Mice that lack astrotactin have slowed neuronal migration
about
Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)Timing neurogenesis and differentiation: insights from quantitative clonal analyses of cerebellar granule cellsCellullar insights into cerebral cortical development: focusing on the locomotion mode of neuronal migrationEffects of Transforming Growth Factor Beta 1 in Cerebellar Development: Role in Synapse FormationBrinp1(-/-) mice exhibit autism-like behaviour, altered memory, hyperactivity and increased parvalbumin-positive cortical interneuron densityAstn2, a novel member of the astrotactin gene family, regulates the trafficking of ASTN1 during glial-guided neuronal migration.Cerebellum development and medulloblastomaAltered cerebellar development in nuclear receptor TAK1/ TR4 null mice is associated with deficits in GLAST(+) glia, alterations in social behavior, motor learning, startle reactivity, and microgliaIdentification of Astrotactin2 as a Genetic Modifier That Regulates the Global Orientation of Mammalian Hair FolliclesThe MACPF/CDC family of pore-forming toxins.Replicated Risk Nicotinic Cholinergic Receptor Genes for Nicotine Dependence.A rapid screening method for population-specific neuronal motogens, substrates and associated signaling pathwaysFour distinct phases of basket/stellate cell migration after entering their final destination (the molecular layer) in the developing cerebellum.Vav3-deficient mice exhibit a transient delay in cerebellar developmentDownregulation of genes with a function in axon outgrowth and synapse formation in motor neurones of the VEGFdelta/delta mouse model of amyotrophic lateral sclerosis.Characterization of biological pathways associated with a 1.37 Mbp genomic region protective of hypertension in Dahl S rats.Deficits in motor coordination with aberrant cerebellar development in mice lacking testicular orphan nuclear receptor 4.Huwe1 ubiquitin ligase is essential to synchronize neuronal and glial differentiation in the developing cerebellumPostnatal Migration of Cerebellar Interneurons.Long noncoding RNA HOTAIR is relevant to cellular proliferation, invasiveness, and clinical relapse in small-cell lung cancerA marked paucity of granule cells in the developing cerebellum of the Npc1(-/-) mouse is corrected by a single injection of hydroxypropyl-β-cyclodextrinFoxa1 and Foxa2 maintain the metabolic and secretory features of the mature beta-cellCompletion of neuronal migration regulated by loss of Ca(2+) transientsPAPPA2, an enzyme that cleaves an insulin-like growth-factor-binding protein, is a candidate gene for a quantitative trait locus affecting body size in miceIdentification of piRNAs in the central nervous system.Neuronal migration and molecular conservation with leukocyte chemotaxisThe role of Rho GTPase proteins in CNS neuronal migration.Neuron-derived FGF9 is essential for scaffold formation of Bergmann radial fibers and migration of granule neurons in the cerebellum.Pathway-Based Genome-Wide Association Studies for Plasma Triglycerides in Obese Females and Normal-Weight Controls.Impaired motor coordination and disrupted cerebellar architecture in Fgfr1 and Fgfr2 double knockout miceSticky situations: recent advances in control of cell adhesion during neuronal migrationASTN1 and alcohol dependence: family-based association analysis in multiplex alcohol dependence familiesConsensus Paper: Cerebellar Development.N-myc alters the fate of preneoplastic cells in a mouse model of medulloblastoma.Cell biology in neuroscience: mechanisms of cell migration in the nervous system.1q25.2-q31.3 Deletion in a female with mental retardation, clinodactyly, minor facial anomalies but no growth retardation.piRNAs and Their Functions in the Brain.Molecular genetics of addiction and related heritable phenotypes: genome-wide association approaches identify "connectivity constellation" and drug target genes with pleiotropic effects.Guiding neuronal cell migrations.Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.
P2860
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P2860
Mice that lack astrotactin have slowed neuronal migration
description
2002 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2002
@ast
im Februar 2002 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2002/02/01)
@sk
vědecký článek publikovaný v roce 2002
@cs
wetenschappelijk artikel (gepubliceerd op 2002/02/01)
@nl
наукова стаття, опублікована в лютому 2002
@uk
مقالة علمية (نشرت في فبراير 2002)
@ar
name
Mice that lack astrotactin have slowed neuronal migration
@ast
Mice that lack astrotactin have slowed neuronal migration
@en
Mice that lack astrotactin have slowed neuronal migration
@nl
type
label
Mice that lack astrotactin have slowed neuronal migration
@ast
Mice that lack astrotactin have slowed neuronal migration
@en
Mice that lack astrotactin have slowed neuronal migration
@nl
prefLabel
Mice that lack astrotactin have slowed neuronal migration
@ast
Mice that lack astrotactin have slowed neuronal migration
@en
Mice that lack astrotactin have slowed neuronal migration
@nl
P2093
P3181
P1433
P1476
Mice that lack astrotactin have slowed neuronal migration
@en
P2093
Gunnar Dietz
Margaret Cooper
Mary E. Hatten
Niels C. Adams
Toshifumi Tomoda
P304
P3181
P407
P577
2002-02-01T00:00:00Z