Associated Papers
Proteomic profiling of TBC1 domain family member 21-null sperms reveals the critical roles of TEKT 1 in their tail defects.
Pan PY et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists, 2024
Genetic aspects of idiopathic asthenozoospermia as a cause of male infertility.
Heidary Z et al.
Human Fertility (cambridge, England), 2020
Association of polymorphisms in tektin-t gene with idiopathic asthenozoospermia in Sichuan, China.
Zhang SH et al.
Journal of Assisted Reproduction and Genetics, 2016
Endothelial nitric oxide synthase (eNOS) T-786C, 4a4b, and G894T polymorphisms and male infertility: study for idiopathic asthenozoospermia and meta-analysis.
Song P et al.
Biology of Reproduction, 2015
A possible association of a human tektin-t gene mutation (A229V) with isolated non-syndromic asthenozoospermia: case report.
Zuccarello D et al.
Human Reproduction (oxford, England), 2008
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