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Journal Articles

Mechanism-Based Targeting of Sickle Cell Pathobiology and Pain with Novel Transdermal Curcumin

Yugal Goel, Mya Angela Arellano, Raghda T Fouda, Daniel Kerr, Sirsendu Jana, Reina Alexis Lomeli, Graham J Velasco, Probal Banerjee, Donovan Alexander Argueta, Mihir Gupta, Richard Prince, Abdu Alayash, Joel Friedman, Kalpna Gupta

Blood (2023) 142 (Supplement 1): 2490.

https://doi.org/10.1182/blood-2023-182512

Published: 2023

Journal Articles

Hydroxyurea Reverses Dysfunctional Ubiquitin-Proteasomal System in Sickle CELL Disease and Suppresses Posttranslational Alterations in Hemoglobin and CELL Membranes

Swee Lay Thein, DSc, MBBS, Arun S Shet, MD, Michael Brad Strader, PhD, Fanato Meng, PhD, Michael Heaven, PhD, Jana Sirsendu, PhD, Abdu Alayash, PhD

Blood (2019) 134 (Supplement_1): 4822.

https://doi.org/10.1182/blood-2019-122840

Published: 2019

Journal Articles

Hemoglobin S Oxidation Promotes Plasma-Derived Microparticle Membrane Alterations and Toxicity

Sirsendu Jana, PhD, Michael B Strader, PhD, Tigist Kassa, PhD, Fantao Meng, PhD, Wayne Hicks, PhD, Ivan Tarandovskiy, PhD, Silvia De Paoli, PhD, Jan Simak, PhD, Jeffery L Miller, MD, Laurel Mendelsohn, BSc., Jim Nichols, RSN, Swee Lay Thein, MD, John D. Belcher, PhD, Gregory M Vercellotti, MD, Abdu Alayash, PhD

Blood (2016) 128 (22): 856.

https://doi.org/10.1182/blood.V128.22.856.856

Published: 2016

Journal Articles

Three Months of Human Haptoglobin Treatment Decreases Iron Deposition in the Kidneys of Townes Sickle Mice

Patricia A Shi, MD, Erika Choi, BA, Julia Nguyen, BS, Xinhua Guo, BS, Narla Mohandas, DSc, Abdu Alayash, PhD, Elizabeth Manci, MD, John D. Belcher, PhD, Gregory M Vercellotti

Blood (2015) 126 (23): 2163.

https://doi.org/10.1182/blood.V126.23.2163.2163

Published: 2015

Journal Articles

Investigation of the Molecular Basis of High Oxygen Affinity Hemoglobin Brigham (α 2 A β 2 100 Pro→Leu ) In a Subject with Familial Erythrocytosis

Bindu Abraham, Yiping Jia, Francine Wood, Chad Reiter, Jay Nelson Lozier, Jeffery L. Miller, Abdu Alayash

Blood (2010) 116 (21): 4806.

https://doi.org/10.1182/blood.V116.21.4806.4806

Published: 2010

NARROW

Mechanism-Based Targeting of Sickle Cell Pathobiology and Pain with Novel Transdermal Curcumin

Hydroxyurea Reverses Dysfunctional Ubiquitin-Proteasomal System in Sickle CELL Disease and Suppresses Posttranslational Alterations in Hemoglobin and CELL Membranes

Hemoglobin S Oxidation Promotes Plasma-Derived Microparticle Membrane Alterations and Toxicity

Three Months of Human Haptoglobin Treatment Decreases Iron Deposition in the Kidneys of Townes Sickle Mice

Investigation of the Molecular Basis of High Oxygen Affinity Hemoglobin Brigham (α 2 A β 2 100 Pro→Leu ) In a Subject with Familial Erythrocytosis

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ASH Publications

American Society of Hematology

Mechanism-Based Targeting of Sickle Cell Pathobiology and Pain with Novel Transdermal Curcumin

Hydroxyurea Reverses Dysfunctional Ubiquitin-Proteasomal System in Sickle CELL Disease and Suppresses Posttranslational Alterations in Hemoglobin and CELL Membranes

Hemoglobin S Oxidation Promotes Plasma-Derived Microparticle Membrane Alterations and Toxicity

Three Months of Human Haptoglobin Treatment Decreases Iron Deposition in the Kidneys of Townes Sickle Mice

Investigation of the Molecular Basis of High Oxygen Affinity Hemoglobin Brigham (α 2 A β 2 100 Pro→Leu ) In a Subject with Familial Erythrocytosis

Email alerts

ASH Publications

American Society of Hematology

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