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PMC2045105_F1_14457.jpg | What can you see in this picture? | Renal biopsy specimen obtained at the time of clinical presentation with advanced renal impairment. There is severe tubular atrophy and interstitial changes consistent with an advanced chronic interstitial nephropathy. A) Low power haematoxylin and eosin stain demonstrating chronic interstitial nephropathy. B) High pow... |
PMC2045105_F1_14458.jpg | Describe the main subject of this image. | Renal biopsy specimen obtained at the time of clinical presentation with advanced renal impairment. There is severe tubular atrophy and interstitial changes consistent with an advanced chronic interstitial nephropathy. A) Low power haematoxylin and eosin stain demonstrating chronic interstitial nephropathy. B) High pow... |
PMC2045105_F1_14455.jpg | Can you identify the primary element in this image? | Renal biopsy specimen obtained at the time of clinical presentation with advanced renal impairment. There is severe tubular atrophy and interstitial changes consistent with an advanced chronic interstitial nephropathy. A) Low power haematoxylin and eosin stain demonstrating chronic interstitial nephropathy. B) High pow... |
PMC2045107_F2_14469.jpg | Can you identify the primary element in this image? | Connective tissue in the lamina propria of theolfactory system in vivo expresses calponin. Sections of olfactory mucosa were immunolabeled with antibodies to connective tissue and glia together with calponin and visualized using confocal microscopy. A, B) Calponin immunoreactivity was associated with markers of connect... |
PMC2045107_F2_14464.jpg | What does this image primarily show? | Connective tissue in the lamina propria of theolfactory system in vivo expresses calponin. Sections of olfactory mucosa were immunolabeled with antibodies to connective tissue and glia together with calponin and visualized using confocal microscopy. A, B) Calponin immunoreactivity was associated with markers of connect... |
PMC2045107_F2_14466.jpg | What is the central feature of this picture? | Connective tissue in the lamina propria of theolfactory system in vivo expresses calponin. Sections of olfactory mucosa were immunolabeled with antibodies to connective tissue and glia together with calponin and visualized using confocal microscopy. A, B) Calponin immunoreactivity was associated with markers of connect... |
PMC2045107_F2_14468.jpg | What is the core subject represented in this visual? | Connective tissue in the lamina propria of theolfactory system in vivo expresses calponin. Sections of olfactory mucosa were immunolabeled with antibodies to connective tissue and glia together with calponin and visualized using confocal microscopy. A, B) Calponin immunoreactivity was associated with markers of connect... |
PMC2045107_F2_14467.jpg | What is the central feature of this picture? | Connective tissue in the lamina propria of theolfactory system in vivo expresses calponin. Sections of olfactory mucosa were immunolabeled with antibodies to connective tissue and glia together with calponin and visualized using confocal microscopy. A, B) Calponin immunoreactivity was associated with markers of connect... |
PMC2045107_F2_14463.jpg | What's the most prominent thing you notice in this picture? | Connective tissue in the lamina propria of theolfactory system in vivo expresses calponin. Sections of olfactory mucosa were immunolabeled with antibodies to connective tissue and glia together with calponin and visualized using confocal microscopy. A, B) Calponin immunoreactivity was associated with markers of connect... |
PMC2045107_F3_14461.jpg | What object or scene is depicted here? | Calponin is not expressed in embryonic tissue. The olfactory mucosa was immunolabeled with antibodies to identify A) ORNs (TUJ1-red, Fn-green, DAPI-blue), B) connective tissue (Fn-red, calponin-green, DAPI-blue), C) OECs (p75NTR-red, calponin-green, DAPI-blue) and D) control tissue omitting the primary antibody. Images... |
PMC2045107_F3_14460.jpg | What can you see in this picture? | Calponin is not expressed in embryonic tissue. The olfactory mucosa was immunolabeled with antibodies to identify A) ORNs (TUJ1-red, Fn-green, DAPI-blue), B) connective tissue (Fn-red, calponin-green, DAPI-blue), C) OECs (p75NTR-red, calponin-green, DAPI-blue) and D) control tissue omitting the primary antibody. Images... |
PMC2045107_F3_14459.jpg | What is being portrayed in this visual content? | Calponin is not expressed in embryonic tissue. The olfactory mucosa was immunolabeled with antibodies to identify A) ORNs (TUJ1-red, Fn-green, DAPI-blue), B) connective tissue (Fn-red, calponin-green, DAPI-blue), C) OECs (p75NTR-red, calponin-green, DAPI-blue) and D) control tissue omitting the primary antibody. Images... |
