Associated Papers
Novel genetic variants of sperm chromatin compaction regulators are associated with non-obstructive azoospermia in Indian men.
Dutta S et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology, 2025
Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations.
Fragoza R et al.
Nature Communications, 2019
31515488 (PubMed )
Supplement: 41467_2019_11959_MOESM11_ESM.xlsx › SD7_-_Drug_Targets
The association between TNP2 gene polymorphisms and Iranian infertile men with varicocele: A case-control study.
Heidari MM et al.
International Journal of Reproductive Biomedicine, 2019
Association study of six SNPs in PRM1, PRM2 and TNP2 genes in iranian infertile men with idiopathic azoospermia.
Siasi E et al.
Iranian Journal of Reproductive Medicine, 2012
Analysis of sperm nuclear protein gene polymorphisms and DNA integrity in infertile men.
Venkatesh S et al.
Systems Biology in Reproductive Medicine, 2011
Mutations in the protamine locus: association with spermatogenic failure?
Imken L et al.
Molecular Human Reproduction, 2009
Identification of novel polymorphisms in the nuclear protein genes and their relationship with human sperm protamine deficiency and severe male infertility.
Aoki VW et al.
Fertility and Sterility, 2006
Single-nucleotide polymorphisms and mutation analyses of the TNP1 and TNP2 genes of fertile and infertile human male populations.
Miyagawa Y et al.
Journal of Andrology, 0
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