurpose catheter in the LV (B); the distal disc device opening (orange asterisk) (C–E) and the 14 × 6 mm rectangular waist PLD correctly positioned and still anchored to the delivery cable (F). MP, multipurpose catheter; PLD, Occlutech Parvalvular Leak Device; RW, rectangular waist.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272523-3-fcvm-09-839159-g0002.jpg"
} | 009232 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
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{
"caption": "Baseline two-dimensional (2D) X-plane imaging Transoeophageal Echocardiogram (TEE) color Doppler (A) and ascending aorta angiography (B) showing the presence of a huge crescent-shaped 17 × 6 mm aortic PVL located at non coronary cusp (NCC) 9-12 o'clock, with moderate-to-severe regurgitation. Fluoro-angiographic image confirming the stable position of the mechanical tilting disc aortic prosthetic valve (white asterisk) with moderate regurgitation (black arrow).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272523-4-fcvm-09-839159-g0001.jpg"
} | 009233 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
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{
"caption": "Representative PET/CT images of rat hearts at different time points from ischemia/reperfusion injury model",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272551-1-12872_2022_2750_Fig4_HTML.jpg"
} | 009234 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
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{
"caption": "Representative HE staining of myocardial tissues in Control group and Met group after day 30th imaging acquisition in the ischemia center (×10) and remote area (×20)",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272551-3-12872_2022_2750_Fig5_HTML.jpg"
} | 009235 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
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{
"caption": "Proximal intestine histological sections of fish fed different test diets. A CF diet, well preserved intestinal morphology with elongated and regularly branched complex villi. B FH10 diet, similar to the CF diet, intestinal morphology was well preserved with elongated and regularly branched complex villi. C CV diet, elongated, irregularly branched complex villi with extensive multifocal detachment of lamina epithelialis from the lamina propria (arrows). D Detail of area indicated by the rectangle in panel C; note the pronounced vacuolisation of enterocytes (arrow heads) and notable number of neutral goblet cells (NGC). E VH10 diet, elongated, irregularly and highly branched complex villi with multifocal moderate to extensive detachment of lamina epithelialis from the lamina propria (arrows). F Detail of area indicated with by the rectangle in panel E; note the moderate vacuolisation of enterocytes (arrow heads) with the predominance of acid goblet cells (AGC) over neutral goblet cells (NGC). G VH10P30 diet, elongated and irregularly branched complex villi with multifocal moderate to extensive detachment of lamina epithelialis from the lamina propria (arrows). Alcian blue/PAS staining, pH = 2.5. Scale bar: A, B, C, E, G = 500 μm, D, F = 100 μm",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272557-5-40104_2022_725_Fig2_HTML.jpg"
} | 009236 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Pharmacological antagonism of OXTR in dCA2 blocks chemogenetic enhancement of long-term SRM. A Schematic representation of the experimental design. B Schematic representation of viral injection and CNO administration. Three weeks after stereotaxic injection of AAV5-mOXT-hM3D(Gq)-mCherry into the PVN, mice were subjected to three-chamber paradigm test and long-term SRM retention was tested 7 days after the initial interaction. Mice were bilaterally administered of vehicle (Veh) or an OXTR antagonist L-368,899 into dCA2 10 min before CNO injection, followed by three-chamber paradigm test 20 min after CNO injection. Representative images showing the co-expression of hM3D(Gq)-mCherry and OXT immunoreactivity in the PVN. mCherry signals of axonal projections were observed in dCA2. Scale bar represents 50 μm. C Top, schematic representation of the three-chamber sociability test. Bottom left, time spent by the subject mouse in sniffing directed at the wire cage containing the juvenile stimulus mouse or the empty wire cage. hM3D(Gq)/CNO/Veh and hM3D(Gq)/CNO/L-368,899 subject mice spent significantly more time interacting with the wire cage containing the juvenile stimulus mouse than the empty wire cage. Bottom right, discrimination index (stimulus minus empty) was similar between groups in the sociability test. D Top, schematic representation of the three-chamber social novelty preference test. Bottom left, time spent by the subject mouse in sniffing directed at the wire cage containing a familiar mouse or a novel 1 mouse, 10 min after the sociability test. hM3D(Gq)/CNO/Veh and hM3D(Gq)/CNO/L-368,899 subject mice spent significantly more time sniffing the cage containing the novel mouse than the familiar mouse. Bottom right, discrimination index (novel 1 minus familiar) was comparable between groups in the social novelty preference test. E Top, schematic representation of the three-chamber long-term SRM test. Bottom, time spent by the subject mouse in sniffing directed at the wire cage containing a familiar mouse or a novel 2 mouse, 7 days after the initial interaction. hM3D(Gq)/CNO/Veh, but not hM3D(Gq)/CNO/L-368,899, subject mice spent significantly more time sniffing the cage containing the novel mouse than the familiar mouse. Bottom right, discrimination index (novel 2 minus familiar) of hM3D(Gq)/CNO/Veh subject mice was significantly higher than that of hM3D(Gq)/CNO/L-368,899 subject mice in 7-day long-term SRM test. The total number of animal examined is indicated by n in parenthesis. Error bars represent the SEM; *P < 0.05, **P < 0.01, ***P < 0.001",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272559-0-12929_2022_834_Fig4_HTML.jpg"
