Recurrent deletions of ULK4 in schizophrenia: a gene crucial for neuritogenesis and neuronal motility
about
The human CHRNA7 and CHRFAM7A genes: A review of the genetics, regulation, and functionThe Tribbles 2 (TRB2) pseudokinase binds to ATP and autophosphorylates in a metal-independent mannerHigh-resolution copy number variation analysis of schizophrenia in Japan.Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsyGenome-wide alterations in hippocampal 5-hydroxymethylcytosine links plasticity genes to acute stress.Transcriptomics analysis of iPSC-derived neurons and modeling of neuropsychiatric disorders.Genetic Variants in LRP1 and ULK4 Are Associated with Acute Aortic Dissections.Control of cortex development by ULK4, a rare risk gene for mental disorders including schizophreniaThe schizophrenia risk gene MIR137 acts as a hippocampal gene network node orchestrating the expression of genes relevant to nervous system development and function.Microtubule and microtubule associated protein anomalies in psychiatric disease.Psychiatric behaviors associated with cytoskeletal defects in radial neuronal migration.Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.Potential Role of Microtubule Stabilizing Agents in Neurodevelopmental Disorders.Loss of Apela Peptide in Mice Causes Low Penetrance Embryonic Lethality and Defects in Early Mesodermal Derivatives.De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.Ulk4 deficiency leads to hypomyelination in mice.Ulk4 regulates GABAergic signaling and anxiety-related behavior.No Time to Waste: Transcriptome Study Reveals that Drought Tolerance in Barley May Be Attributed to Stressed-Like Expression Patterns that Exist before the Occurrence of Stress.A novel relationship for schizophrenia, bipolar and major depressive disorder Part 3: Evidence from chromosome 3 high density association screen.Multiple roles of Ulk4 in neurogenesis and brain function.Genetic Programming of Hypertension.Chromosomal microarray analysis in the genetic evaluation of 279 patients with syndromic obesity.
P2860
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P2860
Recurrent deletions of ULK4 in schizophrenia: a gene crucial for neuritogenesis and neuronal motility
description
2014 nî lūn-bûn
@nan
2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Recurrent deletions of ULK4 in ...... ogenesis and neuronal motility
@ast
Recurrent deletions of ULK4 in ...... ogenesis and neuronal motility
@en
Recurrent deletions of ULK4 in ...... ogenesis and neuronal motility
@en-gb
Recurrent deletions of ULK4 in ...... ogenesis and neuronal motility
@nl
type
label
Recurrent deletions of ULK4 in ...... ogenesis and neuronal motility
@ast
Recurrent deletions of ULK4 in ...... ogenesis and neuronal motility
@en
Recurrent deletions of ULK4 in ...... ogenesis and neuronal motility
@en-gb
Recurrent deletions of ULK4 in ...... ogenesis and neuronal motility
@nl
prefLabel
Recurrent deletions of ULK4 in ...... ogenesis and neuronal motility
@ast
Recurrent deletions of ULK4 in ...... ogenesis and neuronal motility
@en
Recurrent deletions of ULK4 in ...... ogenesis and neuronal motility
@en-gb
Recurrent deletions of ULK4 in ...... ogenesis and neuronal motility
@nl
P2093
P50
P921
P3181
P356
P1476
Recurrent deletions of ULK4 in ...... ogenesis and neuronal motility
@en
P2093
Colin D McCaig
Cristina Martin-Granados
David St Clair
Douglas H Blackwood
Guo-Dong Gao
Irene Hunter
P304
P3181
P356
10.1242/JCS.137604
P407
P577
2013-11-27T00:00:00Z