Zhang GH - Search Results

1

The mutation spectrum of Parkinson-disease-related genes in early-onset Parkinson's disease in ethnic Chinese.

Chen YP, Yu SH, Zhang GH, Hou YB, Gu XJ, Ou RW, Shen Y, Song W, Chen XP, Zhao B, Cao B, Zhang LY, Sun MM, Liu FF, Wei QQ, Liu KC, Lin JY, Yang TM, Yang J, Wu Y, Jiang Z, Liu J, Cheng YF, Xiao Y, Su WM, Feng F, Cai YY, Li SR, Hu T, Yuan XQ, Zhou QQ, Shao N, Ma S, Shang HF. Chen YP, et al. Among authors: zhang ly, zhang gh. Eur J Neurol. 2022 Nov;29(11):3218-3228. doi: 10.1111/ene.15509. Epub 2022 Aug 4. Eur J Neurol. 2022. PMID: 35861376

2

A novel missense variant in the CASK gene causes intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia.

Wu S, Jiang C, Li J, Zhang G, Shen Y, Wang J. Wu S, et al. BMC Med Genomics. 2022 Jun 6;15(1):127. doi: 10.1186/s12920-022-01275-z. BMC Med Genomics. 2022. PMID: 35668446 Free PMC article.

3

PRSS55 is a novel potential causative gene for human male infertility.

Liu M, Jiang C, Zhang X, Zhang G, Liu M, Zheng R, Yang Y, Shen Y. Liu M, et al. Reprod Biomed Online. 2022 Sep;45(3):553-562. doi: 10.1016/j.rbmo.2022.05.016. Epub 2022 May 29. Reprod Biomed Online. 2022. PMID: 35821214

4

A novel missense mutation in GREB1L identified in a three-generation family with renal hypodysplasia/aplasia-3.

Wu S, Wang X, Dai S, Zhang G, Zhou J, Shen Y. Wu S, et al. Orphanet J Rare Dis. 2022 Nov 12;17(1):413. doi: 10.1186/s13023-022-02553-w. Orphanet J Rare Dis. 2022. PMID: 36371238 Free PMC article.

5

Deficiency of cancer/testis antigen gene CT55 causes male infertility in humans and mice.

Zhang G, Jiang C, Yang Y, Wang Y, Zhou H, Dai S, Liu M, Yang Y, Yang L, Shen Q, Zhang T, Zhang X, Yang Y, Shen Y. Zhang G, et al. Cell Death Differ. 2023 Feb;30(2):500-514. doi: 10.1038/s41418-022-01098-6. Epub 2022 Dec 8. Cell Death Differ. 2023. PMID: 36481789 Free PMC article.

6

A loss-of-function variant in ZCWPW1 causes human male infertility with sperm head defect and high DNA fragmentation.

Song Y, Guo J, Zhou Y, Wei X, Li J, Zhang G, Wang H. Song Y, et al. Reprod Health. 2024 Feb 3;21(1):18. doi: 10.1186/s12978-024-01746-9. Reprod Health. 2024. PMID: 38310235 Free PMC article.

7

Identification of a novel mutation in chibby family member 2 in a non-obstructive azoospermic patient.

Zhang G, Ye F, Yang Y, Xiong D, Zhi W, Wu Y, Sun Y, Zeng J, Liu W. Zhang G, et al. Reprod Biol. 2024 Jun;24(2):100891. doi: 10.1016/j.repbio.2024.100891. Epub 2024 May 10. Reprod Biol. 2024. PMID: 38733656

8

Novel PLCZ1 compound heterozygous mutations indicate gene dosage effect involved in total fertilisation failure after ICSI.

Li Q, Guo J, Huang G, Wu N, Chen S, Dai J, Zhang X, Zhang G, Zhi W, Yan J, Zheng R, Yan F, Yan Z, Wu L, Wu S, Ji Z, Zeng J, Lin G, Li B, Xu W. Li Q, et al. Reproduction. 2024 Sep 16;168(4):e230466. doi: 10.1530/REP-23-0466. Print 2024 Oct 1. Reproduction. 2024. PMID: 39042720 Free PMC article.

9

Metabolic profiling identifies Qrich2 as a novel glutamine sensor that regulates microtubule glutamylation and mitochondrial function in mouse sperm.

Zhang G, Guo J, Yang H, Li Q, Ye F, Song Y, Xiong D, Zeng J, Zhi W, Yuan S, Lv Y, Li T, Wang Y, Liao L, Deng D, Liu W, Xu W. Zhang G, et al. Cell Mol Life Sci. 2024 Apr 10;81(1):170. doi: 10.1007/s00018-024-05177-4. Cell Mol Life Sci. 2024. PMID: 38597976 Free PMC article.

10

CEP112 coordinates translational regulation of essential fertility genes during spermiogenesis through phase separation in humans and mice.

Zhang X, Huang G, Jiang T, Meng L, Li T, Zhang G, Wu N, Chen X, Zhao B, Li N, Wu S, Guo J, Zheng R, Ji Z, Xu Z, Wang Z, Deng D, Tan Y, Xu W. Zhang X, et al. Nat Commun. 2024 Sep 30;15(1):8465. doi: 10.1038/s41467-024-52705-8. Nat Commun. 2024. PMID: 39349455 Free PMC article.

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