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Impact of cold storage on the oxygenation and oxidation reactions of red blood cells

Frontiers in physiology, 2024-08, Vol.15, p.1427094

2024

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Changes in hemoglobin oxidation and band 3 during blood storage impact oxygen sensing and mitochondrial bioenergetic pathways in the human pulmonary arterial endothelial cell model

Frontiers in physiology, 2023-10, Vol.14, p.1278763-1278763

2023

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Differential heme release from various hemoglobin redox states and the upregulation of cellular heme oxygenase‐1

FEBS open bio, 2016-09, Vol.6 (9), p.876-884

2016

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Antisickling Drugs Targeting βCys93 Reduce Iron Oxidation and Oxidative Changes in Sickle Cell Hemoglobin

Frontiers in physiology, 2019-07, Vol.10, p.931-931

2019

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Caffeic acid: an antioxidant with novel antisickling properties

FEBS open bio, 2021-12, Vol.11 (12), p.3293-3303

2021

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Effects of α subunit substitutions on the oxidation of βCys93 and the stability of sickle cell hemoglobin

Redox report : communications in free radical research, 2020-01, Vol.25 (1), p.95-103

2020

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Sexual and reproductive health of young people with disability in Ethiopia: a study on knowledge, attitude and practice: a cross-sectional study

Globalization and health, 2016-02, Vol.12 (5), p.5-5, Article 5

2016

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Oxidative instability of hemoglobin E (β26 Glu→Lys) is increased in the presence of free α subunits and reversed by α-hemoglobin stabilizing protein (AHSP): Relevance to HbE/β-thalassemia

Redox biology, 2016-08, Vol.8 (C), p.363-374

2016

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Appropriate complementary feeding practices and associated factors among mothers of children age 6-23 months in Southern Ethiopia, 2015

BMC pediatrics, 2016-08, Vol.16 (1), p.131, Article 131

2016

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Design, synthesis, and activity of 2,3-diphosphoglycerate analogs as allosteric modulators of hemoglobin O2 affinity

Artificial cells, nanomedicine, and biotechnology, 2013-04, Vol.41 (2), p.109-115

2013

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Comprehensive Biochemical and Biophysical Characterization of Hemoglobin-Based Oxygen Carrier Therapeutics: All HBOCs Are Not Created Equally

Bioconjugate chemistry, 2018-05, Vol.29 (5), p.1560-1575

2018

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Sickle Cell Hemoglobin in the Ferryl State Promotes βCys-93 Oxidation and Mitochondrial Dysfunction in Epithelial Lung Cells (E10)

The Journal of biological chemistry, 2015-11, Vol.290 (46), p.27939-27958

2015

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Substitutions in the β subunits of sickle-cell hemoglobin improve oxidative stability and increase the delay time of sickle-cell fiber formation

The Journal of biological chemistry, 2019-03, Vol.294 (11), p.4145-4159

2019

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Sexuality and sexual reproductive health of disabled young people in Ethiopia

Sexually transmitted diseases, 2014-10, Vol.41 (10), p.583-588

2014

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Targeting βCys93 in hemoglobin S with an antisickling agent possessing dual allosteric and antioxidant effects

Metallomics, 2017-09, Vol.9 (9), p.1260-1270

2017

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Hemoglobin oxidation-dependent reactions promote interactions with band 3 and oxidative changes in sickle cell-derived microparticles

JCI insight, 2018-11, Vol.3 (21)

2018

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Post-translational transformation of methionine to aspartate is catalyzed by heme iron and driven by peroxide: a novel subunit-specific mechanism in hemoglobin

The Journal of biological chemistry, 2014-08, Vol.289 (32), p.22342-22357

2014

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

Blood, 2016-12, Vol.128 (22), p.856-856

2016

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Post-translational Transformation of Methionine to Aspartate Is Catalyzed by Heme Iron and Driven by Peroxide

The Journal of biological chemistry, 2014-08, Vol.289 (32), p.22342-22357

2014

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Crystallographic evidence for oxidative Met→Asp conversion in human hemoglobin

