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Impact of a deletion of p75NTR on the neuronal lineage . Mitotically active young neuronal cells were determined using NeuroD as a specific marker ( A ; the NeuroD positive cells are shown in red. DAPI-staining (in blue) was used to visualize cell nuclei). No significant differences in the number of NeuroD positive cells was noted (B) . The analysis of the postmitotical DCX-positive neurons revealed that adult p75NTR ExIV−/− mice display significant more DCX neurons of that subpopulation than age-matched controls (C) . A comparison of images of late DCX-positive neurons in the adult DG that extents its dendrites towards the molecular layer of adult p75NTR ExIV+/+ mice (D) and p75NTR ExIV+/+ mice (E) hinted for a possible difference in their morphologies <t>(NeuroLucida:</t> deep projection of a z-stack). Sholl analysis revealed that the morphologies of those DCX-positive neurons were different [concerning intersections (F) , nodes (G) and endings (H) ]. Scalebars: 100 μm.
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Autodesk Inc inventor technical drawing software
Impact of a deletion of p75NTR on the neuronal lineage . Mitotically active young neuronal cells were determined using NeuroD as a specific marker ( A ; the NeuroD positive cells are shown in red. DAPI-staining (in blue) was used to visualize cell nuclei). No significant differences in the number of NeuroD positive cells was noted (B) . The analysis of the postmitotical DCX-positive neurons revealed that adult p75NTR ExIV−/− mice display significant more DCX neurons of that subpopulation than age-matched controls (C) . A comparison of images of late DCX-positive neurons in the adult DG that extents its dendrites towards the molecular layer of adult p75NTR ExIV+/+ mice (D) and p75NTR ExIV+/+ mice (E) hinted for a possible difference in their morphologies <t>(NeuroLucida:</t> deep projection of a z-stack). Sholl analysis revealed that the morphologies of those DCX-positive neurons were different [concerning intersections (F) , nodes (G) and endings (H) ]. Scalebars: 100 μm.
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Impact of a deletion of p75NTR on the neuronal lineage . Mitotically active young neuronal cells were determined using NeuroD as a specific marker ( A ; the NeuroD positive cells are shown in red. DAPI-staining (in blue) was used to visualize cell nuclei). No significant differences in the number of NeuroD positive cells was noted (B) . The analysis of the postmitotical DCX-positive neurons revealed that adult p75NTR ExIV−/− mice display significant more DCX neurons of that subpopulation than age-matched controls (C) . A comparison of images of late DCX-positive neurons in the adult DG that extents its dendrites towards the molecular layer of adult p75NTR ExIV+/+ mice (D) and p75NTR ExIV+/+ mice (E) hinted for a possible difference in their morphologies <t>(NeuroLucida:</t> deep projection of a z-stack). Sholl analysis revealed that the morphologies of those DCX-positive neurons were different [concerning intersections (F) , nodes (G) and endings (H) ]. Scalebars: 100 μm.
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Impact of a deletion of p75NTR on the neuronal lineage . Mitotically active young neuronal cells were determined using NeuroD as a specific marker ( A ; the NeuroD positive cells are shown in red. DAPI-staining (in blue) was used to visualize cell nuclei). No significant differences in the number of NeuroD positive cells was noted (B) . The analysis of the postmitotical DCX-positive neurons revealed that adult p75NTR ExIV−/− mice display significant more DCX neurons of that subpopulation than age-matched controls (C) . A comparison of images of late DCX-positive neurons in the adult DG that extents its dendrites towards the molecular layer of adult p75NTR ExIV+/+ mice (D) and p75NTR ExIV+/+ mice (E) hinted for a possible difference in their morphologies <t>(NeuroLucida:</t> deep projection of a z-stack). Sholl analysis revealed that the morphologies of those DCX-positive neurons were different [concerning intersections (F) , nodes (G) and endings (H) ]. Scalebars: 100 μm.
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Biofluids Inc three dimensional printed ise
Impact of a deletion of p75NTR on the neuronal lineage . Mitotically active young neuronal cells were determined using NeuroD as a specific marker ( A ; the NeuroD positive cells are shown in red. DAPI-staining (in blue) was used to visualize cell nuclei). No significant differences in the number of NeuroD positive cells was noted (B) . The analysis of the postmitotical DCX-positive neurons revealed that adult p75NTR ExIV−/− mice display significant more DCX neurons of that subpopulation than age-matched controls (C) . A comparison of images of late DCX-positive neurons in the adult DG that extents its dendrites towards the molecular layer of adult p75NTR ExIV+/+ mice (D) and p75NTR ExIV+/+ mice (E) hinted for a possible difference in their morphologies <t>(NeuroLucida:</t> deep projection of a z-stack). Sholl analysis revealed that the morphologies of those DCX-positive neurons were different [concerning intersections (F) , nodes (G) and endings (H) ]. Scalebars: 100 μm.
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BioMimetic Therapeutics three-dimensional scaffold
Impact of a deletion of p75NTR on the neuronal lineage . Mitotically active young neuronal cells were determined using NeuroD as a specific marker ( A ; the NeuroD positive cells are shown in red. DAPI-staining (in blue) was used to visualize cell nuclei). No significant differences in the number of NeuroD positive cells was noted (B) . The analysis of the postmitotical DCX-positive neurons revealed that adult p75NTR ExIV−/− mice display significant more DCX neurons of that subpopulation than age-matched controls (C) . A comparison of images of late DCX-positive neurons in the adult DG that extents its dendrites towards the molecular layer of adult p75NTR ExIV+/+ mice (D) and p75NTR ExIV+/+ mice (E) hinted for a possible difference in their morphologies <t>(NeuroLucida:</t> deep projection of a z-stack). Sholl analysis revealed that the morphologies of those DCX-positive neurons were different [concerning intersections (F) , nodes (G) and endings (H) ]. Scalebars: 100 μm.
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TOSHIBA Medical adaptive iterative dose reduction using three dimensional processing (aidr3d)
Impact of a deletion of p75NTR on the neuronal lineage . Mitotically active young neuronal cells were determined using NeuroD as a specific marker ( A ; the NeuroD positive cells are shown in red. DAPI-staining (in blue) was used to visualize cell nuclei). No significant differences in the number of NeuroD positive cells was noted (B) . The analysis of the postmitotical DCX-positive neurons revealed that adult p75NTR ExIV−/− mice display significant more DCX neurons of that subpopulation than age-matched controls (C) . A comparison of images of late DCX-positive neurons in the adult DG that extents its dendrites towards the molecular layer of adult p75NTR ExIV+/+ mice (D) and p75NTR ExIV+/+ mice (E) hinted for a possible difference in their morphologies <t>(NeuroLucida:</t> deep projection of a z-stack). Sholl analysis revealed that the morphologies of those DCX-positive neurons were different [concerning intersections (F) , nodes (G) and endings (H) ]. Scalebars: 100 μm.
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Impact of a deletion of p75NTR on the neuronal lineage . Mitotically active young neuronal cells were determined using NeuroD as a specific marker ( A ; the NeuroD positive cells are shown in red. DAPI-staining (in blue) was used to visualize cell nuclei). No significant differences in the number of NeuroD positive cells was noted (B) . The analysis of the postmitotical DCX-positive neurons revealed that adult p75NTR ExIV−/− mice display significant more DCX neurons of that subpopulation than age-matched controls (C) . A comparison of images of late DCX-positive neurons in the adult DG that extents its dendrites towards the molecular layer of adult p75NTR ExIV+/+ mice (D) and p75NTR ExIV+/+ mice (E) hinted for a possible difference in their morphologies <t>(NeuroLucida:</t> deep projection of a z-stack). Sholl analysis revealed that the morphologies of those DCX-positive neurons were different [concerning intersections (F) , nodes (G) and endings (H) ]. Scalebars: 100 μm.
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Impact of a deletion of p75NTR on the neuronal lineage . Mitotically active young neuronal cells were determined using NeuroD as a specific marker ( A ; the NeuroD positive cells are shown in red. DAPI-staining (in blue) was used to visualize cell nuclei). No significant differences in the number of NeuroD positive cells was noted (B) . The analysis of the postmitotical DCX-positive neurons revealed that adult p75NTR ExIV−/− mice display significant more DCX neurons of that subpopulation than age-matched controls (C) . A comparison of images of late DCX-positive neurons in the adult DG that extents its dendrites towards the molecular layer of adult p75NTR ExIV+/+ mice (D) and p75NTR ExIV+/+ mice (E) hinted for a possible difference in their morphologies <t>(NeuroLucida:</t> deep projection of a z-stack). Sholl analysis revealed that the morphologies of those DCX-positive neurons were different [concerning intersections (F) , nodes (G) and endings (H) ]. Scalebars: 100 μm.
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Image Search Results


