Bu D - Search Results

1

[Analysis of the relationship between mitochondrial DNA deletion and clinical complexity of mitochondrial disease].

Zhang Y, Ma Y, Bu D, Liu H, Xia C, Zhang Y, Zhu S, Zheng X, Pei P, Wang S, Xu Y, Pan H, Qi Y. Zhang Y, et al. Among authors: bu d. Zhonghua Yi Xue Za Zhi. 2015 Nov 10;95(42):3449-53. Zhonghua Yi Xue Za Zhi. 2015. PMID: 26813137 Chinese.

2

[Molecular genetic analysis of mitochondrial DNA C1494T mutation in non-syndromic hearing loss of Chinese population].

Tian G, Liu YH, Ma YN, Li YJ, Zhang Y, Niu SL, Xu YE, Pei P, Wang ST, Bu DF, Du BR, Zhou X, Ke XM, Qi Y. Tian G, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Aug;24(4):464-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 17680545 Chinese.

3

[Identification of an ideal noninvasive method to detect A3243G gene mutation in MELAS syndrome].

Ma YN, Fang F, Yang YL, Zhang Y, Wang ST, Xu YF, Pei P, Yuan Y, Bu DF, Qi Y. Ma YN, et al. Zhonghua Yi Xue Za Zhi. 2008 Dec 16;88(46):3250-3. Zhonghua Yi Xue Za Zhi. 2008. PMID: 19159547 Chinese.

4

[Mitochondrial DNA mutation analysis in 97 Chinese patients with mitochondrial cephalomyopathy].

Wang ZX, Luan XH, Zhang Y, Yang YL, Qi Y, Bu DF, Yuan Y. Wang ZX, et al. Zhonghua Yi Xue Za Zhi. 2008 Dec 16;88(46):3254-6. Zhonghua Yi Xue Za Zhi. 2008. PMID: 19159548 Chinese.

5

[Screening of mitochondrial deoxyribonucleic acid 3271T > C, 8356T > C, 9176T > C/G and 13513G > A mutations in mitochondrial encephalomyopathies].

Xu JB, Ma YN, Pan H, Zheng XF, Zhang Y, Wang ST, Bu DF, Qi Y. Xu JB, et al. Zhonghua Yi Xue Za Zhi. 2011 Apr 12;91(14):969-72. Zhonghua Yi Xue Za Zhi. 2011. PMID: 21609548 Chinese.

6

Deletion of a 4977-bp Fragment in the Mitochondrial Genome Is Associated with Mitochondrial Disease Severity.

Zhang Y, Ma Y, Bu D, Liu H, Xia C, Zhang Y, Zhu S, Pan H, Pei P, Zheng X, Wang S, Xu Y, Qi Y. Zhang Y, et al. Among authors: bu d. PLoS One. 2015 May 29;10(5):e0128624. doi: 10.1371/journal.pone.0128624. eCollection 2015. PLoS One. 2015. PMID: 26024530 Free PMC article. Clinical Trial.

7

[The diagnostic value of chromosome microarray analysis technique in the genetic causes of children with intellectual disability or global developmental delay].

Wu HR, Li L, Ma YN, Liu CL, Pei P, Zheng XF, Wang ST, Xiao Y, Bu DF, Xu YF, Pan H, Qi Y. Wu HR, et al. Among authors: bu df. Zhonghua Yi Xue Za Zhi. 2021 Jan 19;101(3):224-228. doi: 10.3760/cma.j.cn112137-20200422-01275. Zhonghua Yi Xue Za Zhi. 2021. PMID: 33455150 Chinese.

8

[Detection of mtDNA 11778 (G-->A) point mutation in a family with Leber's hereditary optic neuropathy by site-specific polymerase chain reaction].

Niu SL, Zhang Y, Xu YF, Bu DF, Ren ZQ, Wang SY, Liu GH, Qi Y. Niu SL, et al. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2003 Apr;25(2):153-5. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2003. PMID: 12905709 Chinese.

9

[Development of IgHV family specific nucleic acid vaccine against lymphoma by construction of fusion gene of immunoglobulin heavy chain variable region and cytokine].

Liu H, Zhu P, Lin NJ, Zhang Y, Bu DF, Wang YJ, Wang YQ, Yang Y. Liu H, et al. Zhonghua Yi Xue Za Zhi. 2004 Jan 2;84(1):48-53. Zhonghua Yi Xue Za Zhi. 2004. PMID: 14990159 Chinese.

10

[Five single nucleotide polymorphisms of casein kinase I gamma 2 gene in children with familial febrile convulsions].

Ma YN, Hao L, Niu SL, Xu YF, Zhang Y, Pei P, Bu DF, Qi Y. Ma YN, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Aug;21(4):347-50. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15300631 Chinese.

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