About: A chorionic gonadotropin-sensitive mutation in the follicle-stimulating hormone receptor as a cause of familial gestational spontaneous ovarian hyperstimulation syndrome

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About: A chorionic gonadotropin-sensitive mutation in the follicle-stimulating hormone receptor as a cause of familial gestational spontaneous ovarian hyperstimulation syndrome Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в серпні 2003 (uk) im August 2003 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q55671001-522D1370-5F20-4C60-8CB4-5BC65BE0B567
publication date	2003-08-21 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q55671001-526003FA-07EB-4DFB-AFCC-813E602C6B91
language of work or name	English
author name string	wds:Q55671001-0E781A25-90E9-4839-ABEA-5487B4812B82 wds:Q55671001-1AE0B8AD-44A1-4995-BC1E-83755B79E760 wds:Q55671001-1E2B04DE-787B-42DB-9570-420599F9456D wds:Q55671001-1FC7D491-A8C7-45B8-8C3C-85A30290C438 wds:Q55671001-2E9E1A88-455E-4E04-A63E-C1DB7A8AD058 wds:Q55671001-6D138B75-CB9F-4DCB-8E86-86CBBC633B99 wds:Q55671001-81F4E77B-379F-4689-A206-FBE10B593ED8 wds:Q55671001-89888D9F-B1E6-4ED6-8B70-DCEB254420C4 wds:Q55671001-B2EFAF8B-B896-4E66-AC50-7D350479288C wds:Q55671001-B3CCE92E-498F-4EEE-AA80-AD26C7D28026 wds:Q55671001-D92BF7A0-2A47-4425-B203-A352EF94D8BA wds:Q55671001-DD81D5D2-7B83-46DF-9317-C41F7CF19AC0
author name string	Philippe Descamps Isabelle Beau Micheline Misrahi Patrice Rodien Loïc de Poncheville Frédérique Savagner Elisabeth Mathieu Anne Croué Agnès Desroches Claudine Vasseur Capucine Gérard Stéphanie Chaplot
rdfs:label	A chorionic gonadotropin-sensitive mutation in the follicle-stimulating hormone receptor as a cause of familial gestational spontaneous ovarian hyperstimulation syndrome (en) A chorionic gonadotropin-sensitive mutation in the follicle-stimulating hormone receptor as a cause of familial gestational spontaneous ovarian hyperstimulation syndrome (nl)
skos:prefLabel	A chorionic gonadotropin-sensitive mutation in the follicle-stimulating hormone receptor as a cause of familial gestational spontaneous ovarian hyperstimulation syndrome (en) A chorionic gonadotropin-sensitive mutation in the follicle-stimulating hormone receptor as a cause of familial gestational spontaneous ovarian hyperstimulation syndrome (nl)
name	A chorionic gonadotropin-sensitive mutation in the follicle-stimulating hormone receptor as a cause of familial gestational spontaneous ovarian hyperstimulation syndrome (en) A chorionic gonadotropin-sensitive mutation in the follicle-stimulating hormone receptor as a cause of familial gestational spontaneous ovarian hyperstimulation syndrome (nl)
author	wds:Q55671001-19B16206-38D9-4844-A84C-C66F1D069C91
author	Najiba Lahlou
title	wds:Q55671001-3D5D745F-EA97-4EDE-8C62-F980F2FF2C0C
title	A chorionic gonadotropin-sensitive mutation in the follicle-stimulating hormone receptor as a cause of familial gestational spontaneous ovarian hyperstimulation syndrome (en)
page(s)	wds:Q55671001-C6A4AC75-D09F-42EF-A340-0AFE58791DBC
page(s)	753-9
instance of	wds:Q55671001-1E483BF4-D6C7-4121-A47A-C2E4F4B9840F
instance of	scholarly article
main subject	wds:Q55671001-7ABCD9A9-4CD3-49FB-B5AA-2637DE9EE819
main subject	ovarian hyperstimulation syndrome
PubMed ID	wds:Q55671001-52E8235B-FA35-40AC-9B48-40AA1C52E573
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12930927
PubMed ID	12930927
published in	wds:Q55671001-5FC55542-F00D-4367-B59E-BF3CBBD51570
published in	The New England Journal of Medicine
issue	wds:Q55671001-4F600A57-A34B-4C83-90D1-5A291DAD11E1
volume	wds:Q55671001-47B5EF11-AC8A-4C27-8004-D6B7F3474152
issue	8
volume	349
DOI	wds:Q55671001-56E2D286-8626-4C01-A5AC-E9D1D91B27FA
DOI	http://dx.doi.org/10.1056/NEJMOA030065
DOI	10.1056/NEJMOA030065
ResearchGate publication ID	wds:Q55671001-4AFAEC8B-C9DD-40DF-A4D9-822A1FCFB38F
ResearchGate publication ID	10603548
