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PMC1976115_F1_13634.jpg | What key item or scene is captured in this photo? | MRI of brain. (A) Initial MRI on February 16, 2005, shows a tumor in the right and left frontal lobe as well as the right thalamus. (B) MRI after surgery, radiation and chemotherapy. The tumor has completely disappeared except for slight enhancement adjacent to the surgical margin. (C) Recurrence of the thalamic tumor ... |
PMC1976115_F1_13633.jpg | What object or scene is depicted here? | MRI of brain. (A) Initial MRI on February 16, 2005, shows a tumor in the right and left frontal lobe as well as the right thalamus. (B) MRI after surgery, radiation and chemotherapy. The tumor has completely disappeared except for slight enhancement adjacent to the surgical margin. (C) Recurrence of the thalamic tumor ... |
PMC1976115_F1_13629.jpg | What is the main focus of this visual representation? | MRI of brain. (A) Initial MRI on February 16, 2005, shows a tumor in the right and left frontal lobe as well as the right thalamus. (B) MRI after surgery, radiation and chemotherapy. The tumor has completely disappeared except for slight enhancement adjacent to the surgical margin. (C) Recurrence of the thalamic tumor ... |
PMC1976134_F1_13635.jpg | What is the focal point of this photograph? | Examples of tissue-specific molecular markers in the E14.5 mouse embryo. A and B. Prostaglandin D2 synthase (brain) (Ptgds) (Genepaint set ID HD33, image 2C) expression is exclusive to the meninges (me), choroid plexi (cp, A) and gonads (g, B). C. Lysyl oxidase-like 3 (Lox13) (MH1813, 4A) is exclusively expressed in ca... |
PMC1976134_F1_13641.jpg | Describe the main subject of this image. | Examples of tissue-specific molecular markers in the E14.5 mouse embryo. A and B. Prostaglandin D2 synthase (brain) (Ptgds) (Genepaint set ID HD33, image 2C) expression is exclusive to the meninges (me), choroid plexi (cp, A) and gonads (g, B). C. Lysyl oxidase-like 3 (Lox13) (MH1813, 4A) is exclusively expressed in ca... |
PMC1976134_F1_13646.jpg | What key item or scene is captured in this photo? | Examples of tissue-specific molecular markers in the E14.5 mouse embryo. A and B. Prostaglandin D2 synthase (brain) (Ptgds) (Genepaint set ID HD33, image 2C) expression is exclusive to the meninges (me), choroid plexi (cp, A) and gonads (g, B). C. Lysyl oxidase-like 3 (Lox13) (MH1813, 4A) is exclusively expressed in ca... |
PMC1976134_F1_13645.jpg | Can you identify the primary element in this image? | Examples of tissue-specific molecular markers in the E14.5 mouse embryo. A and B. Prostaglandin D2 synthase (brain) (Ptgds) (Genepaint set ID HD33, image 2C) expression is exclusive to the meninges (me), choroid plexi (cp, A) and gonads (g, B). C. Lysyl oxidase-like 3 (Lox13) (MH1813, 4A) is exclusively expressed in ca... |
PMC1976134_F1_13639.jpg | What is the core subject represented in this visual? | Examples of tissue-specific molecular markers in the E14.5 mouse embryo. A and B. Prostaglandin D2 synthase (brain) (Ptgds) (Genepaint set ID HD33, image 2C) expression is exclusive to the meninges (me), choroid plexi (cp, A) and gonads (g, B). C. Lysyl oxidase-like 3 (Lox13) (MH1813, 4A) is exclusively expressed in ca... |
PMC1976134_F1_13636.jpg | What can you see in this picture? | Examples of tissue-specific molecular markers in the E14.5 mouse embryo. A and B. Prostaglandin D2 synthase (brain) (Ptgds) (Genepaint set ID HD33, image 2C) expression is exclusive to the meninges (me), choroid plexi (cp, A) and gonads (g, B). C. Lysyl oxidase-like 3 (Lox13) (MH1813, 4A) is exclusively expressed in ca... |
PMC1976134_F1_13638.jpg | What is the focal point of this photograph? | Examples of tissue-specific molecular markers in the E14.5 mouse embryo. A and B. Prostaglandin D2 synthase (brain) (Ptgds) (Genepaint set ID HD33, image 2C) expression is exclusive to the meninges (me), choroid plexi (cp, A) and gonads (g, B). C. Lysyl oxidase-like 3 (Lox13) (MH1813, 4A) is exclusively expressed in ca... |
PMC1976134_F1_13643.jpg | What can you see in this picture? | Examples of tissue-specific molecular markers in the E14.5 mouse embryo. A and B. Prostaglandin D2 synthase (brain) (Ptgds) (Genepaint set ID HD33, image 2C) expression is exclusive to the meninges (me), choroid plexi (cp, A) and gonads (g, B). C. Lysyl oxidase-like 3 (Lox13) (MH1813, 4A) is exclusively expressed in ca... |
PMC1976134_F1_13637.jpg | What object or scene is depicted here? | Examples of tissue-specific molecular markers in the E14.5 mouse embryo. A and B. Prostaglandin D2 synthase (brain) (Ptgds) (Genepaint set ID HD33, image 2C) expression is exclusive to the meninges (me), choroid plexi (cp, A) and gonads (g, B). C. Lysyl oxidase-like 3 (Lox13) (MH1813, 4A) is exclusively expressed in ca... |
