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PMC1082913_F1_1787.jpg | What's the most prominent thing you notice in this picture? | Electron microscope morphological observations of DEN2 virus particles. A) Typical viral particle in the extracellular environment (arrow; bar: 200 nm). B) Viral particles engulfed in an intracytoplasmic vacuole (arrow; bar: 50 nm). C) Membrane disruption of a vesicle containing a virus (arrow; bar: 100 nm). D) Fuzzy c... |
PMC1082913_F1_1783.jpg | What stands out most in this visual? | Electron microscope morphological observations of DEN2 virus particles. A) Typical viral particle in the extracellular environment (arrow; bar: 200 nm). B) Viral particles engulfed in an intracytoplasmic vacuole (arrow; bar: 50 nm). C) Membrane disruption of a vesicle containing a virus (arrow; bar: 100 nm). D) Fuzzy c... |
PMC1082913_F1_1785.jpg | What is the core subject represented in this visual? | Electron microscope morphological observations of DEN2 virus particles. A) Typical viral particle in the extracellular environment (arrow; bar: 200 nm). B) Viral particles engulfed in an intracytoplasmic vacuole (arrow; bar: 50 nm). C) Membrane disruption of a vesicle containing a virus (arrow; bar: 100 nm). D) Fuzzy c... |
PMC1082913_F1_1786.jpg | What is the focal point of this photograph? | Electron microscope morphological observations of DEN2 virus particles. A) Typical viral particle in the extracellular environment (arrow; bar: 200 nm). B) Viral particles engulfed in an intracytoplasmic vacuole (arrow; bar: 50 nm). C) Membrane disruption of a vesicle containing a virus (arrow; bar: 100 nm). D) Fuzzy c... |
PMC1082913_F1_1782.jpg | What's the most prominent thing you notice in this picture? | Electron microscope morphological observations of DEN2 virus particles. A) Typical viral particle in the extracellular environment (arrow; bar: 200 nm). B) Viral particles engulfed in an intracytoplasmic vacuole (arrow; bar: 50 nm). C) Membrane disruption of a vesicle containing a virus (arrow; bar: 100 nm). D) Fuzzy c... |
PMC1082913_F1_1784.jpg | What object or scene is depicted here? | Electron microscope morphological observations of DEN2 virus particles. A) Typical viral particle in the extracellular environment (arrow; bar: 200 nm). B) Viral particles engulfed in an intracytoplasmic vacuole (arrow; bar: 50 nm). C) Membrane disruption of a vesicle containing a virus (arrow; bar: 100 nm). D) Fuzzy c... |
PMC1082913_F2_1781.jpg | What can you see in this picture? | Electron microscope morphological observations of dense particles. A) Dense particles close to the cell surface (arrow; bar: 200 nm). B) Aggregated dense particles in the extracellular space (arrow). Note the nucleocapsid like center and the electron dense envelopes (bar: 100 nm). C) Dense particles showing a nucleocap... |
PMC1082913_F2_1780.jpg | What key item or scene is captured in this photo? | Electron microscope morphological observations of dense particles. A) Dense particles close to the cell surface (arrow; bar: 200 nm). B) Aggregated dense particles in the extracellular space (arrow). Note the nucleocapsid like center and the electron dense envelopes (bar: 100 nm). C) Dense particles showing a nucleocap... |
PMC1082913_F2_1779.jpg | What is shown in this image? | Electron microscope morphological observations of dense particles. A) Dense particles close to the cell surface (arrow; bar: 200 nm). B) Aggregated dense particles in the extracellular space (arrow). Note the nucleocapsid like center and the electron dense envelopes (bar: 100 nm). C) Dense particles showing a nucleocap... |
PMC1084330_pbio-0030156-g005_1788.jpg | Describe the main subject of this image. | Simultaneous Visualization of GFP-LC3 Localization and MDC Staining (Red) in Uninfected and Poliovirus-Infected CellsForty-eight hours posttransfection of MCF-7 cells with a plasmid that expresses a GFP-LC3 fusion protein, cells were mock-infected or infected with poliovirus at an MOI of 50 PFU/cell for 5 h at 37 °C. A... |
PMC1084330_pbio-0030156-g005_1789.jpg | What is the focal point of this photograph? | Simultaneous Visualization of GFP-LC3 Localization and MDC Staining (Red) in Uninfected and Poliovirus-Infected CellsForty-eight hours posttransfection of MCF-7 cells with a plasmid that expresses a GFP-LC3 fusion protein, cells were mock-infected or infected with poliovirus at an MOI of 50 PFU/cell for 5 h at 37 °C. A... |
PMC1084330_pbio-0030156-g005_1791.jpg | What is the focal point of this photograph? | Simultaneous Visualization of GFP-LC3 Localization and MDC Staining (Red) in Uninfected and Poliovirus-Infected CellsForty-eight hours posttransfection of MCF-7 cells with a plasmid that expresses a GFP-LC3 fusion protein, cells were mock-infected or infected with poliovirus at an MOI of 50 PFU/cell for 5 h at 37 °C. A... |
