Genetics of puberty (Q37050042)

17 August 2017

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title

Genetics of puberty (English)

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17 August 2017

Allan E Herbison

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publication date

10 December 2007

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17 August 2017

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17 August 2017

68 Suppl 5

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17 August 2017

75-79

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Variation in the timing of puberty: clinical spectrum and genetic investigation

17 August 2017

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Developmental aspect of the gonadotropin-releasing hormone system.

21 January 2018

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Kallmann syndrome: adhesion, afferents, and anosmia

21 January 2018

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Neurobiological mechanisms of the onset of puberty in primates

21 January 2018

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Activating Gsalpha mutations: analysis of 113 patients with signs of McCune-Albright syndrome--a European Collaborative Study

21 January 2018

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Molecular pathogenesis of Kallmann's syndrome.

21 January 2018

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The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics.

21 January 2018

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Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome

21 January 2018

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Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.

21 January 2018

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Characterization of the human nasal embryonic LHRH factor gene, NELF, and a mutation screening among 65 patients with idiopathic hypogonadotropic hypogonadism (IHH)

21 January 2018

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Abnormal development of the olfactory bulb and reproductive system in mice lacking prokineticin receptor PKR2

21 January 2018

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Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism

21 January 2018

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A leptin missense mutation associated with hypogonadism and morbid obesity.

21 January 2018

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

21 January 2018

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Delayed puberty and hypogonadism caused by mutations in the follicle-stimulating hormone beta-subunit gene

21 January 2018

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Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency

21 January 2018

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Mutations in PROP1 cause familial combined pituitary hormone deficiency

21 January 2018

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Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

21 January 2018

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Clinical and molecular genetics of the human GnRH receptor.

21 January 2018

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Hypogonadotropic hypogonadism.

21 January 2018

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Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54

21 January 2018

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The GPR54 gene as a regulator of puberty

21 January 2018

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Activation of gonadotropin-releasing hormone neurons by kisspeptin as a neuroendocrine switch for the onset of puberty.

21 January 2018

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Advanced vaginal opening and precocious activation of the reproductive axis by KiSS-1 peptide, the endogenous ligand of GPR54.

21 January 2018

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Two novel missense mutations in g protein-coupled receptor 54 in a patient with hypogonadotropic hypogonadism.

21 January 2018

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21 January 2018

Identifiers

DOI

10.1159/000110583

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17 August 2017

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PubMed ID

18174715