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Journal Articles

RUNX1 Deficiency and SRSF2 Mutation Cooperate to Promote Myelodysplastic Syndrome Development

Yi-Jou Huang, BS, Ming Yan, PhD, Eunhee Kim, PhD, Amanda G Davis, BS, Takahiro Shima, MD PhD, Sayuri Miyauchi, DDS, PhD, Xiang-Dong Fu, PhD, Omar Abdel-Wahab, MD, Dong-Er Zhang, PhD
Journal: Blood
Blood (2017) 130 (Supplement 1): 119.
https://doi.org/10.1182/blood.V130.Suppl_1.119.119
Published: 2017
Journal Articles

Modeling ASXL1 Mutation Revealed Myelodysplasia Caused By Derepression of p16Ink4a through Aberrant PRC1-Mediated Histone Modification

Masahiro Uni, MD PhD, Yosuke Masamoto, MD PhD, Tomohiko Sato, MD PhD, Shunya Arai, MD PhD, Eiji Hara, PhD, Mineo Kurokawa, MD PhD
Journal: Blood
Blood (2017) 130 (Supplement 1): 118.
https://doi.org/10.1182/blood.V130.Suppl_1.118.118
Published: 2017
Journal Articles

Myelodysplastic Syndrome Caused By Activating Kras Mutation in the Non-Hematopoietic Bone Marrow Microenvironment

Lena Osswald, Cornelius Miething, MD, Justus Duyster, MD PhD, Tilman Brummer, PhD, Robert Zeiser, MD
Journal: Blood
Blood (2015) 126 (23): 359.
https://doi.org/10.1182/blood.V126.23.359.359
Published: 2015
Journal Articles

Hypersegmented Neutrophil Percentage Using Automated Digital Cell Morphology: A Simple Laboratory Parameter to Monitor Hydroxyurea Therapy in Sickle Cell Disease Patients

Kleber Yotsumoto Fertrin, MD, PhD, Elza Miyuki Kimura, B.Sc., Fernanda Madureira de Oliveira Araujo, B.Sc., Maria de Fatima Pereira Gilberti, MD, Sara T.O. Saad, MD, PhD, Fernando F Costa, MD, PhD
Journal: Blood
Blood (2015) 126 (23): 2188.
https://doi.org/10.1182/blood.V126.23.2188.2188
Published: 2015
Journal Articles

Megaloblastic Anemia and Mitochondriopathy Caused by a Homozygous Mutation in Sideroflexin-4.

Jeffrey D. Cooney, Gordon J. Hildick-Smith, Caterina Garone, M.D., Jonathan N. Thon, Ph.D., Orhan H. Akman, Ph.D., Caiyong Chen, Ph.D., Dhvanit I. Shah, Ph.D., Diana Santos Branco, M. Sc., Non Miyata, Ph.D., Matthew L. Freedman, M.D., Sarah E. Calvo, Ph.D., Vamsi K. Mootha, M.D., Carla M. Koehler, Ph.D., Joseph E. Italiano, Jr., PhD, M. Alice Donati, M.D., Salvatore DiMauro, M.D., Barry H. Paw, M.D., Ph.D.
Journal: Blood
Blood (2012) 120 (21): 79.
https://doi.org/10.1182/blood.V120.21.79.79
Published: 2012
Journal Articles

A NUP98-HOXD13 Fusion Gene Induces a Transplantable Myelodysplastic Syndrome in Mice.

Yang Jo Chung, PhD, Chul Won Choi, MD, Ph.D, Christopher Slape, Ph.D, Terry Fry, MD, Peter D. Aplan, MD
Journal: Blood
Blood (2007) 110 (11): 401.
https://doi.org/10.1182/blood.V110.11.401.401
Published: 2007
Journal Articles

Mutant CXCR4 Identified in Neutropenic Patients with Myelokathexis Impairs Survival of Human Myeloid Cells.

Vahagn Makaryan, MD, David C. Dale, MD, Andrew A. Aprikyan, PhD
Journal: Blood
Blood (2005) 106 (11): 3071.
https://doi.org/10.1182/blood.V106.11.3071.3071
Published: 2005
Journal Articles

Oncogenic TLS-ERG Fusion Protein Promotes Differentiation of Myeloid Progenitors into Myeloblasts but Blocks Their Terminal Differentiation.

Junhui Zou, MD, Anna Zielinska-Kwiatkowska, MS, Michael L. Blackburn, BS, Hitoshi Ichikawa, PhD, Liu Yang, PhD
Journal: Blood
Blood (2005) 106 (11): 1383.
https://doi.org/10.1182/blood.V106.11.1383.1383
Published: 2005
Journal Articles

NUP98-HOXD13 Transgenic Mice Develop Myelodysplastic Syndrome, Acute Myeloid Leukemia, and Pre-T Lymphoblastic Leukemia.

Yingwei Lin, MD, PhD, Christopher Slape, PhD, Zhenhua Zhang, Peter D. Aplan, MD
Journal: Blood
Blood (2004) 104 (11): 345.
https://doi.org/10.1182/blood.V104.11.345.345
Published: 2004