PMC1976134_F1_13640.jpg | What is the core subject represented in this visual? | Examples of tissue-specific molecular markers in the E14.5 mouse embryo. A and B. Prostaglandin D2 synthase (brain) (Ptgds) (Genepaint set ID HD33, image 2C) expression is exclusive to the meninges (me), choroid plexi (cp, A) and gonads (g, B). C. Lysyl oxidase-like 3 (Lox13) (MH1813, 4A) is exclusively expressed in ca... |
PMC1976134_F1_13644.jpg | What does this image primarily show? | Examples of tissue-specific molecular markers in the E14.5 mouse embryo. A and B. Prostaglandin D2 synthase (brain) (Ptgds) (Genepaint set ID HD33, image 2C) expression is exclusive to the meninges (me), choroid plexi (cp, A) and gonads (g, B). C. Lysyl oxidase-like 3 (Lox13) (MH1813, 4A) is exclusively expressed in ca... |
PMC1976312_F1_13647.jpg | What object or scene is depicted here? | Abdominal X-Ray on the day of A&E admission showing small bowel dilation. |
PMC1976386_fig02_13664.jpg | What is the focal point of this photograph? | Initial loss of CaKIP1 is deleteriousA. Morphology over time of cells (CKFY288) in which CaKIP1 had been excised. Following excision in YCB-BSA, cells were back-diluted into fresh YPD medium and incubated at 30°C. Aliquots were examined at various time points under the microscope.B. Morphology of control cells (CKFY286... |
PMC1976386_fig02_13655.jpg | What is the principal component of this image? | Initial loss of CaKIP1 is deleteriousA. Morphology over time of cells (CKFY288) in which CaKIP1 had been excised. Following excision in YCB-BSA, cells were back-diluted into fresh YPD medium and incubated at 30°C. Aliquots were examined at various time points under the microscope.B. Morphology of control cells (CKFY286... |
PMC1976386_fig02_13669.jpg | What is the principal component of this image? | Initial loss of CaKIP1 is deleteriousA. Morphology over time of cells (CKFY288) in which CaKIP1 had been excised. Following excision in YCB-BSA, cells were back-diluted into fresh YPD medium and incubated at 30°C. Aliquots were examined at various time points under the microscope.B. Morphology of control cells (CKFY286... |
PMC1976386_fig02_13651.jpg | What is shown in this image? | Initial loss of CaKIP1 is deleteriousA. Morphology over time of cells (CKFY288) in which CaKIP1 had been excised. Following excision in YCB-BSA, cells were back-diluted into fresh YPD medium and incubated at 30°C. Aliquots were examined at various time points under the microscope.B. Morphology of control cells (CKFY286... |
PMC1976386_fig02_13666.jpg | What is being portrayed in this visual content? | Initial loss of CaKIP1 is deleteriousA. Morphology over time of cells (CKFY288) in which CaKIP1 had been excised. Following excision in YCB-BSA, cells were back-diluted into fresh YPD medium and incubated at 30°C. Aliquots were examined at various time points under the microscope.B. Morphology of control cells (CKFY286... |
PMC1976386_fig02_13649.jpg | What object or scene is depicted here? | Initial loss of CaKIP1 is deleteriousA. Morphology over time of cells (CKFY288) in which CaKIP1 had been excised. Following excision in YCB-BSA, cells were back-diluted into fresh YPD medium and incubated at 30°C. Aliquots were examined at various time points under the microscope.B. Morphology of control cells (CKFY286... |
PMC1976386_fig02_13653.jpg | What is the central feature of this picture? | Initial loss of CaKIP1 is deleteriousA. Morphology over time of cells (CKFY288) in which CaKIP1 had been excised. Following excision in YCB-BSA, cells were back-diluted into fresh YPD medium and incubated at 30°C. Aliquots were examined at various time points under the microscope.B. Morphology of control cells (CKFY286... |
PMC1976386_fig02_13656.jpg | Can you identify the primary element in this image? | Initial loss of CaKIP1 is deleteriousA. Morphology over time of cells (CKFY288) in which CaKIP1 had been excised. Following excision in YCB-BSA, cells were back-diluted into fresh YPD medium and incubated at 30°C. Aliquots were examined at various time points under the microscope.B. Morphology of control cells (CKFY286... |
PMC1976386_fig02_13667.jpg | What is being portrayed in this visual content? | Initial loss of CaKIP1 is deleteriousA. Morphology over time of cells (CKFY288) in which CaKIP1 had been excised. Following excision in YCB-BSA, cells were back-diluted into fresh YPD medium and incubated at 30°C. Aliquots were examined at various time points under the microscope.B. Morphology of control cells (CKFY286... |
PMC1976386_fig02_13660.jpg | What is shown in this image? | Initial loss of CaKIP1 is deleteriousA. Morphology over time of cells (CKFY288) in which CaKIP1 had been excised. Following excision in YCB-BSA, cells were back-diluted into fresh YPD medium and incubated at 30°C. Aliquots were examined at various time points under the microscope.B. Morphology of control cells (CKFY286... |
PMC1976386_fig02_13652.jpg | What object or scene is depicted here? | Initial loss of CaKIP1 is deleteriousA. Morphology over time of cells (CKFY288) in which CaKIP1 had been excised. Following excision in YCB-BSA, cells were back-diluted into fresh YPD medium and incubated at 30°C. Aliquots were examined at various time points under the microscope.B. Morphology of control cells (CKFY286... |
