Results 201 to 203 of about 4,038 (203)

Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism

Molecular Human Reproduction, 2000
exaly  

A novel INSL3 mutation associated with human cryptorchidism

2001
MARIN P., FERLIN, ALBERTO, MORO, ENRICO, ROSSI A. BARTOLONI L., ROSSATO, MARCO, FORESTA, CARLO   +5 more
openaire   +3 more sources

INSL3 promotes macrophage polarization to an immunosuppressive phenotype via the cAMP downstream signaling pathway and Akt/mTOR pathway

International Immunopharmacology
exaly