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MAGEL2 gene

Known as: nM15, NDNL1, MAGEL2 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
MON-103 Chromosome 15q13.3 Microdeletion And MAGEL2 Gene Mutation In A Pediatric Patient With Extreme Obesity And Tall Stature: A Case Report
Abstract Background: Clinical practice guidelines call for consideration of genetic syndromes in evaluation of pediatric patients… 
2018
2018
The role of obesity in the fatal outcome of Schaaf–Yang syndrome: Early onset morbid obesity in a patient with a MAGEL2 mutation
Schaaf–Yang syndrome (SYS) was recently identified as a genetic condition resembling Prader–Willi syndrome. It is caused by… 
2018
2018
Magel2 Gene Mutation and Its Associated Phenotypic Features in A Five-Month-Old Female
Melanoma antigen L2 (MAGE-L2) belongs to the approximately 60 gene MAGE family, which is divided into two subsets based on… 
2014
2014
Promoter characterization and functional association with placenta of porcine MAGEL2.
2013
2013
Knockdown of CDKN1C (p57kip2) and PHLDA2 Results in Developmental Changes in Bovine Pre-implantation Embryos
Imprinted genes have been implicated in early embryonic, placental, and neonatal development and alterations in expression levels… 
2011
2011
Imprinting analysis of porcine MAGEL2 gene in two fetal stages and association analysis with carcass traits
Imprinted genes play an essential role in the regulation of fetal growth, development and function of the placenta, however only… 
2011
2011
Neural stem cell‐like gene expression in a mouse ependymoma cell line transformed by human BK polyomavirus
Ependymomas often show characteristics similar to those of neural stem cells in vivo and in vitro. However, few ependymoma cell… 
2010
2010
Lack of Association Between MAGEL2 and Schizophrenia and Mood Disorders in the Japanese Population
Several investigations have reported that abnormalities in circadian rhythms might be related with the pathophysiology of… 
2010
2010
Precise microdeletion detection of Prader-Willi Syndrome with array comparative genome hybridization.
Highly Cited
2000
Highly Cited
2000
De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch
Prader-Willi syndrome (PWS) is a neurogenetic disease characterized by infantile hypotonia, gonadal hypoplasia, obsessive… 
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