PMC1976386_fig02_13668.jpg | What's the most prominent thing you notice in this picture? | Initial loss of CaKIP1 is deleteriousA. Morphology over time of cells (CKFY288) in which CaKIP1 had been excised. Following excision in YCB-BSA, cells were back-diluted into fresh YPD medium and incubated at 30°C. Aliquots were examined at various time points under the microscope.B. Morphology of control cells (CKFY286... |
PMC1976386_fig02_13657.jpg | What is the core subject represented in this visual? | Initial loss of CaKIP1 is deleteriousA. Morphology over time of cells (CKFY288) in which CaKIP1 had been excised. Following excision in YCB-BSA, cells were back-diluted into fresh YPD medium and incubated at 30°C. Aliquots were examined at various time points under the microscope.B. Morphology of control cells (CKFY286... |
PMC1976386_fig02_13658.jpg | What stands out most in this visual? | Initial loss of CaKIP1 is deleteriousA. Morphology over time of cells (CKFY288) in which CaKIP1 had been excised. Following excision in YCB-BSA, cells were back-diluted into fresh YPD medium and incubated at 30°C. Aliquots were examined at various time points under the microscope.B. Morphology of control cells (CKFY286... |
PMC1976425_F7_13673.jpg | What is the core subject represented in this visual? | Immunohistochemical localisation of MSX1 protein in bovine ovarian sections at day of estrus (b, d), day of ovulation (f, h), growth phase (j, l), dominance phase (m, q). Cumulus cells are marked with Cc and oocytes are marked with Oo. Negative controls were processed without addition of primary anti-MSX1 antibody (r, ... |
PMC1976425_F7_13675.jpg | What is the main focus of this visual representation? | Immunohistochemical localisation of MSX1 protein in bovine ovarian sections at day of estrus (b, d), day of ovulation (f, h), growth phase (j, l), dominance phase (m, q). Cumulus cells are marked with Cc and oocytes are marked with Oo. Negative controls were processed without addition of primary anti-MSX1 antibody (r, ... |
PMC1976425_F7_13683.jpg | What is the principal component of this image? | Immunohistochemical localisation of MSX1 protein in bovine ovarian sections at day of estrus (b, d), day of ovulation (f, h), growth phase (j, l), dominance phase (m, q). Cumulus cells are marked with Cc and oocytes are marked with Oo. Negative controls were processed without addition of primary anti-MSX1 antibody (r, ... |
PMC1976425_F7_13681.jpg | What is the principal component of this image? | Immunohistochemical localisation of MSX1 protein in bovine ovarian sections at day of estrus (b, d), day of ovulation (f, h), growth phase (j, l), dominance phase (m, q). Cumulus cells are marked with Cc and oocytes are marked with Oo. Negative controls were processed without addition of primary anti-MSX1 antibody (r, ... |
PMC1976425_F7_13678.jpg | What does this image primarily show? | Immunohistochemical localisation of MSX1 protein in bovine ovarian sections at day of estrus (b, d), day of ovulation (f, h), growth phase (j, l), dominance phase (m, q). Cumulus cells are marked with Cc and oocytes are marked with Oo. Negative controls were processed without addition of primary anti-MSX1 antibody (r, ... |
PMC1976425_F7_13671.jpg | What's the most prominent thing you notice in this picture? | Immunohistochemical localisation of MSX1 protein in bovine ovarian sections at day of estrus (b, d), day of ovulation (f, h), growth phase (j, l), dominance phase (m, q). Cumulus cells are marked with Cc and oocytes are marked with Oo. Negative controls were processed without addition of primary anti-MSX1 antibody (r, ... |
PMC1976425_F7_13684.jpg | What is the central feature of this picture? | Immunohistochemical localisation of MSX1 protein in bovine ovarian sections at day of estrus (b, d), day of ovulation (f, h), growth phase (j, l), dominance phase (m, q). Cumulus cells are marked with Cc and oocytes are marked with Oo. Negative controls were processed without addition of primary anti-MSX1 antibody (r, ... |
PMC1976425_F7_13674.jpg | Can you identify the primary element in this image? | Immunohistochemical localisation of MSX1 protein in bovine ovarian sections at day of estrus (b, d), day of ovulation (f, h), growth phase (j, l), dominance phase (m, q). Cumulus cells are marked with Cc and oocytes are marked with Oo. Negative controls were processed without addition of primary anti-MSX1 antibody (r, ... |
PMC1976425_F7_13676.jpg | What is the core subject represented in this visual? | Immunohistochemical localisation of MSX1 protein in bovine ovarian sections at day of estrus (b, d), day of ovulation (f, h), growth phase (j, l), dominance phase (m, q). Cumulus cells are marked with Cc and oocytes are marked with Oo. Negative controls were processed without addition of primary anti-MSX1 antibody (r, ... |
