Relationship of SNP of H2BFWT gene to male infertility in a Chinese population with idiopathic spermatogenesis impairment
Author:
Publisher
Informa UK Limited
Subject
Health, Toxicology and Mutagenesis,Clinical Biochemistry,Biochemistry
Link
http://www.tandfonline.com/doi/pdf/10.3109/1354750X.2012.677066
Reference25 articles.
1. Histone variants--the structure behind the function
2. The NH 2 Tail of the Novel Histone Variant H2BFWT Exhibits Properties Distinct from Conventional H2B with Respect to the Assembly of Mitotic Chromosomes
3. The search for SNPs, CNVs, and epigenetic variants associated with the complex disease of male infertility
4. Novel human testis-specific histone H2B encoded by the interrupted gene on the X chromosome
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2. H2BFWT Variations in Sperm DNA and Its Correlation to Pregnancy;International Journal of Molecular Sciences;2024-05-31
3. Proteomic and genetic dissection of testis-specific histone 2B in infertile men reveals its contribution to meiosis and sperm motility;F&S Science;2022-11
4. Impact of tobacco smoking in association with H2BFWT , PRM1 and PRM2 genes variants on male infertility;Andrologia;2022-10-10
5. Correlation of Single Nucleotide Polymorphisms of PRM1, PRM2, PYGO2, and DAZL Genes with Male Infertility in North West of Iran;Türk Üroloji Dergisi/Turkish Journal of Urology;2022-10-03
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