Disruption of the mouse necdin gene results in early post-natal lethality
about
Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardationNecdin-related MAGE proteins differentially interact with the E2F1 transcription factor and the p75 neurotrophin receptorMAGE-RING protein complexes comprise a family of E3 ubiquitin ligasesMAGE-A1 interacts with adaptor SKIP and the deacetylase HDAC1 to repress transcriptionSmall evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brainIdentification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting controlThe comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13Separate necdin domains bind ARNT2 and HIF1alpha and repress transcriptionA necdin/MAGE-like gene in the chromosome 15 autism susceptibility region: expression, imprinting, and mapping of the human and mouse orthologuesThe Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin geneA Novel Mutant Allele of Pw1/Peg3 Does Not Affect Maternal Behavior or Nursing BehaviorThe postmitotic growth suppressor necdin interacts with a calcium-binding protein (NEFA) in neuronal cytoplasmPrader-Willi and Angelman syndromes: sister imprinted disordersA RING finger protein Praja1 regulates Dlx5-dependent transcription through its ubiquitin ligase activity for the Dlx/Msx-interacting MAGE/Necdin family protein, Dlxin-1Cancer/testis antigens: an expanding family of targets for cancer immunotherapyEctopic expression of necdin induces differentiation of mouse neuroblastoma cellshNRAGE, a human neurotrophin receptor interacting MAGE homologue, regulates p53 transcriptional activity and inhibits cell proliferationNecdin interacts with the Msx2 homeodomain protein via MAGE-D1 to promote myogenic differentiation of C2C12 cellsThe trophinin gene encodes a novel group of MAGE proteins, magphinins, and regulates cell proliferation during gametogenesis in the mouseDevelopmental abnormalities of neuronal structure and function in prenatal mice lacking the prader-willi syndrome gene necdinEpigenetic functions of smchd1 repress gene clusters on the inactive X chromosome and on autosomesNSCL-1 and NSCL-2 synergistically determine the fate of GnRH-1 neurons and control necdin gene expressionDNA methylation and human diseaseStochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences.Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death.Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint regionNecdin promotes ubiquitin-dependent degradation of PIAS1 SUMO E3 ligasep53 regulates hematopoietic stem cell quiescence.The function of non-coding RNAs in genomic imprinting.Mice with altered serotonin 2C receptor RNA editing display characteristics of Prader-Willi syndrome.Necdin protects embryonic motoneurons from programmed cell death.Necdin controls proliferation of white adipocyte progenitor cells.The Necdin-Wnt pathway causes epigenetic peroxisome proliferator-activated receptor gamma repression in hepatic stellate cells.The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome.An unexpected function of the Prader-Willi syndrome imprinting center in maternal imprinting in miceA paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndromeThe MAGE proteins: emerging roles in cell cycle progression, apoptosis, and neurogenetic disease.Spermatogenesis in Bclw-deficient miceNon-coding RNAs in imprinted gene clusters.Chromosome-wide identification of novel imprinted genes using microarrays and uniparental disomies.
P2860
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P2860
Disruption of the mouse necdin gene results in early post-natal lethality
description
1999 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
articolo scientifico
@it
artículu científicu espublizáu en 1999
@ast
im Oktober 1999 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1999/10/01)
@sk
vědecký článek publikovaný v roce 1999
@cs
wetenschappelijk artikel (gepubliceerd op 1999/10/01)
@nl
наукова стаття, опублікована в жовтні 1999
@uk
name
Disruption of the mouse necdin gene results in early post-natal lethality
@ast
Disruption of the mouse necdin gene results in early post-natal lethality
@en
Disruption of the mouse necdin gene results in early post-natal lethality
@nl
type
label
Disruption of the mouse necdin gene results in early post-natal lethality
@ast
Disruption of the mouse necdin gene results in early post-natal lethality
@en
Disruption of the mouse necdin gene results in early post-natal lethality
@nl
prefLabel
Disruption of the mouse necdin gene results in early post-natal lethality
@ast
Disruption of the mouse necdin gene results in early post-natal lethality
@en
Disruption of the mouse necdin gene results in early post-natal lethality
@nl
P2093
P3181
P356
P1433
P1476
Disruption of the mouse necdin gene results in early post-natal lethality
@en
P2093
C. L. Stewart
L. Hernandez
P2888
P304
P3181
P356
10.1038/13828
P407
P577
1999-10-01T00:00:00Z