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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| Principais autores: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2023-01-01
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| coleção: | Frontiers in Neuroanatomy |
| Assuntos: | |
| Acesso em linha: | https://www.frontiersin.org/articles/10.3389/fnana.2022.1057727/full |
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