Wang CQ - Search Results

1

RUNX1 point mutations potentially identify a subset of early immature T-cell acute lymphoblastic leukaemia that may originate from differentiated T-cells.

Mok MM, Du L, Wang CQ, Tergaonkar V, Liu TC, Yin Kham SK, Sanda T, Yeoh AE, Osato M. Mok MM, et al. Among authors: wang cq. Gene. 2014 Jul 15;545(1):111-6. doi: 10.1016/j.gene.2014.04.074. Epub 2014 May 2. Gene. 2014. PMID: 24792891

2

Stem cell exhaustion due to Runx1 deficiency is prevented by Evi5 activation in leukemogenesis.

Jacob B, Osato M, Yamashita N, Wang CQ, Taniuchi I, Littman DR, Asou N, Ito Y. Jacob B, et al. Among authors: wang cq. Blood. 2010 Feb 25;115(8):1610-20. doi: 10.1182/blood-2009-07-232249. Epub 2009 Dec 14. Blood. 2010. PMID: 20008790 Free PMC article.

3

Runx family genes, niche, and stem cell quiescence.

Wang CQ, Jacob B, Nah GS, Osato M. Wang CQ, et al. Blood Cells Mol Dis. 2010 Apr 15;44(4):275-86. doi: 10.1016/j.bcmd.2010.01.006. Epub 2010 Feb 9. Blood Cells Mol Dis. 2010. PMID: 20144877 Review.

4

Runx3 deficiency results in myeloproliferative disorder in aged mice.

Wang CQ, Motoda L, Satake M, Ito Y, Taniuchi I, Tergaonkar V, Osato M. Wang CQ, et al. Blood. 2013 Jul 25;122(4):562-6. doi: 10.1182/blood-2012-10-460618. Epub 2013 Jun 5. Blood. 2013. PMID: 23741011 Free article.

5

Disruption of Runx1 and Runx3 leads to bone marrow failure and leukemia predisposition due to transcriptional and DNA repair defects.

Wang CQ, Krishnan V, Tay LS, Chin DW, Koh CP, Chooi JY, Nah GS, Du L, Jacob B, Yamashita N, Lai SK, Tan TZ, Mori S, Tanuichi I, Tergaonkar V, Ito Y, Osato M. Wang CQ, et al. Cell Rep. 2014 Aug 7;8(3):767-82. doi: 10.1016/j.celrep.2014.06.046. Epub 2014 Jul 24. Cell Rep. 2014. PMID: 25066130 Free article.

6

Hematopoietic stem cell enhancer: a powerful tool in stem cell biology.

Koh CP, Ng CE, Nah GS, Wang CQ, Tergaonkar V, Matsumura T, Yokomizo T, Suda T, Osato M. Koh CP, et al. Among authors: wang cq. Histol Histopathol. 2015 Jun;30(6):661-72. doi: 10.14670/HH-30.661. Epub 2015 Jan 9. Histol Histopathol. 2015. PMID: 25574754 Review.

7

Hematopoiesis specific loss of Cdk2 and Cdk4 results in increased erythrocyte size and delayed platelet recovery following stress.

Jayapal SR, Wang CQ, Bisteau X, Caldez MJ, Lim S, Tergaonkar V, Osato M, Kaldis P. Jayapal SR, et al. Among authors: wang cq. Haematologica. 2015 Apr;100(4):431-8. doi: 10.3324/haematol.2014.106468. Epub 2015 Jan 23. Haematologica. 2015. PMID: 25616574 Free PMC article.

8

Cyclin A2 regulates erythrocyte morphology and numbers.

Jayapal SR, Ang HY, Wang CQ, Bisteau X, Caldez MJ, Xuan GX, Yu W, Tergaonkar V, Osato M, Lim B, Kaldis P. Jayapal SR, et al. Among authors: wang cq. Cell Cycle. 2016 Nov 16;15(22):3070-3081. doi: 10.1080/15384101.2016.1234546. Epub 2016 Sep 22. Cell Cycle. 2016. PMID: 27657745 Free PMC article.

9

Runx Family Genes in Tissue Stem Cell Dynamics.

Wang CQ, Mok MM, Yokomizo T, Tergaonkar V, Osato M. Wang CQ, et al. Adv Exp Med Biol. 2017;962:117-138. doi: 10.1007/978-981-10-3233-2_9. Adv Exp Med Biol. 2017. PMID: 28299655 Review.

10

TUBB1 dysfunction in inherited thrombocytopenia causes genome instability.

Matsumura T, Nakamura-Ishizu A, Takaoka K, Maki H, Muddineni SSNA, Wang CQ, Suzushima H, Kawakita M, Asou N, Matsuoka M, Kurokawa M, Osato M, Suda T. Matsumura T, et al. Among authors: wang cq. Br J Haematol. 2019 Jun;185(5):888-902. doi: 10.1111/bjh.15835. Epub 2019 Mar 10. Br J Haematol. 2019. PMID: 30854628 Free article.

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