PMC1084331_pbio-0030159-g002_1805.jpg | What is the focal point of this photograph? | Rescue of Ia Proprioceptive Afferent Projections into the Ventral Spinal Cord in Er81EWS-Pea3 Mutants(A–F) Morphological analysis of central projections at lumbar level L3 of PV+ DRG neurons (A–C) or all DRG sensory afferents after application of fluorescently labeled dextran to individual dorsal roots (D–F) in P0.5 (A... |
PMC1084331_pbio-0030159-g002_1800.jpg | What is shown in this image? | Rescue of Ia Proprioceptive Afferent Projections into the Ventral Spinal Cord in Er81EWS-Pea3 Mutants(A–F) Morphological analysis of central projections at lumbar level L3 of PV+ DRG neurons (A–C) or all DRG sensory afferents after application of fluorescently labeled dextran to individual dorsal roots (D–F) in P0.5 (A... |
PMC1084331_pbio-0030159-g002_1802.jpg | What does this image primarily show? | Rescue of Ia Proprioceptive Afferent Projections into the Ventral Spinal Cord in Er81EWS-Pea3 Mutants(A–F) Morphological analysis of central projections at lumbar level L3 of PV+ DRG neurons (A–C) or all DRG sensory afferents after application of fluorescently labeled dextran to individual dorsal roots (D–F) in P0.5 (A... |
PMC1084331_pbio-0030159-g002_1804.jpg | Describe the main subject of this image. | Rescue of Ia Proprioceptive Afferent Projections into the Ventral Spinal Cord in Er81EWS-Pea3 Mutants(A–F) Morphological analysis of central projections at lumbar level L3 of PV+ DRG neurons (A–C) or all DRG sensory afferents after application of fluorescently labeled dextran to individual dorsal roots (D–F) in P0.5 (A... |
PMC1084331_pbio-0030159-g002_1796.jpg | What object or scene is depicted here? | Rescue of Ia Proprioceptive Afferent Projections into the Ventral Spinal Cord in Er81EWS-Pea3 Mutants(A–F) Morphological analysis of central projections at lumbar level L3 of PV+ DRG neurons (A–C) or all DRG sensory afferents after application of fluorescently labeled dextran to individual dorsal roots (D–F) in P0.5 (A... |
PMC1084331_pbio-0030159-g002_1803.jpg | What does this image primarily show? | Rescue of Ia Proprioceptive Afferent Projections into the Ventral Spinal Cord in Er81EWS-Pea3 Mutants(A–F) Morphological analysis of central projections at lumbar level L3 of PV+ DRG neurons (A–C) or all DRG sensory afferents after application of fluorescently labeled dextran to individual dorsal roots (D–F) in P0.5 (A... |
PMC1084331_pbio-0030159-g002_1801.jpg | What object or scene is depicted here? | Rescue of Ia Proprioceptive Afferent Projections into the Ventral Spinal Cord in Er81EWS-Pea3 Mutants(A–F) Morphological analysis of central projections at lumbar level L3 of PV+ DRG neurons (A–C) or all DRG sensory afferents after application of fluorescently labeled dextran to individual dorsal roots (D–F) in P0.5 (A... |
PMC1084331_pbio-0030159-g002_1799.jpg | What can you see in this picture? | Rescue of Ia Proprioceptive Afferent Projections into the Ventral Spinal Cord in Er81EWS-Pea3 Mutants(A–F) Morphological analysis of central projections at lumbar level L3 of PV+ DRG neurons (A–C) or all DRG sensory afferents after application of fluorescently labeled dextran to individual dorsal roots (D–F) in P0.5 (A... |
PMC1084331_pbio-0030159-g002_1798.jpg | What is the principal component of this image? | Rescue of Ia Proprioceptive Afferent Projections into the Ventral Spinal Cord in Er81EWS-Pea3 Mutants(A–F) Morphological analysis of central projections at lumbar level L3 of PV+ DRG neurons (A–C) or all DRG sensory afferents after application of fluorescently labeled dextran to individual dorsal roots (D–F) in P0.5 (A... |
PMC1084335_pbio-0030157-g001_1813.jpg | What is the main focus of this visual representation? | 24-Color 3D FISH Representation and Classification of Chromosomes in a Human G0 Fibroblast Nucleus(A) A deconvoluted mid-plane nuclear section recorded by wide-field microscopy in eight channels: one channel for DAPI (DNA counterstain) and seven channels for the following fluorochromes: diethylaminocoumarin (Deac), Spe... |
PMC1084335_pbio-0030157-g001_1806.jpg | What is the focal point of this photograph? | 24-Color 3D FISH Representation and Classification of Chromosomes in a Human G0 Fibroblast Nucleus(A) A deconvoluted mid-plane nuclear section recorded by wide-field microscopy in eight channels: one channel for DAPI (DNA counterstain) and seven channels for the following fluorochromes: diethylaminocoumarin (Deac), Spe... |
PMC1084335_pbio-0030157-g001_1807.jpg | What is being portrayed in this visual content? | 24-Color 3D FISH Representation and Classification of Chromosomes in a Human G0 Fibroblast Nucleus(A) A deconvoluted mid-plane nuclear section recorded by wide-field microscopy in eight channels: one channel for DAPI (DNA counterstain) and seven channels for the following fluorochromes: diethylaminocoumarin (Deac), Spe... |
