Zhan Y - Search Results

1

A novel de novo PDE4D gene mutation identified in a Chinese patient with acrodysostosis.

Zhan Y, Chen W, Feng Z, Tan C, Li M, Song Y, Zhao Z, Sheng W, Huang G. Zhan Y, et al. Genesis. 2019 Nov;57(11-12):e23336. doi: 10.1002/dvg.23336. Epub 2019 Sep 14. Genesis. 2019. PMID: 31520578

2

Engineering human ventricular heart muscles based on a highly efficient system for purification of human pluripotent stem cell-derived ventricular cardiomyocytes.

Li B, Yang H, Wang X, Zhan Y, Sheng W, Cai H, Xin H, Liang Q, Zhou P, Lu C, Qian R, Chen S, Yang P, Zhang J, Shou W, Huang G, Liang P, Sun N. Li B, et al. Among authors: zhan y. Stem Cell Res Ther. 2017 Sep 29;8(1):202. doi: 10.1186/s13287-017-0651-x. Stem Cell Res Ther. 2017. PMID: 28962583 Free PMC article.

3

Establishment of a PRKAG2 cardiac syndrome disease model and mechanism study using human induced pluripotent stem cells.

Zhan Y, Sun X, Li B, Cai H, Xu C, Liang Q, Lu C, Qian R, Chen S, Yin L, Sheng W, Huang G, Sun A, Ge J, Sun N. Zhan Y, et al. J Mol Cell Cardiol. 2018 Apr;117:49-61. doi: 10.1016/j.yjmcc.2018.02.007. Epub 2018 Feb 13. J Mol Cell Cardiol. 2018. PMID: 29452156

4

DNAH11 variants and its association with congenital heart disease and heterotaxy syndrome.

Liu S, Chen W, Zhan Y, Li S, Ma X, Ma D, Sheng W, Huang G. Liu S, et al. Among authors: zhan y. Sci Rep. 2019 Apr 30;9(1):6683. doi: 10.1038/s41598-019-43109-6. Sci Rep. 2019. PMID: 31040315 Free PMC article.

5

Functional analysis of rare variants of GATA4 identified in Chinese patients with congenital heart defect.

Zhao Z, Zhan Y, Chen W, Ma X, Sheng W, Huang G. Zhao Z, et al. Among authors: zhan y. Genesis. 2019 Nov;57(11-12):e23333. doi: 10.1002/dvg.23333. Epub 2019 Sep 12. Genesis. 2019. PMID: 31513339

6

Rapid detection of twenty-nine common Chinese glucose-6-phosphate dehydrogenase variants using a matrix-assisted laser desorption/ionization-time of flight mass spectrometry assay on dried blood spots.

Dai W, Yang T, Wang Y, Zhao Q, Zhan Y, Ye J, Han L, Qiu W, Zhang H, Liang L, Gu X, Yu Y. Dai W, et al. Among authors: zhan y. Clin Biochem. 2021 Aug;94:27-34. doi: 10.1016/j.clinbiochem.2021.04.012. Epub 2021 Apr 18. Clin Biochem. 2021. PMID: 33882285

7

Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy.

Li B, Zhan Y, Liang Q, Xu C, Zhou X, Cai H, Zheng Y, Guo Y, Wang L, Qiu W, Cui B, Lu C, Qian R, Zhou P, Chen H, Liu Y, Chen S, Li X, Sun N. Li B, et al. Among authors: zhan y. Protein Cell. 2022 Jan;13(1):65-71. doi: 10.1007/s13238-021-00843-w. Epub 2021 Apr 22. Protein Cell. 2022. PMID: 33884582 Free PMC article. No abstract available.

8

Establishing a new human hypertrophic cardiomyopathy-specific model using human embryonic stem cells.

Cai H, Li B, Bai A, Huang J, Zhan Y, Sun N, Liang Q, Xu C. Cai H, et al. Among authors: zhan y. Exp Cell Res. 2020 Feb 1;387(1):111736. doi: 10.1016/j.yexcr.2019.111736. Epub 2019 Nov 20. Exp Cell Res. 2020. PMID: 31759053

9

HPDL deficiency causes a neuromuscular disease by impairing the mitochondrial respiration.

Sun Y, Wei X, Fang F, Shen Y, Wei H, Li J, Ye X, Zhan Y, Ye X, Liu X, Yang W, Li Y, Geng X, Huang X, Ruan Y, Qin Z, Yi S, Lyu J, Fang H, Yu Y. Sun Y, et al. Among authors: zhan y. J Genet Genomics. 2021 Aug 20;48(8):727-736. doi: 10.1016/j.jgg.2021.01.009. Epub 2021 Jun 17. J Genet Genomics. 2021. PMID: 34334354

10

A 29 Mainland Chinese cohort of patients with Phelan-McDermid syndrome: genotype-phenotype correlations and the role of SHANK3 haploinsufficiency in the important phenotypes.

Xu N, Lv H, Yang T, Du X, Sun Y, Xiao B, Fan Y, Luo X, Zhan Y, Wang L, Li F, Yu Y. Xu N, et al. Among authors: zhan y. Orphanet J Rare Dis. 2020 Nov 30;15(1):335. doi: 10.1186/s13023-020-01592-5. Orphanet J Rare Dis. 2020. PMID: 33256793 Free PMC article.

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