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Chaofeng Tu

Showing results (31-40 of 64) with videos related to

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Scientific Reports|November 3, 2019
Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagellaChaofeng Tu, Hongchuan Nie, Lanlan Meng, et al.
Clinical Genetics|December 17, 2022
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotypeJiaxin He, Qiang Liu, Weili Wang, et al.
Journal of Medical Genetics|April 7, 2022
Biallelic <i>CFAP61</i> variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermiaTongyao Hu, Lanlan Meng, Chen Tan, et al.
Autophagy|February 23, 2021
TDRD7 participates in lens development and spermiogenesis by mediating autophagosome maturationChaofeng Tu, Haiyu Li, Xuyang Liu, et al.
Journal of Assisted Reproduction and Genetics|March 16, 2024
Identification of novel homozygous asthenoteratospermia-causing ARMC2 mutations associated with multiple morphological abnormalities of the sperm flagellaSiyi Zhao, Qiong Liu, Lilan Su, et al.
Journal of Assisted Reproduction and Genetics|April 3, 2024
Novel SPEF2 variants cause male infertility and likely primary ciliary dyskinesiaWenqing Lu, Yong Li, Lanlan Meng, et al.
Carcinogenesis|August 14, 2018
Identification of genomic alterations in nasopharyngeal carcinoma and nasopharyngeal carcinoma-derived Epstein-Barr virus by whole-genome sequencingChaofeng Tu, Zhaoyang Zeng, Peng Qi, et al.
Human Molecular Genetics|August 20, 2021
Loss-of-function missense variant of AKAP4 induced male infertility through reduced interaction with QRICH2 during sperm flagella developmentGuohui Zhang, Dongyan Li, Chaofeng Tu, et al.
Molecular Cytogenetics|February 15, 2018
Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literatureHaiyu Li, Juan Du, Wen Li, et al.
Journal of Assisted Reproduction and Genetics|December 14, 2022
Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertilityYunhao Li, Yong Li, Ying Wang, et al.
Pageof 7

Showing results (31-40 of 64) with videos related to

Sort By:
Pageof 7
Scientific Reports|November 3, 2019
Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagellaChaofeng Tu, Hongchuan Nie, Lanlan Meng, et al.
Clinical Genetics|December 17, 2022
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotypeJiaxin He, Qiang Liu, Weili Wang, et al.
Journal of Medical Genetics|April 7, 2022
Biallelic <i>CFAP61</i> variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermiaTongyao Hu, Lanlan Meng, Chen Tan, et al.
Autophagy|February 23, 2021
TDRD7 participates in lens development and spermiogenesis by mediating autophagosome maturationChaofeng Tu, Haiyu Li, Xuyang Liu, et al.
Journal of Assisted Reproduction and Genetics|March 16, 2024
Identification of novel homozygous asthenoteratospermia-causing ARMC2 mutations associated with multiple morphological abnormalities of the sperm flagellaSiyi Zhao, Qiong Liu, Lilan Su, et al.
Journal of Assisted Reproduction and Genetics|April 3, 2024
Novel SPEF2 variants cause male infertility and likely primary ciliary dyskinesiaWenqing Lu, Yong Li, Lanlan Meng, et al.
Carcinogenesis|August 14, 2018
Identification of genomic alterations in nasopharyngeal carcinoma and nasopharyngeal carcinoma-derived Epstein-Barr virus by whole-genome sequencingChaofeng Tu, Zhaoyang Zeng, Peng Qi, et al.
Human Molecular Genetics|August 20, 2021
Loss-of-function missense variant of AKAP4 induced male infertility through reduced interaction with QRICH2 during sperm flagella developmentGuohui Zhang, Dongyan Li, Chaofeng Tu, et al.
Molecular Cytogenetics|February 15, 2018
Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literatureHaiyu Li, Juan Du, Wen Li, et al.
Journal of Assisted Reproduction and Genetics|December 14, 2022
Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertilityYunhao Li, Yong Li, Ying Wang, et al.
Pageof 7