PMC1084335_pbio-0030157-g001_1812.jpg | Describe the main subject of this image. | 24-Color 3D FISH Representation and Classification of Chromosomes in a Human G0 Fibroblast Nucleus(A) A deconvoluted mid-plane nuclear section recorded by wide-field microscopy in eight channels: one channel for DAPI (DNA counterstain) and seven channels for the following fluorochromes: diethylaminocoumarin (Deac), Spe... |
PMC1084335_pbio-0030157-g001_1810.jpg | Can you identify the primary element in this image? | 24-Color 3D FISH Representation and Classification of Chromosomes in a Human G0 Fibroblast Nucleus(A) A deconvoluted mid-plane nuclear section recorded by wide-field microscopy in eight channels: one channel for DAPI (DNA counterstain) and seven channels for the following fluorochromes: diethylaminocoumarin (Deac), Spe... |
PMC1084335_pbio-0030157-g001_1808.jpg | What stands out most in this visual? | 24-Color 3D FISH Representation and Classification of Chromosomes in a Human G0 Fibroblast Nucleus(A) A deconvoluted mid-plane nuclear section recorded by wide-field microscopy in eight channels: one channel for DAPI (DNA counterstain) and seven channels for the following fluorochromes: diethylaminocoumarin (Deac), Spe... |
PMC1084356_F1_1816.jpg | What is the dominant medical problem in this image? | Example of a DTI curve analysis. It was manually positioned a region of interest (ROI) at the level of the mitral annulus and three others in the 3 segments of each wall (following the ASE left ventricular segmentation) IVC: peak of velocity recorded at the isivolumic contraction time S: peak of velocity recorded in sy... |
PMC1084356_F1_1815.jpg | What is the core subject represented in this visual? | Example of a DTI curve analysis. It was manually positioned a region of interest (ROI) at the level of the mitral annulus and three others in the 3 segments of each wall (following the ASE left ventricular segmentation) IVC: peak of velocity recorded at the isivolumic contraction time S: peak of velocity recorded in sy... |
PMC1084359_F3_1817.jpg | What key item or scene is captured in this photo? | IDR/A and IDR/B-specific anti TPO aAbs mainly recognize the same regions on hTPO: the binding strength makes the difference. IDR/A- and IDR/B- specific epitopes (left and right panel respectively) are globally composed by the same peptidic regions on hTPO. Region 599–617 (in orange) represents the amino acid sequence p... |
PMC1084363_F5_1819.jpg | What is being portrayed in this visual content? | Histology following hyperoxic injury. Hematoxylin-eosin stained lung sections of (a) IGF-1R+/+, and (b) IGF-1Rneo/- mice following 72 h of hyperoxic exposure, illustrating perivascular and peribronchiolar edema as indicated by asterisks. Magnification: 10× objective. Representative histology of lung sections demonstrat... |
PMC1084363_F5_1821.jpg | What key item or scene is captured in this photo? | Histology following hyperoxic injury. Hematoxylin-eosin stained lung sections of (a) IGF-1R+/+, and (b) IGF-1Rneo/- mice following 72 h of hyperoxic exposure, illustrating perivascular and peribronchiolar edema as indicated by asterisks. Magnification: 10× objective. Representative histology of lung sections demonstrat... |
PMC1084363_F5_1820.jpg | What is shown in this image? | Histology following hyperoxic injury. Hematoxylin-eosin stained lung sections of (a) IGF-1R+/+, and (b) IGF-1Rneo/- mice following 72 h of hyperoxic exposure, illustrating perivascular and peribronchiolar edema as indicated by asterisks. Magnification: 10× objective. Representative histology of lung sections demonstrat... |
PMC1087208_pmed-0020103-g002_1830.jpg | What is the main focus of this visual representation? | Immunohistochemical Detection of Neural Markers and Insulin during Stages 1–4 of Human Neural Progenitor Cell DifferentiationImmunofluorescent images were obtained by confocal microscopy and are representative of at least ten samples for each antibody. We detected insulin in only stage 4 IPCs, consistent with RT-PCR re... |
PMC1087208_pmed-0020103-g002_1827.jpg | What is the focal point of this photograph? | Immunohistochemical Detection of Neural Markers and Insulin during Stages 1–4 of Human Neural Progenitor Cell DifferentiationImmunofluorescent images were obtained by confocal microscopy and are representative of at least ten samples for each antibody. We detected insulin in only stage 4 IPCs, consistent with RT-PCR re... |
PMC1087208_pmed-0020103-g002_1825.jpg | What key item or scene is captured in this photo? | Immunohistochemical Detection of Neural Markers and Insulin during Stages 1–4 of Human Neural Progenitor Cell DifferentiationImmunofluorescent images were obtained by confocal microscopy and are representative of at least ten samples for each antibody. We detected insulin in only stage 4 IPCs, consistent with RT-PCR re... |
PMC1087480_F3_1831.jpg | What object or scene is depicted here? | Intracellular localization of recombinant Δ51CB. LCLC-103H cells with transient Δ51CB-EGFP expression revealed an intensive mitochondrial distribution of the fluorescence signals. Beside a slight cytoplasmic background there was also a signal level in the nucleoplasm, which reached ~40% of the mitochondrial fluorescenc... |
