Yang H - Search Results

1

Phenotype-Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy.

Tan D, Yang H, Yuan Y, Bonnemann C, Chang X, Wang S, Wu Y, Wu X, Xiong H. Tan D, et al. Among authors: yang h. PLoS One. 2015 Jun 22;10(6):e0129699. doi: 10.1371/journal.pone.0129699. eCollection 2015. PLoS One. 2015. PMID: 26098624 Free PMC article.

2

[Study on hsp 70 gene level in cultured smooth muscle cells and aorta from SHR and WKY rats].

Yang HP, Wang SN, Yang H, Zhou H, Yang YZ, Tang J, Zhou AR. Yang HP, et al. Among authors: yang yz, yang h. Shi Yan Sheng Wu Xue Bao. 1995 Mar;28(1):31-5. Shi Yan Sheng Wu Xue Bao. 1995. PMID: 7597867 Chinese.

3

Wild-type p53 gene expression in cultured smooth muscle cells from SHR and WKY rats.

Yang HP, Tang NM, Wang SH, Tang J. Yang HP, et al. Chin Med J (Engl). 1993 Jun;106(6):471-3. Chin Med J (Engl). 1993. PMID: 8222901 No abstract available.

4

[Clinical and mutation analyses of a Chinese family with Bethlem myopathy].

Yang HP, Zhang YZ, Ding J, Jiao H, Lü JL, Xiong H. Yang HP, et al. Zhonghua Yi Xue Za Zhi. 2012 Oct 30;92(40):2820-4. Zhonghua Yi Xue Za Zhi. 2012. PMID: 23290209 Chinese.

5

Novel collagen VI mutations identified in Chinese patients with Ullrich congenital muscular dystrophy.

Zhang YZ, Zhao DH, Yang HP, Liu AJ, Chang XZ, Hong DJ, Bonnemann C, Yuan Y, Wu XR, Xiong H. Zhang YZ, et al. Among authors: yang hp. World J Pediatr. 2014 May;10(2):126-32. doi: 10.1007/s12519-014-0481-1. Epub 2014 May 7. World J Pediatr. 2014. PMID: 24801232

6

Founder mutation causes classical Fukuyama congenital muscular dystrophy (FCMD) in Chinese patients.

Yang H, Kobayashi K, Wang S, Jiao H, Xiao J, Toda T, Wu X, Xiong H. Yang H, et al. Brain Dev. 2015 Oct;37(9):880-6. doi: 10.1016/j.braindev.2015.02.010. Epub 2015 Mar 23. Brain Dev. 2015. PMID: 25814170

7

Clinical and molecular genetic analysis of a family with late-onset LAMA2-related muscular dystrophy.

Ding J, Zhao D, Du R, Zhang Y, Yang H, Liu J, Yan C, Zhang F, Xiong H. Ding J, et al. Among authors: yang h. Brain Dev. 2016 Feb;38(2):242-9. doi: 10.1016/j.braindev.2015.08.005. Epub 2015 Aug 21. Brain Dev. 2016. PMID: 26304763

8

[Analysis of clinical features of 6 patients with infantile type glycogen storage disease type II].

Ding J, Huang Y, Yang H, Zhang Q, Hou X, Liu X, Yang Y, Xiong H. Ding J, et al. Among authors: yang h, yang y. Zhonghua Er Ke Za Zhi. 2015 Jun;53(6):436-41. Zhonghua Er Ke Za Zhi. 2015. PMID: 26310554 Chinese.

9

[Application of targeted capture technology and next generation sequencing in molecular diagnosis of inherited myopathy].

Fu X, Liu A, Yang H, Wei C, Ding J, Wang S, Wang J, Yuan Y, Jiang Y, Xiong H. Fu X, et al. Among authors: yang h. Zhonghua Er Ke Za Zhi. 2015 Oct;53(10):741-6. Zhonghua Er Ke Za Zhi. 2015. PMID: 26758109 Chinese.

10

Analysis of phenotype, enzyme activity and genotype of Chinese patients with POMT1 mutation.

Yang H, Manya H, Kobayashi K, Jiao H, Fu X, Xiao J, Li X, Wang J, Jiang Y, Toda T, Endo T, Wu X, Xiong H. Yang H, et al. J Hum Genet. 2016 Aug;61(8):753-9. doi: 10.1038/jhg.2016.42. Epub 2016 May 19. J Hum Genet. 2016. PMID: 27193224

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