} | 009237 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Subcellular localization of GFP-fused PeCER32 protein based on transient expression assays in onion epidermal cells. (A) (a) Structure of CaMV35S-GFP as empty vector. (b) Structure of CaMV35S-PeCER32-GFP as construct. (B) (a–c) Onion cells transformed with CaMV35S-GFP as control (scale bar = 100 μm). (d–f) Onion cells transformed with CaMV35S-PeCER32-GFP (scale bar = 50 μm). (a,d) GFP signals visualized under dark field. (b,e) Onion epidermal cells under bright light. (c,f) represent merging of (a,b,d,e).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272567-11-fpls-13-898307-g0009.jpg"
} | 009238 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "CT scan of the chest with arrows showing multiple bilateral pulmonary masses of varying sizes.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272580-0-cureus-0014-00000025843-i02.jpg"
} | 009239 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Arrow showing an ill-defined low-attenuation in the left internal jugular vein on CT angiogram of the head and neck.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272580-1-cureus-0014-00000025843-i03.jpg"
} | 009240 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "X-ray of the chest showing ill-defined ground-glass opacities in both lungs suspicious for pneumonia/pneumonitis.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272580-2-cureus-0014-00000025843-i01.jpg"
} | 009241 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Immediate postoperative view",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272581-4-cureus-0014-00000025844-i06.jpg"
} | 009242 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Scrotal hemangioma on presentation",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272581-5-cureus-0014-00000025844-i01.jpg"
} | 009243 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Rbfox1 expression in GABAergic ACs(A) The vast majority GABAergic ACs in the INL were Rbfox1-positive. Some GABA/Rbfox2-positive ACs are pointed with yellow arrows. Rbfox1-negative GABAergic ACs and Rbfox1-positve/GABA-negative cells are pointed with green and red arrows, respectively. (B) Rbfox1 is expressed in all cholinergic (ChAT-positive) starburst ACs both in the INL and GCL. (C) Extensive overlap of Rbfox1 with NPY expression was also observed (yellow arrows). Very few NPY-positive cells had very faint staining for Rbfox1 (pointed by green arrows).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272594-0-bsr-42-bsr20220497-g3.jpg"
} | 009244 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Expression of Rbfox1 in glycinergic ACs(A) Rbfox1 is expressed in very few GlyT1-positve ACs (yellow arrows). Rbfox1-positive/GlyT1-negative and GlyT1-positive/Rbfox1-negative cells are pointed with red and green arrows, respectively. (B) Rbfox1 is expressed in sparse population of VGlut3-positve glycinergic ACs (yellow arrows). Red arrows point at Rbfox1-positive cells that not immunostained for GlyT1 (A) or for VGlut3 (B). The boxed areas of the vertical retinal sections are shown at higher magnification.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272594-1-bsr-42-bsr20220497-g2.jpg"
} | 009245 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Rbfox1 is expressed in RGCs and ACs(A) In the GCL, all Rbpms-positive cells, RGCs, were also stained for Rbfox1 (yellow arrows point at some Rbpms/Rbfox1-positive cells). Red arrows point at some Rbfox1-positive/Rbpms-negative cells that are most likely displaced ACs. (B) In the INL, virtually all clabindin-positive cells were also Rbfox1-positive cells (yellow arrows). Very few Rbfox1-immunostained cells appeared to be calbindin-negative (red arrows). In the GCL, Rbfox1 is expressed in calbindin-positive displaced ACs (yellow arrows), as well as in calbindin-negative cells, many of which are RGCs (red arrows). (C) Colocalization of Rbfox1 expression with RGCs in whole mount retinas. All Rbpms-positive cells were immunostained with Rbfof1. Rbfox1-positive/Rbpms-negative cells (presumably displaced ACs) are indicated by white arrows. (D) A significant overlap in Rbfox1 and calbindin expression within GCL was observed in whole mount retinas (yellow arrows). Rbfox1-positive/calbindin-negative and calbindin-positive/Rbfox1-negative cells are pointed with red and green arrows, respectively. DAPI; 4',6-diamidino-2-phenylindole; GCL; ganglion cell layer, INL; inner nuclear layer, IPL; inner plexiform layer, ONL; outer nuclear layer, OPL; outer plexiform layer.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272594-2-bsr-42-bsr20220497-g1.jpg"
} | 009246 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Near-infrared fluorescence lymphatic imaging (NIRF-LI) images of the left axilla (left to right) before axillary lymph node dissection (ALND), 4 weeks after ALND, 6 months after radiotherapy (RT), 12 months after RT, and 18 months after RT in study subject number 13. Dermal backflow appears as a cloudy dispersion of lymph (seen at 6, 12, and 18 months after RT), as opposed to linear lymphatic collector vessels (seen before and at 4 weeks after ALND). This study subject received physiotherapy for breast cancer-related lymphedema beginning at 6 months after RT. RVC, relative volume change (from baseline)",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272652-2-10549_2022_6667_Fig1_HTML.jpg"