PMC1087480_F4_1841.jpg | What stands out most in this visual? | Intracellular localization of recombinant CB(SC). Transient overexpression in LCLC-103H cells visualized by WFM (A-F) or OPM (G, H). A, B. Cells expressing CB(SC)-EGFP (green) were counterstained with Hoechst33342 (blue) and LysoTracker Red (red). Diffuse, vesicular, and granular EGFP fluorescence signals were found in... |
PMC1087480_F4_1840.jpg | What object or scene is depicted here? | Intracellular localization of recombinant CB(SC). Transient overexpression in LCLC-103H cells visualized by WFM (A-F) or OPM (G, H). A, B. Cells expressing CB(SC)-EGFP (green) were counterstained with Hoechst33342 (blue) and LysoTracker Red (red). Diffuse, vesicular, and granular EGFP fluorescence signals were found in... |
PMC1087480_F4_1843.jpg | What's the most prominent thing you notice in this picture? | Intracellular localization of recombinant CB(SC). Transient overexpression in LCLC-103H cells visualized by WFM (A-F) or OPM (G, H). A, B. Cells expressing CB(SC)-EGFP (green) were counterstained with Hoechst33342 (blue) and LysoTracker Red (red). Diffuse, vesicular, and granular EGFP fluorescence signals were found in... |
PMC1087480_F4_1837.jpg | What is the dominant medical problem in this image? | Intracellular localization of recombinant CB(SC). Transient overexpression in LCLC-103H cells visualized by WFM (A-F) or OPM (G, H). A, B. Cells expressing CB(SC)-EGFP (green) were counterstained with Hoechst33342 (blue) and LysoTracker Red (red). Diffuse, vesicular, and granular EGFP fluorescence signals were found in... |
PMC1087480_F4_1839.jpg | What object or scene is depicted here? | Intracellular localization of recombinant CB(SC). Transient overexpression in LCLC-103H cells visualized by WFM (A-F) or OPM (G, H). A, B. Cells expressing CB(SC)-EGFP (green) were counterstained with Hoechst33342 (blue) and LysoTracker Red (red). Diffuse, vesicular, and granular EGFP fluorescence signals were found in... |
PMC1087480_F4_1838.jpg | What can you see in this picture? | Intracellular localization of recombinant CB(SC). Transient overexpression in LCLC-103H cells visualized by WFM (A-F) or OPM (G, H). A, B. Cells expressing CB(SC)-EGFP (green) were counterstained with Hoechst33342 (blue) and LysoTracker Red (red). Diffuse, vesicular, and granular EGFP fluorescence signals were found in... |
PMC1087480_F5_1835.jpg | Describe the main subject of this image. | Nuclear diffusion and binding of recombinant CB(SC). Fluorescence was extinguished by TPM within distinct nuclear regions and the diffusion and binding characteristics of GFP-tagged constructs were determined. A. The approach is described by means of the GFP-tagged histone-construct H2A-EGFP. In the continuous photoble... |
PMC1087488_F1_1860.jpg | Describe the main subject of this image. | Laminin stimulation elicits lamellopodia and process formation in adult sensory neurons. DRG neurons plated on polylysine were stimulated with laminin in solution for 5 min, 15 min, 30 min, 1 hr, 6 hrs, 24 hrs. After fixation, neurons were stained with rhodamine-phalloidin to detect actin and images obtained using conf... |
PMC1087488_F1_1861.jpg | What stands out most in this visual? | Laminin stimulation elicits lamellopodia and process formation in adult sensory neurons. DRG neurons plated on polylysine were stimulated with laminin in solution for 5 min, 15 min, 30 min, 1 hr, 6 hrs, 24 hrs. After fixation, neurons were stained with rhodamine-phalloidin to detect actin and images obtained using conf... |
PMC1087488_F1_1858.jpg | What is the central feature of this picture? | Laminin stimulation elicits lamellopodia and process formation in adult sensory neurons. DRG neurons plated on polylysine were stimulated with laminin in solution for 5 min, 15 min, 30 min, 1 hr, 6 hrs, 24 hrs. After fixation, neurons were stained with rhodamine-phalloidin to detect actin and images obtained using conf... |
PMC1087488_F1_1856.jpg | What object or scene is depicted here? | Laminin stimulation elicits lamellopodia and process formation in adult sensory neurons. DRG neurons plated on polylysine were stimulated with laminin in solution for 5 min, 15 min, 30 min, 1 hr, 6 hrs, 24 hrs. After fixation, neurons were stained with rhodamine-phalloidin to detect actin and images obtained using conf... |
PMC1087488_F1_1859.jpg | What is being portrayed in this visual content? | Laminin stimulation elicits lamellopodia and process formation in adult sensory neurons. DRG neurons plated on polylysine were stimulated with laminin in solution for 5 min, 15 min, 30 min, 1 hr, 6 hrs, 24 hrs. After fixation, neurons were stained with rhodamine-phalloidin to detect actin and images obtained using conf... |
