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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Frontiers Media S.A.,
2023-01-01T00:00:00Z.
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A1234.567 |
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