Zhang H - Search Results

1

Different mutations in the MMUT gene are associated with the effect of vitamin B12 in a cohort of 266 Chinese patients with mut-type methylmalonic acidemia: A retrospective study.

Yu Y, Shuai R, Liang L, Qiu W, Shen L, Wu S, Wei H, Chen Y, Yang C, Xu P, Chen X, Zou H, Feng J, Niu T, Hu H, Ye J, Zhang H, Lu D, Gong Z, Zhan X, Ji W, Gu X, Han L. Yu Y, et al. Among authors: zhang h. Mol Genet Genomic Med. 2021 Nov;9(11):e1822. doi: 10.1002/mgg3.1822. Epub 2021 Oct 20. Mol Genet Genomic Med. 2021. PMID: 34668645 Free PMC article.

2

[Alteration of gene expression profiles of cultured embryo rat cortex induced by phenylalanine].

Zhang HW, Gu XF. Zhang HW, et al. Sheng Li Xue Bao. 2004 Apr 25;56(2):183-91. Sheng Li Xue Bao. 2004. PMID: 15127128 Free article. Chinese.

3

[Effect of phenylalanine on genes expression of Rho GTPases: possible relevance to neuron damage induced by phenylalanine].

Zhang YJ, Zhang HW, Gu XF. Zhang YJ, et al. Zhonghua Er Ke Za Zhi. 2005 Mar;43(3):210-1. Zhonghua Er Ke Za Zhi. 2005. PMID: 15833199 Chinese. No abstract available.

4

Differential effects of phenylalanine on Rac1, Cdc42, and RhoA expression and activity in cultured cortical neurons.

Zhang Y, Zhang H, Yuan X, Gu X. Zhang Y, et al. Among authors: zhang h. Pediatr Res. 2007 Jul;62(1):8-13. doi: 10.1203/PDR.0b013e31806772be. Pediatr Res. 2007. PMID: 17515837

5

[Treatment of 2 children with mucopolysaccharidosis by allogeneic hematopoietic stem cell transplantation].

Chen J, Jiang H, Dong L, Wang Y, Luo C, Zhou M, Zhang W, Huang S, Gu X, Qiu W, Zhang H, Gu L. Chen J, et al. Among authors: zhang w, zhang h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Dec;25(6):675-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 19065530 Chinese.

6

[Diagnosis, treatment and gene mutation analysis of the first case with dihydropteridine reductase deficiency in the mainland of China].

Ye J, Qiu WJ, Han LS, Zhang HW, Zhou JD, Gao XL, Wang Y, Gu XF. Ye J, et al. Zhonghua Er Ke Za Zhi. 2008 Apr;46(4):281-5. Zhonghua Er Ke Za Zhi. 2008. PMID: 19099731 Chinese.

7

[Clinical and mutational study of a Chinese infant with isovaleric acidemia].

Qiu WJ, Gu XF, Ye J, Han LS, Bai HT, Wang X, Gao XL, Wang Y, Jin J, Zhang HW. Qiu WJ, et al. Zhonghua Er Ke Za Zhi. 2008 Jul;46(7):526-30. Zhonghua Er Ke Za Zhi. 2008. PMID: 19099814 Chinese.

8

Homozygous LMNA mutation R527C in atypical Hutchinson-Gilford progeria syndrome: evidence for autosomal recessive inheritance.

Liang L, Zhang H, Gu X. Liang L, et al. Among authors: zhang h. Acta Paediatr. 2009 Aug;98(8):1365-8. doi: 10.1111/j.1651-2227.2009.01324.x. Epub 2009 May 6. Acta Paediatr. 2009. PMID: 19432833

9

[Enzymatic diagnosis of 47 cases with mucopolysaccharidosis].

Zhang HW, Wang Y, Ye J, Qiu WJ, Han LS, Gao XL, Gu XF. Zhang HW, et al. Zhonghua Er Ke Za Zhi. 2009 Apr;47(4):276-80. Zhonghua Er Ke Za Zhi. 2009. PMID: 19555566 Chinese.

10

Recurring G12S mutation of HRAS in a Chinese child with Costello syndrome with high alkaline phosphatase level.

Zhang H, Ye J, Gu X. Zhang H, et al. Biochem Genet. 2009 Dec;47(11-12):868-72. doi: 10.1007/s10528-009-9286-7. Biochem Genet. 2009. PMID: 19669404 No abstract available.

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