PMC1087488_F1_1857.jpg | What is the main focus of this visual representation? | Laminin stimulation elicits lamellopodia and process formation in adult sensory neurons. DRG neurons plated on polylysine were stimulated with laminin in solution for 5 min, 15 min, 30 min, 1 hr, 6 hrs, 24 hrs. After fixation, neurons were stained with rhodamine-phalloidin to detect actin and images obtained using conf... |
PMC1087488_F2_1852.jpg | Can you identify the primary element in this image? | Hsp27 co-localizes with actin and tubulin at early stages of neurite growth. Neurons were plated on polylysine and stimulated with laminin for 1–6 hrs. Following fixation, neurons were labelled with rhodamine-phalloidin (red-A, D) or immunostained with antibodies directed against total tubulin (red – G, J) or Hsp27 (gr... |
PMC1087488_F2_1848.jpg | What stands out most in this visual? | Hsp27 co-localizes with actin and tubulin at early stages of neurite growth. Neurons were plated on polylysine and stimulated with laminin for 1–6 hrs. Following fixation, neurons were labelled with rhodamine-phalloidin (red-A, D) or immunostained with antibodies directed against total tubulin (red – G, J) or Hsp27 (gr... |
PMC1087488_F2_1844.jpg | Can you identify the primary element in this image? | Hsp27 co-localizes with actin and tubulin at early stages of neurite growth. Neurons were plated on polylysine and stimulated with laminin for 1–6 hrs. Following fixation, neurons were labelled with rhodamine-phalloidin (red-A, D) or immunostained with antibodies directed against total tubulin (red – G, J) or Hsp27 (gr... |
PMC1087488_F2_1849.jpg | What can you see in this picture? | Hsp27 co-localizes with actin and tubulin at early stages of neurite growth. Neurons were plated on polylysine and stimulated with laminin for 1–6 hrs. Following fixation, neurons were labelled with rhodamine-phalloidin (red-A, D) or immunostained with antibodies directed against total tubulin (red – G, J) or Hsp27 (gr... |
PMC1087488_F2_1845.jpg | What's the most prominent thing you notice in this picture? | Hsp27 co-localizes with actin and tubulin at early stages of neurite growth. Neurons were plated on polylysine and stimulated with laminin for 1–6 hrs. Following fixation, neurons were labelled with rhodamine-phalloidin (red-A, D) or immunostained with antibodies directed against total tubulin (red – G, J) or Hsp27 (gr... |
PMC1087488_F2_1855.jpg | What does this image primarily show? | Hsp27 co-localizes with actin and tubulin at early stages of neurite growth. Neurons were plated on polylysine and stimulated with laminin for 1–6 hrs. Following fixation, neurons were labelled with rhodamine-phalloidin (red-A, D) or immunostained with antibodies directed against total tubulin (red – G, J) or Hsp27 (gr... |
PMC1087488_F2_1850.jpg | What is the principal component of this image? | Hsp27 co-localizes with actin and tubulin at early stages of neurite growth. Neurons were plated on polylysine and stimulated with laminin for 1–6 hrs. Following fixation, neurons were labelled with rhodamine-phalloidin (red-A, D) or immunostained with antibodies directed against total tubulin (red – G, J) or Hsp27 (gr... |
PMC1087488_F2_1853.jpg | Can you identify the primary element in this image? | Hsp27 co-localizes with actin and tubulin at early stages of neurite growth. Neurons were plated on polylysine and stimulated with laminin for 1–6 hrs. Following fixation, neurons were labelled with rhodamine-phalloidin (red-A, D) or immunostained with antibodies directed against total tubulin (red – G, J) or Hsp27 (gr... |
PMC1087488_F2_1846.jpg | What is the principal component of this image? | Hsp27 co-localizes with actin and tubulin at early stages of neurite growth. Neurons were plated on polylysine and stimulated with laminin for 1–6 hrs. Following fixation, neurons were labelled with rhodamine-phalloidin (red-A, D) or immunostained with antibodies directed against total tubulin (red – G, J) or Hsp27 (gr... |
PMC1087488_F2_1847.jpg | What is shown in this image? | Hsp27 co-localizes with actin and tubulin at early stages of neurite growth. Neurons were plated on polylysine and stimulated with laminin for 1–6 hrs. Following fixation, neurons were labelled with rhodamine-phalloidin (red-A, D) or immunostained with antibodies directed against total tubulin (red – G, J) or Hsp27 (gr... |
PMC1087489_F1_1864.jpg | Describe the main subject of this image. | Camera lucida drawings of anterior coronal brain sections. Dots represent BrdU+ cells. No difference in number or spatial and temporal distribution of BrdU+ cells was seen in the contralateral and control hemispheres at corresponding time points (corresponding time points: 10 h = P9, 3d = P12, 5d = P14, 7d = P16, 14d =... |
PMC1087489_F1_1863.jpg | What object or scene is depicted here? | Camera lucida drawings of anterior coronal brain sections. Dots represent BrdU+ cells. No difference in number or spatial and temporal distribution of BrdU+ cells was seen in the contralateral and control hemispheres at corresponding time points (corresponding time points: 10 h = P9, 3d = P12, 5d = P14, 7d = P16, 14d =... |