} | 009247 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Isolation of MPXV-IMBmuc1 on Vero E6 cells and serology results. VeroE6 cells were inoculated with sample material from a lanced pustule of Patient #1 following standard procedure [17]. A Typical plaque formation of MPXV IMBmuc 1 on Vero E6 2 days post-infection of the sample material. B Vero E6 mock infected. C Plaque morphology of vaccinia virus (VACV) Elstree (1), VACV WR (2), MPXV IMBmuc 1 (3; most similar to VACV Elstree), MPXV IMBdrc 2510 (4), on MA104 cells 3 dpi—size bar refers to (1–4). D Reactivity of VACV Elstree in immunofluorescence assay with sera from patient #1 at hospital admission (1; non-reactive) and 11 days later (2; reactive, titre 80), sera of MVA unvaccinated (3; non-reactive), and MVA vaccinated (4; reactive) controls",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272654-2-15010_2022_1874_Fig3_HTML.jpg"
} | 009248 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "A Enoral lesions (right tonsil) visible already at first presentation of patient #1. B–D Both patients developed 10–12 initially vesicular, later pustular skin lesions distributed over the entire body. Many of these lesions were umbilicated, and all were at the same general stage of development. Upon opening of the lesions, the typical septate structure of pox lesions became apparent",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272654-3-15010_2022_1874_Fig1_HTML.jpg"
} | 009249 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Preoperative MRI (T1 sequence) showing the osteoarthritis of the proximal tibiofibular joint",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272732-0-cureus-0014-00000025849-i02.jpg"
} | 009250 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Preoperative MRI (T2 sequence) showing the osteoarthritis of the proximal tibiofibular joint",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272732-1-cureus-0014-00000025849-i01.jpg"
} | 009251 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Histology results of rumen explant tissue with different media and culture time. Hematoxylin–eosin staining (HE) or HE staining is a common method for observing the morphology and structural integrity of tissue cells. Normal physiological changes of animal explants in general or morphological changes after the addition of certain stimuli can be observed by the HE staining method. MA is rumen explant cultured in medium A containing 10% serum, and MB is rumen explant cultured in medium B without serum. The effect of different media and cultural times on the growth of rumen explants was observed by the integrity of the flat cut structure of the rumen epithelial tissue. The explant maintained a complete organizational structure at 12 h but started to disintegrate after 16 h and festering increased with longer cultural time.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272757-2-fvets-09-852321-g0005.jpg"
} | 009252 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Segmentation tools.A) Thresholdmann is a brain extraction tool that creates a mask from those voxels that are brighter than a spatially varying threshold. The threshold is constrained by control points (blue dots flagged with number arrows) that are added by clicking at locations in the web viewer (left). Adjustable sliders to the right control the threshold in the vicinity of each control point. In the examples shown to the right, the mask initially (top) excludes ventral brain areas but is filled out (bottom) by the addition of ventral control points. B) Brainbox is a web-based tool for collaborative brain segmentation. In the interface, each MRI (left) has a page where information on all projects utilizing this dataset is centralized. Under project settings (right), users can assemble datasets into projects, add collaborators, manage access rights, and add annotation layers. C) The UNet tool uses a neural network model approach for brain extraction. Local accuracy at each voxel is estimated by the regional Dice coefficient (top). Bottom panels show results for three example subjects from the PRIME-DE repository, with regions assessed to be brain tissue shown in red.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272762-4-nihms-1800568-f0004.jpg"
} | 009253 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Anatomical MRI pipelines.A) Six sagittal slices illustrating the D99 atlas transformed to the native space of a macaque subject using @animal_warper. B) CIVET-macaque results for the D99 subject. Top row (left to right): anatomical scan, brain mask (red) from brain extraction, tissue classification (CSF in dark blue, cortical GM in green, portions of non-cortical GM in white, WM and other non-cortical GM in yellow) from segmentation, and generated cortical surfaces overlaid on the anatomical scan (WM surface in red, pial surface in green). Bottom row (left to right): 3D-renderings of the white and pial surfaces; cortical thickness indication from morphometric analysis (1.0 mm in light blue to 3.5 mm in red) and D99 surface parcellation (atlas) viewed on the pial surface. C) PREEMACS results. Top row: brainmask (red) created by a Deep Learning convolutional neural network model (left) and volumetric tissue segmentation (right). Middle row: white matter and pial surface estimation (left) and rendered white matter surface (right). Bottom row left: surface registration to the PREEMACS Rhesus parameterization template to obtain vertex correspondence (i.e., surface coregistration) between subjects. Bottom row right: individual cortical thickness estimation from morphometric analysis. The resulting surfaces can be analyzed in the geometric space of the PREEMACS average surface.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272762-5-nihms-1800568-f0005.jpg"
