Yuan J - Search Results

1

A COL4A5 Missense Variant in a Han-Chinese Family with X-linked Alport Syndrome.

Wu Y, Guo Y, Yuan J, Xu H, Chen Y, Zhang H, Yuan M, Deng H, Yuan L. Wu Y, et al. Among authors: yuan j, yuan l, yuan m. Curr Mol Med. 2019;19(10):758-765. doi: 10.2174/1566524019666190906144214. Curr Mol Med. 2019. PMID: 31490752

2

[Evaluation of the renal replacement therapy on the liver transplant patients with acute renal failure].

YUAN JZ, YE QF, ZHANG H, MING YZ, GUI M, JI Y, Sun J, WANG JW, REN ZH, CHENG K, ZHAO YJ, SUN PL, WU K, JI LZ. YUAN JZ, et al. Zhonghua Gan Zang Bing Za Zhi. 2009 May;17(5):334-7. Zhonghua Gan Zang Bing Za Zhi. 2009. PMID: 19497196 Chinese.

3

Identification of a novel COL4A5 mutation in a Chinese family with X-linked Alport syndrome using exome sequencing.

Guo Y, Yuan J, Liang H, Xiao J, Xu H, Yuan L, Gao K, Wu B, Tang Y, Li X, Deng H. Guo Y, et al. Among authors: yuan j, yuan l. Mol Biol Rep. 2014 Jun;41(6):3631-5. doi: 10.1007/s11033-014-3227-1. Epub 2014 Feb 13. Mol Biol Rep. 2014. PMID: 24522658

4

A novel COL4A5 mutation identified in a Chinese Han family using exome sequencing.

Xiu X, Yuan J, Deng X, Xiao J, Xu H, Zeng Z, Guan L, Xu F, Deng S. Xiu X, et al. Among authors: yuan j. Biomed Res Int. 2014;2014:186048. doi: 10.1155/2014/186048. Epub 2014 Jul 6. Biomed Res Int. 2014. PMID: 25110662 Free PMC article.

5

Identification of a novel GJA3 mutation in congenital nuclear cataract.

Yuan L, Guo Y, Yi J, Xiao J, Yuan J, Xiong W, Xu H, Yang Z, Zhang J, Deng H. Yuan L, et al. Among authors: yuan j. Optom Vis Sci. 2015 Mar;92(3):337-42. doi: 10.1097/OPX.0000000000000518. Optom Vis Sci. 2015. PMID: 25635993

6

A novel FN1 variant associated with familial hematuria: TBMN?

Yuan L, Xu H, Yuan J, Deng X, Xiong W, Yang Z, Huang Y, Deng H. Yuan L, et al. Among authors: yuan j. Clin Biochem. 2016 Jul;49(10-11):816-20. doi: 10.1016/j.clinbiochem.2016.01.026. Epub 2016 Mar 9. Clin Biochem. 2016. PMID: 26968105

7

A novel heterozygous COL4A4 missense mutation in a Chinese family with focal segmental glomerulosclerosis.

Wu Y, Hu P, Xu H, Yuan J, Yuan L, Xiong W, Deng X, Deng H. Wu Y, et al. Among authors: yuan j, yuan l. J Cell Mol Med. 2016 Dec;20(12):2328-2332. doi: 10.1111/jcmm.12924. Epub 2016 Jul 29. J Cell Mol Med. 2016. PMID: 27469977 Free PMC article.

8

Identification of a novel collagen type IV alpha-4 (COL4A4) mutation in a Chinese family with autosomal dominant Alport syndrome using exome sequencing.

Deng S, Xu H, Yuan J, Xiao J, Yuan L, Deng X, Guan L, Zhu A, Rong P, Zhang J, Deng H. Deng S, et al. Among authors: yuan j, yuan l. Indian J Med Res. 2016 Aug;144(2):200-205. doi: 10.4103/0971-5916.195026. Indian J Med Res. 2016. PMID: 27934798 Free PMC article.

9

Identification of a Missense Mutation in the α-galactosidase A Gene in a Chinese Family with Fabry Disease.

Wu Y, Xia H, Yuan J, Xu H, Deng X, Liu J, Zhang H, Deng H. Wu Y, et al. Among authors: yuan j. Curr Genomics. 2018 Jan;19(1):70-75. doi: 10.2174/1389202918666170915155033. Curr Genomics. 2018. PMID: 29491734 Free PMC article. Review.

10

Identification of COL4A4 variants in Chinese patients with familial hematuria.

Gao Y, Yuan L, Yuan J, Yang Y, Wang J, Chen Y, Zhang H, Ai Y, Deng H. Gao Y, et al. Among authors: yuan j, yuan l. Front Genet. 2023 Jan 9;13:1064491. doi: 10.3389/fgene.2022.1064491. eCollection 2022. Front Genet. 2023. PMID: 36699462 Free PMC article.

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