The puzzles of the prokineticin 2 pathway in human reproduction-Reference-Cited by-同舟云学术

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The puzzles of the prokineticin 2 pathway in human reproduction

Published:2011-10 Issue:1-2 Volume:346 Page:44-50
ISSN:0303-7207
Container-title:Molecular and Cellular Endocrinology
language:en
Short-container-title:Molecular and Cellular Endocrinology

Author:

Balasubramanian Ravikumar,Plummer Lacey,Sidis Yisrael,Pitteloud Nelly,Martin Cecilia,Zhou Qun-Yong,Crowley William F.

Publisher

Elsevier BV

Subject

Endocrinology,Molecular Biology,Biochemistry

Reference47 articles.

1. Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome;Abreu;J. Clin. Endocrinol. Metab.,2008

2. Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia;Aston;J. Androl.,2009

3. Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1;Canto;J. Androl.,2009

4. Identification and pharmacological characterization of prokineticin 2 beta as a selective ligand for prokineticin receptor 1;Chen;Mol. Pharmacol.,2005

5. Regulation of prokineticin 2 expression by light and the circadian clock;Cheng;BMC Neurosci.,2005

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4. Increased expression of prokineticin 2 and its receptor in endometrium of recurrent implantation failure patients decreased the expression of MMP9 important for decidualization;Reproductive Biology and Endocrinology;2022-05-02

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