PMC1976425_F7_13682.jpg | What is shown in this image? | Immunohistochemical localisation of MSX1 protein in bovine ovarian sections at day of estrus (b, d), day of ovulation (f, h), growth phase (j, l), dominance phase (m, q). Cumulus cells are marked with Cc and oocytes are marked with Oo. Negative controls were processed without addition of primary anti-MSX1 antibody (r, ... |
PMC1976425_F7_13679.jpg | What stands out most in this visual? | Immunohistochemical localisation of MSX1 protein in bovine ovarian sections at day of estrus (b, d), day of ovulation (f, h), growth phase (j, l), dominance phase (m, q). Cumulus cells are marked with Cc and oocytes are marked with Oo. Negative controls were processed without addition of primary anti-MSX1 antibody (r, ... |
PMC1976425_F7_13670.jpg | What stands out most in this visual? | Immunohistochemical localisation of MSX1 protein in bovine ovarian sections at day of estrus (b, d), day of ovulation (f, h), growth phase (j, l), dominance phase (m, q). Cumulus cells are marked with Cc and oocytes are marked with Oo. Negative controls were processed without addition of primary anti-MSX1 antibody (r, ... |
PMC1976425_F7_13672.jpg | Can you identify the primary element in this image? | Immunohistochemical localisation of MSX1 protein in bovine ovarian sections at day of estrus (b, d), day of ovulation (f, h), growth phase (j, l), dominance phase (m, q). Cumulus cells are marked with Cc and oocytes are marked with Oo. Negative controls were processed without addition of primary anti-MSX1 antibody (r, ... |
PMC1976425_F7_13677.jpg | What stands out most in this visual? | Immunohistochemical localisation of MSX1 protein in bovine ovarian sections at day of estrus (b, d), day of ovulation (f, h), growth phase (j, l), dominance phase (m, q). Cumulus cells are marked with Cc and oocytes are marked with Oo. Negative controls were processed without addition of primary anti-MSX1 antibody (r, ... |
PMC1976620_F5_13705.jpg | What object or scene is depicted here? | Nucleolin depletion induces the formation of micronuclei and multinuclear cells. A. Images of HeLa cells or human primary fibroblasts transfected for 4 days with scrambled siRNA #1 or with nucleolin siRNA mix #2 and #4 were counterstained with DAPI and visualized at the same magnification. Micronuclei are observed on A... |
PMC1976620_F5_13701.jpg | What can you see in this picture? | Nucleolin depletion induces the formation of micronuclei and multinuclear cells. A. Images of HeLa cells or human primary fibroblasts transfected for 4 days with scrambled siRNA #1 or with nucleolin siRNA mix #2 and #4 were counterstained with DAPI and visualized at the same magnification. Micronuclei are observed on A... |
PMC1976620_F5_13706.jpg | What is the central feature of this picture? | Nucleolin depletion induces the formation of micronuclei and multinuclear cells. A. Images of HeLa cells or human primary fibroblasts transfected for 4 days with scrambled siRNA #1 or with nucleolin siRNA mix #2 and #4 were counterstained with DAPI and visualized at the same magnification. Micronuclei are observed on A... |
PMC1976620_F5_13700.jpg | What is the dominant medical problem in this image? | Nucleolin depletion induces the formation of micronuclei and multinuclear cells. A. Images of HeLa cells or human primary fibroblasts transfected for 4 days with scrambled siRNA #1 or with nucleolin siRNA mix #2 and #4 were counterstained with DAPI and visualized at the same magnification. Micronuclei are observed on A... |
PMC1976620_F6_13693.jpg | What does this image primarily show? | Depletion of nucleolin induces hyper amplification of centrosome and multipolar mitotic spindle formation. HeLa cells transfected for 4 days with control siRNA # 1 or with the nucleolin siRNA mix #2 and #4 were processed for immunofluorescence. Centromeres were stained with a CREST antiserum (CEN), microtubules with an... |
PMC1976620_F6_13696.jpg | What is the principal component of this image? | Depletion of nucleolin induces hyper amplification of centrosome and multipolar mitotic spindle formation. HeLa cells transfected for 4 days with control siRNA # 1 or with the nucleolin siRNA mix #2 and #4 were processed for immunofluorescence. Centromeres were stained with a CREST antiserum (CEN), microtubules with an... |
PMC1976620_F6_13697.jpg | What stands out most in this visual? | Depletion of nucleolin induces hyper amplification of centrosome and multipolar mitotic spindle formation. HeLa cells transfected for 4 days with control siRNA # 1 or with the nucleolin siRNA mix #2 and #4 were processed for immunofluorescence. Centromeres were stained with a CREST antiserum (CEN), microtubules with an... |
PMC1976620_F6_13686.jpg | What can you see in this picture? | Depletion of nucleolin induces hyper amplification of centrosome and multipolar mitotic spindle formation. HeLa cells transfected for 4 days with control siRNA # 1 or with the nucleolin siRNA mix #2 and #4 were processed for immunofluorescence. Centromeres were stained with a CREST antiserum (CEN), microtubules with an... |
