Septins at the annulus of mammalian sperm
Abstract
Arachidonic acid ω-hydroxylase CYP4A11: inter-ethnic variations in the 8590T>C loss-of-function variant
Abstract
[Human asthenozoospermia and structural defects of the annulus]
Abstract
Functional interaction of the cystic fibrosis transmembrane conductance regulator with members of the SLC26 family of anion transporters (SLC26A8 and SLC26A9): physiological and pathophysiological relevance
Abstract
SSTY proteins co-localize with the post-meiotic sex chromatin and interact with regulators of its expression
Abstract
Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella
Abstract
Deletion of MgcRacGAP in the male germ cells impairs spermatogenesis and causes male sterility in the mouse
Abstract
Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia
Abstract
Loss-of-function mutations in LRRC6, a gene essential for proper axonemal assembly of inner and outer dynein arms, cause primary ciliary dyskinesia
Abstract
[Morphological defects of sperm flagellum implicated in human male infertility]
Abstract