Impact of a deletion of p75NTR on the neuronal lineage . Mitotically active young neuronal cells were determined using NeuroD as a specific marker ( A ; the NeuroD positive cells are shown in red. DAPI-staining (in blue) was used to visualize cell nuclei). No significant differences in the number of NeuroD positive cells was noted (B) . The analysis of the postmitotical DCX-positive neurons revealed that adult p75NTR ExIV−/− mice display significant more DCX neurons of that subpopulation than age-matched controls (C) . A comparison of images of late DCX-positive neurons in the adult DG that extents its dendrites towards the molecular layer of adult p75NTR ExIV+/+ mice (D) and p75NTR ExIV+/+ mice (E) hinted for a possible difference in their morphologies (NeuroLucida: deep projection of a z-stack). Sholl analysis revealed that the morphologies of those DCX-positive neurons were different [concerning intersections (F) , nodes (G) and endings (H) ]. Scalebars: 100 μm.

Journal: Frontiers in Neuroanatomy

Article Title: Impact of a deletion of the full-length and short isoform of p75NTR on cholinergic innervation and the population of postmitotic doublecortin positive cells in the dentate gyrus

doi: 10.3389/fnana.2015.00063

Figure Lengend Snippet: Impact of a deletion of p75NTR on the neuronal lineage . Mitotically active young neuronal cells were determined using NeuroD as a specific marker ( A ; the NeuroD positive cells are shown in red. DAPI-staining (in blue) was used to visualize cell nuclei). No significant differences in the number of NeuroD positive cells was noted (B) . The analysis of the postmitotical DCX-positive neurons revealed that adult p75NTR ExIV−/− mice display significant more DCX neurons of that subpopulation than age-matched controls (C) . A comparison of images of late DCX-positive neurons in the adult DG that extents its dendrites towards the molecular layer of adult p75NTR ExIV+/+ mice (D) and p75NTR ExIV+/+ mice (E) hinted for a possible difference in their morphologies (NeuroLucida: deep projection of a z-stack). Sholl analysis revealed that the morphologies of those DCX-positive neurons were different [concerning intersections (F) , nodes (G) and endings (H) ]. Scalebars: 100 μm.

Article Snippet: From these z-stacks DCX-positive neurons within the granular layer of the DG were reconstructed using NeuroLucida (MBF Biosciences, USA) and the reconstructions were analyzed with the help of NeuroExplorer (MBF Biosciences, USA) using the module “Sholl analysis” for the analysis of the three-dimensional vector-based Neurolucida data sets.

Techniques: Marker, Staining