PMC1976620_F6_13692.jpg | Describe the main subject of this image. | Depletion of nucleolin induces hyper amplification of centrosome and multipolar mitotic spindle formation. HeLa cells transfected for 4 days with control siRNA # 1 or with the nucleolin siRNA mix #2 and #4 were processed for immunofluorescence. Centromeres were stained with a CREST antiserum (CEN), microtubules with an... |
PMC1976620_F6_13691.jpg | What is the central feature of this picture? | Depletion of nucleolin induces hyper amplification of centrosome and multipolar mitotic spindle formation. HeLa cells transfected for 4 days with control siRNA # 1 or with the nucleolin siRNA mix #2 and #4 were processed for immunofluorescence. Centromeres were stained with a CREST antiserum (CEN), microtubules with an... |
PMC1976620_F6_13689.jpg | What does this image primarily show? | Depletion of nucleolin induces hyper amplification of centrosome and multipolar mitotic spindle formation. HeLa cells transfected for 4 days with control siRNA # 1 or with the nucleolin siRNA mix #2 and #4 were processed for immunofluorescence. Centromeres were stained with a CREST antiserum (CEN), microtubules with an... |
PMC1976620_F6_13698.jpg | What is the dominant medical problem in this image? | Depletion of nucleolin induces hyper amplification of centrosome and multipolar mitotic spindle formation. HeLa cells transfected for 4 days with control siRNA # 1 or with the nucleolin siRNA mix #2 and #4 were processed for immunofluorescence. Centromeres were stained with a CREST antiserum (CEN), microtubules with an... |
PMC1976620_F6_13688.jpg | What does this image primarily show? | Depletion of nucleolin induces hyper amplification of centrosome and multipolar mitotic spindle formation. HeLa cells transfected for 4 days with control siRNA # 1 or with the nucleolin siRNA mix #2 and #4 were processed for immunofluorescence. Centromeres were stained with a CREST antiserum (CEN), microtubules with an... |
PMC1976620_F6_13690.jpg | What does this image primarily show? | Depletion of nucleolin induces hyper amplification of centrosome and multipolar mitotic spindle formation. HeLa cells transfected for 4 days with control siRNA # 1 or with the nucleolin siRNA mix #2 and #4 were processed for immunofluorescence. Centromeres were stained with a CREST antiserum (CEN), microtubules with an... |
PMC1976622_F2_13726.jpg | What stands out most in this visual? | Comparison between phantom data and reconstruction. Slices 44, 54, 64, 74, and 84 of every volume are shown. Reconstructions were performed on noisy projections of a phantom (range: -50° to +50°, every 1°, vertical tilt axis). A: Original phantom. B: Reconstruction using the ART with 10 iterations and a relaxation coef... |
PMC1976622_F2_13725.jpg | What is the central feature of this picture? | Comparison between phantom data and reconstruction. Slices 44, 54, 64, 74, and 84 of every volume are shown. Reconstructions were performed on noisy projections of a phantom (range: -50° to +50°, every 1°, vertical tilt axis). A: Original phantom. B: Reconstruction using the ART with 10 iterations and a relaxation coef... |
PMC1976622_F2_13716.jpg | What is the core subject represented in this visual? | Comparison between phantom data and reconstruction. Slices 44, 54, 64, 74, and 84 of every volume are shown. Reconstructions were performed on noisy projections of a phantom (range: -50° to +50°, every 1°, vertical tilt axis). A: Original phantom. B: Reconstruction using the ART with 10 iterations and a relaxation coef... |
PMC1976622_F2_13727.jpg | What object or scene is depicted here? | Comparison between phantom data and reconstruction. Slices 44, 54, 64, 74, and 84 of every volume are shown. Reconstructions were performed on noisy projections of a phantom (range: -50° to +50°, every 1°, vertical tilt axis). A: Original phantom. B: Reconstruction using the ART with 10 iterations and a relaxation coef... |
PMC1976622_F2_13717.jpg | What key item or scene is captured in this photo? | Comparison between phantom data and reconstruction. Slices 44, 54, 64, 74, and 84 of every volume are shown. Reconstructions were performed on noisy projections of a phantom (range: -50° to +50°, every 1°, vertical tilt axis). A: Original phantom. B: Reconstruction using the ART with 10 iterations and a relaxation coef... |
PMC1976622_F2_13711.jpg | What is the core subject represented in this visual? | Comparison between phantom data and reconstruction. Slices 44, 54, 64, 74, and 84 of every volume are shown. Reconstructions were performed on noisy projections of a phantom (range: -50° to +50°, every 1°, vertical tilt axis). A: Original phantom. B: Reconstruction using the ART with 10 iterations and a relaxation coef... |
PMC1976622_F2_13714.jpg | What is shown in this image? | Comparison between phantom data and reconstruction. Slices 44, 54, 64, 74, and 84 of every volume are shown. Reconstructions were performed on noisy projections of a phantom (range: -50° to +50°, every 1°, vertical tilt axis). A: Original phantom. B: Reconstruction using the ART with 10 iterations and a relaxation coef... |