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55671001
is cites work of	Mutations in human gonadotropin and gonadotropin-receptor genes Comparative sequence and structural analyses of G-protein-coupled receptor crystal structures and implications for molecular models Ovarian hyperstimulation, hyperprolactinaemia and LH gonadotroph adenoma Action of molecular switches in GPCRs--theoretical and experimental studies. Novel insights on thyroid-stimulating hormone receptor signal transduction Ignored adult primary hypothyroidism presenting chiefly with persistent ovarian cysts: a need for increased awareness A case of ovarian enlargement in severe primary hypothyroidism and review of the literature. Constitutive activation of G protein-coupled receptors and diseases: insights into mechanisms of activation and therapeutics Follicle stimulating hormone receptor mutations and reproductive disorders Evidence for activity-regulated hormone-binding cooperativity across glycoprotein hormone receptor homomers New insights into the pathophysiology of ovarian hyperstimulation syndrome. What makes the difference between spontaneous and iatrogenic syndrome? G protein-coupled receptors: mutations and endocrine diseases Plasma levels of soluble vascular endothelial growth factor receptor-1 may determine the onset of early and late ovarian hyperstimulation syndrome. The genetic basis of female reproductive disorders: etiology and clinical testing Understanding ovarian hyperstimulation syndrome Endocrinology: fertility hormone in repose Phenotypic and pharmacogenetic aspects of ovulation induction in WHO II anovulatory women Thrombosis of subclavian and internal jugular veins following severe ovarian hyperstimulation syndrome: a case report Pharmacogenetics of controlled ovarian hyperstimulation. Fish FSH receptors bind LH: how to make the human FSH receptor to be more fishy? Female mice expressing constitutively active mutants of FSH receptor present with a phenotype of premature follicle depletion and estrogen excess Nephrotic sydrome developing in severe ovarian hyperstimulation syndrome The molecular basis of impaired follicle-stimulating hormone action: evidence from human mutations and mouse models Intrinsic differences in the response of the human lutropin receptor versus the human follitropin receptor to activating mutations. Identification of the first germline mutation in the extracellular domain of the follitropin receptor responsible for spontaneous ovarian hyperstimulation syndrome Symposium: Update on prediction and management of OHSS. Genetics of ovarian hyperstimulation syndrome Diseases associated with mutations of the human lutropin receptor Cullen's sign and massive ovarian enlargement secondary to primary hypothyroidism in a patient with a normal FSH receptor. The pathophysiology of ovarian hyperstimulation syndrome: an unrecognized compartment syndrome Identification and in vitro characterization of follicle stimulating hormone (FSH) receptor variants associated with abnormal ovarian response to FSH Novel FSH receptor mutation in a case of spontaneous ovarian hyperstimulation syndrome with successful pregnancy outcome The Follitropin Receptor: Matching Structure and Function In Vitro Effects of the Endocrine Disruptor p,p'-DDT on Human Follitropin Receptor. Hyperplasia in glands with hormone excess An intracellular loop (IL2) residue confers different basal constitutive activities to the human lutropin receptor and human thyrotropin receptor through structural communication between IL2 and helix 6, via helix 3. Multicystic ovaries and pituitary pseudo-adenoma associated with primary hypothyroidism. Transgenic mutant D567G but not wild-type human FSH receptor overexpression provides FSH-independent and promiscuous glycoprotein hormone Sertoli cell signaling

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