Wei W - Search Results

1

Identification of functional cooperative mutations of SETD2 in human acute leukemia.

Zhu X, He F, Zeng H, Ling S, Chen A, Wang Y, Yan X, Wei W, Pang Y, Cheng H, Hua C, Zhang Y, Yang X, Lu X, Cao L, Hao L, Dong L, Zou W, Wu J, Li X, Zheng S, Yan J, Zhou J, Zhang L, Mi S, Wang X, Zhang L, Zou Y, Chen Y, Geng Z, Wang J, Zhou J, Liu X, Wang J, Yuan W, Huang G, Cheng T, Wang QF. Zhu X, et al. Among authors: wei w. Nat Genet. 2014 Mar;46(3):287-93. doi: 10.1038/ng.2894. Epub 2014 Feb 9. Nat Genet. 2014. PMID: 24509477 Free PMC article.

2

[Regulatory mechanisms of PI3K/AKT signaling pathway in acute leukemia].

Wang WL, Zhang YC, Zeng HM, Hua CL, Wei W, Xu J, Zhu XF, Cheng T, Yuan WP. Wang WL, et al. Among authors: wei w. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2012 Feb;20(1):18-21. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2012. PMID: 22391157 Chinese.

3

Whole exome sequencing reveals concomitant mutations of multiple FA genes in individual Fanconi anemia patients.

Chang L, Yuan W, Zeng H, Zhou Q, Wei W, Zhou J, Li M, Wang X, Xu M, Yang F, Yang Y, Cheng T, Zhu X. Chang L, et al. Among authors: wei w. BMC Med Genomics. 2014 May 15;7:24. doi: 10.1186/1755-8794-7-24. BMC Med Genomics. 2014. PMID: 24885126 Free PMC article.

4

[Type III familial hemophagocytic lymphohistiocytosis susceptibility gene UNC13D involves in homologous recombination repair].

Chang LX, Zeng HM, Zhou QQ, Gao M, Wei W, Zhou JF, An WB, Yuan WP, Zhu XF. Chang LX, et al. Among authors: wei w. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2013 Jun;21(3):692-5. doi: 10.7534/j.issn.1009-2137.2013.03.031. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2013. PMID: 23815924 Chinese.

5

[Significance of ikaros family zinc finger 1 deletion in pediatric B-acute lymphoblastic leukemia without reproducible cytogenetic abnormalities].

Liu X, Zhang L, Zou Y, Chang L, Wei W, Ruan M, Chen Y, Yang W, Chen X, Guo Y, Wang S, Liu T, Zhang J, Liu F, Qi B, An W, Zhu X. Liu X, et al. Among authors: wei w. Zhonghua Er Ke Za Zhi. 2016 Feb;54(2):126-30. doi: 10.3760/cma.j.issn.0578-1310.2016.02.011. Zhonghua Er Ke Za Zhi. 2016. PMID: 26875463 Chinese.

6

Prediction of outcomes by early treatment responses in childhood T-cell acute lymphoblastic leukemia: a retrospective study in China.

Wei W, Chen X, Zou Y, Chang L, An W, Wan Y, Liu T, Yang W, Chen Y, Guo Y, Zhu X. Wei W, et al. BMC Pediatr. 2015 Jul 15;15:80. doi: 10.1186/s12887-015-0390-z. BMC Pediatr. 2015. PMID: 26174476 Free PMC article.

7

[Research progress of pathogenic mechanism of congenital neutropenia].

Wei W, Zhu XF. Wei W, et al. Zhonghua Er Ke Za Zhi. 2012 Nov;50(11):868-71. Zhonghua Er Ke Za Zhi. 2012. PMID: 23302623 Review. Chinese. No abstract available.

8

[WHIM syndrome: a case report and literature review].

Chen XJ, Yang WY, Wang SC, Guo Y, Liu F, Qi BQ, Chang LX, Zhou JF, An WB, Wei W, Wan Y, Zhu XF. Chen XJ, et al. Among authors: wei w. Zhonghua Er Ke Za Zhi. 2013 Mar;51(3):178-82. Zhonghua Er Ke Za Zhi. 2013. PMID: 23751577 Review. Chinese.

9

Missense mutations near the N-glycosylation site of the A2 domain lead to various intracellular trafficking defects in coagulation factor VIII.

Wei W, Zheng C, Zhu M, Zhu X, Yang R, Misra S, Zhang B. Wei W, et al. Sci Rep. 2017 Mar 22;7:45033. doi: 10.1038/srep45033. Sci Rep. 2017. PMID: 28327546 Free PMC article.

10

CALR mutation screening in pediatric primary myelofibrosis.

An W, Wan Y, Guo Y, Chen X, Ren Y, Zhang J, Chang L, Wei W, Zhang P, Zhu X. An W, et al. Among authors: wei w. Pediatr Blood Cancer. 2014 Dec;61(12):2256-62. doi: 10.1002/pbc.25211. Epub 2014 Aug 30. Pediatr Blood Cancer. 2014. PMID: 25176567

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