PMC1976622_F2_13713.jpg | What is being portrayed in this visual content? | Comparison between phantom data and reconstruction. Slices 44, 54, 64, 74, and 84 of every volume are shown. Reconstructions were performed on noisy projections of a phantom (range: -50° to +50°, every 1°, vertical tilt axis). A: Original phantom. B: Reconstruction using the ART with 10 iterations and a relaxation coef... |
PMC1976622_F2_13721.jpg | What is the main focus of this visual representation? | Comparison between phantom data and reconstruction. Slices 44, 54, 64, 74, and 84 of every volume are shown. Reconstructions were performed on noisy projections of a phantom (range: -50° to +50°, every 1°, vertical tilt axis). A: Original phantom. B: Reconstruction using the ART with 10 iterations and a relaxation coef... |
PMC1976622_F2_13719.jpg | What key item or scene is captured in this photo? | Comparison between phantom data and reconstruction. Slices 44, 54, 64, 74, and 84 of every volume are shown. Reconstructions were performed on noisy projections of a phantom (range: -50° to +50°, every 1°, vertical tilt axis). A: Original phantom. B: Reconstruction using the ART with 10 iterations and a relaxation coef... |
PMC1976622_F2_13712.jpg | What key item or scene is captured in this photo? | Comparison between phantom data and reconstruction. Slices 44, 54, 64, 74, and 84 of every volume are shown. Reconstructions were performed on noisy projections of a phantom (range: -50° to +50°, every 1°, vertical tilt axis). A: Original phantom. B: Reconstruction using the ART with 10 iterations and a relaxation coef... |
PMC1976622_F2_13709.jpg | What does this image primarily show? | Comparison between phantom data and reconstruction. Slices 44, 54, 64, 74, and 84 of every volume are shown. Reconstructions were performed on noisy projections of a phantom (range: -50° to +50°, every 1°, vertical tilt axis). A: Original phantom. B: Reconstruction using the ART with 10 iterations and a relaxation coef... |
PMC1976622_F2_13720.jpg | What can you see in this picture? | Comparison between phantom data and reconstruction. Slices 44, 54, 64, 74, and 84 of every volume are shown. Reconstructions were performed on noisy projections of a phantom (range: -50° to +50°, every 1°, vertical tilt axis). A: Original phantom. B: Reconstruction using the ART with 10 iterations and a relaxation coef... |
PMC1976622_F2_13722.jpg | What's the most prominent thing you notice in this picture? | Comparison between phantom data and reconstruction. Slices 44, 54, 64, 74, and 84 of every volume are shown. Reconstructions were performed on noisy projections of a phantom (range: -50° to +50°, every 1°, vertical tilt axis). A: Original phantom. B: Reconstruction using the ART with 10 iterations and a relaxation coef... |
PMC1976628_pbio-0050251-g001_13729.jpg | What's the most prominent thing you notice in this picture? | Mutations in cul3Testis Block Caspase Activation and Spermatid Individualization, but Not Axonemal Tubulin Polyglycylation(A–H) Visualization of active drICE with anti-cleaved caspase-3 antibody (CM1; green) and axonemal tubulin polyglycylation with anti-glycylated tubulin monoclonal antibody (AXO 49; red). These figur... |
PMC1976628_pbio-0050251-g001_13737.jpg | What is the principal component of this image? | Mutations in cul3Testis Block Caspase Activation and Spermatid Individualization, but Not Axonemal Tubulin Polyglycylation(A–H) Visualization of active drICE with anti-cleaved caspase-3 antibody (CM1; green) and axonemal tubulin polyglycylation with anti-glycylated tubulin monoclonal antibody (AXO 49; red). These figur... |
PMC1976628_pbio-0050251-g001_13734.jpg | What can you see in this picture? | Mutations in cul3Testis Block Caspase Activation and Spermatid Individualization, but Not Axonemal Tubulin Polyglycylation(A–H) Visualization of active drICE with anti-cleaved caspase-3 antibody (CM1; green) and axonemal tubulin polyglycylation with anti-glycylated tubulin monoclonal antibody (AXO 49; red). These figur... |
PMC1976628_pbio-0050251-g001_13735.jpg | What is the dominant medical problem in this image? | Mutations in cul3Testis Block Caspase Activation and Spermatid Individualization, but Not Axonemal Tubulin Polyglycylation(A–H) Visualization of active drICE with anti-cleaved caspase-3 antibody (CM1; green) and axonemal tubulin polyglycylation with anti-glycylated tubulin monoclonal antibody (AXO 49; red). These figur... |
PMC1976628_pbio-0050251-g001_13730.jpg | What does this image primarily show? | Mutations in cul3Testis Block Caspase Activation and Spermatid Individualization, but Not Axonemal Tubulin Polyglycylation(A–H) Visualization of active drICE with anti-cleaved caspase-3 antibody (CM1; green) and axonemal tubulin polyglycylation with anti-glycylated tubulin monoclonal antibody (AXO 49; red). These figur... |