} | 009254 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Macaque Templates and Atlases.The symmetric variant of the NIMH Macaque Template v2 (NMT v2), with tissue segmentation (top row) and anatomical regions (middle and bottom rows) depicted in color on a coronal slice (11 mm anterior to ear bar zero) and the pial surface (right column). The NMT v2 includes A) the population average volume; B) a manually refined brain mask that indicates which voxels contain brain tissue; C) a 5-class tissue segmentation that differentiates cerebrospinal fluid (green), gray matter (dark blue), white matter (light blue), subcortex (purple), and vasculature (red); and D) rendering of surfaces. The middle row shows the Cortical Hierarchy Atlas of the Rhesus Macaque (CHARM) and the bottom row shows the Subcortical Atlas of the Rhesus Macaque (SARM). The atlases provide anatomical labeling of cortical and subcortical regions, respectively, at six progressively finer spatial scales. Parcellations for E,I) Level 2, F,J) Level 4, and G,K) Level 6 are shown. H,L) Surface representation of the finest (Level 6) parcellations.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272762-6-nihms-1800568-f0002.jpg"
} | 009255 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Magnetic resonance imaging of the spinal cord revealed a lesion showing a hyperintense signal on sagittal tbl2-weighted imaging (A), sagittal short tau inversion recovery sequence (B), and axial tbl2-weighted imaging (C), indicating a longitudinally extensive demyelinating lesion from the C5 to the D4 level.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272764-0-qmj-2022-029-g001.jpg"
} | 009256 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Tulp3 and Pkd1 double knockout models of PKD. (A) Kidneys from postnatal day 5 (P5). Tulp3 cko (HoxB7-cre; Tulp3\n\nfl/fl\n), Pkd1 cko (HoxB7-cre; Pkd1\n\nfl/fl\n), Tulp3 cko;Pkd1 cko (HoxB7-cre; Tulp3\n\nfl/fl\n\n;Pkd1\n\nfl/fl\n). cko: conditional knockout. Scale bar, 1 mm. Images adapted from (Hwang et al., 2019). (B) Adult-onset models. Pax8\n\nrtTA\n\n; tetO-cre doxycycline inducible mice were given doxycycline (Dox) starting at P28 for 2 weeks and analyzed at 18 weeks. Control (mice without tetO-cre), Tulp3 cko (Pax8\n\nrtTA\n\n; tetO-cre; Tulp3\n\nfl/fl\n), Pkd1 cko (Pax8\n\nrtTA\n\n; tetO-cre; Pkd1\n\nfl/fl\n), Tulp3 cko;Pkd1 cko (Pax8\n\nrtTA\n\n; tetO-cre; Tulp3\n\nfl/fl\n\n;Pkd1\n\nfl/fl\n). Images adapted from (Legue and Liem, 2019) with permission.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272769-1-fmolb-09-936070-g004.jpg"
} | 009257 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Complex roles of cilia in cystogenesis. Cysts from PC1 loss are severe and only partially suppressed from cilia loss. Images adapted from (Ma et al., 2013) with permission. Postnatal day 24 (P24) kidneys from (A)\nPkd1 cko (Pkhd1-cre;Pkd1\n\nfl/fl\n),\n(B)\nPkd1 cko; cilia cko (Pkhd1-cre;Kif3a\n\nfl/-\n\n;pkd1\n\nfl/fl\n), and (C) cilia cko (Pkhd1-cre;Kif3a\n\nfl/-\n) mice. Abbreviations: cko, conditional knockout.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272769-4-fmolb-09-936070-g001.jpg"
} | 009258 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "The contouring process of the m. quadriceps femoris for MV estimation of the individual muscle heads.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272772-1-fphys-13-830216-g002.jpg"
} | 009259 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "(A). Ultrasonographic measurement of the m. rectus femoris and m. vastus intermedius. (B) Ultrasonographic measurement of the m. vastus lateralis and m. vastus intermedius. (C) Ultrasonographic measurement of the m. vastus medialis. The white indicator shows the length of 1 cm.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272772-4-fphys-13-830216-g001.jpg"
} | 009260 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Gonads of adult medaka at 2 months post-hatching. (A) XY male, control, (B) XX female, control, (C) sex-reversal XX male, (D) no sex-reversal XX female with H2O2 treatment, (E) H2O2 + metyrapone, (F) H2O2 + NAC, (G)\ngsdf KO XX female, (H)\npparaa KO XX female with H2O2 treatment. SC, spermatocytes; SG, spermatogonia; O, oocytes; OC, ovarian cavities; Scale bars: 100 μm.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272773-3-fendo-13-878286-g001.jpg"
} | 009261 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
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{
"caption": "Results of morphological processing. (A) Type-1 field (illumination: 130800 lx). (B) Type-2 field (illumination: 101700 lx).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272774-0-fpls-13-916474-g0010.jpg"
} | 009262 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
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{
"caption": "Binary images. (A) Type-1 field (illumination: 130800 lx). (B) Type-2 field (illumination: 101700 lx).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272774-10-fpls-13-916474-g0009.jpg"
} | 009263 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
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{
"caption": "(A) Synthesis procedures of UCNPs, (B)TEM images of core (a), core–shell (b) nanoparticles for NaYF4:Tm/Yb and NaYF4:Tm/Yb@NaYF4 UCNPs, respectively. UCNPs@SiO2 NPs (c).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272789-1-fbioe-10-891727-g001.jpg"
} | 009264 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Reproductive characterization of 12-week-old InhaR233A/R233A males. Testis weights (A), representative histology (B), and daily sperm production counts (C) in wild-type and InhaR233A/R233A males. Body (D), fat (E), and lean mass (F) were measured weekly by EchoMRI. Serum levels of follicle-stimulating hormone (G), inhibin B (H), activin B (I), and testosterone (J) were measured by enzyme-linked immunosorbent assay. Bars represent mean ± SE of the mean.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272799-3-bqac025_fig4.jpg"
