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An association study of the single-nucleotide polymorphism c190C〉T (Arg64Cys) in the human testis-specific histone variant, H3t, of Japanese patients with Sertoli cell-only syndrome 被引量:1
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作者 Toshinobu Miyamoto Masashi Iijima +5 位作者 Takeshi Shin Gaku Minase hiroto ueda Yasuaki Saijo Hiroshi Okada Kazuo Sengoku 《Asian Journal of Andrology》 SCIE CAS CSCD 2018年第5期527-528,共2页
Dear Editor,Approximately 20% of men with nonobstructive azoospermia (NOA) are diagnosed with infertility caused by genetic defects.1 These include chromosomal abnormalities, Y-chromosome microdeletions, and several... Dear Editor,Approximately 20% of men with nonobstructive azoospermia (NOA) are diagnosed with infertility caused by genetic defects.1 These include chromosomal abnormalities, Y-chromosome microdeletions, and several specific gene mutations/deletions, such as in DAZ, RBMY, USP9Y, SYCP3, HSF2, PLK4, and TEX11.1,2 Several histones have been detected in mammalian testes, and testis-specific variants are specifically and highly expressed during spermatogenesis^3. 展开更多
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