Abnormalities in neuronal process extension, hippocampal development, and the ventricular system of L1 knockout mice.
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Structural plasticity of climbing fibers and the growth-associated protein GAP-43FAK-MAPK-dependent adhesion disassembly downstream of L1 contributes to semaphorin3A-induced collapseTargeted ablation of NrCAM or ankyrin-B results in disorganized lens fibers leading to cataract formationFunctional binding interaction identified between the axonal CAM L1 and members of the ERM familyThe role of neuronal complexes in human X-linked brain diseasesCD146 deletion in the nervous system impairs appetite, locomotor activity and spatial learning in miceL1cam is crucial for cell locomotion and terminal translocation of the Soma in radial migration during murine corticogenesisRecycling of the cell adhesion molecule L1 in axonal growth cones.Flotillin-mediated endocytic events dictate cell type-specific responses to semaphorin 3AMisguided axonal projections, neural cell adhesion molecule 180 mRNA upregulation, and altered behavior in mice deficient for the close homolog of L1Neural recognition molecules CHL1 and NB-3 regulate apical dendrite orientation in the neocortex via PTP alphaCortical thinning and hydrocephalus in mice lacking the immunoglobulin superfamily member CDOABI2-deficient mice exhibit defective cell migration, aberrant dendritic spine morphogenesis, and deficits in learning and memoryThe 14-3-3ζ protein binds to the cell adhesion molecule L1, promotes L1 phosphorylation by CKII and influences L1-dependent neurite outgrowthDevelopmental regulation of GABAergic interneuron branching and synaptic development in the prefrontal cortex by soluble neural cell adhesion moleculePolarized targeting of L1-CAM regulates axonal and dendritic bundling in vitroCerebellar defects in a mouse model of juvenile neuronal ceroid lipofuscinosis.Skin-derived cues control arborization of sensory dendrites in Caenorhabditis elegansThe systematic functional characterisation of Xq28 genes prioritises candidate disease genes.Mouse olfactory ensheathing glia enhance axon outgrowth on a myelin substrate in vitroClinical, genetic and imaging findings identify new causes for corpus callosum development syndromes.Human genetic disorders of axon guidance.ADAM10 is expressed in human podocytes and found in urinary vesicles of patients with glomerular kidney diseasesSpatiotemporal maturation patterns of murine brain quantified by diffusion tensor MRI and deformation-based morphometry.L1 and CHL1 Cooperate in Thalamocortical Axon TargetingNrCAM deletion causes topographic mistargeting of thalamocortical axons to the visual cortex and disrupts visual acuityThe Drosophila L1CAM homolog Neuroglian signals through distinct pathways to control different aspects of mushroom body axon developmentThe cell adhesion molecule L1 regulates the expression of choline acetyltransferase and the development of septal cholinergic neurons.Perinatal asphyxia: current status and approaches towards neuroprotective strategies, with focus on sentinel proteins.Gene expression analysis of nuclear factor I-A deficient mice indicates delayed brain maturationThe neural cell adhesion molecules L1 and CHL1 are cleaved by BACE1 protease in vivoOverlapping functions of the cell adhesion molecules Nr-CAM and L1 in cerebellar granule cell developmentSemaphorin 3A activates the guanosine triphosphatase Rab5 to promote growth cone collapse and organize callosal axon projections.Brain development in mice lacking L1-L1 homophilic adhesion.Uncovering multiple axonal targeting pathways in hippocampal neurons.Plasmin-sensitive dibasic sequences in the third fibronectin-like domain of L1-cell adhesion molecule (CAM) facilitate homomultimerization and concomitant integrin recruitmentNCAM Regulates Inhibition and Excitability in Layer 2/3 Pyramidal Cells of Anterior Cingulate CortexL1 cell adhesion molecule overexpression in hepatocellular carcinoma associates with advanced tumor progression and poor patient survival.β-Site amyloid precursor protein (APP)-cleaving enzyme 1 (BACE1)-deficient mice exhibit a close homolog of L1 (CHL1) loss-of-function phenotype involving axon guidance defectsPolysialylated NCAM and ephrinA/EphA regulate synaptic development of GABAergic interneurons in prefrontal cortex.
P2860
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P2860
Abnormalities in neuronal process extension, hippocampal development, and the ventricular system of L1 knockout mice.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh
1999年學術文章
@zh-hant
name
Abnormalities in neuronal proc ...... ar system of L1 knockout mice.
@en
Abnormalities in neuronal proc ...... ar system of L1 knockout mice.
@nl
type
label
Abnormalities in neuronal proc ...... ar system of L1 knockout mice.
@en
Abnormalities in neuronal proc ...... ar system of L1 knockout mice.
@nl
prefLabel
Abnormalities in neuronal proc ...... ar system of L1 knockout mice.
@en
Abnormalities in neuronal proc ...... ar system of L1 knockout mice.
@nl
P2093
P1476
Abnormalities in neuronal proc ...... ar system of L1 knockout mice.
@en
P2093
P304
P407
P577
1999-06-01T00:00:00Z