Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype.
about
Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndromeNecdin-related MAGE proteins differentially interact with the E2F1 transcription factor and the p75 neurotrophin receptorIdentification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking dupliconsSmall 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 brainThe comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13A necdin/MAGE-like gene in the chromosome 15 autism susceptibility region: expression, imprinting, and mapping of the human and mouse orthologuesGenetics of Prader-Willi syndrome and Prader-Will-Like syndromeMagel2 is required for leptin-mediated depolarization of POMC neurons in the hypothalamic arcuate nucleus in miceMagel2, a Prader-Willi syndrome candidate gene, modulates the activities of circadian rhythm proteins in cultured cellsUSP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental DisorderLoss of magel2, a candidate gene for features of Prader-Willi syndrome, impairs reproductive function in mice.Necdin promotes ubiquitin-dependent degradation of PIAS1 SUMO E3 ligaseThe role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome.The human obesity gene map: the 2001 update.The MAGE proteins: emerging roles in cell cycle progression, apoptosis, and neurogenetic disease.Regulatory elements associated with paternally-expressed genes in the imprinted murine Angelman/Prader-Willi syndrome domain.The Smc5/Smc6/MAGE complex confers resistance to caffeine and genotoxic stress in Drosophila melanogaster.The human obesity gene map: the 2002 update.Impaired hypothalamic regulation of endocrine function and delayed counterregulatory response to hypoglycemia in Magel2-null mice.High concentrations of long interspersed nuclear element sequence distinguish monoallelically expressed genes.Biological functions of melanoma-associated antigensRumMAGE-D the members: structure and function of a new adaptor family of MAGE-D proteins.Targeting the endocannabinoid/CB1 receptor system for treating obesity in Prader-Willi syndrome.Leptin signaling defects in a mouse model of Prader-Willi syndrome: An orphan genetic obesity syndrome no more?Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.A Comprehensive Guide to the MAGE Family of Ubiquitin Ligases.Relative expression of type II MAGE genes during retinoic acid-induced neural differentiation of mouse embryonic carcinoma P19 cells: a comparative real-time PCR analysis.Cellular and disease functions of the Prader-Willi Syndrome gene MAGEL2.Magel2-null mice are hyper-responsive to setmelanotide, a melanocortin 4 receptor agonist.Loss of Magel2 impairs the development of hypothalamic Anorexigenic circuits.Imprinting analysis of porcine MAGEL2 gene in two fetal stages and association analysis with carcass traits.Recommendations for the investigation of animal models of Prader-Willi syndrome.Oxytocin and Prader-Willi Syndrome.Progressive postnatal decline in leptin sensitivity of arcuate hypothalamic neurons in the Magel2-null mouse model of Prader-Willi syndrome.Genome-wide analysis of gene transcription in the hypothalamus.Muscle dysfunction caused by loss of Magel2 in a mouse model of Prader-Willi and Schaaf-Yang syndromes.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.The Human Obesity Gene Map: The 2004 Update
P2860
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P2860
Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
2000年學術文章
@zh
2000年學術文章
@zh-hant
name
Expression and imprinting of M ...... s murine imprinting phenotype.
@en
Expression and imprinting of M ...... s murine imprinting phenotype.
@nl
type
label
Expression and imprinting of M ...... s murine imprinting phenotype.
@en
Expression and imprinting of M ...... s murine imprinting phenotype.
@nl
prefLabel
Expression and imprinting of M ...... s murine imprinting phenotype.
@en
Expression and imprinting of M ...... s murine imprinting phenotype.
@nl
P2093
P356
P1476
Expression and imprinting of M ...... s murine imprinting phenotype.
@en
P2093
Brannan CI
Chamberlain SJ
Hernandez L
Stewart CL
P304
P356
10.1093/HMG/9.12.1813
P577
2000-07-01T00:00:00Z