Liu Y - Search Results

1

SINO Syndrome Causative KIDINS220/ARMS Gene Regulates Adipocyte Differentiation.

Zhang K, Sun W, Liu Y, Lv Y, Hou D, Lin Y, Xu W, Zhao J, Gai Z, Zhao S, Yuan Y. Zhang K, et al. Among authors: liu y. Front Cell Dev Biol. 2021 Mar 4;9:619475. doi: 10.3389/fcell.2021.619475. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33763417 Free PMC article.

2

Mutational Characteristics of Causative Genes in Chinese Hereditary Spherocytosis Patients: a Report on Fourteen Cases and a Review of the Literature.

Wang D, Song L, Shen L, Zhang K, Lv Y, Gao M, Ma J, Wan Y, Gai Z, Liu Y. Wang D, et al. Among authors: liu y. Front Pharmacol. 2021 Jul 16;12:644352. doi: 10.3389/fphar.2021.644352. eCollection 2021. Front Pharmacol. 2021. PMID: 34335240 Free PMC article.

3

Transmission of a Novel Imprinting Center Deletion Associated With Prader-Willi Syndrome Through Three Generations of a Chinese Family: Case Presentation, Differential Diagnosis, and a Lesson Worth Thinking About.

Zhang K, Liu S, Gu W, Lv Y, Yu H, Gao M, Wang D, Zhao J, Li X, Gai Z, Zhao S, Liu Y, Yuan Y. Zhang K, et al. Among authors: liu y, liu s. Front Genet. 2021 Aug 24;12:630650. doi: 10.3389/fgene.2021.630650. eCollection 2021. Front Genet. 2021. PMID: 34504512 Free PMC article.

4

[A case with autosomal dominant mental retardation type 5 due to de novo SYNGAP1 variant].

Gao Z, Lyu Y, Zhang K, Gao M, Ma J, Wang D, Gai Z, Liu Y. Gao Z, et al. Among authors: liu y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Jun 10;37(6):661-664. doi: 10.3760/cma.j.issn.1003-9406.2020.06.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32472547 Chinese.

5

[Genetic analysis of a case with Pitt-Hopkins syndrome due to variant of TCF4 gene].

Ma J, Zhang H, Zhang K, Lyu Y, Gao M, Wang D, Gai Z, Liu Y. Ma J, et al. Among authors: liu y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Nov 10;37(11):1253-1256. doi: 10.3760/cma.j.cn511374-20190725-00372. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 33179233 Chinese.

6

Generation and characterization of an induced pluripotent stem cell line SDQLCHi018-A from a congenital myasthenic syndrome patient carrying compound heterozygote mutations in RAPSN gene.

Zhang H, Zhang H, Ma Y, Lv Y, Gai Z, Liu Y. Zhang H, et al. Among authors: liu y. Stem Cell Res. 2021 Mar;51:102160. doi: 10.1016/j.scr.2021.102160. Epub 2021 Jan 8. Stem Cell Res. 2021. PMID: 33465529 Free article.

7

Reprogramming of human peripheral blood mononuclear cell (PBMC) from a patient suffering from hearing loss into iPSC line (SDQLCHi035-A) maintaining compound heterozygous variations in GJB2 gene.

Yang X, Liu N, Mu H, Lv Y, Zhang H, Li Y, Guan J, Gai Z, Liu Y. Yang X, et al. Among authors: liu y, liu n. Stem Cell Res. 2021 Mar;51:102188. doi: 10.1016/j.scr.2021.102188. Epub 2021 Jan 21. Stem Cell Res. 2021. PMID: 33517119 Free article.

8

[Analysis of ADNP gene variant in a child with Helsmoortel-van der Aa syndrome].

Ma J, Ma H, Zhang K, Lyu Y, Gao M, Wang D, Gai Z, Liu Y. Ma J, et al. Among authors: liu y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Apr 10;39(4):428-432. doi: 10.3760/cma.j.cn511374-20201113-00797. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35446982 Chinese.

9

Genotypic and phenotypic characteristics of 12 chinese children with glycogen storage diseases.

Dong R, Wei X, Zhang K, Song F, Lv Y, Gao M, Wang D, Ma J, Gai Z, Liu Y. Dong R, et al. Among authors: liu y. Front Genet. 2022 Aug 29;13:932760. doi: 10.3389/fgene.2022.932760. eCollection 2022. Front Genet. 2022. PMID: 36105079 Free PMC article.

10

Generation of an induced pluripotent stem cell line (SDQLCHi044-A) from a patient with autosomal dominant mental retardation type 5 harboring heterozygous mutation in SYNGAP1 gene.

Wang Y, Lv Y, Yang X, Li Y, Li Z, Gao Z, Gai Z, Liu Y. Wang Y, et al. Among authors: liu y. Stem Cell Res. 2022 Oct;64:102922. doi: 10.1016/j.scr.2022.102922. Epub 2022 Sep 17. Stem Cell Res. 2022. PMID: 36183676 Free article.

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