} | 009265 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Subcellular localization of Ycf 1 protein.Ycf 1 antibody coupled with Alexa Fluor 488 (green) labeled secondary antibody. DAPI (blue) was used to stain the nuclei of host cells and N. bombycis. (A) Sporoplasm. (B) Meront. (C) Sporont. (D) Sporoblasts. (E) Mouse IgG; red arrow: Ycf 1; Scale bars, 5 µm.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272817-0-peerj-10-13530-g004.jpg"
} | 009266 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Co-localization of Ycf 1 with SWP30 or Nb-actin in dormant spores of N. bombycis.(A) Dormant spore; white arrow: Ycf 1; yellow arrow: SWP30. (B) Mouse IgG. (C) Dormant spore; white arrow: Ycf 1; yellow arrow: Nb-actin. (D) Mouse IgG; Scale bars, 5 µm.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272817-1-peerj-10-13530-g003.jpg"
} | 009267 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Colocalization of Ycf 1 with Nb-actin during the proliferative phase of N. bombycis.Ycf 1 antibody coupled with Alexa Fluor 488 (green) labeled secondary antibody. Nb-actin antibody coupled with Cy5 (red) labeled secondary antibody. DAPI (blue) was used to stain the nuclei of host cells and N. bombycis. (A) Sporoplasm. (B) Meront. (C) Sporont. (D) Sporoblasts. (E) Mouse IgG; white arrow: Ycf 1; yellow arrow: Nb-actin; Scale bars, 5 µm.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272817-3-peerj-10-13530-g005.jpg"
} | 009268 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Optimal TCID50 method for the titration of HCoV-OC43.A common viral stock produced on MRC-5 cells was used to infect VeroE6 or HRT-18. (A) Typical images of the infected cells by bright field (CPE, IPA) or fluorescence microscopy (IFA). (B) Quantification of the viral yields by TCID50-CPE, TCID50-IPA and TCID50-IFA. Error bars represent SEM (n = 3). Statistical analyses were done by one-way ANOVA with Dunnett multiple comparisons (*p < 0.05; ****p < 0.0001).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272819-0-peerj-10-13721-g005.jpg"
} | 009269 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Optimal propagation of HCoV-OC43 at 33 °C.MRC-5 cells were grown to 80% confluence on 6-well plates before being mock treated or infected at an MOI of 0.7 and grown for 3 days at either 33 °C or 37 °C in DMEM supplemented with 2% serum. (A) Monitoring of the cells by bright field microscopy over time. Note that the infection leads to more CPE at 33 °C compared to 37 °C. (B) Extracellular virus harvested at 3 dpi were titered by the TCID50-IPA method as in Fig. 1. Error bars represent SEM (n = 3). Statistical analyses were done with a Student t-test (*p < 0.05).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272819-1-peerj-10-13721-g002.jpg"
} | 009270 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "HCoV-OC43 can be grown in serum free media.MRC-5 cells were grown to 80% confluence on six-well plates then mock treated or infected at an MOI of 0.7 in serum free media. After a 1h adsorption period, cells were incubated for up to 3 days at 33 °C in the presence of EMEM containing different concentrations of serum (0%, 2% or 10%) or Optipro, a serum-free media (SFM-Optipro). (A) Bright field monitoring over the course of the infection indicated the lack of noticeable effect of the serum. (B) Extracellular virus harvested on at 3 dpi were titered by the TCID50-IPA method. Error bars represent SEM. Statistical analyses were done by one-way ANOVA with Dunnett multiple comparisons (n = 3).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272819-2-peerj-10-13721-g003.jpg"
} | 009271 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "TEM of embryonic cells at stage IIIwith different GA3 concentrations treatment (10 mol/L, 50 mol/L, CK: no treatment). (a, b) TEM of embryonic cells at stage III treated with 10 mol/L GA3;(c, d) TEM of embryonic cells at stage III treated with 50 mol/L GA3; (e, f) TEM of embryonic cells in Stage III without treatment. Abbreviations: sg, starch grain; m, mitochondria; g, Golgi apparatus; lb, lipid body; m, mitochondrion; n, nucleus; v, vacuole; mb, multivesicular bodies.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272834-1-KPSB_A_2091305_F0003_B.jpg"
} | 009272 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "TEM of embryonic cells at stage II with different GA3 concentrations treatment(10 mol/L, 50 mol/L, CK: no treatment). (a, b) TEM of embryonic cells at stage II treated with 10 mol/L GA3;(c, d) TEM of embryonic cells at stage II treated with 50 mol/L GA3; (e, f) TEM of embryonic cells at stage II without treatment. Abbreviations: sg, starch grain; m, mitochondria; g, Golgi apparatus; lb, lipid body; m, mitochondrion; n, nucleus; v, vacuole; mb, multivesicular bodies; ce, cell edge.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272834-3-KPSB_A_2091305_F0002_B.jpg"
} | 009273 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "TEM of embryonic cells at stageIV with different GA3 concentrations treatment (10 mol/L, 50 mol/L, CK: no treatment). (a, b) TEM of embryonic cells at stage IV treated with 10 mol/L GA3;(c, d) TEM of embryonic cells at stage IV treated with 50 mol/L GA3; (e, f) TEM of embryonic cells in stage IVwithout treatment. Abbreviations: sg, starch grain; m, mitochondria; g, Golgi apparatus; lb, lipid body; m, mitochondrion; n, nucleus; v, vacuole; mb, multivesicular bodies.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272834-9-KPSB_A_2091305_F0004_B.jpg"
} | 009274 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "a Glomerular mesangial expansion and hypercellularity (periodic acid–Schiff, ×400). b Moderate-to-intense mesangial staining for IgA (immunofluorescence, ×200). c Moderate-to-intense mesangial staining for C3c (immunofluorescence, ×200). d Mesangial electron-dense deposits (electron microscopy, ×3000)",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272869-0-13256_2022_3514_Fig1_HTML.jpg"
