Functional consequences of AXL sequence variants in hypogonadotropic hypogonadism. - Wikidata - awgldk - TriplyDB

Functional consequences of AXL sequence variants in hypogonadotropic hypogonadism.

Functional consequences of AXL sequence variants in hypogonadotropic hypogonadism.

http://www.wikidata.org/entity/Q37681140

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Novel Interaction of Class IIb Histone Deacetylase 6 (HDAC6) with Class IIa HDAC9 Controls Gonadotropin Releasing Hormone (GnRH) Neuronal Cell Survival and Movement Discovering Genes Essential to the Hypothalamic Regulation of Human Reproduction Using a Human Disease Model: Adjusting to Life in the "-Omics" Era.DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development.

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Functional consequences of AXL sequence variants in hypogonadotropic hypogonadism.

http://www.wikidata.org/entity/Q37681140

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 29 January 2014

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Functional consequences of AXL sequence variants in hypogonadotropic hypogonadism.

@en

Functional consequences of AXL sequence variants in hypogonadotropic hypogonadism.

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Functional consequences of AXL sequence variants in hypogonadotropic hypogonadism.

@en

Functional consequences of AXL sequence variants in hypogonadotropic hypogonadism.

@nl

prefLabel

Functional consequences of AXL sequence variants in hypogonadotropic hypogonadism.

@en

Functional consequences of AXL sequence variants in hypogonadotropic hypogonadism.

@nl

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The Journal of Clinical Endocrinology and Metabolism

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Functional consequences of AXL sequence variants in hypogonadotropic hypogonadism.

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A J Knox

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D Slavov

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L Plummer

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M E Wierman

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M Taylor

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M Xu

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R S Hodges

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S Bevers

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S Salian-Mehta

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W F Crowley

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P2860

Predicting deleterious amino acid substitutions

Structural basis for Gas6-Axl signalling.

Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism

axl, a transforming gene isolated from primary human myeloid leukemia cells, encodes a novel receptor tyrosine kinase

PROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activity

A genetic basis for functional hypothalamic amenorrhea

Growth arrest-specific gene 6 (Gas6)/adhesion related kinase (Ark) signaling promotes gonadotropin-releasing hormone neuronal survival via extracellular signal-regulated kinase (ERK) and Akt

Axl and Tyro3 modulate female reproduction by influencing gonadotropin-releasing hormone neuron survival and migration

Tyro-3 family receptors are essential regulators of mammalian spermatogenesis

Human non-synonymous SNPs: server and survey

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1452-1460

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10.1210/JC.2013-3426

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