PMC2045107_F4_14477.jpg | What is shown in this image? | Purified OECs and Schwann cells in vitro do not express calponin. OECs and Schwann cells were immunolabeled with calponin in the presence and absence of proteinase K and no differences were found. A, B) OECs and Schwann cells were immuolabelled with p75NTR (red) and calponin (green). Greater than 99% of the cells immun... |
PMC2045107_F4_14473.jpg | Can you identify the primary element in this image? | Purified OECs and Schwann cells in vitro do not express calponin. OECs and Schwann cells were immunolabeled with calponin in the presence and absence of proteinase K and no differences were found. A, B) OECs and Schwann cells were immuolabelled with p75NTR (red) and calponin (green). Greater than 99% of the cells immun... |
PMC2045107_F4_14479.jpg | What is the principal component of this image? | Purified OECs and Schwann cells in vitro do not express calponin. OECs and Schwann cells were immunolabeled with calponin in the presence and absence of proteinase K and no differences were found. A, B) OECs and Schwann cells were immuolabelled with p75NTR (red) and calponin (green). Greater than 99% of the cells immun... |
PMC2045107_F4_14480.jpg | What is the dominant medical problem in this image? | Purified OECs and Schwann cells in vitro do not express calponin. OECs and Schwann cells were immunolabeled with calponin in the presence and absence of proteinase K and no differences were found. A, B) OECs and Schwann cells were immuolabelled with p75NTR (red) and calponin (green). Greater than 99% of the cells immun... |
PMC2045107_F4_14476.jpg | What is the core subject represented in this visual? | Purified OECs and Schwann cells in vitro do not express calponin. OECs and Schwann cells were immunolabeled with calponin in the presence and absence of proteinase K and no differences were found. A, B) OECs and Schwann cells were immuolabelled with p75NTR (red) and calponin (green). Greater than 99% of the cells immun... |
PMC2045107_F4_14475.jpg | What key item or scene is captured in this photo? | Purified OECs and Schwann cells in vitro do not express calponin. OECs and Schwann cells were immunolabeled with calponin in the presence and absence of proteinase K and no differences were found. A, B) OECs and Schwann cells were immuolabelled with p75NTR (red) and calponin (green). Greater than 99% of the cells immun... |
PMC2045107_F4_14481.jpg | What does this image primarily show? | Purified OECs and Schwann cells in vitro do not express calponin. OECs and Schwann cells were immunolabeled with calponin in the presence and absence of proteinase K and no differences were found. A, B) OECs and Schwann cells were immuolabelled with p75NTR (red) and calponin (green). Greater than 99% of the cells immun... |
PMC2045107_F4_14472.jpg | What is the principal component of this image? | Purified OECs and Schwann cells in vitro do not express calponin. OECs and Schwann cells were immunolabeled with calponin in the presence and absence of proteinase K and no differences were found. A, B) OECs and Schwann cells were immuolabelled with p75NTR (red) and calponin (green). Greater than 99% of the cells immun... |
PMC2045107_F4_14474.jpg | What is shown in this image? | Purified OECs and Schwann cells in vitro do not express calponin. OECs and Schwann cells were immunolabeled with calponin in the presence and absence of proteinase K and no differences were found. A, B) OECs and Schwann cells were immuolabelled with p75NTR (red) and calponin (green). Greater than 99% of the cells immun... |
PMC2045107_F4_14471.jpg | What is the central feature of this picture? | Purified OECs and Schwann cells in vitro do not express calponin. OECs and Schwann cells were immunolabeled with calponin in the presence and absence of proteinase K and no differences were found. A, B) OECs and Schwann cells were immuolabelled with p75NTR (red) and calponin (green). Greater than 99% of the cells immun... |
PMC2045107_F6_14486.jpg | What is being portrayed in this visual content? | Confrontation assays illustrate astrocytes express calponin. Confrontation assays were set up between OECs/astrocytes (A, B) and Schwann cells/astrocytes (C, D). A) OECs mingled with astrocytes while B) Schwann cells formed a boundary with astrocytes. Astrocytes expressed GFAP (red) and OECs or Schwann cells expressed ... |
PMC2045107_F6_14483.jpg | What is the focal point of this photograph? | Confrontation assays illustrate astrocytes express calponin. Confrontation assays were set up between OECs/astrocytes (A, B) and Schwann cells/astrocytes (C, D). A) OECs mingled with astrocytes while B) Schwann cells formed a boundary with astrocytes. Astrocytes expressed GFAP (red) and OECs or Schwann cells expressed ... |
PMC2045107_F6_14485.jpg | What is the central feature of this picture? | Confrontation assays illustrate astrocytes express calponin. Confrontation assays were set up between OECs/astrocytes (A, B) and Schwann cells/astrocytes (C, D). A) OECs mingled with astrocytes while B) Schwann cells formed a boundary with astrocytes. Astrocytes expressed GFAP (red) and OECs or Schwann cells expressed ... |