} | 009275 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Feeding progression of Rhimi-PKR silenced ticks. Photographs of open cotton sleeves showing shaved patches on cattle where the confined R.\nmicroplus female ticks fed, photographed at 6, 8 and 10 days (numbers on the left side of the figure). Additional pictures of ticks feeding throughout the course of the experiment are shown in Additional file 3: Figure S3. Abbreviations: D, Days feeding on the animals; NI, non-injected ticks; β-Lac, beta-lactamase dsRNA-injected ticks (negative controls); PKR, Rhimi-PKR dsRNA-injected ticks; β-Act, Rhimi-ACTB dsRNA-injected ticks (positive control)",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272880-2-13071_2022_5349_Fig4_HTML.jpg"
} | 009276 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Adhesion morphology of cells after co-culture of hydrogel and cells.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272884-2-fbioe-10-906835-g006.jpg"
} | 009277 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Morphology and diameter distribution of hydrogel. (A–D) SEM images of CP50, OCP50, CP100, and OCP100 hydrogels (200×); (E–H) SEM images of CP50, OCP50, CP100, and OCP100 hydrogels (500×); (I–L) Pore statistics of cross-section of CP50, OCP50, CP100, and OCP100 hydrogels.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272884-4-fbioe-10-906835-g003.jpg"
} | 009278 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Photo of OCP100 hydrogel adhered to the pigskin. (A) Side bending, twisting, and curling; (B) folding and twisting; (C) lateral water flow impact; (D) double water flow impact.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272884-5-fbioe-10-906835-g004.jpg"
} | 009279 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "COG treatment ameliorated DSS-induced experimental colitis. (A) Body weight. (B) Disease activity index (DAI) score. (C) Representative pictures of colon gross appearance and colon length. (D) Colon length. (E) Colon weight index. (F) Representative microscopic pictures of H&E-stained sections (magnifications: ×40 and ×100). (G) Pathological injury score. Data were presented as mean ± SEM (n = 8–12). #p < 0.05 and ##p < 0.01 compared to the normal group; *p < 0.05 and **p < 0.01 compared to the DSS group.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_49-PMC9272890-7-fcimb-12-907813-g003.jpg"
} | 009280 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "SEM images of cell plastics. Cell plastics with intracellular contents (0% ~ 25%) were prepared without heat treatment. Scale bars were 500 μm and 10 μm in low (× 20) and high (× 1000) magnification levels, respectively",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259522-4-253_2022_12000_Fig5_HTML.jpg"
} | 009281 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Thrombus burden classification. RVD reference vessel diameter. The Thrombolysis In the Myocardial Infarction (TIMI) thrombus classification consists of six grades from grade 0 (no thrombus) to grade 5 (total occlusion). Grade 5 represents an occluded infarct related artery and prevents thrombus size assessment. Grade 5 was reclassified after guidewire crossing or small (diameter 1.5 mm) deflated balloon passage. After G5 reclassification, large thrombus burden (LTB) was defined as being greater than or equal to two vessel diameters or greater (G4) and small thrombus burden (STB) defined by thrombus grade < G4",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259523-0-11239_2021_2603_Fig1_HTML.jpg"
} | 009282 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "KPNB1 modulation affects ataxin-3 aggregation levels. a, b Fluorescence microscopy was conducted to visualize the alteration of polyQ-expanded ataxin-3 aggregation in KPNB1 overexpressing cells. ATXN3 KO HEK 293T cells co-expressing EGFP ataxin-3 148Q and KPNB1 were fixed 72 h post-transfection, and the number of GFP-positive (EGFP+) cells with and without aggregates was counted manually in 20 fields of vision. The analysis showed a decrease of cells with ataxin-3 aggregates upon KPNB1 overexpression. Blue, green, and red channels show DAPI as nuclear counterstain, GFP, and KPNB1 signals, respectively. White arrowheads mark ataxin-3 aggregates. 400 × magnification, scale bar = 20 µm. The diagram shows the percentage of aggregates in EGFP+ cells. n = 4, unpaired t-test, p = 0.0123. c Filter retardation assay of ATXN3 KO HEK 293T cells co-expressing polyQ-expanded (148Q) ataxin-3 and KPNB1 for 72 h demonstrated a reduction of polyQ-expanded ataxin-3 aggregates compared with control. n = 6, one sample t-test, p = 0.0004. d PrestoBlue assay of ATXN3 KO HEK 293T cells cotransfected with either 15Q or 148Q ataxin-3 and KPNB1 or empty vectors. The viability of cells expressing 148Q ataxin-3 was rescued upon KPNB1 overexpression. Viability was normalized to 15Q ataxin-3 expressing cells. n = 4, one sample t-test, 15Q + CTRL vs 148Q + CTRL, p = 0.0144; 15Q + CTRL vs 148Q + KPNB1, p = 0.0882; paired t-test, 148Q + CTRL vs 148Q + KPNB1, p = 0.0138. e Filter retardation assay of ATXN3 KO HEK 293T cells co-expressing 148Q ataxin-3 and either wild-type or KPNB1 I178D indicates a decrease in the aggregation of 148Q ataxin-3. n = 6, one sample t-test, CTRL vs KPNB1, p = 0.0030; CTRL vs KPNB1 I178D, p = 0.0247; unpaired t-test, KPNB1 vs KPNB1 I178D, p = 0.1883. f Knockdown of KPNB1 using esiRNA shows an increased load of aggregated 148Q ataxin-3 using filter retardation assay. ATXN3 KO HEK 293T cells were cotransfected for 72 h with 148Q ataxin-3 and esiKPNB1 or esiLUC as control. n = 5, one sample t-test, p = 0.0054. g Filter retardation assay shows increased ataxin-3 aggregation in ATXN3 KO HEK 293T cells expressing 148Q ataxin-3 for 72 h and treated with 16 µM IPZ for 48 h. Values were normalized to DMSO-treated cells. n = 5, one sample t-test, p = 0.0279. CTRL empty vector, IPZ importazole, Rel. relative. Values are displayed as means ± SEM. ns not significant; *p ≤ 0.05; **p ≤ 0.01; ***p ≤ 0.001",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259533-1-18_2022_4372_Fig5_HTML.jpg"
