Rong Hua

发表

Bi-allelic variants in human TCTE1/DRC5 cause asthenospermia and male infertility

P. Zhou, Yunxia Cao, Siyu Liu, 2022, European Journal of Human Genetics.

Loss of DRC1 function leads to multiple morphological abnormalities of the sperm flagella and male infertility in human and mouse

Yunxia Cao, Siyu Liu, Jintao Zhang, 2021, Human molecular genetics.

In vitro testicular organogenesis from human fetal gonads produces fertilization-competent spermatids

Qi Zhou, Hao Zhang, Xuejiang Guo, 2020, Cell Research.

Sexual Dimorphism in Mouse Meiosis

Mingxi Liu, Rong Hua, 2021, Frontiers in Cell and Developmental Biology.

In vitro testicular organogenesis from human fetal gonads produces fertilization-competent spermatids

Hao Zhang, Xuejiang Guo, Zuo-min Zhou, 2020, Cell Research.

Single-cell RNA-seq uncovers dynamic processes and critical regulators in mouse spermatogenesis

Fuchou Tang, Yuxuan Zheng, Jiahao Sha, 2018, Cell Research.

FBXO47 regulates telomere-inner nuclear envelope integration by stabilizing TRF2 during meiosis

Xuejiang Guo, Yiqiang Cui, Yueshuai Guo, 2019, Nucleic acids research.

Novel FSIP2 Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans

Kuokuo Li, Yu-xia Cao, P. Zhou, 2023, International journal of biological sciences.

T-complex protein 1 subunit zeta-2 (CCT6B) deficiency induces murine teratospermia

W. Tang, Yiqiang Cui, J. Sha, 2021, PeerJ.

TCTE1 is a conserved component of the dynein regulatory complex and is required for motility and metabolism in mouse spermatozoa

R. Ramirez-Solis, Zhibin Hu, M. Matzuk, 2017, Proceedings of the National Academy of Sciences.

DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath

Kuokuo Li, Yu-xia Cao, P. Zhou, 2023, Cell Death & Disease.

Biallelic loss‐of‐function mutations in SEPTIN4 (C17ORF47), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humans

Kuokuo Li, F. Tao, P. Zhou, 2022, Human mutation.

A homozygous loss‐of‐function mutation in FBXO43 causes human non‐obstructive azoospermia

F. Tao, P. Zhou, Yiyuan Liu, 2021, Clinical genetics.

Novel HYDIN variants associated with male infertility in two Chinese families

Kuokuo Li, Yu-xia Cao, P. Zhou, 2023, Frontiers in Endocrinology.

Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humans

Kuokuo Li, Yiyuan Liu, Yunxia Cao, 2022, Human Genetics.

Bi-allelic human TEKT3 mutations cause male infertility with oligoasthenoteratozoospermia due to acrosomal hypoplasia and reduced progressive motility.

Kuokuo Li, P. Zhou, Yiyuan Liu, 2023, Human molecular genetics.

ACROSIN deficiency causes total fertilization failure in humans by preventing the sperm from penetrating the zona pellucida.

Kuokuo Li, Yiyuan Liu, Yunxia Cao, 2023, Human reproduction.

Prioritizing de novo potential non-canonical splicing variants in neurodevelopmental disorders

Kuokuo Li, Xiaomeng Wang, Guihu Zhao, 2023, EBioMedicine.

Adenylate kinase phosphate energy shuttle underlies energetic communication in flagellar axonemes.

P. Zhou, Xin Zhang, Shushu Zhou, 2024, Science China. Life sciences.