PMC1976628_pbio-0050251-g001_13731.jpg | Describe the main subject of this image. | Mutations in cul3Testis Block Caspase Activation and Spermatid Individualization, but Not Axonemal Tubulin Polyglycylation(A–H) Visualization of active drICE with anti-cleaved caspase-3 antibody (CM1; green) and axonemal tubulin polyglycylation with anti-glycylated tubulin monoclonal antibody (AXO 49; red). These figur... |
PMC1978209_F2_13742.jpg | What key item or scene is captured in this photo? | Lack of growth restriction between the embryonic and extra-embryonic regions of the VE. Examples of labelled conceptuses recovered after microinjection of single cells at the surface of the ICM at the blastocyst stage. They are shown as a fluorescent projection of a confocal z series merged with a transmitted light sec... |
PMC1978209_F2_13746.jpg | What's the most prominent thing you notice in this picture? | Lack of growth restriction between the embryonic and extra-embryonic regions of the VE. Examples of labelled conceptuses recovered after microinjection of single cells at the surface of the ICM at the blastocyst stage. They are shown as a fluorescent projection of a confocal z series merged with a transmitted light sec... |
PMC1978209_F2_13739.jpg | What is the focal point of this photograph? | Lack of growth restriction between the embryonic and extra-embryonic regions of the VE. Examples of labelled conceptuses recovered after microinjection of single cells at the surface of the ICM at the blastocyst stage. They are shown as a fluorescent projection of a confocal z series merged with a transmitted light sec... |
PMC1978209_F2_13744.jpg | What is being portrayed in this visual content? | Lack of growth restriction between the embryonic and extra-embryonic regions of the VE. Examples of labelled conceptuses recovered after microinjection of single cells at the surface of the ICM at the blastocyst stage. They are shown as a fluorescent projection of a confocal z series merged with a transmitted light sec... |
PMC1978209_F2_13743.jpg | What is the core subject represented in this visual? | Lack of growth restriction between the embryonic and extra-embryonic regions of the VE. Examples of labelled conceptuses recovered after microinjection of single cells at the surface of the ICM at the blastocyst stage. They are shown as a fluorescent projection of a confocal z series merged with a transmitted light sec... |
PMC1978209_F2_13741.jpg | What key item or scene is captured in this photo? | Lack of growth restriction between the embryonic and extra-embryonic regions of the VE. Examples of labelled conceptuses recovered after microinjection of single cells at the surface of the ICM at the blastocyst stage. They are shown as a fluorescent projection of a confocal z series merged with a transmitted light sec... |
PMC1978209_F2_13745.jpg | What is the dominant medical problem in this image? | Lack of growth restriction between the embryonic and extra-embryonic regions of the VE. Examples of labelled conceptuses recovered after microinjection of single cells at the surface of the ICM at the blastocyst stage. They are shown as a fluorescent projection of a confocal z series merged with a transmitted light sec... |
PMC1978209_F2_13740.jpg | What is the core subject represented in this visual? | Lack of growth restriction between the embryonic and extra-embryonic regions of the VE. Examples of labelled conceptuses recovered after microinjection of single cells at the surface of the ICM at the blastocyst stage. They are shown as a fluorescent projection of a confocal z series merged with a transmitted light sec... |
PMC1978530_pone-0000960-g001_13749.jpg | What is the dominant medical problem in this image? | Schematic diagram of the assessment of actinomycete antagonism.The resident actinomycete was inoculated in the center of a Petri dish and left at room temperature for three weeks, after which a suspension of the intruder actinomycete was inoculated to the entire unoccupied Petri dish area (top). One week after the intr... |
PMC1978530_pone-0000960-g001_13747.jpg | What is the dominant medical problem in this image? | Schematic diagram of the assessment of actinomycete antagonism.The resident actinomycete was inoculated in the center of a Petri dish and left at room temperature for three weeks, after which a suspension of the intruder actinomycete was inoculated to the entire unoccupied Petri dish area (top). One week after the intr... |
PMC1978530_pone-0000960-g001_13750.jpg | What object or scene is depicted here? | Schematic diagram of the assessment of actinomycete antagonism.The resident actinomycete was inoculated in the center of a Petri dish and left at room temperature for three weeks, after which a suspension of the intruder actinomycete was inoculated to the entire unoccupied Petri dish area (top). One week after the intr... |
PMC1978531_pone-0000961-g002_13751.jpg | What does this image primarily show? | ID elements do not mark EGFP reporter mRNA for dendritic transport.