PMC2045107_F6_14484.jpg | What is the main focus of this visual representation? | Confrontation assays illustrate astrocytes express calponin. Confrontation assays were set up between OECs/astrocytes (A, B) and Schwann cells/astrocytes (C, D). A) OECs mingled with astrocytes while B) Schwann cells formed a boundary with astrocytes. Astrocytes expressed GFAP (red) and OECs or Schwann cells expressed ... |
PMC2045107_F6_14487.jpg | What is being portrayed in this visual content? | Confrontation assays illustrate astrocytes express calponin. Confrontation assays were set up between OECs/astrocytes (A, B) and Schwann cells/astrocytes (C, D). A) OECs mingled with astrocytes while B) Schwann cells formed a boundary with astrocytes. Astrocytes expressed GFAP (red) and OECs or Schwann cells expressed ... |
PMC2045107_F6_14488.jpg | What can you see in this picture? | Confrontation assays illustrate astrocytes express calponin. Confrontation assays were set up between OECs/astrocytes (A, B) and Schwann cells/astrocytes (C, D). A) OECs mingled with astrocytes while B) Schwann cells formed a boundary with astrocytes. Astrocytes expressed GFAP (red) and OECs or Schwann cells expressed ... |
PMC2045117_F4_14490.jpg | Can you identify the primary element in this image? | The hot-spots are detected by HOTTOR algorithm in fMRI data (from [13]). Three slices are shown at different orientations and identifying significant altered activity in (A) the medial thalamus, (B) the right amygdala, (C) the head of the caudate nucleus and (D) the right retrosplenial cortex. |
PMC2045117_F4_14491.jpg | What key item or scene is captured in this photo? | The hot-spots are detected by HOTTOR algorithm in fMRI data (from [13]). Three slices are shown at different orientations and identifying significant altered activity in (A) the medial thalamus, (B) the right amygdala, (C) the head of the caudate nucleus and (D) the right retrosplenial cortex. |
PMC2045117_F4_14492.jpg | What is the focal point of this photograph? | The hot-spots are detected by HOTTOR algorithm in fMRI data (from [13]). Three slices are shown at different orientations and identifying significant altered activity in (A) the medial thalamus, (B) the right amygdala, (C) the head of the caudate nucleus and (D) the right retrosplenial cortex. |
PMC2045632_fig2_14495.jpg | What is the focal point of this photograph? | UNC-34 localizes to the leading edge of cell protrusions and to apical junctions.(A and A′) Confocal projections of dorsolateral (A) and ventrolateral (A′) surfaces (anterior is to the left) of the same embryo stained at mid-enclosure with anti-UNC-34 show broad expression throughout the embryo with enrichment at apica... |
PMC2045632_fig2_14493.jpg | What is being portrayed in this visual content? | UNC-34 localizes to the leading edge of cell protrusions and to apical junctions.(A and A′) Confocal projections of dorsolateral (A) and ventrolateral (A′) surfaces (anterior is to the left) of the same embryo stained at mid-enclosure with anti-UNC-34 show broad expression throughout the embryo with enrichment at apica... |
PMC2045632_fig2_14499.jpg | What is the main focus of this visual representation? | UNC-34 localizes to the leading edge of cell protrusions and to apical junctions.(A and A′) Confocal projections of dorsolateral (A) and ventrolateral (A′) surfaces (anterior is to the left) of the same embryo stained at mid-enclosure with anti-UNC-34 show broad expression throughout the embryo with enrichment at apica... |
PMC2045632_fig2_14498.jpg | What can you see in this picture? | UNC-34 localizes to the leading edge of cell protrusions and to apical junctions.(A and A′) Confocal projections of dorsolateral (A) and ventrolateral (A′) surfaces (anterior is to the left) of the same embryo stained at mid-enclosure with anti-UNC-34 show broad expression throughout the embryo with enrichment at apica... |
PMC2045632_fig2_14501.jpg | What is being portrayed in this visual content? | UNC-34 localizes to the leading edge of cell protrusions and to apical junctions.(A and A′) Confocal projections of dorsolateral (A) and ventrolateral (A′) surfaces (anterior is to the left) of the same embryo stained at mid-enclosure with anti-UNC-34 show broad expression throughout the embryo with enrichment at apica... |
PMC2045632_fig2_14497.jpg | What is the core subject represented in this visual? | UNC-34 localizes to the leading edge of cell protrusions and to apical junctions.(A and A′) Confocal projections of dorsolateral (A) and ventrolateral (A′) surfaces (anterior is to the left) of the same embryo stained at mid-enclosure with anti-UNC-34 show broad expression throughout the embryo with enrichment at apica... |
PMC2045632_fig2_14503.jpg | What is the focal point of this photograph? | UNC-34 localizes to the leading edge of cell protrusions and to apical junctions.(A and A′) Confocal projections of dorsolateral (A) and ventrolateral (A′) surfaces (anterior is to the left) of the same embryo stained at mid-enclosure with anti-UNC-34 show broad expression throughout the embryo with enrichment at apica... |
