The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules
about
Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2Reproduction, smell, and neurodevelopmental disorders: genetic defects in different hypogonadotropic hypogonadal syndromesNELF is a nuclear protein involved in hypothalamic GnRH neuronal migrationWDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndromeHeparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadismPROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activityNovel mechanisms of fibroblast growth factor receptor 1 regulation by extracellular matrix protein anosmin-1Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinismA locus on human chromosome 20 contains several genes expressing protease inhibitor domains with homology to whey acidic proteinKisspeptin directly stimulates gonadotropin-releasing hormone release via G protein-coupled receptor 54.CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndromeHuman GnRH deficiency: a unique disease model to unravel the ontogeny of GnRH neuronsFrom nose to brain: development of gonadotrophin-releasing hormone-1 neuronesMutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndromeDigenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadismHypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54Clinical and inheritance profiles of Kallmann syndrome in JordanCreation of non-human primate neurogenetic disease models by gene targeting and nuclear transferCell migration in the developing rodent olfactory systemThe role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndromeThe genetic basis of female reproductive disorders: etiology and clinical testingThe Regulation and Function of Fibroblast Growth Factor 8 and Its Function during Gonadotropin-Releasing Hormone Neuron DevelopmentExtracellular matrix protein anosmin promotes neural crest formation and regulates FGF, BMP, and WNT activitiesMolecular modelling and experimental studies of mutation and cell-adhesion sites in the fibronectin type III and whey acidic protein domains of human anosmin-1The role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutationsCommentary: the year in endocrine genetics for basic scientistsAxl and Tyro3 modulate female reproduction by influencing gonadotropin-releasing hormone neuron survival and migrationMolecular cloning and expression of ps20 growth inhibitor. A novel WAP-type "four-disulfide core" domain protein expressed in smooth muscleFunctional dissection of the Drosophila Kallmann's syndrome protein DmKal-1.Cellular signaling by fibroblast growth factors (FGFs) and their receptors (FGFRs) in male reproduction.Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadismThe new dysmorphology: application of insights from basic developmental biology to the understanding of human birth defects.Advances in the molecular genetics of hypogonadotropic hypogonadism.Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.Renal abnormalities in patients with Kallmann syndrome.Human genetic disorders of axon guidance.Kallmann syndrome and the link between olfactory and reproductive development.How is the Human Genome Project doing, and what have we learned so far?The genetic and molecular basis of idiopathic hypogonadotropic hypogonadism.Kisspeptin and GPR54: discovery of a novel pathway in reproduction.
P2860
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P2860
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules
description
1991 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 1991
@ast
im Oktober 1991 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1991/10/18)
@sk
vědecký článek publikovaný v roce 1991
@cs
wetenschappelijk artikel (gepubliceerd op 1991/10/18)
@nl
наукова стаття, опублікована в жовтні 1991
@uk
научни чланак (објављен 1991/10/18)
@sr
name
The candidate gene for the X-l ...... related to adhesion molecules
@ast
The candidate gene for the X-l ...... related to adhesion molecules
@en
The candidate gene for the X-l ...... related to adhesion molecules
@nl
type
label
The candidate gene for the X-l ...... related to adhesion molecules
@ast
The candidate gene for the X-l ...... related to adhesion molecules
@en
The candidate gene for the X-l ...... related to adhesion molecules
@nl
prefLabel
The candidate gene for the X-l ...... related to adhesion molecules
@ast
The candidate gene for the X-l ...... related to adhesion molecules
@en
The candidate gene for the X-l ...... related to adhesion molecules
@nl
P2093
P3181
P1433
P1476
The candidate gene for the X-l ...... related to adhesion molecules
@en
P2093
D. Caterina
D. Le Paslier
J. Levilliers
J. M. Claverie
J. P. Hardelin
P. Millasseau
S. Compain
V. Wunderle
P304
P3181
P356
10.1016/0092-8674(91)90193-3
P407
P577
1991-10-18T00:00:00Z