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Qu, Ronggui
38
results:
Search for persons
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Online (38)
Mediatypes
Articles (Online) (22)
OpenAccess-fulltext (16)
Sorted by: Relevance
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1
CCDC28A deficiency causes sperm head defects, reduced sperm..:
Zhou, Hongbin
;
Zhang, Zhihua
;
Qu, Ronggui
...
Cellular and Molecular Life Sciences. 81 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1007/..
?
2
ADGB variants cause asthenozoospermia and male infertility:
Qu, Ronggui
;
Zhang, Zhihua
;
Wu, Ling
...
Human Genetics. 142 (2023) 6 - p. 735-748 , 2023
Link:
https://doi.org/10.1007/..
?
3
Bi‐allelic pathogenic variants in PABPC1L cause oocyte matu..:
Wang, Weijie
;
Guo, Jing
;
Shi, Juanzi
...
EMBO Molecular Medicine. 15 (2023) 6 - p. , 2023
Link:
https://doi.org/10.15252..
?
4
Genetic screening in patients with ovarian dysfunction:
Zeng, Yang
;
Li, Lin
;
Li, Qingchun
...
Clinical Genetics. 103 (2022) 3 - p. 352-357 , 2022
Link:
https://doi.org/10.1111/..
?
5
IQUB deficiency causes male infertility by affecting the ac..:
Zhang, Zhihua
;
Zhou, Hongbin
;
Deng, Xujing
...
Human Reproduction. 38 (2022) 1 - p. 168-179 , 2022
Link:
https://doi.org/10.1093/..
?
6
Bi-allelic variants in KCNU1 cause impaired acrosome reacti..:
Liu, Ruyi
;
Yan, Zheng
;
Fan, Yong
...
Human Reproduction. 37 (2022) 7 - p. 1394-1405 , 2022
Link:
https://doi.org/10.1093/..
?
7
Homozygous variants in PANX1 cause human oocyte death and f..:
Wang, Weijie
;
Qu, Ronggui
;
Dou, Qian
...
European Journal of Human Genetics. 29 (2021) 9 - p. 1396-1404 , 2021
Link:
https://doi.org/10.1038/..
?
8
Cryo-EM structure of human heptameric Pannexin 1 channel:
Qu, Ronggui
;
Dong, Lili
;
Zhang, Jilin
...
Cell Research. 30 (2020) 5 - p. 446-448 , 2020
Link:
https://doi.org/10.1038/..
?
9
Resolvin E1 in Follicular Fluid Acts as a Potential Biomark..:
Zhang, Yijing
;
Zhu, Zhongyi
;
Li, He
...
Frontiers in Endocrinology. 11 (2020) - p. , 2020
Link:
https://doi.org/10.3389/..
?
10
Disruption inACTL7Acauses acrosomal ultrastructural defects..:
Xin, Aijie
;
Qu, Ronggui
;
Chen, Guowu
...
Science Advances. 6 (2020) 35 - p. , 2020
Link:
https://doi.org/10.1126/..
?
11
A homozygous mutation in CMAS causes autosomal recessive in..:
Qu, Ronggui
;
Sang, Qing
;
Wang, Xueqian
...
Annals of Human Genetics. 84 (2019) 1 - p. 46-53 , 2019
Link:
https://doi.org/10.1111/..
?
12
MicroRNA-451 is downregulated in the follicular fluid of wo..:
Li, Xiong
;
Zhang, Wenbi
;
Fu, Jing
...
Reproductive Biology and Endocrinology. 17 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/..
?
13
Screening of miRNAs in human follicular fluid reveals an in..:
Fu, Jing
;
Qu, Rong-gui
;
Zhang, Yi-jing
...
Reproductive BioMedicine Online. 37 (2018) 1 - p. 25-32 , 2018
Link:
https://doi.org/10.1016/..
?
14
Identification of a novel homozygous mutation in MYO3A in a..:
Qu, Ronggui
;
Sang, Qing
;
Xu, Yao
...
International Journal of Pediatric Otorhinolaryngology. 84 (2016) - p. 43-47 , 2016
Link:
https://doi.org/10.1016/..
?
15
ILDR1 deficiency causes degeneration of cochlear outer hair..:
Sang, Qing
;
Li, Wen
;
Xu, Yao
...
Biology Open. 4 (2015) 4 - p. 411-418 , 2015
Link:
https://doi.org/10.1242/..
1-15