Direct regulation of p53 by miR-142a-3p mediates the survival of hematopoietic stem and progenitor cells in zebrafish

by Lu, Xinyan, Wei, Yonglong, Liu, Feng
Published 2015

Retrospective Review of MET Gene Mutations

by Zenali, Maryam, deKay, James, Liu, Zesheng, Hamilton, Stanley, Zuo, Zhuang, Lu, Xinyan, Bakkar, Rania, Mills, Gordon, Broaddus, Russell
Published 2015

Sex chromosome loss after allogeneic hematopoietic stem cell transplant in patients with hematologic neoplasms: a diagnostic dilemma for clinical cytogeneticists

by Tang, Zhenya, Medeiros, L. Jeffrey, Yin, C. Cameron, Wang, Wei, Lu, Xinyan, Young, Ken H., Khoury, Joseph D., Tang, Guilin
Published 2016

A Familial Cri-du-Chat/5p Deletion Syndrome Resulted from Rare Maternal Complex Chromosomal Rearrangements (CCRs) and/or Possible Chromosome 5p Chromothripsis

by Gu, Heng, Jiang, Jian-hui, Li, Jian-ying, Zhang, Ya-nan, Dong, Xing-sheng, Huang, Yang-yu, Son, Xin-ming, Lu, Xinyan, Chen, Zheng
Published 2013

Double inv(3)(q21q26.2) in acute myeloid leukemia is resulted from an acquired copy neutral loss of heterozygosity of chromosome 3q and associated with disease progression

by Gu, Jun, Patel, Keyur P., Bai, Bing, Liu, Ching-Hua, Tang, Guilin, Kantarjian, Hagop M., Tang, Zhenya, Abraham, Ronald, Luthra, Rajyalakshmi, Medeiros, L. Jeffrey, Lin, Pei, Lu, Xinyan
Published 2015

Coexistence of iAMP21 and ETV6-RUNX1 fusion in an adolescent with B cell acute lymphoblastic leukemia: literature review of six additional cases

by Gu, Jun, Reynolds, Alexandra, Fang, Lianghua, DeGraffenreid, Corrie, Sterns, Kenneth, Patel, Keyur P., Medeiros, L. Jeffrey, Lin, Pei, Lu, Xinyan
Published 2016

Simultaneous deletion of 3′ETV6 and 5′EWSR1 genes in blastic plasmacytoid dendritic cell neoplasm: case report and literature review

by Tang, Zhenya, Tang, Guilin, Wang, Sa A., Lu, Xinyan, Young, Ken H., Bueso-Ramos, Carlos E., Alvarado, Yesid, Medeiros, L. Jeffrey, Khoury, Joseph D.
Published 2016

Clinical Implementation of Chromosomal Microarray Analysis: Summary of 2513 Postnatal Cases

by Lu, Xinyan, Shaw, Chad A., Patel, Ankita, Li, Jiangzhen, Cooper, M. Lance, Wells, William R., Sullivan, Cathy M., Sahoo, Trilochan, Yatsenko, Svetlana A., Bacino, Carlos A., Stankiewicz, Pawel, Ou, Zhishu, Chinault, A. Craig, Beaudet, Arthur L., Lupski, James R., Cheung, Sau W., Ward, Patricia A.
Published 2007

Myeloid neoplasms with isolated isochromosome 17q demonstrate a high frequency of mutations in SETBP1, SRSF2, ASXL1 and NRAS

by Kanagal-Shamanna, Rashmi, Luthra, Rajyalakshmi, Yin, Cameron C., Patel, Keyur P., Takahashi, Koichi, Lu, Xinyan, Lee, John, Zhao, Chong, Stingo, Francesco, Zuo, Zhuang, Routbort, Mark J., Singh, Rajesh R., Fox, Patricia, Ravandi, Farhad, Garcia-Manero, Guillermo, Medeiros, L. Jeffrey, Bueso-Ramos, Carlos E.
Published 2016