Lyu J - Search Results

1

[Variant analysis for a pedigree affected with limb-girdle muscular dystrophy type 2D].

Ding L, Tang S, Li H, Xu X, Luan Z, Zhang Q, Lyu J. Ding L, et al. Among authors: lyu j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Feb 10;36(2):136-139. doi: 10.3760/cma.j.issn.1003-9406.2019.02.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30703231 Chinese.

2

[Establishment and application of quantitative detection for heteroplasmic mtDNA mutation 3243A→G].

Zhang X, Chen L, Yang Y, Zheng C, Yan J, Lu Z, Lyu J, Li W. Zhang X, et al. Among authors: lyu j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Aug;31(4):438-43. doi: 10.3760/cma.j.issn.1003-9406.2014.04.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25119906 Chinese.

3

[Investigation of a family with Kennedy disease by genetic analysis].

Fan R, Zhang L, Zhang J, Shao B, Pan D, Lyu J. Fan R, et al. Among authors: lyu j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Dec;31(6):750-3. doi: 10.3760/cma.j.issn.1003-9406.2014.06.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25449081 Chinese.

4

[Effect of mitochondrial DNA 5178 C/A polymorphism on risks for type 2 diabetes mellitus and its complications].

Yang X, Zhang Y, Ma Y, Zhao Q, Lyu J. Yang X, et al. Among authors: lyu j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Dec;32(6):855-60. doi: 10.3760/cma.j.issn.1003-9406.2015.06.023. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26663065 Chinese.

5

[Analysis of genome-wide copy number variations among fetuses with abnormalities detected by prenatal ultrasouography].

Wu K, Tang S, Chen C, Li H, Zhou L, Lyu J. Wu K, et al. Among authors: lyu j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Apr 10;34(2):178-182. doi: 10.3760/cma.j.issn.1003-9406.2017.02.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28397213 Chinese.

6

[Whole exome sequencing analysis for a Chinese pedigree affected with X-Linked intellectual disability].

Tang S, Jia M, Chen C, Li H, Hu L, Luan Z, Xu X, Lyu J. Tang S, et al. Among authors: lyu j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Jun 10;35(3):403-407. doi: 10.3760/cma.j.issn.1003-9406.2018.03.022. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29896742 Chinese.

7

[Analysis of TWNK variant in a family affected with Perrault syndrome].

Chen Z, Tang S, Li H, Xu X, Lyu J. Chen Z, et al. Among authors: lyu j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Jul 10;37(7):739-742. doi: 10.3760/cma.j.issn.1003-9406.2020.07.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32619254 Chinese.

8

[NK4 growth inhibition of human Raji lymphoma xenografts by competitive interrupting HGF/Met signal pathway].

Gao Z, Zheng X, Shen R, Zhao H, Cen D, Luo J, Hua S, Pei R, Lyu J. Gao Z, et al. Among authors: lyu j. Zhonghua Bing Li Xue Za Zhi. 2014 Aug;43(8):551-5. Zhonghua Bing Li Xue Za Zhi. 2014. PMID: 25346127 Chinese.

9

Dataset of mitochondrial genome variants in oncocytic tumors.

Lyu L, Wang Q, Song S, Zhou H, Li M, Zhou C, Jiang Z, Li L, Lyu J, Chen G, Bai Y. Lyu L, et al. Among authors: lyu j. Data Brief. 2018 Feb 16;17:1149-1152. doi: 10.1016/j.dib.2018.02.040. eCollection 2018 Apr. Data Brief. 2018. PMID: 29876471 Free PMC article.

10

Mutations in TOMM70 lead to multi-OXPHOS deficiencies and cause severe anemia, lactic acidosis, and developmental delay.

Wei X, Du M, Xie J, Luo T, Zhou Y, Zhang K, Li J, Chen D, Xu P, Jia M, Zhou H, Fang H, Lyu J, Yang Y. Wei X, et al. Among authors: lyu j. J Hum Genet. 2020 Mar;65(3):231-240. doi: 10.1038/s10038-019-0714-1. Epub 2020 Jan 6. J Hum Genet. 2020. PMID: 31907385

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