PMC2045632_fig2_14500.jpg | What is the principal component of this image? | UNC-34 localizes to the leading edge of cell protrusions and to apical junctions.(A and A′) Confocal projections of dorsolateral (A) and ventrolateral (A′) surfaces (anterior is to the left) of the same embryo stained at mid-enclosure with anti-UNC-34 show broad expression throughout the embryo with enrichment at apica... |
PMC2045632_fig3_14516.jpg | What stands out most in this visual? | Loss of unc-34 Function Enhances the Penetrance and Severity of hmp-1(fe4) Morphogenetic Defects(A–C) Time-lapse images showing the morphogenesis of representative embryos for each genotype: hmp-1(fe4) (A), unc-34(gm104) (B), and unc-34(gm104) hmp-1(fe4) double mutant (C). Anterior is to the left in all panels. The lea... |
PMC2045632_fig3_14524.jpg | What is the main focus of this visual representation? | Loss of unc-34 Function Enhances the Penetrance and Severity of hmp-1(fe4) Morphogenetic Defects(A–C) Time-lapse images showing the morphogenesis of representative embryos for each genotype: hmp-1(fe4) (A), unc-34(gm104) (B), and unc-34(gm104) hmp-1(fe4) double mutant (C). Anterior is to the left in all panels. The lea... |
PMC2045632_fig3_14522.jpg | What is the main focus of this visual representation? | Loss of unc-34 Function Enhances the Penetrance and Severity of hmp-1(fe4) Morphogenetic Defects(A–C) Time-lapse images showing the morphogenesis of representative embryos for each genotype: hmp-1(fe4) (A), unc-34(gm104) (B), and unc-34(gm104) hmp-1(fe4) double mutant (C). Anterior is to the left in all panels. The lea... |
PMC2045632_fig3_14513.jpg | Describe the main subject of this image. | Loss of unc-34 Function Enhances the Penetrance and Severity of hmp-1(fe4) Morphogenetic Defects(A–C) Time-lapse images showing the morphogenesis of representative embryos for each genotype: hmp-1(fe4) (A), unc-34(gm104) (B), and unc-34(gm104) hmp-1(fe4) double mutant (C). Anterior is to the left in all panels. The lea... |
PMC2045632_fig3_14518.jpg | What stands out most in this visual? | Loss of unc-34 Function Enhances the Penetrance and Severity of hmp-1(fe4) Morphogenetic Defects(A–C) Time-lapse images showing the morphogenesis of representative embryos for each genotype: hmp-1(fe4) (A), unc-34(gm104) (B), and unc-34(gm104) hmp-1(fe4) double mutant (C). Anterior is to the left in all panels. The lea... |
PMC2045632_fig3_14520.jpg | Can you identify the primary element in this image? | Loss of unc-34 Function Enhances the Penetrance and Severity of hmp-1(fe4) Morphogenetic Defects(A–C) Time-lapse images showing the morphogenesis of representative embryos for each genotype: hmp-1(fe4) (A), unc-34(gm104) (B), and unc-34(gm104) hmp-1(fe4) double mutant (C). Anterior is to the left in all panels. The lea... |
PMC2045632_fig3_14525.jpg | What stands out most in this visual? | Loss of unc-34 Function Enhances the Penetrance and Severity of hmp-1(fe4) Morphogenetic Defects(A–C) Time-lapse images showing the morphogenesis of representative embryos for each genotype: hmp-1(fe4) (A), unc-34(gm104) (B), and unc-34(gm104) hmp-1(fe4) double mutant (C). Anterior is to the left in all panels. The lea... |
PMC2045632_fig3_14517.jpg | What key item or scene is captured in this photo? | Loss of unc-34 Function Enhances the Penetrance and Severity of hmp-1(fe4) Morphogenetic Defects(A–C) Time-lapse images showing the morphogenesis of representative embryos for each genotype: hmp-1(fe4) (A), unc-34(gm104) (B), and unc-34(gm104) hmp-1(fe4) double mutant (C). Anterior is to the left in all panels. The lea... |
PMC2045632_fig3_14521.jpg | What can you see in this picture? | Loss of unc-34 Function Enhances the Penetrance and Severity of hmp-1(fe4) Morphogenetic Defects(A–C) Time-lapse images showing the morphogenesis of representative embryos for each genotype: hmp-1(fe4) (A), unc-34(gm104) (B), and unc-34(gm104) hmp-1(fe4) double mutant (C). Anterior is to the left in all panels. The lea... |
PMC2045632_fig3_14526.jpg | What is being portrayed in this visual content? | Loss of unc-34 Function Enhances the Penetrance and Severity of hmp-1(fe4) Morphogenetic Defects(A–C) Time-lapse images showing the morphogenesis of representative embryos for each genotype: hmp-1(fe4) (A), unc-34(gm104) (B), and unc-34(gm104) hmp-1(fe4) double mutant (C). Anterior is to the left in all panels. The lea... |
PMC2045632_fig3_14519.jpg | What key item or scene is captured in this photo? | Loss of unc-34 Function Enhances the Penetrance and Severity of hmp-1(fe4) Morphogenetic Defects(A–C) Time-lapse images showing the morphogenesis of representative embryos for each genotype: hmp-1(fe4) (A), unc-34(gm104) (B), and unc-34(gm104) hmp-1(fe4) double mutant (C). Anterior is to the left in all panels. The lea... |
