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Yan-wei Sha

Showing results (21-30 of 31) with videos related to

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Gene|April 24, 2018
Two cases of complex balanced autosomal translocations associated with severe oligozoospermiaYan-Wei Sha, Li-Bin Mei, Zhi-Yong Ji, et al.
Systems Biology in Reproductive Medicine|April 17, 2018
Identification of a novel mutation in FGFR1 gene in patients with Kallmann syndrome by high throughput sequencingBao-Fang Jin, Zhi-Yong Ji, Zhi-Ying Su, et al.
Oncotarget|February 9, 2018
Sperm-egg fusion disorder in a Chinese male patient was associated with a rare <i>ADAM20</i> variantYan-Wei Sha, Xiaohui Xu, Zhi-Yong Ji, et al.
International Journal of Fertility & Sterility|March 18, 2016
A Case of Bilateral Testicular Tumors Subsequently Diagnosed as Congenital Adrenal Hyperplasia Due to 21-Hydroxylase DeficiencyYan-Kun Sha, Yan-Wei Sha, Lu Ding, et al.
Molecular Genetics & Genomic Medicine|August 10, 2019
Novel IFT140 variants cause spermatogenic dysfunction in humansXiong Wang, Yan-Wei Sha, Wen-Ting Wang, et al.
Gene|January 15, 2018
Genetic contribution of SUN5 mutations to acephalic spermatozoa in Fujian ChinaYan-Wei Sha, Xiaohui Xu, Zhi-Yong Ji, et al.
Gene|October 12, 2017
A novel mutation in HAUS7 results in severe oligozoospermia in two brothersLin Li, Yan-Wei Sha, Zhi-Ying Su, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|December 27, 2017
Novel Mutations in CFAP44 and CFAP43 Cause Multiple Morphological Abnormalities of the Sperm Flagella (MMAF)Yan-Wei Sha, Xiong Wang, Xiaohui Xu, et al.
Asian Journal of Andrology|July 2, 2021
Biallelic mutations in spermatogenesis and centriole-associated 1 like (<i>SPATC1L</i>) cause acephalic spermatozoa syndrome and male infertilityYou-Zhu Li, Na Li, Wen-Sheng Liu, et al.
Clinical Genetics|October 10, 2018
Biallelic mutations in PMFBP1 cause acephalic spermatozoaYan-Wei Sha, Xiong Wang, Xiaohui Xu, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Gene|April 24, 2018
Two cases of complex balanced autosomal translocations associated with severe oligozoospermiaYan-Wei Sha, Li-Bin Mei, Zhi-Yong Ji, et al.
Systems Biology in Reproductive Medicine|April 17, 2018
Identification of a novel mutation in FGFR1 gene in patients with Kallmann syndrome by high throughput sequencingBao-Fang Jin, Zhi-Yong Ji, Zhi-Ying Su, et al.
Oncotarget|February 9, 2018
Sperm-egg fusion disorder in a Chinese male patient was associated with a rare <i>ADAM20</i> variantYan-Wei Sha, Xiaohui Xu, Zhi-Yong Ji, et al.
International Journal of Fertility & Sterility|March 18, 2016
A Case of Bilateral Testicular Tumors Subsequently Diagnosed as Congenital Adrenal Hyperplasia Due to 21-Hydroxylase DeficiencyYan-Kun Sha, Yan-Wei Sha, Lu Ding, et al.
Molecular Genetics & Genomic Medicine|August 10, 2019
Novel IFT140 variants cause spermatogenic dysfunction in humansXiong Wang, Yan-Wei Sha, Wen-Ting Wang, et al.
Gene|January 15, 2018
Genetic contribution of SUN5 mutations to acephalic spermatozoa in Fujian ChinaYan-Wei Sha, Xiaohui Xu, Zhi-Yong Ji, et al.
Gene|October 12, 2017
A novel mutation in HAUS7 results in severe oligozoospermia in two brothersLin Li, Yan-Wei Sha, Zhi-Ying Su, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|December 27, 2017
Novel Mutations in CFAP44 and CFAP43 Cause Multiple Morphological Abnormalities of the Sperm Flagella (MMAF)Yan-Wei Sha, Xiong Wang, Xiaohui Xu, et al.
Asian Journal of Andrology|July 2, 2021
Biallelic mutations in spermatogenesis and centriole-associated 1 like (<i>SPATC1L</i>) cause acephalic spermatozoa syndrome and male infertilityYou-Zhu Li, Na Li, Wen-Sheng Liu, et al.
Clinical Genetics|October 10, 2018
Biallelic mutations in PMFBP1 cause acephalic spermatozoaYan-Wei Sha, Xiong Wang, Xiaohui Xu, et al.
Pageof 4