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Dive into the research topics where Wu Wm is active.

Publication


Featured researches published by Wu Wm.


Chinese Journal of Hematology | 2003

[Identification of two novel factor XI non-sense mutation Trp228stop and Trp383stop in a Chinese pedigree of congenital factor XI deficiency].

Wu Wm; Wang H; Wang Xf; Chu H; Fu Qh; Ding Ql; Hu Yq; Zhi-Xiang Shen; Zhaoyue Wang


Chinese Journal of Hematology | 2005

[The inherited coagulation factor XI deficiency caused by intronic mutation IVS J-4delgttg].

Xie S; Wang H; Wang Xf; Wu Wm; Zhou Rf; Wang Wb; Hu Yq; Zhaoyue Wang


Chinese Journal of Hematology | 2005

Study on the molecular mechanism of antithrombin gene C2759T (Leu99Phe) mutation causing antithrombin deficiency

Fu Qh; Wang Wb; Ding Ql; Zhou Rf; Wu Wm; Hu Yq; Wang Xf; Yan Lx; Zhaoyue Wang; Wang H


Chinese Journal of Hematology | 2006

Studies on inherited coagulation factor VII deficiency and tissue factor abnormality in a pedigree

Ding Ql; Wang Xf; Xu Gq; Huang Xp; Hu Yq; Wu Wm; Fu Qh; Wang H; Zhaoyue Wang


Chinese Journal of Hematology | 2005

Severe hereditary coagulation factor V deficiency caused by two novel heterozygous mutations

Zhou Rf; Fu Qh; Xu Xc; Wang Wb; Wu Wm; Ding Ql; Xie S; Zhai Zm; Hu Yq; Wang Xf; Wu Js; Wang H


Chinese Journal of Hematology | 2004

[Hereditary hemorrhagic telangiectasia resulted from a nonsense mutation Arg479 Stop in the ALK-1 gene].

Xie Bs; Xie S; Chen P; Zhu My; Zheng Jy; Wang Xf; Fu Qh; Zhou Rf; Wang Wb; Wu Wm; Ding Ql; Wang H; Hu Lm


Chinese Journal of Hematology | 2004

[Double heterozygous mutations of non-canonical splice (IVS1a + 5g > a) and His348Gln caused inherited coagulation factor VII deficiency].

Ding Ql; Wang H; Wang Xf; Wang Ms; Fu Qh; Wu Wm; Hu Yq; Zhaoyue Wang


Chinese Journal of Hematology | 2004

FXI gene mutations in two pedigrees of congenital clotting factor XI deficiency

Wu Wm; Ding Ql; Wang Xf; Fu Qh; Wang Wb; Dai J; Fang Y; Zhou Rf; Xie S; Hu Yq; Sheng Zx; Wang H; Zhaoyue Wang


Chinese Journal of Hematology | 2003

Analysis of an inherited FVII deficiency pedigree caused by homozygosity of Thr359Met

Chu H; Wang H; Qiurong Ding; Wang Xf; Qu B; Wu F; Kang W; Duan B; Yin J; Fu Qh; Wu Wm; Zhaoyue Wang


Chinese Journal of Hematology | 2003

Prothrombin deficiency resulted from a homozygous Glu29 to Gly mutation in the prothrombin gene

Wang Wb; Wang H; Huang Cy; Fang Y; Fu Qh; Zhou Rf; Xie S; Ding Ql; Wu Wm; Wang Xf; Hu Yq; Zhaoyue Wang

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Wang H

Chinese Academy of Sciences

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Wang Xf

University of Pennsylvania

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Qiurong Ding

Chinese Academy of Sciences

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Zhi-Xiang Shen

Shanghai Jiao Tong University

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