PMC2045633_fig1_14506.jpg | What is being portrayed in this visual content? | DSpd-2 Localizes to the Centrioles throughout the Cell Cycle and to the PCM in Mitosis(A) WT mitotic third-instar larval neuroblast stained for DSpd-2 (green), γ-tubulin (red), and DNA (blue). DSpd-2 localizes to a broad spot at the mitotic centrosome and largely colocalizes with the PCM marker γ-tubulin.(B) The behavi... |
PMC2045633_fig1_14512.jpg | What's the most prominent thing you notice in this picture? | DSpd-2 Localizes to the Centrioles throughout the Cell Cycle and to the PCM in Mitosis(A) WT mitotic third-instar larval neuroblast stained for DSpd-2 (green), γ-tubulin (red), and DNA (blue). DSpd-2 localizes to a broad spot at the mitotic centrosome and largely colocalizes with the PCM marker γ-tubulin.(B) The behavi... |
PMC2045633_fig1_14511.jpg | What is the core subject represented in this visual? | DSpd-2 Localizes to the Centrioles throughout the Cell Cycle and to the PCM in Mitosis(A) WT mitotic third-instar larval neuroblast stained for DSpd-2 (green), γ-tubulin (red), and DNA (blue). DSpd-2 localizes to a broad spot at the mitotic centrosome and largely colocalizes with the PCM marker γ-tubulin.(B) The behavi... |
PMC2045633_fig1_14507.jpg | What is shown in this image? | DSpd-2 Localizes to the Centrioles throughout the Cell Cycle and to the PCM in Mitosis(A) WT mitotic third-instar larval neuroblast stained for DSpd-2 (green), γ-tubulin (red), and DNA (blue). DSpd-2 localizes to a broad spot at the mitotic centrosome and largely colocalizes with the PCM marker γ-tubulin.(B) The behavi... |
PMC2045633_fig1_14508.jpg | What is the main focus of this visual representation? | DSpd-2 Localizes to the Centrioles throughout the Cell Cycle and to the PCM in Mitosis(A) WT mitotic third-instar larval neuroblast stained for DSpd-2 (green), γ-tubulin (red), and DNA (blue). DSpd-2 localizes to a broad spot at the mitotic centrosome and largely colocalizes with the PCM marker γ-tubulin.(B) The behavi... |
PMC2045633_fig1_14509.jpg | Can you identify the primary element in this image? | DSpd-2 Localizes to the Centrioles throughout the Cell Cycle and to the PCM in Mitosis(A) WT mitotic third-instar larval neuroblast stained for DSpd-2 (green), γ-tubulin (red), and DNA (blue). DSpd-2 localizes to a broad spot at the mitotic centrosome and largely colocalizes with the PCM marker γ-tubulin.(B) The behavi... |
PMC2045633_fig4_14537.jpg | What can you see in this picture? | DSpd-2 Is Essential for PCM Recruitment and MT Nucleation from the Sperm CentrioleWT or DSpd-2 embryos expressing Asl-GFP (centriole marker) were stained to reveal the distribution of GFP, MTs, DNA, and Cnn.(A) The first mitotic spindle in a WT embryo. Shown are MTs (red), centrioles (green), and DNA (blue). A single c... |
PMC2045633_fig4_14530.jpg | What is the focal point of this photograph? | DSpd-2 Is Essential for PCM Recruitment and MT Nucleation from the Sperm CentrioleWT or DSpd-2 embryos expressing Asl-GFP (centriole marker) were stained to reveal the distribution of GFP, MTs, DNA, and Cnn.(A) The first mitotic spindle in a WT embryo. Shown are MTs (red), centrioles (green), and DNA (blue). A single c... |
PMC2045633_fig4_14533.jpg | What is the core subject represented in this visual? | DSpd-2 Is Essential for PCM Recruitment and MT Nucleation from the Sperm CentrioleWT or DSpd-2 embryos expressing Asl-GFP (centriole marker) were stained to reveal the distribution of GFP, MTs, DNA, and Cnn.(A) The first mitotic spindle in a WT embryo. Shown are MTs (red), centrioles (green), and DNA (blue). A single c... |
PMC2045633_fig4_14539.jpg | What is being portrayed in this visual content? | DSpd-2 Is Essential for PCM Recruitment and MT Nucleation from the Sperm CentrioleWT or DSpd-2 embryos expressing Asl-GFP (centriole marker) were stained to reveal the distribution of GFP, MTs, DNA, and Cnn.(A) The first mitotic spindle in a WT embryo. Shown are MTs (red), centrioles (green), and DNA (blue). A single c... |
PMC2045633_fig4_14532.jpg | What can you see in this picture? | DSpd-2 Is Essential for PCM Recruitment and MT Nucleation from the Sperm CentrioleWT or DSpd-2 embryos expressing Asl-GFP (centriole marker) were stained to reveal the distribution of GFP, MTs, DNA, and Cnn.(A) The first mitotic spindle in a WT embryo. Shown are MTs (red), centrioles (green), and DNA (blue). A single c... |
PMC2045633_fig4_14540.jpg | What is shown in this image? | DSpd-2 Is Essential for PCM Recruitment and MT Nucleation from the Sperm CentrioleWT or DSpd-2 embryos expressing Asl-GFP (centriole marker) were stained to reveal the distribution of GFP, MTs, DNA, and Cnn.(A) The first mitotic spindle in a WT embryo. Shown are MTs (red), centrioles (green), and DNA (blue). A single c... |
PMC2045633_fig4_14541.jpg | What object or scene is depicted here? | DSpd-2 Is Essential for PCM Recruitment and MT Nucleation from the Sperm CentrioleWT or DSpd-2 embryos expressing Asl-GFP (centriole marker) were stained to reveal the distribution of GFP, MTs, DNA, and Cnn.(A) The first mitotic spindle in a WT embryo. Shown are MTs (red), centrioles (green), and DNA (blue). A single c... |
