Abstract
Tubulin glycylation controls axonemal dynein activity, flagellar beat, and male fertility.
Abstract
Genetics of teratozoospermia: Back to the head.
Abstract
Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility.
Abstract
Biallelic variants in MAATS1 encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertility.
Abstract
TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus Flagella.
Abstract
The genetic architecture of morphological abnormalities of the sperm tail.
Abstract
A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.
Abstract
Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility.
Abstract
The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility.
Abstract