PMC1087489_F1_1865.jpg | Describe the main subject of this image. | Camera lucida drawings of anterior coronal brain sections. Dots represent BrdU+ cells. No difference in number or spatial and temporal distribution of BrdU+ cells was seen in the contralateral and control hemispheres at corresponding time points (corresponding time points: 10 h = P9, 3d = P12, 5d = P14, 7d = P16, 14d =... |
PMC1087489_F1_1862.jpg | What's the most prominent thing you notice in this picture? | Camera lucida drawings of anterior coronal brain sections. Dots represent BrdU+ cells. No difference in number or spatial and temporal distribution of BrdU+ cells was seen in the contralateral and control hemispheres at corresponding time points (corresponding time points: 10 h = P9, 3d = P12, 5d = P14, 7d = P16, 14d =... |
PMC1087489_F5_1879.jpg | Can you identify the primary element in this image? | Phenotypes of proliferating cells in the SVZ. Optical microscope studies of coronal brain sections after double-labeled immunofluorescence showed that there is a characteristic placement of cell phenotypes along the entire length of the ventricular wall (vw). Photographs show TL+ ventricular ependymal cells (arrow, a) ... |
PMC1087489_F5_1877.jpg | What is the central feature of this picture? | Phenotypes of proliferating cells in the SVZ. Optical microscope studies of coronal brain sections after double-labeled immunofluorescence showed that there is a characteristic placement of cell phenotypes along the entire length of the ventricular wall (vw). Photographs show TL+ ventricular ependymal cells (arrow, a) ... |
PMC1087489_F5_1874.jpg | What is the focal point of this photograph? | Phenotypes of proliferating cells in the SVZ. Optical microscope studies of coronal brain sections after double-labeled immunofluorescence showed that there is a characteristic placement of cell phenotypes along the entire length of the ventricular wall (vw). Photographs show TL+ ventricular ependymal cells (arrow, a) ... |
PMC1087489_F5_1880.jpg | What object or scene is depicted here? | Phenotypes of proliferating cells in the SVZ. Optical microscope studies of coronal brain sections after double-labeled immunofluorescence showed that there is a characteristic placement of cell phenotypes along the entire length of the ventricular wall (vw). Photographs show TL+ ventricular ependymal cells (arrow, a) ... |
PMC1087489_F5_1876.jpg | What is the dominant medical problem in this image? | Phenotypes of proliferating cells in the SVZ. Optical microscope studies of coronal brain sections after double-labeled immunofluorescence showed that there is a characteristic placement of cell phenotypes along the entire length of the ventricular wall (vw). Photographs show TL+ ventricular ependymal cells (arrow, a) ... |
PMC1087489_F5_1882.jpg | What's the most prominent thing you notice in this picture? | Phenotypes of proliferating cells in the SVZ. Optical microscope studies of coronal brain sections after double-labeled immunofluorescence showed that there is a characteristic placement of cell phenotypes along the entire length of the ventricular wall (vw). Photographs show TL+ ventricular ependymal cells (arrow, a) ... |
PMC1087489_F5_1875.jpg | What is shown in this image? | Phenotypes of proliferating cells in the SVZ. Optical microscope studies of coronal brain sections after double-labeled immunofluorescence showed that there is a characteristic placement of cell phenotypes along the entire length of the ventricular wall (vw). Photographs show TL+ ventricular ependymal cells (arrow, a) ... |
PMC1087489_F5_1878.jpg | What key item or scene is captured in this photo? | Phenotypes of proliferating cells in the SVZ. Optical microscope studies of coronal brain sections after double-labeled immunofluorescence showed that there is a characteristic placement of cell phenotypes along the entire length of the ventricular wall (vw). Photographs show TL+ ventricular ependymal cells (arrow, a) ... |
PMC1087489_F5_1881.jpg | What key item or scene is captured in this photo? | Phenotypes of proliferating cells in the SVZ. Optical microscope studies of coronal brain sections after double-labeled immunofluorescence showed that there is a characteristic placement of cell phenotypes along the entire length of the ventricular wall (vw). Photographs show TL+ ventricular ependymal cells (arrow, a) ... |
PMC1087489_F7_1871.jpg | What stands out most in this visual? | Double immunohistochemical staining of BrdU+ cell clusters in the striatum. In lesioned animals, from 3 days post lesion until 7 days post lesion grouped BrdU+ cells were found in the parenchyma a short distance away from the ventricular wall. Double labeling immunofluorescence studies followed by confocal imaging reve... |
