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GNRH1 protein, human

Known as: Gonadotropin Releasing Hormone 1, GnRH I, GNRH1 precursor protein, human 
Specifically expressed as a 92-aa 10-kDa precursor in a small population of hypothalamic neurons by human GNRH1 Gene (GnRH Family), Gonadotropin… 
National Institutes of Health

Related topics

Related topics

10 relations
GNRH1 geneGNRH1 wt AlleleHypothalamic HormonesHypothalamic structure

Broader (1)

Gonadorelin

Papers overview

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2020
2020
İdiyopatik Hipogonadotropik Hipogonadizme Neden Olan GNRH1 c.99delA Delesyonunun Klinik ve Genetik İncelemesi
GNRH1 , gonadotropin salgilatici hormon ailesinin uyesi olan bir preprohormonu kodlamaktadir ve idiyopatik hipogonadotropik… 
2017
2017
Explorer R 31 C GNRH 1 mutation and congenital hypogonadotropic hypogonadism
Normosmic congenital hypogonadotropic hypogonadism (nCHH) is a rare reproductive disease leading to lack of puberty and… 
2015
2015
Frequency of Mutations in The GnRH Receptor Gene in Pakistani Patients With Hypogonadotropic Hypogonadism
The hypothalamic gonadotropic releasing hormone (GnRH) is a key regulator in normal puberty, sexual development and function. The… 
2014
2014
Idiopathic Hypogonadotropic Hypogonadism due to a GNRH1 Mutation
Conclusion: We here described a frameshift GNRH1 mutation which is predicted to lead a total failure of GnRH synthesis. This… 
2011
2011
한국인 중추성 성조숙증 여아에서 GNRH1, GNRHR 및 GPR54 유전자의 다형성 분석
2010
2010
New mutations Heterozygous orthodenticle homeobox 2 mutations are associated with variable pituitary phenotype
Significant advances have been made in the field of pituitary development, pituitary tumor biology and pituitary signaling, as… 
2009
2009
Genetics: GNRH1 mutations identified in patients with IHH
idiopathic hypogonadotropic hypogonadism (iHH) is a condition characterized by the failure to undergo puberty in association with… 
2006
2006
Maintenance of Spermatogenesis by the Activated Human (Asp567Gly) FSH Receptor During Testicular Regression Due to Hormonal Withdrawal1
Abstract The first activating mutation of the FSH receptor (FSHR*D567G) was identified in a gonadotropin-deficient… 
2004
2004
Acanthosis nigricans as skin manifestation of polycystic ovariessyndrome in primary infertile females
Objective: The present work is to record the frequency of Acanthosis Nigricans (AN) among patients with Polycystic Ovaries… 
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