Yang K - Search Results

1

[Association of CMA1 gene tag single nucleotide polymorphisms with essential hypertension in Yi population from Yunnan].

Wu Y, Li Q, Yang K, Xiao C. Wu Y, et al. Among authors: yang k. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Aug;31(4):449-54. doi: 10.3760/cma.j.issn.1003-9406.2014.04.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25119908 Chinese.

2

Association of polymorphisms in prolylcarboxypeptidase and chymase genes with essential hypertension in the Chinese Han population.

Wu Y, Yang H, Yang B, Yang K, Xiao C. Wu Y, et al. Among authors: yang b, yang k, yang h. J Renin Angiotensin Aldosterone Syst. 2013 Sep;14(3):263-70. doi: 10.1177/1470320312448949. Epub 2012 Jun 7. J Renin Angiotensin Aldosterone Syst. 2013. PMID: 22679278 Free article.

3

[Predictive value of HLA-DRB1 gene for the treatment of unexplained recurrent spontaneous abortion with paternal lymphocyte alloimmunization therapy in Henan Hans].

Yang K, Zhang B, Liao S, He M, Chu Y, Li Q, Guo Q, Hou Q, Ding X. Yang K, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Jun;31(3):380-2. doi: 10.3760/cma.j.issn.1003-9406.2014.03.027. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24928025 Clinical Trial. Chinese.

4

[Association of polymorphisms of HLA-DRB1 gene with unexplained recurrent spontaneous abortion in ethnic Hans from Henan].

He M, Kang B, Liao S, Yang K, Ding X, Wu D, Guo Q, Hou Q. He M, et al. Among authors: yang k. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Aug;31(4):504-7. doi: 10.3760/cma.j.issn.1003-9406.2014.04.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25119922 Chinese.

5

[Association of MTHFR and MTRR genes polymorphisms with non-disjunctions of chromosomes 18 and 21].

Guo Q, Wang H, Yang K, Zhang B, Li T, Liao S. Guo Q, et al. Among authors: yang k. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Jun;32(3):395-9. doi: 10.3760/cma.j.issn.1003-9406.2015.03.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26037359 Chinese.

6

[Analysis of spinocerebellar ataxia type 31 related mutations among patients from mainland China].

Yang K, Zeng S, Liu Z, Shi S, Sun W, Yuan Y, Weng L, Jiang H, Shen L, Tang B, Wang J. Yang K, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Jun 10;35(3):309-313. doi: 10.3760/cma.j.issn.1003-9406.2018.03.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29896721 Chinese.

7

[Analysis of a Chinese pedigree affected with dyschromatosis symmetrica hereditaria due to a novel variant of ADAR gene].

Yang K, Hou Q, Zhang Y, Lou G, Qi N, Kang B, Zhang B, Liao S. Yang K, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Jan 10;39(1):64-67. doi: 10.3760/cma.j.cn511374-20201015-00720. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 34964970 Chinese.

8

[Analysis of a child with mental retardation due to a de novo variant of the KAT6A gene].

Ren Z, Lei X, Zeng M, Yang K, Guo Q, Yu S, Lou G, Zhang B, Wang L. Ren Z, et al. Among authors: yang k. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Dec 10;39(12):1385-1389. doi: 10.3760/cma.j.cn511374-20210903-00718. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 36453964 Chinese.

9

[Genetic analysis of a pedigree affected with Intellectual disability due to variants of two different genes].

Shi T, Ren Z, Yang K, Qin L, Lei X, Zhang B, Liao S, Wang L. Shi T, et al. Among authors: yang k. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024 Nov 10;41(11):1302-1307. doi: 10.3760/cma.j.cn511374-20240426-00257. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024. PMID: 39528279 Chinese.

10

[Analysis of CYP17A1 gene mutation in a child patient with 17 alpha-hydroxylase/17, 20-lyase deficiency].

Yang K, Zhang B, Cui SX, Guo QN, Hou QF, Li QC, Liao SX. Yang K, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Aug;30(4):439-42. doi: 10.3760/cma.j.issn.1003-9406.2013.04.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23926012 Chinese.

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