PMC1087489_F7_1867.jpg | What can you see in this picture? | Double immunohistochemical staining of BrdU+ cell clusters in the striatum. In lesioned animals, from 3 days post lesion until 7 days post lesion grouped BrdU+ cells were found in the parenchyma a short distance away from the ventricular wall. Double labeling immunofluorescence studies followed by confocal imaging reve... |
PMC1087489_F7_1872.jpg | What is the main focus of this visual representation? | Double immunohistochemical staining of BrdU+ cell clusters in the striatum. In lesioned animals, from 3 days post lesion until 7 days post lesion grouped BrdU+ cells were found in the parenchyma a short distance away from the ventricular wall. Double labeling immunofluorescence studies followed by confocal imaging reve... |
PMC1087489_F7_1873.jpg | What object or scene is depicted here? | Double immunohistochemical staining of BrdU+ cell clusters in the striatum. In lesioned animals, from 3 days post lesion until 7 days post lesion grouped BrdU+ cells were found in the parenchyma a short distance away from the ventricular wall. Double labeling immunofluorescence studies followed by confocal imaging reve... |
PMC1087489_F7_1868.jpg | What is the core subject represented in this visual? | Double immunohistochemical staining of BrdU+ cell clusters in the striatum. In lesioned animals, from 3 days post lesion until 7 days post lesion grouped BrdU+ cells were found in the parenchyma a short distance away from the ventricular wall. Double labeling immunofluorescence studies followed by confocal imaging reve... |
PMC1087489_F7_1870.jpg | What key item or scene is captured in this photo? | Double immunohistochemical staining of BrdU+ cell clusters in the striatum. In lesioned animals, from 3 days post lesion until 7 days post lesion grouped BrdU+ cells were found in the parenchyma a short distance away from the ventricular wall. Double labeling immunofluorescence studies followed by confocal imaging reve... |
PMC1087490_F3_1889.jpg | What object or scene is depicted here? | Differential distribution of Cln8 mRNA in brains of P0, P5, P10 and adult mouse. Dark-field emulsion autoradiographs from frontal sections, shown on the left, were analyzed by in situ hybridization analysis (A-D). Higher magnification in the hippocampal area CA3 is shown on the right. Bright-field views of the cells (a... |
PMC1087490_F3_1884.jpg | What is the central feature of this picture? | Differential distribution of Cln8 mRNA in brains of P0, P5, P10 and adult mouse. Dark-field emulsion autoradiographs from frontal sections, shown on the left, were analyzed by in situ hybridization analysis (A-D). Higher magnification in the hippocampal area CA3 is shown on the right. Bright-field views of the cells (a... |
PMC1087490_F3_1883.jpg | What can you see in this picture? | Differential distribution of Cln8 mRNA in brains of P0, P5, P10 and adult mouse. Dark-field emulsion autoradiographs from frontal sections, shown on the left, were analyzed by in situ hybridization analysis (A-D). Higher magnification in the hippocampal area CA3 is shown on the right. Bright-field views of the cells (a... |
PMC1087490_F3_1888.jpg | What can you see in this picture? | Differential distribution of Cln8 mRNA in brains of P0, P5, P10 and adult mouse. Dark-field emulsion autoradiographs from frontal sections, shown on the left, were analyzed by in situ hybridization analysis (A-D). Higher magnification in the hippocampal area CA3 is shown on the right. Bright-field views of the cells (a... |
PMC1087490_F3_1891.jpg | What is the main focus of this visual representation? | Differential distribution of Cln8 mRNA in brains of P0, P5, P10 and adult mouse. Dark-field emulsion autoradiographs from frontal sections, shown on the left, were analyzed by in situ hybridization analysis (A-D). Higher magnification in the hippocampal area CA3 is shown on the right. Bright-field views of the cells (a... |
PMC1087490_F3_1892.jpg | What key item or scene is captured in this photo? | Differential distribution of Cln8 mRNA in brains of P0, P5, P10 and adult mouse. Dark-field emulsion autoradiographs from frontal sections, shown on the left, were analyzed by in situ hybridization analysis (A-D). Higher magnification in the hippocampal area CA3 is shown on the right. Bright-field views of the cells (a... |
PMC1087490_F3_1886.jpg | Describe the main subject of this image. | Differential distribution of Cln8 mRNA in brains of P0, P5, P10 and adult mouse. Dark-field emulsion autoradiographs from frontal sections, shown on the left, were analyzed by in situ hybridization analysis (A-D). Higher magnification in the hippocampal area CA3 is shown on the right. Bright-field views of the cells (a... |
PMC1087490_F4_1896.jpg | What object or scene is depicted here? | Distribution of Cln8 mRNA in brains of hippocampal kindling induced epileptic mice. Frontal mouse brain sections were analyzed 2 h, 6 h and 24 h after kindling induced epileptic seizures by in situ hybridization. Mice with electrodes implanted but without electrical stimulations were used as controls (0 h). Dark-field ... |