Acta crystallographica. Section A, Foundations and advances, 2014-08, Vol.70 (a1), p.C310-C310

2014

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Design, synthesis, and activity of 2,3-diphosphoglycerate analogs as allosteric modulators of hemoglobin O 2 affinity

Artificial cells, nanomedicine, and biotechnology, 2013-04, Vol.41 (2), p.109-115

2013

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Design and Synthesis of Novel Phosphonate Analogs of 2,3-Diphosphoglycerate as Hemoglobin Modifiers

Kassa, Tigist Wondwossen

2011

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Assessment of drug-related problems in pediatric ward of Zewditu Memorial Referral Hospital, Addis Ababa, Ethiopia

International journal of clinical pharmacy, 2017-10, Vol.39 (5), p.1039-1046

2017

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Readiness of the primary health care units and associated factors for the management of hypertension and type II diabetes mellitus in Sidama, Ethiopia

PeerJ (San Francisco, CA), 2022-08, Vol.10, p.e13797-e13797, Article e13797

2022

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Understanding spatial patterns of soils for sustainable agriculture in northern Ethiopia's tropical mountains

PloS one, 2019-10, Vol.14 (10), p.e0224041

2019

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Impact of cold storage on the oxygenation and oxidation reactions of red blood cells

Changes in hemoglobin oxidation and band 3 during blood storage impact oxygen sensing and mitochondrial bioenergetic pathways in the human pulmonary arterial endothelial cell model

Differential heme release from various hemoglobin redox states and the upregulation of cellular heme oxygenase‐1

Antisickling Drugs Targeting βCys93 Reduce Iron Oxidation and Oxidative Changes in Sickle Cell Hemoglobin

Caffeic acid: an antioxidant with novel antisickling properties

Effects of α subunit substitutions on the oxidation of βCys93 and the stability of sickle cell hemoglobin

Sexual and reproductive health of young people with disability in Ethiopia: a study on knowledge, attitude and practice: a cross-sectional study

Oxidative instability of hemoglobin E (β26 Glu→Lys) is increased in the presence of free α subunits and reversed by α-hemoglobin stabilizing protein (AHSP): Relevance to HbE/β-thalassemia

Appropriate complementary feeding practices and associated factors among mothers of children age 6-23 months in Southern Ethiopia, 2015

Design, synthesis, and activity of 2,3-diphosphoglycerate analogs as allosteric modulators of hemoglobin O2 affinity

Comprehensive Biochemical and Biophysical Characterization of Hemoglobin-Based Oxygen Carrier Therapeutics: All HBOCs Are Not Created Equally

Sickle Cell Hemoglobin in the Ferryl State Promotes βCys-93 Oxidation and Mitochondrial Dysfunction in Epithelial Lung Cells (E10)

Substitutions in the β subunits of sickle-cell hemoglobin improve oxidative stability and increase the delay time of sickle-cell fiber formation

Sexuality and sexual reproductive health of disabled young people in Ethiopia

Targeting βCys93 in hemoglobin S with an antisickling agent possessing dual allosteric and antioxidant effects

Hemoglobin oxidation-dependent reactions promote interactions with band 3 and oxidative changes in sickle cell-derived microparticles

Post-translational transformation of methionine to aspartate is catalyzed by heme iron and driven by peroxide: a novel subunit-specific mechanism in hemoglobin

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

Post-translational Transformation of Methionine to Aspartate Is Catalyzed by Heme Iron and Driven by Peroxide

Crystallographic evidence for oxidative Met→Asp conversion in human hemoglobin

Design, synthesis, and activity of 2,3-diphosphoglycerate analogs as allosteric modulators of hemoglobin O 2 affinity

Design and Synthesis of Novel Phosphonate Analogs of 2,3-Diphosphoglycerate as Hemoglobin Modifiers

Assessment of drug-related problems in pediatric ward of Zewditu Memorial Referral Hospital, Addis Ababa, Ethiopia

Readiness of the primary health care units and associated factors for the management of hypertension and type II diabetes mellitus in Sidama, Ethiopia

Understanding spatial patterns of soils for sustainable agriculture in northern Ethiopia's tropical mountains

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