Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth
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The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13Androgen receptor molecular biology and potential targets in prostate cancerThe odyssey of MeCP2 and parental imprintingAn essential role for DYF-11/MIP-T3 in assembling functional intraflagellar transport complexesAge-dependent modulation of cortical transcriptomes in spinal cord injury and repairPsychosis and autism as diametrical disorders of the social brainMagel2, a Prader-Willi syndrome candidate gene, modulates the activities of circadian rhythm proteins in cultured cellsBhlhb5 and Prdm8 form a repressor complex involved in neuronal circuit assemblyThe ciliary protein cystin forms a regulatory complex with necdin to modulate Myc expressionTwo binding partners cooperate to activate the molecular motor Kinesin-1.Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death.Necdin protects embryonic motoneurons from programmed cell death.The Smc5/Smc6/MAGE complex confers resistance to caffeine and genotoxic stress in Drosophila melanogaster.The neurobiology of mouse models syntenic to human chromosome 15q.Increased EID1 nuclear translocation impairs synaptic plasticity and memory function associated with pathogenesis of Alzheimer's disease.Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules.RNAs of the human chromosome 15q11-q13 imprinted regionPathophysiological mechanisms for actions of the neurotrophins.Assessment of sleep and breathing in adults with prader-willi syndrome: a case control seriesNecdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development.Early childhood obesity is associated with compromised cerebellar developmentNew Perspectives on Genomic Imprinting, an Essential and Multifaceted Mode of Epigenetic Control in the Developing and Adult Brain.Genetic and epigenetic dysregulation of imprinted genes in the brain.Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.Regulation of the metastasis suppressor Nm23-H1 by tumor viruses.Mice lacking the schizophrenia-associated protein FEZ1 manifest hyperactivity and enhanced responsiveness to psychostimulants.Distinct transcriptomes define rostral and caudal serotonin neurons.Loss of Magel2 impairs the development of hypothalamic Anorexigenic circuits.Functional consequences of necdin nucleocytoplasmic localization.Imprinting analysis of porcine MAGEL2 gene in two fetal stages and association analysis with carcass traits.Prader-Willi and Angelman SyndromeRecommendations for the investigation of animal models of Prader-Willi syndrome.Necdin shapes serotonergic development and SERT activity modulating breathing in a mouse model for Prader-Willi syndrome.The Prader-Willi syndrome proteins MAGEL2 and necdin regulate leptin receptor cell surface abundance through ubiquitination pathways.Muscle dysfunction caused by loss of Magel2 in a mouse model of Prader-Willi and Schaaf-Yang syndromes.Subclinical dysphagia in persons with Prader-Willi syndrome.Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome.Whole genome microarray analysis of gene expression in Prader-Willi syndrome.Evaluation of Prader-Willi Syndrome GeneMAGEL2in Severe Childhood-Onset Obesity
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Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth
description
2005 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի մարտին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2005
@ast
im März 2005 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2005/03/01)
@sk
vědecký článek publikovaný v roce 2005
@cs
wetenschappelijk artikel (gepubliceerd op 2005/03/01)
@nl
наукова стаття, опублікована в березні 2005
@uk
مقالة علمية (نشرت في مارس 2005)
@ar
name
Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth
@ast
Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth
@en
Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth
@nl
type
label
Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth
@ast
Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth
@en
Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth
@nl
prefLabel
Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth
@ast
Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth
@en
Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth
@nl
P2093
P921
P356
P1476
Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth
@en
P2093
Alysa A Tennese
Barbara Karten
Christine L Walker
Megan A O'Neill
Sharee L Kuny
P304
P356
10.1093/HMG/DDI059
P577
2005-01-13T00:00:00Z