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Dongdong Tang

Showing results (101-110 of 105) with videos related to

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Science China. Life Sciences|May 18, 2024
Adenylate kinase phosphate energy shuttle underlies energetic communication in flagellar axonemesHuan Wu, Yanman Zhang, Yuqian Li, et al.
Journal of Medical Genetics|November 12, 2018
Novel homozygous <i>CFAP69</i> mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagellaXiaojin He, Weiyu Li, Huan Wu, et al.
Journal of Medical Genetics|February 14, 2020
Homozygous mutations in <i>DZIP1</i> can induce asthenoteratospermia with severe MMAFMingrong Lv, Wangjie Liu, Wangfei Chi, et al.
American Journal of Human Genetics|August 14, 2020
Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and MiceXiaojin He, Chunyu Liu, Xiaoyu Yang, et al.
American Journal of Human Genetics|February 16, 2023
Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew modelsChunyu Liu, Wei Si, Chaofeng Tu, et al.
Pageof 11

Showing results (101-110 of 105) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 105 results.
Science China. Life Sciences|May 18, 2024
Adenylate kinase phosphate energy shuttle underlies energetic communication in flagellar axonemesHuan Wu, Yanman Zhang, Yuqian Li, et al.
Journal of Medical Genetics|November 12, 2018
Novel homozygous <i>CFAP69</i> mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagellaXiaojin He, Weiyu Li, Huan Wu, et al.
Journal of Medical Genetics|February 14, 2020
Homozygous mutations in <i>DZIP1</i> can induce asthenoteratospermia with severe MMAFMingrong Lv, Wangjie Liu, Wangfei Chi, et al.
American Journal of Human Genetics|August 14, 2020
Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and MiceXiaojin He, Chunyu Liu, Xiaoyu Yang, et al.
American Journal of Human Genetics|February 16, 2023
Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew modelsChunyu Liu, Wei Si, Chaofeng Tu, et al.
Pageof 11