PMC1087490_F4_1894.jpg | What's the most prominent thing you notice in this picture? | Distribution of Cln8 mRNA in brains of hippocampal kindling induced epileptic mice. Frontal mouse brain sections were analyzed 2 h, 6 h and 24 h after kindling induced epileptic seizures by in situ hybridization. Mice with electrodes implanted but without electrical stimulations were used as controls (0 h). Dark-field ... |
PMC1087507_F1_1899.jpg | What key item or scene is captured in this photo? | Vibrio cholerae O1 Biotype ElTor bacteriophages AS1-3. Panels A and B show the vibriophage AS1. They are contractile in nature and possess similar pattern as seen in the tail of another O1 ElTor typing vibriophage D10 (Chakrabarti et al., (1993). Panels A and B are shown at the same magnification. Panel C show the vibr... |
PMC1087507_F1_1902.jpg | What key item or scene is captured in this photo? | Vibrio cholerae O1 Biotype ElTor bacteriophages AS1-3. Panels A and B show the vibriophage AS1. They are contractile in nature and possess similar pattern as seen in the tail of another O1 ElTor typing vibriophage D10 (Chakrabarti et al., (1993). Panels A and B are shown at the same magnification. Panel C show the vibr... |
PMC1087507_F1_1901.jpg | What is shown in this image? | Vibrio cholerae O1 Biotype ElTor bacteriophages AS1-3. Panels A and B show the vibriophage AS1. They are contractile in nature and possess similar pattern as seen in the tail of another O1 ElTor typing vibriophage D10 (Chakrabarti et al., (1993). Panels A and B are shown at the same magnification. Panel C show the vibr... |
PMC1087507_F1_1900.jpg | What is the main focus of this visual representation? | Vibrio cholerae O1 Biotype ElTor bacteriophages AS1-3. Panels A and B show the vibriophage AS1. They are contractile in nature and possess similar pattern as seen in the tail of another O1 ElTor typing vibriophage D10 (Chakrabarti et al., (1993). Panels A and B are shown at the same magnification. Panel C show the vibr... |
PMC1087842_F1_1904.jpg | What object or scene is depicted here? | Biopsy specimen of gastric glandular epithelial mucosa showing the presence of intranuclear cytomegalic inclusion bodies (1A, arrow), together with edema and inflammatory infiltrate. CMV infection was confirmed using immunohistochemistry, with a specific anti-CMV antibody (DAB-peroxydase) (1B). |
PMC1087842_F1_1905.jpg | What is the principal component of this image? | Biopsy specimen of gastric glandular epithelial mucosa showing the presence of intranuclear cytomegalic inclusion bodies (1A, arrow), together with edema and inflammatory infiltrate. CMV infection was confirmed using immunohistochemistry, with a specific anti-CMV antibody (DAB-peroxydase) (1B). |
PMC1087842_F2_1906.jpg | What is the principal component of this image? | Abdominal CT scan showing the presence of large and heterogeneous hypodensities (open arrow), surrounding the pancreas (filled arrow) and mildly enhanced following contrast infusion. The spleen (gray arrow) was patchy, demonstrating ischemic zones. |
PMC1087846_F5_1907.jpg | What key item or scene is captured in this photo? | Replaying an examination of slide 2 using the ReplaySuite. |
PMC1087847_F2_1918.jpg | What is shown in this image? | Annexin A7 immunoreactivity in early mouse embryos. (A) Phase contrast, embryo E5: The egg cylinder consists of an inner cell mass (a) representing the ectoderm and an outer layer of endoderm cells (b). (B) Immunostaining of the paraffin section was performed using purified mAb 203–217 and Cy3-conjugated anti-mouse IgG... |
PMC1087847_F2_1921.jpg | What's the most prominent thing you notice in this picture? | Annexin A7 immunoreactivity in early mouse embryos. (A) Phase contrast, embryo E5: The egg cylinder consists of an inner cell mass (a) representing the ectoderm and an outer layer of endoderm cells (b). (B) Immunostaining of the paraffin section was performed using purified mAb 203–217 and Cy3-conjugated anti-mouse IgG... |
PMC1087847_F2_1919.jpg | Can you identify the primary element in this image? | Annexin A7 immunoreactivity in early mouse embryos. (A) Phase contrast, embryo E5: The egg cylinder consists of an inner cell mass (a) representing the ectoderm and an outer layer of endoderm cells (b). (B) Immunostaining of the paraffin section was performed using purified mAb 203–217 and Cy3-conjugated anti-mouse IgG... |
PMC1087847_F2_1922.jpg | What is the main focus of this visual representation? | Annexin A7 immunoreactivity in early mouse embryos. (A) Phase contrast, embryo E5: The egg cylinder consists of an inner cell mass (a) representing the ectoderm and an outer layer of endoderm cells (b). (B) Immunostaining of the paraffin section was performed using purified mAb 203–217 and Cy3-conjugated anti-mouse IgG... |
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