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Sex differences in the coexpression of prokineticin receptor 2 and gonadal steroids receptors in mice

Loss-of-function mutations in prokineticin 2 (PROK2) and the cognate receptor prokineticin receptor 2 (PROKR2) genes have been implicated in reproductive deficits characteristic of Kallmann Syndrome (KS). Knock out of Prokr2 gene produces the KS-like phenotype in mice resulting in impaired migration...

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Detalles Bibliográficos
Autores principales:	Cisneros-Larios, Brenda, Elias, Carol Fuzeti
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2023
Materias:	Neuroscience
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9853983/ https://www.ncbi.nlm.nih.gov/pubmed/36686573 http://dx.doi.org/10.3389/fnana.2022.1057727

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