Arachidonic acid ω-hydroxylase CYP4A11: inter-ethnic variations in the 8590T>C loss-of-function variant
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[Human asthenozoospermia and structural defects of the annulus]
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Septins at the annulus of mammalian sperm
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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
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SSTY proteins co-localize with the post-meiotic sex chromatin and interact with regulators of its expression
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Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella
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Deletion of MgcRacGAP in the male germ cells impairs spermatogenesis and causes male sterility in the mouse
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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