PMC2045633_fig4_14538.jpg | Describe the main subject of this image. | DSpd-2 Is Essential for PCM Recruitment and MT Nucleation from the Sperm CentrioleWT or DSpd-2 embryos expressing Asl-GFP (centriole marker) were stained to reveal the distribution of GFP, MTs, DNA, and Cnn.(A) The first mitotic spindle in a WT embryo. Shown are MTs (red), centrioles (green), and DNA (blue). A single c... |
PMC2045633_fig4_14534.jpg | What key item or scene is captured in this photo? | DSpd-2 Is Essential for PCM Recruitment and MT Nucleation from the Sperm CentrioleWT or DSpd-2 embryos expressing Asl-GFP (centriole marker) were stained to reveal the distribution of GFP, MTs, DNA, and Cnn.(A) The first mitotic spindle in a WT embryo. Shown are MTs (red), centrioles (green), and DNA (blue). A single c... |
PMC2045633_fig4_14535.jpg | What is the core subject represented in this visual? | DSpd-2 Is Essential for PCM Recruitment and MT Nucleation from the Sperm CentrioleWT or DSpd-2 embryos expressing Asl-GFP (centriole marker) were stained to reveal the distribution of GFP, MTs, DNA, and Cnn.(A) The first mitotic spindle in a WT embryo. Shown are MTs (red), centrioles (green), and DNA (blue). A single c... |
PMC2045666_F2_14545.jpg | What object or scene is depicted here? | Electron microscopy observations of MYXV BT infected cells. A. Numerous virions are still adsorbed on the cell surface 8 h p.i.. B. Large cytoplasmic area without organite containing dense particles (5 h p.i.). C. Atypical Immature Virion (IV) (12 h p.i.). D. Intracellular Enveloped Virion (IEV) (12 h p.i.). Microscope... |
PMC2045666_F2_14543.jpg | What does this image primarily show? | Electron microscopy observations of MYXV BT infected cells. A. Numerous virions are still adsorbed on the cell surface 8 h p.i.. B. Large cytoplasmic area without organite containing dense particles (5 h p.i.). C. Atypical Immature Virion (IV) (12 h p.i.). D. Intracellular Enveloped Virion (IEV) (12 h p.i.). Microscope... |
PMC2048497_F3_14547.jpg | What is being portrayed in this visual content? | Central pair defects originate at the basal plate. (A-C) Serial thin section electron micrographs through the basal plate region of non-induced (A) and TbHydin RNAi-induced (B and C) cells. In non-induced cells, the two central pair tubules are nucleated simultaneously (A, arrows), however only a single central pair tu... |
PMC2048497_F3_14554.jpg | What is the dominant medical problem in this image? | Central pair defects originate at the basal plate. (A-C) Serial thin section electron micrographs through the basal plate region of non-induced (A) and TbHydin RNAi-induced (B and C) cells. In non-induced cells, the two central pair tubules are nucleated simultaneously (A, arrows), however only a single central pair tu... |
PMC2048497_F3_14549.jpg | What is the dominant medical problem in this image? | Central pair defects originate at the basal plate. (A-C) Serial thin section electron micrographs through the basal plate region of non-induced (A) and TbHydin RNAi-induced (B and C) cells. In non-induced cells, the two central pair tubules are nucleated simultaneously (A, arrows), however only a single central pair tu... |
PMC2048497_F3_14556.jpg | What stands out most in this visual? | Central pair defects originate at the basal plate. (A-C) Serial thin section electron micrographs through the basal plate region of non-induced (A) and TbHydin RNAi-induced (B and C) cells. In non-induced cells, the two central pair tubules are nucleated simultaneously (A, arrows), however only a single central pair tu... |
PMC2048497_F3_14551.jpg | What is shown in this image? | Central pair defects originate at the basal plate. (A-C) Serial thin section electron micrographs through the basal plate region of non-induced (A) and TbHydin RNAi-induced (B and C) cells. In non-induced cells, the two central pair tubules are nucleated simultaneously (A, arrows), however only a single central pair tu... |
PMC2048497_F3_14555.jpg | What is the core subject represented in this visual? | Central pair defects originate at the basal plate. (A-C) Serial thin section electron micrographs through the basal plate region of non-induced (A) and TbHydin RNAi-induced (B and C) cells. In non-induced cells, the two central pair tubules are nucleated simultaneously (A, arrows), however only a single central pair tu... |
PMC2048497_F3_14553.jpg | What stands out most in this visual? | Central pair defects originate at the basal plate. (A-C) Serial thin section electron micrographs through the basal plate region of non-induced (A) and TbHydin RNAi-induced (B and C) cells. In non-induced cells, the two central pair tubules are nucleated simultaneously (A, arrows), however only a single central pair tu... |
