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Journal Articles

Megakaryocyte Ablation Ameliorates Bone Marrow Fibrosis By Reducing Myofibroblast Differentiation in a Mouse Model of Primary Myelofibrosis

Yutein Chung, PhD, Huiyan Jin, PhD, Claire Trasorras, Francina Gonzalez, Sang Hee Min, MD PhD

Blood (2019) 134 (Supplement_1): 2493.

https://doi.org/10.1182/blood-2019-132186

Published: 2019

Journal Articles

The Phosphoinositide Kinase Pikfyve Regulates Lysosomal Biogenesis in Macrophages By Modulating the Transcription Factor EB (TFEB)

Francina Gonzalez, MSc, Aae Suzuki, Jessica Guzman, Lynn Spruce, Steven H Seeholzer, PhD, Charles S. Abrams, MD, Sang Hee Min, MDhD

Blood (2017) 130 (Supplement 1): 2276.

https://doi.org/10.1182/blood.V130.Suppl_1.2276.2276

Published: 2017

Journal Articles

Pikfyve Deficiency Disrupts Lysosomal Maturation and Degradative Function in Macrophages, and Causes Systemic Inflammation in Mice

Sang Hee Min, MD, Aae Suzuki, Jessica Guzman, Lehn Weaver, MD PhD, Charles S. Abrams, MD

Blood (2016) 128 (22): 704.

https://doi.org/10.1182/blood.V128.22.704.704

Published: 2016

Journal Articles

Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption

Daniel Sanghoon Shin, Sang Hee Min, Laura Russell, Rongbao Zhao, Andras Fiser, I. David Goldman

Blood (2010) 116 (24): 5162–5169.

https://doi.org/10.1182/blood-2010-06-291237

Published: 2010

Journal Articles

The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption

Rongbao Zhao, Sang Hee Min, Andong Qiu, Antoinette Sakaris, Gary L. Goldberg, Claudio Sandoval, J. Jeffrey Malatack, David S. Rosenblatt, I. David Goldman

Blood (2007) 110 (4): 1147–1152.

https://doi.org/10.1182/blood-2007-02-077099

Published: 2007

NARROW

Megakaryocyte Ablation Ameliorates Bone Marrow Fibrosis By Reducing Myofibroblast Differentiation in a Mouse Model of Primary Myelofibrosis

The Phosphoinositide Kinase Pikfyve Regulates Lysosomal Biogenesis in Macrophages By Modulating the Transcription Factor EB (TFEB)

Pikfyve Deficiency Disrupts Lysosomal Maturation and Degradative Function in Macrophages, and Causes Systemic Inflammation in Mice

Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption

The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption

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ASH Publications

American Society of Hematology

Megakaryocyte Ablation Ameliorates Bone Marrow Fibrosis By Reducing Myofibroblast Differentiation in a Mouse Model of Primary Myelofibrosis

The Phosphoinositide Kinase Pikfyve Regulates Lysosomal Biogenesis in Macrophages By Modulating the Transcription Factor EB (TFEB)

Pikfyve Deficiency Disrupts Lysosomal Maturation and Degradative Function in Macrophages, and Causes Systemic Inflammation in Mice

Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption

The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption

Email alerts

ASH Publications

American Society of Hematology

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