Ning Y - Search Results

1

NUP98-PHF23 is a chromatin-modifying oncoprotein that causes a wide array of leukemias sensitive to inhibition of PHD histone reader function.

Gough SM, Lee F, Yang F, Walker RL, Zhu YJ, Pineda M, Onozawa M, Chung YJ, Bilke S, Wagner EK, Denu JM, Ning Y, Xu B, Wang GG, Meltzer PS, Aplan PD. Gough SM, et al. Among authors: ning y. Cancer Discov. 2014 May;4(5):564-77. doi: 10.1158/2159-8290.CD-13-0419. Epub 2014 Feb 17. Cancer Discov. 2014. PMID: 24535671 Free PMC article.

2

A cryptic translocation leading to NUP98-PHF23 fusion in AML.

Ning Y. Ning Y. Best Pract Res Clin Haematol. 2016 Dec;29(4):320-323. doi: 10.1016/j.beha.2016.10.002. Epub 2016 Oct 18. Best Pract Res Clin Haematol. 2016. PMID: 27890253 Review.

3

Regulation of differentiation by a PHD domain in the NUP98-PHF23 fusion protein.

Reader JC, Leng Q, Rassool FV, Ning Y. Reader JC, et al. Among authors: ning y. Leuk Res. 2010 Aug;34(8):1094-7. doi: 10.1016/j.leukres.2010.02.015. Epub 2010 Mar 12. Leuk Res. 2010. PMID: 20219246

4

NUP98-PHF23 fusion is recurrent in acute myeloid leukemia and shares gene expression signature of leukemic stem cells.

Ho H, Skaist AM, Pallavajjala A, Yonescu R, Batista D, Wheelan SJ, Ning Y. Ho H, et al. Among authors: ning y. Leuk Res. 2016 Jun;45:1-7. doi: 10.1016/j.leukres.2016.03.006. Epub 2016 Mar 30. Leuk Res. 2016. PMID: 27060678

5

High frequency of rare structural chromosome abnormalities at relapse of cytogenetically normal acute myeloid leukemia with FLT3 internal tandem duplication.

Gourdin TS, Zou Y, Ning Y, Emadi A, Duong VH, Tidwell ML, Chen C, Rassool FV, Baer MR. Gourdin TS, et al. Among authors: ning y. Cancer Genet. 2014 Oct-Dec;207(10-12):467-73. doi: 10.1016/j.cancergen.2014.09.001. Epub 2014 Sep 16. Cancer Genet. 2014. PMID: 25441683 Free PMC article.

6

Unbalanced 11;18 translocation in an acute erythroid leukemia after radioactive iodine therapy.

Trikalinos NA, Chen Q, Ning Y, Sausville EA, Baer MR. Trikalinos NA, et al. Among authors: ning y. Cancer Genet. 2013 Jun;206(6):252-5. doi: 10.1016/j.cancergen.2013.06.003. Epub 2013 Jul 18. Cancer Genet. 2013. PMID: 23871646

7

Association of acute myeloid leukemia's most immature phenotype with risk groups and outcomes.

Gerber JM, Zeidner JF, Morse S, Blackford AL, Perkins B, Yanagisawa B, Zhang H, Morsberger L, Karp J, Ning Y, Gocke CD, Rosner GL, Smith BD, Jones RJ. Gerber JM, et al. Among authors: ning y. Haematologica. 2016 May;101(5):607-16. doi: 10.3324/haematol.2015.135194. Epub 2016 Jan 27. Haematologica. 2016. PMID: 26819054 Free PMC article.

8

Double minute chromosomes in monoblastic (M5) and myeloblastic (M2) acute myeloid leukemia: two case reports and a review of literature.

Thomas L, Stamberg J, Gojo I, Ning Y, Rapoport AP. Thomas L, et al. Among authors: ning y. Am J Hematol. 2004 Sep;77(1):55-61. doi: 10.1002/ajh.20151. Am J Hematol. 2004. PMID: 15307107 Free article. Review.

9

Identification of a novel KMT2A-SEPT14 fusion in acute myeloid leukemia.

Nguyen D, Haley L, Pallavajjala A, Gojo I, Ning Y. Nguyen D, et al. Among authors: ning y. Leuk Lymphoma. 2018 Jan;59(1):265-267. doi: 10.1080/10428194.2017.1324163. Epub 2017 Jun 2. Leuk Lymphoma. 2018. PMID: 28573893 No abstract available.

10

Genomic characterization of chromosome translocations in patients with T/myeloid mixed-phenotype acute leukemia.

Pallavajjala A, Kim D, Li T, Ghiaur G, Jones RJ, Burns KH, Salzberg SL, Ning Y. Pallavajjala A, et al. Among authors: ning y. Leuk Lymphoma. 2018 May;59(5):1231-1238. doi: 10.1080/10428194.2017.1372577. Epub 2017 Sep 7. Leuk Lymphoma. 2018. PMID: 28882084 Free PMC article.

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