} | 009283 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Unlike O2/glucose deprivation (OGD), bath superfusion of glutamate at pathophysiological concentrations onto a brain slice does not induce SD. A Imaging change in light transmittance (ΔLT) reveals OGD-induced SD and propagation (arrows) along neocortical gray matter (NC) and through striatum (S) with damage arising in the wake of SD (magenta). w = slice weight. B A cocktail of blockers (Mix-1, constituents listed in Fig. D) delays OGD-induced SD onset but not propagation (arrows). By 16.8 min, light scattering in NC caused by dendritic beading indicates acute neuronal damage. C Bath superfusion of glutamate causes slight signal creep from the overlying weight, but no SD. D Superfusion of Mix-1 significantly (p = 0.002) delayed OGD-induced SD onset by 46 ± 11.8%. Adding MK-801 slightly but significantly (p < 0.0001) further delayed SD onset by 52 ± 9.9%. E Percent of slices generating signal creep but no SD in three experimental groups of glutamate application to naïve slices. No SD was observed in slices superfused in aCSF alone (n = 6) or in aCSF + 1 mM glutamate (n = 6)",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259542-1-12028_2021_1429_Fig3_HTML.jpg"
} | 009284 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Dynamics of extracellular glutamate and K+ during SD in vivo. The SD was evoked at a distance by applying a droplet of 1 mM KCl to the surface of the mouse brain. A iGluSnFR, a fluorescent probe, monitors the extracellular glutamate level. B Speed of the extracellular glutamate wave. C Average fluorescence traces with 95% confidence interval, amplitude, and duration of the glutamate transient. D Glutamate trace (blue) aligned to the DC potential below. E Latency between negative DC deflection and glutamate increase. F Relationship between [K+]o, DC potential, and neuronal [Ca2+]i. The latency between 0.25 mM [K+]o rise (arrow over K+ trace) and increase in fluorescence (red vertical line) is indicated to the right. Dashed line indicates start of the negative DC potential shift. G As in F but with [Ca2+]i in astrocytes instead of neurons. H As in F but with [glutamate]e instead of neuronal [Ca2+]i. Images in F–H show positions of electrodes (stippled lines) and sampled regions (white circles). Sampled regions were picked along the front edge of the SD wave as it hit the K+-sensitive microelectrode. Scale bars: 50 μm; error bars, SEM. From [85]",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259542-2-12028_2021_1429_Fig2_HTML.jpg"
} | 009285 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Echocardiogram in the short axis view showing the clot in transit in the right ventricle (star).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259549-0-CRICC2022-3483605p004.jpg"
} | 009286 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Chest computed tomography with contrast showing bilateral pulmonary emboli and multifocal lung consolidations.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259549-2-CRICC2022-3483605p002.jpg"
} | 009287 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Chest X-ray showing bilateral lung opacities.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259549-3-CRICC2022-3483605p001.jpg"
} | 009288 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Microscopic images of (a) T3 formulation, 100×, (b) T1 formulation, 100×.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259567-1-41598_2022_15655_Fig2_HTML.jpg"
} | 009289 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Fifty-eight-year-old man on gadoxetate acid disodium-enhanced liver MR examination using CDT-VIBE sequence. Precontrast phase (A), followed by five subphases of CDT-VIBE at (B)–(F), The portal venous phase (H) and hepatobiliary delay period (G) were shown by VIBE. MR images showed a 2.4 cm mass (white arrows) in S6/8. This mass presents peripheral arterial enhancement and washout in portal venous phase and hepatobiliary delay period. We proved this mass to be hepatocellular carcinoma by Pathologic examination. The scores of artifact degree showed that (A) was 1 point, (B) and (C) were 3 points, and (D)–(G) was 1 point. Respiratory movement artifacts were more likely to occur in the early phase of CDT-VIBE enhancement.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259568-0-41598_2022_15108_Fig6_HTML.jpg"
} | 009290 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "(A) shows the VIBE sequence image, and (B) shows the StarVIBE sequence image. (C)–(G) show the CDT-VIBE images. 1–5 phases of CDT-VIBE sequence, in which (C) and (D) show early arterial phase, only abdominal aorta and hepatic artery are enhanced; (E) Late arterial phase, with an enhancement of the abdominal aorta and hepatic artery and slightly enhancement of hepatic portal vein; (F) and (G) show the portal vein period, with portal vein enhancement and liver parenchyma enhancement. The scores of artefact degree showed that (A) was 4 points, (B) was 1 point, (C) was 2 points, (D)–(F) was 1 point, (G) was 4 points, and the motion artefact in the fifth phase was heavier than that in other phases.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259568-5-41598_2022_15108_Fig5_HTML.jpg"