PMC2048497_F3_14552.jpg | Describe the main subject of this image. | Central pair defects originate at the basal plate. (A-C) Serial thin section electron micrographs through the basal plate region of non-induced (A) and TbHydin RNAi-induced (B and C) cells. In non-induced cells, the two central pair tubules are nucleated simultaneously (A, arrows), however only a single central pair tu... |
PMC2048497_F3_14550.jpg | What is the principal component of this image? | Central pair defects originate at the basal plate. (A-C) Serial thin section electron micrographs through the basal plate region of non-induced (A) and TbHydin RNAi-induced (B and C) cells. In non-induced cells, the two central pair tubules are nucleated simultaneously (A, arrows), however only a single central pair tu... |
PMC2048497_F3_14557.jpg | What is the focal point of this photograph? | Central pair defects originate at the basal plate. (A-C) Serial thin section electron micrographs through the basal plate region of non-induced (A) and TbHydin RNAi-induced (B and C) cells. In non-induced cells, the two central pair tubules are nucleated simultaneously (A, arrows), however only a single central pair tu... |
PMC2048497_F3_14548.jpg | What does this image primarily show? | Central pair defects originate at the basal plate. (A-C) Serial thin section electron micrographs through the basal plate region of non-induced (A) and TbHydin RNAi-induced (B and C) cells. In non-induced cells, the two central pair tubules are nucleated simultaneously (A, arrows), however only a single central pair tu... |
PMC2048497_F3_14546.jpg | Can you identify the primary element in this image? | Central pair defects originate at the basal plate. (A-C) Serial thin section electron micrographs through the basal plate region of non-induced (A) and TbHydin RNAi-induced (B and C) cells. In non-induced cells, the two central pair tubules are nucleated simultaneously (A, arrows), however only a single central pair tu... |
PMC2048498_F2_14563.jpg | What is the core subject represented in this visual? | Examples of CNS Functional Measures. A. Schematic of cortical areas involved with pain processing. The highlighted areas summarize areas found active in previous functional imaging studies. Color-coding reflects the hypothesized role of each area in processing the different psychological dimensions of pain. Numbers in ... |
PMC2048498_F2_14560.jpg | Can you identify the primary element in this image? | Examples of CNS Functional Measures. A. Schematic of cortical areas involved with pain processing. The highlighted areas summarize areas found active in previous functional imaging studies. Color-coding reflects the hypothesized role of each area in processing the different psychological dimensions of pain. Numbers in ... |
PMC2048498_F2_14559.jpg | What is the main focus of this visual representation? | Examples of CNS Functional Measures. A. Schematic of cortical areas involved with pain processing. The highlighted areas summarize areas found active in previous functional imaging studies. Color-coding reflects the hypothesized role of each area in processing the different psychological dimensions of pain. Numbers in ... |
PMC2049047_fig04_14568.jpg | Can you identify the primary element in this image? | Incorporation of BrdU into the DNA of aging nematodes. N2 nematodes at 9 days of age (a,b,c) or 11 days of age (d,e,f) were exposed for 24 h to BrdU. BrdU was detected immunohistochemically using a monoclonal antibody to BrdU, and a fluorescent secondary antibody. In younger worms, incorporation of BrdU is apparent in ... |
PMC2049047_fig04_14564.jpg | What is the central feature of this picture? | Incorporation of BrdU into the DNA of aging nematodes. N2 nematodes at 9 days of age (a,b,c) or 11 days of age (d,e,f) were exposed for 24 h to BrdU. BrdU was detected immunohistochemically using a monoclonal antibody to BrdU, and a fluorescent secondary antibody. In younger worms, incorporation of BrdU is apparent in ... |
PMC2049047_fig04_14570.jpg | Describe the main subject of this image. | Incorporation of BrdU into the DNA of aging nematodes. N2 nematodes at 9 days of age (a,b,c) or 11 days of age (d,e,f) were exposed for 24 h to BrdU. BrdU was detected immunohistochemically using a monoclonal antibody to BrdU, and a fluorescent secondary antibody. In younger worms, incorporation of BrdU is apparent in ... |
PMC2062476_pbio-0050293-g006_14574.jpg | What can you see in this picture? | Spermatogenesis of Double-Mutant dox; nmy Is Normal(A–C) TEM images of sperm maturation.(A) Early post elongation stage of a spermatid head (upper) and tail (lower). Normal nuclear condensation can be seen apposed to rows of microtubules (white arrowheads), while nucleoplasm is eliminated (v).(B) Late post elongation s... |
