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Journal Articles

Lysine-specific demethylase 1A restricts ex vivo propagation of human HSCs and is a target of UM171

Agatheeswaran Subramaniam, Kristijonas Žemaitis, Mehrnaz Safaee Talkhoncheh, David Yudovich, Alexandra Bäckström, Shubhranshu Debnath, Jun Chen, Mayur Vilas Jain, Roman Galeev, Massimiliano Gaetani, Roman A. Zubarev, Jonas Larsson

Blood (2020) 136 (19): 2151–2161.

https://doi.org/10.1182/blood.2020005827

Published: 2020

Includes: Supplemental data

Journal Articles

The common hereditary elliptocytosis-associated α-spectrin L260P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformation

Sandra L. Harper, Sira Sriswasdi, Hsin-Yao Tang, Massimiliano Gaetani, Patrick G. Gallagher, David W. Speicher

Blood (2013) 122 (17): 3045–3053.

https://doi.org/10.1182/blood-2013-02-487702

Published: 2013

Includes: Supplemental data

Journal Articles

Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer site

Massimiliano Gaetani, Sara Mootien, Sandra Harper, Patrick G. Gallagher, David W. Speicher

Blood (2008) 111 (12): 5712–5720.

https://doi.org/10.1182/blood-2007-11-122457

Published: 2008

Includes: Supplemental data

Journal Articles

Dematin and Adducin Provide a Critical Link between the Spectrin Cytoskeleton and the Erythrocyte Membrane Via Glucose Transporter-1.

Anwar A. Khan, PhD, Toshihiko Hanada, Ph.D, Massimiliano Gaetani, Ph.D, Donghai Li, Ph.D, Brent C. Reed, Ph.D, David W. Speicher, Ph.D, Athar H. Chishti, Ph.D

Blood (2007) 110 (11): 1719.

https://doi.org/10.1182/blood.V110.11.1719.1719

Published: 2007

Journal Articles

Identification and Characterization of α-Spectrin Mutations Associated with Inherited Hemolytic Anemia.

Whitney Tolpinrud, BS, Massimiliano Gaetani, PhD, Yelena Maksimova, BS, Sara Mootien, PhD, Sandra Harper, PhD, Bernard G. Forget, MD, David W. Speicher, PhD, Patrick G. Gallagher, MD

Blood (2007) 110 (11): 1706.

https://doi.org/10.1182/blood.V110.11.1706.1706

Published: 2007

Journal Articles

Pathogenic proline mutation in the linker between spectrin repeats: disease caused by spectrin unfolding

Colin P. Johnson, Massimiliano Gaetani, Vanessa Ortiz, Nishant Bhasin, Sandy Harper, Patrick G. Gallagher, David W. Speicher, Dennis E. Discher

Blood (2006) 109 (8): 3538–3543.

https://doi.org/10.1182/blood-2006-07-038588

Published: 2006

Includes: Supplemental data

NARROW

Lysine-specific demethylase 1A restricts ex vivo propagation of human HSCs and is a target of UM171

The common hereditary elliptocytosis-associated α-spectrin L260P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformation

Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer site

Dematin and Adducin Provide a Critical Link between the Spectrin Cytoskeleton and the Erythrocyte Membrane Via Glucose Transporter-1.

Identification and Characterization of α-Spectrin Mutations Associated with Inherited Hemolytic Anemia.

Pathogenic proline mutation in the linker between spectrin repeats: disease caused by spectrin unfolding

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ASH Publications

American Society of Hematology

Lysine-specific demethylase 1A restricts ex vivo propagation of human HSCs and is a target of UM171

The common hereditary elliptocytosis-associated α-spectrin L260P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformation

Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer site

Dematin and Adducin Provide a Critical Link between the Spectrin Cytoskeleton and the Erythrocyte Membrane Via Glucose Transporter-1.

Identification and Characterization of α-Spectrin Mutations Associated with Inherited Hemolytic Anemia.

Pathogenic proline mutation in the linker between spectrin repeats: disease caused by spectrin unfolding

Email alerts

ASH Publications

American Society of Hematology

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