Genetics defects in GNRH1: A paradigm of hypothalamic congenital gonadotropin deficiency-Reference-Cited by-同舟云学术

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Genetics defects in GNRH1: A paradigm of hypothalamic congenital gonadotropin deficiency

Published:2010-12 Issue: Volume:1364 Page:3-9
ISSN:0006-8993
Container-title:Brain Research
language:en
Short-container-title:Brain Research

Author:

Bouligand Jérôme,Ghervan Cristina,Trabado Séverine,Brailly-Tabard Sylvie,Guiochon-Mantel Anne,Young Jacques

Publisher

Elsevier BV

Subject

Developmental Biology,Clinical Neurology,Molecular Biology,General Neuroscience

Reference48 articles.

1. Isolation of the gene and hypothalamic cDNA for the common precursor of gonadotropin-releasing hormone and prolactin release-inhibiting factor in human and rat;Adelman;Proc. Natl Acad. Sci. USA,1986

2. Purification, amino acid composition and N-terminus of the hypothalamic luteinizing hormone releasing factor (LRF) of ovine origin;Amoss;Biochem. Biophys. Res. Commun.,1971

3. Hypophysial responses to continuous and intermittent delivery of hypopthalamic gonadotropin-releasing hormone;Belchetz;Science,1978

4. Isolated familial hypogonadotropic hypogonadism and a GNRH1 mutation;Bouligand;N Engl J. Med.,2009

5. Non-syndromic congenital hypogonadotropic hypogonadism: clinical presentation and genotype–phenotype relationships;Brioude;Eur. J. Endocrinol.,2010

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3. Complete Idiopathic Hypogonadotropic Hypogonadism due to Homozygous GNRH1 Mutations in the Mutational Hot Spots in the Region Encoding the Decapeptide;Hormone Research in Paediatrics;2015-11-24

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