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Nucleic Acids Research
|
August 22, 2022
Performance evaluation of differential splicing analysis methods and splicing analytics platform construction
Kuokuo Li, Tengfei Luo, Yan Zhu, et al.
Reproductive Biomedicine Online
|
March 27, 2021
Novel bi-allelic variants in DNAH2 cause severe asthenoteratozoospermia with multiple morphological abnormalities of the flagella
Yang Gao, Shixiong Tian, Yanwei Sha, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
October 31, 2025
Mapping the Non-Canonical Splicing Variants: Decrypting the Hidden Genetic Architecture of Idiopathic Male Infertility
Kuokuo Li, Yuge Chen, Dongdong Tang, et al.
Ebiomedicine
|
December 19, 2023
Prioritizing de novo potential non-canonical splicing variants in neurodevelopmental disorders
Kuokuo Li, Jifang Xiao, Zhengbao Ling, et al.
Reproductive Biology and Endocrinology : RB&E
|
March 29, 2025
Broadening the ARMC2 mutational phenotype: linking multiple morphological abnormalities of the Flagella to Pulmonary Manifestations in Primary Ciliary Dyskinesia
Baoyan Wu, Wenhao Zhang, Hui Yu, et al.
Human Genomics
|
September 10, 2024
Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility
Senzhao Guo, Dongdong Tang, Yuge Chen, et al.
Journal of Assisted Reproduction and Genetics
|
October 17, 2021
Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility
Kuokuo Li, Guanxiong Wang, Mingrong Lv, et al.
International Journal of Biological Sciences
|
January 12, 2023
Novel <i>FSIP2</i> Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans
Mingrong Lv, Dongdong Tang, Hui Yu, et al.
American Journal of Human Genetics
|
April 2, 2019
Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice
Wangjie Liu, Xiaojin He, Shenmin Yang, et al.
Reproductive Biology and Endocrinology : RB&E
|
January 4, 2022
Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations
Mingrong Lv, Chunyu Liu, Chunjie Ma, et al.
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Search research articles
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Showing results (91-100 of 105) with videos related to
Sort By:
Page
of 11
Nucleic Acids Research
|
August 22, 2022
Performance evaluation of differential splicing analysis methods and splicing analytics platform construction
Kuokuo Li, Tengfei Luo, Yan Zhu, et al.
Reproductive Biomedicine Online
|
March 27, 2021
Novel bi-allelic variants in DNAH2 cause severe asthenoteratozoospermia with multiple morphological abnormalities of the flagella
Yang Gao, Shixiong Tian, Yanwei Sha, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
October 31, 2025
Mapping the Non-Canonical Splicing Variants: Decrypting the Hidden Genetic Architecture of Idiopathic Male Infertility
Kuokuo Li, Yuge Chen, Dongdong Tang, et al.
Ebiomedicine
|
December 19, 2023
Prioritizing de novo potential non-canonical splicing variants in neurodevelopmental disorders
Kuokuo Li, Jifang Xiao, Zhengbao Ling, et al.
Reproductive Biology and Endocrinology : RB&E
|
March 29, 2025
Broadening the ARMC2 mutational phenotype: linking multiple morphological abnormalities of the Flagella to Pulmonary Manifestations in Primary Ciliary Dyskinesia
Baoyan Wu, Wenhao Zhang, Hui Yu, et al.
Human Genomics
|
September 10, 2024
Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility
Senzhao Guo, Dongdong Tang, Yuge Chen, et al.
Journal of Assisted Reproduction and Genetics
|
October 17, 2021
Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility
Kuokuo Li, Guanxiong Wang, Mingrong Lv, et al.
International Journal of Biological Sciences
|
January 12, 2023
Novel <i>FSIP2</i> Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans
Mingrong Lv, Dongdong Tang, Hui Yu, et al.
American Journal of Human Genetics
|
April 2, 2019
Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice
Wangjie Liu, Xiaojin He, Shenmin Yang, et al.
Reproductive Biology and Endocrinology : RB&E
|
January 4, 2022
Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations
Mingrong Lv, Chunyu Liu, Chunjie Ma, et al.
Page
of 11