Publication Year mod 5 Tax: 2020-2021

The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility

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Tubulin glycylation controls axonemal dynein activity, flagellar beat, and male fertility

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Genetics of teratozoospermia: Back to the head

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Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility

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Biallelic variants in <i>MAATS1</i> encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertility

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TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus Flagella

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The genetic architecture of morphological abnormalities of the sperm tail

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Deletions on mouse Yq lead to upregulation of multiple X- and Y-linked transcripts in spermatids

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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

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Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa

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