Zhang YW - Search Results

1

KIR gene presence/absence polymorphisms and global diversity in the Kirgiz ethnic minority and populations distributed worldwide.

Wang HD, Jin XY, Guo YX, Zhang Q, Zhang YW, Wang X, Zhu BF. Wang HD, et al. Among authors: zhang q, zhang yw. Mol Biol Rep. 2019 Feb;46(1):1043-1055. doi: 10.1007/s11033-018-4563-3. Epub 2019 Jan 2. Mol Biol Rep. 2019. PMID: 30603950

2

[Identification of a novel EXT1 mutation in a pedigree affected with hereditary multiple exostosis].

Lou G, Yang K, Qin L, Zhang Y, Wang H, Hou Q, He M, Liao S. Lou G, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Feb 10;35(1):91-95. doi: 10.3760/cma.j.issn.1003-9406.2018.01.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29419870 Chinese.

3

Targeted next-generation sequencing-based molecular diagnosis of congenital hand malformations in Chinese population.

Qin L, Lou G, Guo L, Zhang Y, Wang H, Wang L, Hou Q, Liu H, Li X, Liao S. Qin L, et al. Sci Rep. 2018 Aug 24;8(1):12721. doi: 10.1038/s41598-018-30940-6. Sci Rep. 2018. PMID: 30143665 Free PMC article.

4

Selection and Validation of Reference Genes for RT-PCR Expression Analysis of Candidate Genes Involved in Morphine-Induced Conditioned Place Preference Mice.

Zhang Q, Zhang M, Li J, Xiao H, Wu D, Guo Q, Zhang Y, Wang H, Li S, Liao S. Zhang Q, et al. J Mol Neurosci. 2018 Dec;66(4):587-594. doi: 10.1007/s12031-018-1198-8. Epub 2018 Nov 1. J Mol Neurosci. 2018. PMID: 30386959

5

[A novel compound heterozygous mutation of GNPTAB gene underlying a case with mucolipidosis type II α/β].

Yang K, Lou G, Qi N, Zhang Y, Zhu H, Wang L, Wang X, Zhang B. Yang K, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jun 10;36(6):606-609. doi: 10.3760/cma.j.issn.1003-9406.2019.06.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31055817 Chinese.

6

Stub1 maintains proteostasis of master transcription factors in embryonic stem cells.

Mamun MMA, Khan MR, Zhu Y, Zhang Y, Zhou S, Xu R, Bukhari I, Thorne RF, Li J, Zhang XD, Liu G, Chen S, Wu M, Song X. Mamun MMA, et al. Cell Rep. 2022 Jun 7;39(10):110919. doi: 10.1016/j.celrep.2022.110919. Cell Rep. 2022. PMID: 35675767 Free article.

7

Functional Analysis of a Compound Heterozygous Mutation in the VPS13B Gene in a Chinese Pedigree with Cohen Syndrome.

Lou G, Ke Y, Zhang Y, Liangjie G, Shama SA, Qi N, Qin L, Liao S, Zhao Y. Lou G, et al. J Mol Neurosci. 2021 May;71(5):943-952. doi: 10.1007/s12031-020-01713-6. Epub 2020 Oct 6. J Mol Neurosci. 2021. PMID: 33025479

8

[Analysis of WAS gene mutation in a Chinese family affected with Wiskott-Aldrich syndrome].

Shi W, Hou Q, Zhang H, Lou G, Zhang Y, Liao S. Shi W, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Apr 10;35(2):207-209. doi: 10.3760/cma.j.issn.1003-9406.2018.02.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29652993 Chinese.

9

[Genetic analysis of a pedigree affected with Bartter's syndrome].

Yang K, Huo X, Zhang Y, Zhang M, Gao Y, Wu D, Lou G, Qi N, Zhang B, Wang D. Yang K, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jul 10;36(7):701-703. doi: 10.3760/cma.j.issn.1003-9406.2019.07.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31302915 Chinese.

10

Functional analysis of a novel nonsense variant c.91A>T of the TRAPPC2 gene in a Chinese family with X-linked recessive autosomal spondyloepiphyseal dysplasia tarda.

Lou G, Zhao Y, Zhao H, Zhang Y, Hao B, Qin L, Liu H, Liao S. Lou G, et al. Front Genet. 2023 Aug 25;14:1216592. doi: 10.3389/fgene.2023.1216592. eCollection 2023. Front Genet. 2023. PMID: 37693308 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,630 results

Search Page

Filters