PMC2062476_pbio-0050293-g006_14572.jpg | What is being portrayed in this visual content? | Spermatogenesis of Double-Mutant dox; nmy Is Normal(A–C) TEM images of sperm maturation.(A) Early post elongation stage of a spermatid head (upper) and tail (lower). Normal nuclear condensation can be seen apposed to rows of microtubules (white arrowheads), while nucleoplasm is eliminated (v).(B) Late post elongation s... |
PMC2062476_pbio-0050293-g006_14571.jpg | What is the core subject represented in this visual? | Spermatogenesis of Double-Mutant dox; nmy Is Normal(A–C) TEM images of sperm maturation.(A) Early post elongation stage of a spermatid head (upper) and tail (lower). Normal nuclear condensation can be seen apposed to rows of microtubules (white arrowheads), while nucleoplasm is eliminated (v).(B) Late post elongation s... |
PMC2062476_pbio-0050293-g006_14573.jpg | What is the focal point of this photograph? | Spermatogenesis of Double-Mutant dox; nmy Is Normal(A–C) TEM images of sperm maturation.(A) Early post elongation stage of a spermatid head (upper) and tail (lower). Normal nuclear condensation can be seen apposed to rows of microtubules (white arrowheads), while nucleoplasm is eliminated (v).(B) Late post elongation s... |
PMC2062534_fig01_14576.jpg | What is the focal point of this photograph? | Migration of SCVs to the MTOC/Golgi region of HeLa cells. A. Representative images of HeLa cells infected with wt S. Typhimurium for 2 h, in the presence or absence of nocodazole or BFA. Cells were fixed in ice-cold methanol and coimmunolabelled for giantin (blue in merged images), γ-tubulin (red in merged images) and ... |
PMC2062534_fig01_14577.jpg | What object or scene is depicted here? | Migration of SCVs to the MTOC/Golgi region of HeLa cells. A. Representative images of HeLa cells infected with wt S. Typhimurium for 2 h, in the presence or absence of nocodazole or BFA. Cells were fixed in ice-cold methanol and coimmunolabelled for giantin (blue in merged images), γ-tubulin (red in merged images) and ... |
PMC2062534_fig01_14579.jpg | Can you identify the primary element in this image? | Migration of SCVs to the MTOC/Golgi region of HeLa cells. A. Representative images of HeLa cells infected with wt S. Typhimurium for 2 h, in the presence or absence of nocodazole or BFA. Cells were fixed in ice-cold methanol and coimmunolabelled for giantin (blue in merged images), γ-tubulin (red in merged images) and ... |
PMC2062534_fig04_14583.jpg | What can you see in this picture? | Effect of BFA on SCV association with the MTOC. A. HeLa cells were infected with wt S. Typhimurium and then incubated in the presence or absence of BFA. Cells were then fixed at 8 h post inoculation and coimmunolabelled for γ-tubulin (red in merged images), Salmonella (green in merged images) and giantin (blue in merge... |
PMC2062534_fig04_14585.jpg | What key item or scene is captured in this photo? | Effect of BFA on SCV association with the MTOC. A. HeLa cells were infected with wt S. Typhimurium and then incubated in the presence or absence of BFA. Cells were then fixed at 8 h post inoculation and coimmunolabelled for γ-tubulin (red in merged images), Salmonella (green in merged images) and giantin (blue in merge... |
PMC2062534_fig04_14582.jpg | Can you identify the primary element in this image? | Effect of BFA on SCV association with the MTOC. A. HeLa cells were infected with wt S. Typhimurium and then incubated in the presence or absence of BFA. Cells were then fixed at 8 h post inoculation and coimmunolabelled for γ-tubulin (red in merged images), Salmonella (green in merged images) and giantin (blue in merge... |
PMC2063463_pone-0001158-g001_14587.jpg | What is the principal component of this image? | Microscopic revelation of numerous MLV particles in FDC network with increased PrP expression after immune-stimulation of a C57Bl/6 mouse with IC.(A) Ultrastructure of splenic FDC revealed by TEM. Large panel displays plastic section 70 nm thin, showing lymphocytes with dark round nuclei (L), and part of an FDC with lo... |
PMC2063499_F1_14588.jpg | What is the dominant medical problem in this image? | MRI of the cervical spine. T2-weighted image shows high signal intensity (white arrow) of the right vertebral artery. There is an intramural thrombus plus occlusion of the lumen (Grade four dissection). There is no intraluminal thrombosis. |
PMC2063499_F1_14589.jpg | What is the focal point of this photograph? | MRI of the cervical spine. T2-weighted image shows high signal intensity (white arrow) of the right vertebral artery. There is an intramural thrombus plus occlusion of the lumen (Grade four dissection). There is no intraluminal thrombosis. |
PMC2063502_F5_14595.jpg | What's the most prominent thing you notice in this picture? | Immunohistochemical localization of 14-3-3β (A and B) and mimecan (C and D) in myometrium (A and C) and leiomyomas (B and D) associated with leiomyoma and myometrial smooth muscle cells and cellular components of connective tissue and vasculature with inserts showing a higher magnification portion of these tissues. Inc... |
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