Gu XF - Search Results

1

A study of gene expression profiles of cultured embryonic rat neurons induced by phenylalanine.

Zhang H, Gu XF. Zhang H, et al. Among authors: gu xf. Metab Brain Dis. 2005 Mar;20(1):61-72. doi: 10.1007/s11011-005-2477-y. Metab Brain Dis. 2005. PMID: 15918551

2

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

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

4

Phenylalanine activates the mitochondria-mediated apoptosis through the RhoA/Rho-associated kinase pathway in cortical neurons.

Zhang Y, Gu X, Yuan X. Zhang Y, et al. Eur J Neurosci. 2007 Mar;25(5):1341-8. doi: 10.1111/j.1460-9568.2007.05404.x. Eur J Neurosci. 2007. PMID: 17425560

5

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. Pediatr Res. 2007 Jul;62(1):8-13. doi: 10.1203/PDR.0b013e31806772be. Pediatr Res. 2007. PMID: 17515837

6

[Effect of phenylalanine on the Nogo-66 receptor expression in the cortical neurons of rats].

Huang CJ, Gu XF, Zhang YJ, Ye J, Li D, Huang LS. Huang CJ, et al. Among authors: gu xf. Zhongguo Dang Dai Er Ke Za Zhi. 2008 Apr;10(2):211-5. Zhongguo Dang Dai Er Ke Za Zhi. 2008. PMID: 18433550 Chinese.

7

[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. 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.

8

[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. Among authors: gu xf. Zhonghua Er Ke Za Zhi. 2008 Apr;46(4):281-5. Zhonghua Er Ke Za Zhi. 2008. PMID: 19099731 Chinese.

9

[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. Among authors: gu xf. Zhonghua Er Ke Za Zhi. 2008 Jul;46(7):526-30. Zhonghua Er Ke Za Zhi. 2008. PMID: 19099814 Chinese.

10

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. 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

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