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MKRN3 gene

Known as: MAKORIN 3, MGC88288, ZFP127 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Low Frequency of MKRN3 and DLK1 Variants in Chinese Children with Central Precocious Puberty
Background Central precocious puberty (CPP) is defined by gonadotropin-dependent development of secondary sexual characteristics… 
2018
2018
MKRN3 Levels in Girls with Central Precocious Puberty during GnRHa Treatment: A Longitudinal Study
Background: Recently, mutations of makorin RING finger protein 3 (MKRN3) have been identified in familial central precocious… 
2018
2018
Imprinted gene Zinc finger protein 127 is a novel regulator of master pluripotency transcription factor, Oct4
Induced pluripotent stem cells (iPSCs) show great promise for replacing current stem cell therapies in the field of regenerative… 
2016
2016
Conservation of imprinting of MKRN3 and NAP1L5 in rabbits.
Maternally imprinted genes of makorin ring finger protein 3 (MKRN3) and nucleosome assembly protein 1-like 5 (NAP1L5) have been… 
2016
2016
Circulating makorin ring finger protein 3 levels decline in boys before the clinical onset of puberty.
OBJECTIVE Makorin ring finger protein 3 (MKRN3) gene restrains the hypothalamic-pituitary-gonadal axis. In girls, peripheral… 
2015
2015
Low Frequency of MKRN3 Mutations in Central Precocious Puberty Among Korean Girls
Abstract Mutations of MKRN3, the gene encoding makorin RING-finger protein 3, lead to central precocious puberty (CPP). The aim… 
2015
2015
A missense mutation in MKRN3 in a Danish girl with central precocious puberty and her brother with early puberty
Background:Idiopathic central precocious puberty (ICPP) results from the premature reactivation of the hypothalamic–pituitary… 
Highly Cited
2014
Highly Cited
2014
Central precocious puberty in a girl and early puberty in her brother caused by a novel mutation in the MKRN3 gene.
CONTEXT Central precocious puberty (CPP), defined as the development of secondary sex characteristics prior to age 8 years in… 
Highly Cited
2014
Highly Cited
2014
MKRN3 Mutations in Familial Central Precocious Puberty
Loss-of-function mutations in the gene encoding the makorin RING finger protein 3 (MKRN3) have recently been reported to underlie… 
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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