In situ hybridization using a digoxigenin-labeled antisense (AS) EGFP probe on coronal brain sections from the various transgenic mice. A–D, There are intense hybridization signals in the cell bodies of neurons in the hippocampus and cortex for the ID1... |
PMC1978531_pone-0000961-g002_13755.jpg | What is the main focus of this visual representation? | ID elements do not mark EGFP reporter mRNA for dendritic transport.
In situ hybridization using a digoxigenin-labeled antisense (AS) EGFP probe on coronal brain sections from the various transgenic mice. A–D, There are intense hybridization signals in the cell bodies of neurons in the hippocampus and cortex for the ID1... |
PMC1978531_pone-0000961-g002_13752.jpg | What is shown in this image? | ID elements do not mark EGFP reporter mRNA for dendritic transport.
In situ hybridization using a digoxigenin-labeled antisense (AS) EGFP probe on coronal brain sections from the various transgenic mice. A–D, There are intense hybridization signals in the cell bodies of neurons in the hippocampus and cortex for the ID1... |
PMC1978531_pone-0000961-g002_13756.jpg | Can you identify the primary element in this image? | ID elements do not mark EGFP reporter mRNA for dendritic transport.
In situ hybridization using a digoxigenin-labeled antisense (AS) EGFP probe on coronal brain sections from the various transgenic mice. A–D, There are intense hybridization signals in the cell bodies of neurons in the hippocampus and cortex for the ID1... |
PMC1978531_pone-0000961-g002_13760.jpg | What is being portrayed in this visual content? | ID elements do not mark EGFP reporter mRNA for dendritic transport.
In situ hybridization using a digoxigenin-labeled antisense (AS) EGFP probe on coronal brain sections from the various transgenic mice. A–D, There are intense hybridization signals in the cell bodies of neurons in the hippocampus and cortex for the ID1... |
PMC1978531_pone-0000961-g002_13753.jpg | What key item or scene is captured in this photo? | ID elements do not mark EGFP reporter mRNA for dendritic transport.
In situ hybridization using a digoxigenin-labeled antisense (AS) EGFP probe on coronal brain sections from the various transgenic mice. A–D, There are intense hybridization signals in the cell bodies of neurons in the hippocampus and cortex for the ID1... |
PMC1978531_pone-0000961-g003_13761.jpg | Describe the main subject of this image. | The 3′ UTR of α-CaMKII targets EGFP reporter mRNA to dendrites, whereas full-length BC1 RNA does not.
In situ hybridization with a DIG-riboprobe against EGFP in coronal brain sections through the hippocampus of transgenic mice harboring chimeric RNAs with EGFP plus full length BC1 RNA or the 3′ UTR of α-CaMKII mRNA (po... |
PMC1978531_pone-0000961-g003_13765.jpg | What key item or scene is captured in this photo? | The 3′ UTR of α-CaMKII targets EGFP reporter mRNA to dendrites, whereas full-length BC1 RNA does not.
In situ hybridization with a DIG-riboprobe against EGFP in coronal brain sections through the hippocampus of transgenic mice harboring chimeric RNAs with EGFP plus full length BC1 RNA or the 3′ UTR of α-CaMKII mRNA (po... |
PMC1978531_pone-0000961-g003_13762.jpg | What key item or scene is captured in this photo? | The 3′ UTR of α-CaMKII targets EGFP reporter mRNA to dendrites, whereas full-length BC1 RNA does not.
In situ hybridization with a DIG-riboprobe against EGFP in coronal brain sections through the hippocampus of transgenic mice harboring chimeric RNAs with EGFP plus full length BC1 RNA or the 3′ UTR of α-CaMKII mRNA (po... |
PMC1978531_pone-0000961-g003_13764.jpg | What is the central feature of this picture? | The 3′ UTR of α-CaMKII targets EGFP reporter mRNA to dendrites, whereas full-length BC1 RNA does not.
In situ hybridization with a DIG-riboprobe against EGFP in coronal brain sections through the hippocampus of transgenic mice harboring chimeric RNAs with EGFP plus full length BC1 RNA or the 3′ UTR of α-CaMKII mRNA (po... |
PMC1978531_pone-0000961-g003_13763.jpg | What is the principal component of this image? | The 3′ UTR of α-CaMKII targets EGFP reporter mRNA to dendrites, whereas full-length BC1 RNA does not.
In situ hybridization with a DIG-riboprobe against EGFP in coronal brain sections through the hippocampus of transgenic mice harboring chimeric RNAs with EGFP plus full length BC1 RNA or the 3′ UTR of α-CaMKII mRNA (po... |
PMC1988786_F1_13772.jpg | What does this image primarily show? | Left side: angiography by direct splenic puncture shows the physiological venous drainage through the splenic vein to the portal vein; neo formed capillaries connect the spleen with the superior vena cava through thoraco-epigastric vein, and the inferior vena cava through the superficial epigastric vein. Right side: ma... |
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