Bu DF - Search Results

1

[Proteins structure changes of COL4A5 gene point mutations and structure-phenotype relations in Alport syndrome].

Wang YF, Ding J, Wang F, Bu DF. Wang YF, et al. Among authors: bu df. Zhonghua Er Ke Za Zhi. 2004 Aug;42(8):589-94. Zhonghua Er Ke Za Zhi. 2004. PMID: 15347445 Chinese.

2

[Genealogical research of hereditary nonpolyposis colorectal cancer].

Wang Z, Zhao B, Xu Y, Wan Y, Bu D, Huang Y. Wang Z, et al. Zhonghua Wai Ke Za Zhi. 2002 Jun;40(6):411-3. Zhonghua Wai Ke Za Zhi. 2002. PMID: 12139794 Chinese.

3

Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia.

Yang Y, Wang Y, Li S, Xu Z, Li H, Ma L, Fan J, Bu D, Liu B, Fan Z, Wu G, Jin J, Ding B, Zhu X, Shen Y. Yang Y, et al. J Med Genet. 2004 Mar;41(3):171-4. doi: 10.1136/jmg.2003.012153. J Med Genet. 2004. PMID: 14985375 Free PMC article.

4

Effect of glycine substitutions on alpha5(IV) chain structure and structure-phenotype correlations in Alport syndrome.

Wang YF, Ding J, Wang F, Bu DF. Wang YF, et al. Among authors: bu df. Biochem Biophys Res Commun. 2004 Apr 16;316(4):1143-9. doi: 10.1016/j.bbrc.2004.02.168. Biochem Biophys Res Commun. 2004. PMID: 15044104

5

[Expression of the partial protein encoded by mutated COL4A5 gene and analysis of the structure by circular dichroism].

Wang YF, Ding J, Bu DF, Wang F. Wang YF, et al. Among authors: bu df. Beijing Da Xue Xue Bao Yi Xue Ban. 2004 Apr;36(2):185-9. Beijing Da Xue Xue Bao Yi Xue Ban. 2004. PMID: 15100740 Free article. Chinese.

6

[NOTCH3 gene mutations in four Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].

Wang ZX, Lu H, Zhang Y, Bu DF, Niu XY, Zhang Z, Huang YN, Yuan Y. Wang ZX, et al. Among authors: bu df. Zhonghua Yi Xue Za Zhi. 2004 Jul 17;84(14):1175-80. Zhonghua Yi Xue Za Zhi. 2004. PMID: 15387979 Chinese.

7

Novel GLA gene mutations in two Chinese families with classic Fabry disease.

Wang ZX, Zhang Y, Bu DF, Zhang W, Yuan Y. Wang ZX, et al. Among authors: bu df. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Oct;22(5):489-92. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16215932

8

[NPHS1 mutations in a Chinese family with congenital nephrotic syndrome].

Shi Y, Ding J, Liu JC, Wang H, Bu DF. Shi Y, et al. Among authors: bu df. Zhonghua Er Ke Za Zhi. 2005 Nov;43(11):805-9. Zhonghua Er Ke Za Zhi. 2005. PMID: 16316524 Chinese.

9

A novel CFTR mutation found in a Chinese patient with cystic fibrosis.

Li N, Pei P, Bu DF, He B, Wang GF. Li N, et al. Among authors: bu df. Chin Med J (Engl). 2006 Jan 20;119(2):103-9. doi: 10.3901/jme.2006.11.103. Chin Med J (Engl). 2006. PMID: 16454991

10

[Two novel mutations in palmitoyl-protein thioesterase gene in two Chinese babies with infantile neuronal ceroid lipofuscinosis].

Bi HY, Yao S, Bu DF, Wang ZX, Zhang Y, Qin J, Yang YL, Yuan Y. Bi HY, et al. Among authors: bu df. Zhonghua Er Ke Za Zhi. 2006 Jul;44(7):496-9. Zhonghua Er Ke Za Zhi. 2006. PMID: 17044973 Chinese.

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