Ronggui Qu

发表

Mutations in TUBB8 and Human Oocyte Meiotic Arrest.

B. Li, E. Nogales, Mohan L Gupta, 2016, The New England journal of medicine.

Disruption in ACTL7A causes acrosomal ultrastructural defects in human and mouse sperm as a novel male factor inducing early embryonic arrest

F. Zhang, Ling Zhang, Xiaoxi Sun, 2020, Science Advances.

Identification of a novel homozygous mutation in MYO3A in a Chinese family with DFNB30 non-syndromic hearing impairment.

Lei Wang, Li Jin, Ruizhi Feng, 2016, International journal of pediatric otorhinolaryngology.

Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest.

Y. Kuang, Zheng Yan, Ruizhi Feng, 2016, American journal of human genetics.

Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos

Zhaogui Sun, Y. Kuang, Zheng Yan, 2016, Journal of Medical Genetics.

Cryo-EM structure of human heptameric Pannexin 1 channel

Xuekui Yu, Ronggui Qu, Lei Wang, 2020, Cell Research.

Expression of ENPP3 in human cyclic endometrium: a novel molecule involved in embryo implantation.

Xiaoxi Sun, Ronggui Qu, Yongwei Gu, 2018, Reproduction, fertility, and development.

MiRNA-320 in the human follicular fluid is associated with embryo quality in vivo and affects mouse embryonic development in vitro

R. Chai, Ruizhi Feng, Qing Sang, 2015, Scientific Reports.

Homozygous variants in PANX1 cause human oocyte death and female infertility

Qiaoli Li, Qing Sang, Ronggui Qu, 2021, European Journal of Human Genetics.

Screening of miRNAs in human follicular fluid reveals an inverse relationship between microRNA-663b expression and blastocyst formation.

Qing Sang, Ronggui Qu, Lei Wang, 2018, Reproductive biomedicine online.

Resolvin E1 in Follicular Fluid Acts as a Potential Biomarker and Improves Oocyte Developmental Competence by Optimizing Cumulus Cells

Mingjiang Zhu, Xiaoxi Sun, Ronggui Qu, 2020, Frontiers in Endocrinology.

MicroRNA-451 is downregulated in the follicular fluid of women with endometriosis and influences mouse and human embryonic potential

Xiaoxi Sun, Ronggui Qu, Yijuan Sun, 2019, Reproductive Biology and Endocrinology.

Genetic screening in patients with ovarian dysfunction

K. Choy, Ling Wu, Qingyuan Li, 2022, Clinical genetics.

A homozygous mutation in CMAS causes autosomal recessive intellectual disability in a Kazakh family

Qing Sang, Yao Xu, Ronggui Qu, 2020, Annals of human genetics.

Identification of a novel compound heterozygous mutation in PTPRQ in a DFNB84 family with prelingual sensorineural hearing impairment

Huawei Li, Ruizhi Feng, Qing Sang, 2015, Molecular Genetics and Genomics.

Cryo-EM structure of human heptameric Pannexin 1 channel

Xuekui Yu, Ronggui Qu, Lei Wang, 2020, Cell Research.

ILDR1 deficiency causes degeneration of cochlear outer hair cells and disrupts the structure of the organ of Corti: a mouse model for human DFNB42

Huawei Li, Ruizhi Feng, Qing Sang, 2015, Biology Open.

ILDR 1 deficiency causes degeneration of cochlear outer hair cells and disrupts the structure of the organ of Corti : a mouse model for human DFNB 42

Huawei Li, Ruizhi Feng, Qing Sang, 2015 .

ADGB variants cause asthenozoospermia and male infertility

Ling Wu, Qiaoli Li, Y. Kuang, 2023, Human Genetics.

Identification of a novel compound heterozygous mutation in PTPRQ in a DFNB84 family with prelingual sensorineural hearing impairment

Huawei Li, Ruizhi Feng, Qing Sang, 2015, Molecular Genetics and Genomics.

Bi‐allelic pathogenic variants in PABPC1L cause oocyte maturation arrest and female infertility

Qiaoli Li, Juan-zi Shi, Qing Sang, 2023, EMBO molecular medicine.

CCDC28A deficiency causes sperm head defects, reduced sperm motility and male infertility in mice

Qing Sang, Ronggui Qu, Biaobang Chen, 2024, Cellular and molecular life sciences : CMLS.