Disruption of the mouse L1 gene leads to malformations of the nervous system.
about
Spectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissuesFAK-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 formationDisruption of the murine nuclear factor I-A gene (Nfia) results in perinatal lethality, hydrocephalus, and agenesis of the corpus callosumDissection of complex molecular interactions of neurofascin with axonin-1, F11, and tenascin-R, which promote attachment and neurite formation of tectal cellsCD146 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.RanBPM is an L1-interacting protein that regulates L1-mediated mitogen-activated protein kinase activationThe neural cell adhesion molecule L1 interacts with the AP-2 adaptor and is endocytosed via the clathrin-mediated pathway.Subcommissural organ, cerebrospinal fluid circulation, and hydrocephalusLearning/memory impairment and reduced expression of the HNK-1 carbohydrate in beta4-galactosyltransferase-II-deficient miceFlotillin-mediated endocytic events dictate cell type-specific responses to semaphorin 3AEffects of ethanol on axon outgrowth and branching in developing rat cortical neuronsShootin1 interacts with actin retrograde flow and L1-CAM to promote axon outgrowthMisguided axonal projections, neural cell adhesion molecule 180 mRNA upregulation, and altered behavior in mice deficient for the close homolog of L1Cortical thinning and hydrocephalus in mice lacking the immunoglobulin superfamily member CDOImpaired motor coordination in mice that lack puncEthanol disrupts axon outgrowth stimulated by netrin-1, GDNF, and L1 by blocking their convergent activation of Src family kinase signalingThe 14-3-3ζ protein binds to the cell adhesion molecule L1, promotes L1 phosphorylation by CKII and influences L1-dependent neurite outgrowthDifferential effects of human L1CAM mutations on complementing guidance and synaptic defects in Drosophila melanogasterNeural cell adhesion molecule-associated polysialic acid regulates synaptic plasticity and learning by restraining the signaling through GluN2B-containing NMDA receptors.Mice deficient in transmembrane prostatic acid phosphatase display increased GABAergic transmission and neurological alterations.Neuronal Ig/Caspr recognition promotes the formation of axoaxonic synapses in mouse spinal cord.Cross talk between tetanus neurotoxin-insensitive vesicle-associated membrane protein-mediated transport and L1-mediated adhesion.Polarized targeting of L1-CAM regulates axonal and dendritic bundling in vitroMigration of nerve growth cones requires detergent-resistant membranes in a spatially defined and substrate-dependent manner.Micro-scale chromophore-assisted laser inactivation of nerve growth cone proteins.Cloning and expression of a zebrafish SCN1B ortholog and identification of a species-specific splice variant.Cellular and molecular bases of axonal pathfinding during embryogenesis of the fish central nervous system.An integrin-contactin complex regulates CNS myelination by differential Fyn phosphorylation.Hirschsprung disease and other enteric dysganglionoses.Human genetic disorders of axon guidance.L1-mediated branching is regulated by two ezrin-radixin-moesin (ERM)-binding sites, the RSLE region and a novel juxtamembrane ERM-binding region.A modifier locus on chromosome 5 contributes to L1 cell adhesion molecule X-linked hydrocephalus in mice.Cellular signaling by neural cell adhesion molecules of the immunoglobulin superfamily.Dynamic regulation of cell adhesion molecules during axon outgrowth.A neuronal form of the cell adhesion molecule L1 contains a tyrosine-based signal required for sorting to the axonal growth cone.Genetic and clinical aspects of X-linked hydrocephalus (L1 disease): Mutations in the L1CAM gene.Progressive renal papillary calcification and ureteral stone formation in mice deficient for Tamm-Horsfall protein
P2860
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P2860
Disruption of the mouse L1 gene leads to malformations of the nervous system.
description
1997 nî lūn-bûn
@nan
1997 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Disruption of the mouse L1 gene leads to malformations of the nervous system.
@ast
Disruption of the mouse L1 gene leads to malformations of the nervous system.
@en
Disruption of the mouse L1 gene leads to malformations of the nervous system.
@nl
type
label
Disruption of the mouse L1 gene leads to malformations of the nervous system.
@ast
Disruption of the mouse L1 gene leads to malformations of the nervous system.
@en
Disruption of the mouse L1 gene leads to malformations of the nervous system.
@nl
prefLabel
Disruption of the mouse L1 gene leads to malformations of the nervous system.
@ast
Disruption of the mouse L1 gene leads to malformations of the nervous system.
@en
Disruption of the mouse L1 gene leads to malformations of the nervous system.
@nl
P2093
P2860
P356
P1433
P1476
Disruption of the mouse L1 gene leads to malformations of the nervous system.
@en
P2093
P2860
P2888
P304
P356
10.1038/NG1197-346
P407
P577
1997-11-01T00:00:00Z
P6179
1030804758