The role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutations - Wikidata - thesis-toulmin - TriplyDB

The role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutations

The role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutations

http://www.wikidata.org/entity/Q28385113

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Genetics of isolated hypogonadotropic hypogonadism: role of GnRH receptor and other genes Modeling of human prokineticin receptors: interactions with novel small-molecule binders and potential off-target drugs Signaling role of prokineticin 2 on the estrous cycle of female mice.Discovery and cardioprotective effects of the first non-Peptide agonists of the G protein-coupled prokineticin receptor-1 The Concise Guide to PHARMACOLOGY 2013/14: G protein-coupled receptors Combined pituitary hormone deficiency: current and future status.Chaperoning G protein-coupled receptors: from cell biology to therapeutics Absence of colony stimulation factor-1 receptor results in loss of microglia, disrupted brain development and olfactory deficits GnRH, anosmia and hypogonadotropic hypogonadism--where are we?Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment.Combined pituitary hormone deficiency with unique pituitary dysplasia and morning glory syndrome related to a heterozygous PROKR2 mutation.G protein-coupled receptors involved in GnRH regulation: molecular insights from human disease.The puzzles of the prokineticin 2 pathway in human reproduction Isolated GnRH deficiency: a disease model serving as a unique prism into the systems biology of the GnRH neuronal network Clocks on top: the role of the circadian clock in the hypothalamic and pituitary regulation of endocrine physiology.Olfactory phenotypic spectrum in idiopathic hypogonadotropic hypogonadism: pathophysiological and genetic implications Novel FGFR1 and KISS1R Mutations in Chinese Kallmann Syndrome Males with Cleft Lip/Palate Evidence of the importance of the first intracellular loop of prokineticin receptor 2 in receptor function.An ancient founder mutation in PROKR2 impairs human reproduction.PK2/PKR1 Signaling Regulates Bladder Function and Sensation in Rats with Cyclophosphamide-Induced Cystitis Variations in PROKR2, but not PROK2, are associated with hypopituitarism and septo-optic dysplasia.PROK2/PROKR2 Signaling and Kallmann Syndrome.Mutation analyses in pedigrees and sporadic cases of ethnic Han Chinese Kallmann syndrome patients.Prokineticin-2 upregulation during neuronal injury mediates a compensatory protective response against dopaminergic neuronal degeneration.Absence of central circadian pacemaker abnormalities in humans with loss of function mutation in prokineticin 2 Kallmann syndrome in women: from genes to diagnosis and treatment.Olfactory system and demyelination.Paradoxical gain-of-function mutant of the G-protein-coupled receptor PROKR2 promotes early puberty Transcription Factors Sp8 and Sp9 Coordinately Regulate Olfactory Bulb Interneuron Development.Sexually dimorphic distribution of Prokr2 neurons revealed by the Prokr2-Cre mouse model.Resistance to Anti-Angiogenic Therapy in Cancer-Alterations to Anti-VEGF Pathway.Modeling mutant/wild-type interactions to ascertain pathogenicity of PROKR2 missense variants in patients with isolated GnRH deficiency.Prokr2-deficient mice display vascular dysmorphology of the fetal testes: potential implications for Kallmann syndrome aetiology.Mutation screening of SEMA3A and SEMA7A in patients with congenital hypogonadotropic hypogonadism

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The role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutations

http://www.wikidata.org/entity/Q28385113

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2011 nî lūn-bûn

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2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2011 թվականի ապրիլին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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The role of the prokineticin 2 ...... uman and murine gene mutations

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The role of the prokineticin 2 ...... uman and murine gene mutations

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Endocrine Reviews

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The role of the prokineticin 2 ...... uman and murine gene mutations

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Cecilia Martin

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Margaret G Au

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Qun-Yong Zhou

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Ravikumar Balasubramanian

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Stephanie B Seminara

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Ursula B Kaiser

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William F Crowley

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Yisrael Sidis

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Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2

The mammalian homologues of frog Bv8 are mainly expressed in spermatocytes

Human puberty - simultaneous augmented secretion of luteinizing hormone and testosterone during sleep

Identification of two prokineticin cDNAs: recombinant proteins potently contract gastrointestinal smooth muscle

The endocrine-gland-derived VEGF homologue Bv8 promotes angiogenesis in the testis: Localization of Bv8 receptors to endothelial cells

The AVIT protein family. Secreted cysteine-rich vertebrate proteins with diverse functions

Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

PROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activity

Nociceptive sensitization by the secretory protein Bv8

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3142106

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10.1210/ER.2010-0007

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2

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32

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Nelly Pitteloud

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2010-10-29T00:00:00Z

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21037178

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