Hu Z - Search Results

1

GIGYF1 disruption associates with autism and impaired IGF-1R signaling.

Chen G, Yu B, Tan S, Tan J, Jia X, Zhang Q, Zhang X, Jiang Q, Hua Y, Han Y, Luo S, Hoekzema K, Bernier RA, Earl RK, Kurtz-Nelson EC, Idleburg MJ, Madan-Khetarpal S, Clark R, Sebastian J, Fernandez-Jaen A, Alvarez S, King SD, Ramos LL, Santos MLS, Martin DM, Brooks D, Symonds JD, Cutcutache I, Pan Q, Hu Z, Yuan L, Eichler EE, Xia K, Guo H. Chen G, et al. Among authors: hu z. J Clin Invest. 2022 Oct 3;132(19):e159806. doi: 10.1172/JCI159806. J Clin Invest. 2022. PMID: 35917186 Free PMC article.

2

[A mutation IVS2+1G>A in EXT2 gene causes hereditary multiple exostoses].

Hu ZM, Zheng D, Pan Q, Yang YF, Zhao TL, Liu XP, Wu LQ, Jiang DG, Xia K, Xia JH. Hu ZM, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Apr;21(2):97-100. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15079787 Chinese.

3

[Mutation analysis of ganglioside-induced differentiation associated protein-1 gene in Chinese Charcot-Marie-Tooth disease].

Zhang RX, Tang BS, Zi XH, Luo W, Xia K, Pan Q, Long ZG, Hu ZM, Li XB. Zhang RX, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Jun;21(3):207-10. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15192818 Chinese.

4

[Mutation screening in selected exons of myosin 7a gene in prelingual non-syndromic hearing impairment patients].

Hu P, Xie DH, Xiao ZA, Wu WJ, Ge SL, Hu ZM, Xia K. Hu P, et al. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2004 Sep;39(9):538-42. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2004. PMID: 15606003 Chinese.

5

[ATM gene mutations in Chinese patients with ataxia telangiectasia].

Jiang H, Tang B, Hu Z, Xia K, Xu B, Tang J, Shen L. Jiang H, et al. Among authors: hu z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Apr;22(2):121-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15793768 Chinese.

6

[Studies on PANK2 gene mutations in Chinese patients with Hallervorden-Spatz syndrome].

Zhang Y, Tang B, Guo J, Long Z, Xia K, Pan Q, Hu Z, Wu D, Tang J, Chen T, Yan X. Zhang Y, et al. Among authors: hu z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Apr;22(2):189-91. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15793782 Chinese.

7

[Research on clinical characteristics and ATM gene mutations in Chinese patients with ataxia-telangiectasia].

Jiang H, Tang BS, Hu ZM, Xia K, Xu B, Tang JG. Jiang H, et al. Zhonghua Yi Xue Za Zhi. 2005 Apr 27;85(16):1117-20. Zhonghua Yi Xue Za Zhi. 2005. PMID: 16029571 Chinese.

8

Mutation analysis of the small heat shock protein 27 gene in chinese patients with Charcot-Marie-Tooth disease.

Tang B, Liu X, Zhao G, Luo W, Xia K, Pan Q, Cai F, Hu Z, Zhang C, Chen B, Zhang F, Shen L, Zhang R, Jiang H. Tang B, et al. Among authors: hu z. Arch Neurol. 2005 Aug;62(8):1201-7. doi: 10.1001/archneur.62.8.1201. Arch Neurol. 2005. PMID: 16087758

9

[Mutation analysis of small heat shock protein 27 gene in Chinese patients with Charcot-Marie-Tooth disease].

Liu XM, Tang BS, Zhao GH, Xia K, Zhang FF, Pan Q, Cai F, Hu ZM, Zhang C, Chen B, Shen L, Zhang RX, Jiang H. Liu XM, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Oct;22(5):510-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16215937 Chinese.

10

[Genetic linkage analysis in localizing a gene of autosomal dominant familial dilated cardiomyopathy with conduction defect].

Xu W, Zhang BR, Hu ZM, Pan Q, Liu XP, Liang DS, Wu LQ, Cai F, Long ZG, Xia K, Xia JH. Xu W, et al. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2005 Oct;30(5):510-4. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2005. PMID: 16320577 Chinese.

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