Pubertal development and regulation. - Wikidata - awgldk - TriplyDB

Pubertal development and regulation.

Pubertal development and regulation.

http://www.wikidata.org/entity/Q37538376

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Nakalanga Syndrome: Clinical Characteristics, Potential Causes, and Its Relationship with Recently Described Nodding Syndrome.Loss of microRNA-7a2 induces hypogonadotropic hypogonadism and infertility.Improved final predicted height with the injection of leuprolide in children with earlier puberty: A retrospective cohort study.Reproductive and metabolic features during puberty in sons of women with polycystic ovary syndrome.Mkrn3 functions as a novel ubiquitin E3 ligase to inhibit Nptx1 during puberty initiation.Birth weight and prepubertal body size predict menarcheal age in India, Peru, and Vietnam.Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty.Effect of puberty on multiple sclerosis risk and course.Global DNA methylation changes spanning puberty are near predicted estrogen-responsive genes and enriched for genes involved in endocrine and immune processes.Complex genetics of female fertility Central Precocious Puberty in a Child With Metachromatic Leukodystrophy Circulating Pro-Uroguanylin Levels In Children And Their Relation To Obesity, Sex And Puberty

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Pubertal development and regulation.

http://www.wikidata.org/entity/Q37538376

description

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 03 February 2016

@en

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

Pubertal development and regulation.

@en

Pubertal development and regulation.

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type

label

Pubertal development and regulation.

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Pubertal development and regulation.

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prefLabel

Pubertal development and regulation.

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Pubertal development and regulation.

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S2213-8587(15)00418-0

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The Lancet: Diabetes & Endocrinology

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Pubertal development and regulation.

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Ana Paula Abreu

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Ursula B Kaiser

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P2860

A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region

WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome

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

A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction

Variations in pattern of pubertal changes in girls

Variations in the pattern of pubertal changes in boys

Meta-analysis of genome-wide association data identifies two loci influencing age at menarche

Mutations of the KISS1 gene in disorders of puberty

Genetic variation in LIN28B is associated with the timing of puberty

Genome-wide association studies identify loci associated with age at menarche and age at natural menopause

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254-264

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scholarly article

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10.1016/S2213-8587(15)00418-0

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3

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4

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2016-02-03T00:00:00Z

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26852256

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5192018

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