} | 009291 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "sample image data of kidney cysts, normal, stone and tumor findings.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259587-1-41598_2022_15634_Fig2_HTML.jpg"
} | 009292 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "GradCam analysis of kidney Cyst, Normal, Stone and Tumor class photos at the final convolution layer in the Inception v3, Vgg16, and Resnet models. First row: shows the Gradcam images from inception v3 model for different classes. Second row: shows the Gradcam images from Resnet50 model for different classes. Third row: shows the Gradcam images from Vgg16 model for different classes. The GradCam activation mapping for the xray image is shown in the second row. The first, second, third, and fourth columns are for kidney cysts, normal, stone, and tumor classes respectively.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259587-2-41598_2022_15634_Fig14_HTML.jpg"
} | 009293 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "BBR reduced the plaque size in patients with atherosclerosis. a The ultrasonic images of atherosclerotic plaques (circle in white) of the patients at different positions of carotid arteries before (1) and after (2) 4-month BBR therapy are shown, including the common carotid artery (A: participate No. 1, plaque No. 1), the carotid bifurcation (B: participate No. 16, plaque No. 38), the internal carotid artery (C: participate No. 6, plaque No. 19) and the subclavian artery (D: participate No. 19, plaque No. 44). Also, please see Table S9 in the supplemental material. b The average plaque score in patients was decreased by 3.2% after oral BBR (0.5 g, bid) for 4 months (*P < 0.05, n = 21); the score value was slightly increased (by +1.9%) after treatment with conventional drug combination, including rosuvastatin, aspirin, as well as clopidogrel sulfate or ticagrelor (n = 12) if needed. c The average carotid intima-media thickness was reduced by 3.2% after oral treatment with BBR (P = 0.067), and the value was slightly increased (by +2.0%) in the combination therapy. d The average carotid plaque length in patients was decreased by 2.2% in either oral BBR (0.5 g/bid) group or combination drug group after 4 months on therapy. e TMA and TMAO level in faeces and plasma samples of patients went down after 4 months BBR treatment; the TMA/TMAO levels in plasma were lowered by 37% / 35% (***P < 0.001; *P < 0.05), and TMA/TMAO levels in faeces decreased by 38%/29% (*P < 0.05; *P < 0.05). Data shown are the mean ± SEM and analysed with one-tailed paired t test",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259588-0-41392_2022_1027_Fig6_HTML.jpg"
} | 009294 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Chemical treatment of tachyzoites infecting the EC monolayer. (a–d) Images after 60 h of processing each chemical; (a) control, (b) Genistein, (c) Blebbistatin, and (d) calcium ionophore. (e) Proliferation of tachyzoites in the EC monolayer, and (f) their cluster size. Scale bar indicates 100 μm. Statistical significance was analyzed by one-way ANOVA with Holm-Sidak method and is indicated by asterisks as follows: *P < 0.05, **P < 0.01, ***P < 0.001.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259589-0-41598_2022_15305_Fig6_HTML.jpg"
} | 009295 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Tachyzoite infection of the EC monolayer co-cultured with neurons. (a) Time line for EC monolayer formation (with neurons) and tachyzoite infection. (b) Confocal image of neurons (rhodamine-phalloidin (red) and DAPI (blue)) on ECM shows the 3D migration of axons into ECM. Fluorescent images after 60 h of tachyzoite infection (c) without and (d) with neurons. Scale bars indicates 100 μm.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259589-5-41598_2022_15305_Fig4_HTML.jpg"
} | 009296 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "Effect of calycosin on bone histomorphology.a Representative fluorescence micrographs of trabecular bone sections showing green calcein labels within various groups (scale bar: 200 μm). b Quantitative analysis of the mineral deposition rate (MAR). The results are represented as the mean ± SD; n = 3/group. P-values calculated using a two-tailed Student’s t test (^P < 0.05, ^^P < 0.01 v.s. baseline; #P < 0.05, ##P < 0.01 v.s. control; *P < 0.05, **P < 0.01 v.s. HLU).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259590-4-41526_2022_210_Fig4_HTML.jpg"
} | 009297 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "MN formation promoted by cypermethrin. Buccal mucosal epithelium normal appearance (a), buccal mucosal epithelium with MN (b), erythrocyte cell normal appearance (c), erythrocyte cell with MN (d), leukocyte cell normal appearance-basophil (e), leukocyte cell-basophil with MN (f).",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259609-6-41598_2022_15800_Fig4_HTML.jpg"
} | 009298 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
|
{
"caption": "(a) Illustration showing the general relationship of the baleen racks, soft tissue, and bony palate. (b) Close up photograph highlighting the relationship between zwischensubstanz (baleen mat) and its relationship to the soft tissue ventral to the bony palate in Balaenoptera physalus. (c) Palatal morphology of extant mysticetes, from left to right: Balaenoptera borealis, Eschrichtius robustus, Caperea marginata, and Eubalaena glacialis. White brackets surround lateral palatal foramina and their associated sulci. Art by Alex Boersma.",
"subfigure_path": "/datasets/PMC-15M/filtered_biomedica/filtered_v4/subfigures_final/subfig_0_filelist_commercial_batch_124_5-PMC9259611-0-41598_2022_15684_Fig1_HTML.jpg"
} | 009299 | hf://datasets/vector-institute/open-pmc-18m@6109d453e9b8e2de3564869941b2e622faddd8d3/data_00028.tar |
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