Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Chaofeng Tu

Showing results (51-60 of 64) with videos related to

Pageof 7
Sort By:
Journal of Virology|June 23, 2017
Genome-Wide Analysis of 18 Epstein-Barr Viruses Isolated from Primary Nasopharyngeal Carcinoma Biopsy SpecimensChaofeng Tu, Zhaoyang Zeng, Peng Qi, et al.
American Journal of Human Genetics|December 21, 2021
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and miceChen Tan, Lanlan Meng, Mingrong Lv, et al.
Journal of Assisted Reproduction and Genetics|February 18, 2026
A common cause of non-obstructive azoospermia: biallelic MEI1 variants and implications for infertility diagnosticsChen Tan, Tiantian Wang, Chaofeng Tu, et al.
Cell Discovery|August 21, 2023
Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progressionChaofeng Tu, Junfei Wen, Weili Wang, et al.
Biology of Reproduction|April 24, 2026
SPEM2 deficiency disrupts spermiation leading to oligoasthenoteratozoospermia and male infertility†Yong Li, Wenqing Lu, Lanlan Meng, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|June 25, 2026
The KIF6-RBP Complex Orchestrates mRNA Transport Required for Sperm Flagellar AssemblyChunbo Xie, Sibing Yi, Xinle Lin, et al.
Reproductive Biomedicine Online|April 13, 2025
Women with FSHR-inactivating mutations causing resistant ovarian syndrome benefit from oocyte in-vitro maturationXiao-Feng Li, Jing Hu, Ling Liu, et al.
Science China. Life Sciences|February 3, 2026
Deficiency of primate-specific TFDP3 causes male infertility with oligoasthenoteratozoospermia in humans and cynomolgus monkeysChunyu Liu, Chaofeng Tu, Peng Li, et al.
Human Reproduction Open|February 5, 2024
Bi-allelic variants in <i>DNAH3</i> cause male infertility with asthenoteratozoospermia in humans and miceGui-Quan Meng, Yaling Wang, Chen Luo, et al.
American Journal of Human Genetics|July 8, 2021
Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and miceChaofeng Tu, Jiangshan Cong, Qianjun Zhang, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
Journal of Virology|June 23, 2017
Genome-Wide Analysis of 18 Epstein-Barr Viruses Isolated from Primary Nasopharyngeal Carcinoma Biopsy SpecimensChaofeng Tu, Zhaoyang Zeng, Peng Qi, et al.
American Journal of Human Genetics|December 21, 2021
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and miceChen Tan, Lanlan Meng, Mingrong Lv, et al.
Journal of Assisted Reproduction and Genetics|February 18, 2026
A common cause of non-obstructive azoospermia: biallelic MEI1 variants and implications for infertility diagnosticsChen Tan, Tiantian Wang, Chaofeng Tu, et al.
Cell Discovery|August 21, 2023
Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progressionChaofeng Tu, Junfei Wen, Weili Wang, et al.
Biology of Reproduction|April 24, 2026
SPEM2 deficiency disrupts spermiation leading to oligoasthenoteratozoospermia and male infertility†Yong Li, Wenqing Lu, Lanlan Meng, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|June 25, 2026
The KIF6-RBP Complex Orchestrates mRNA Transport Required for Sperm Flagellar AssemblyChunbo Xie, Sibing Yi, Xinle Lin, et al.
Reproductive Biomedicine Online|April 13, 2025
Women with FSHR-inactivating mutations causing resistant ovarian syndrome benefit from oocyte in-vitro maturationXiao-Feng Li, Jing Hu, Ling Liu, et al.
Science China. Life Sciences|February 3, 2026
Deficiency of primate-specific TFDP3 causes male infertility with oligoasthenoteratozoospermia in humans and cynomolgus monkeysChunyu Liu, Chaofeng Tu, Peng Li, et al.
Human Reproduction Open|February 5, 2024
Bi-allelic variants in <i>DNAH3</i> cause male infertility with asthenoteratozoospermia in humans and miceGui-Quan Meng, Yaling Wang, Chen Luo, et al.
American Journal of Human Genetics|July 8, 2021
Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and miceChaofeng Tu, Jiangshan Cong, Qianjun Zhang, et al.
Pageof 7