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

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Oxidized Mutant Human Hemoglobins S and E Induce Oxidative Stress and Bioenergetic Dysfunction in Human Pulmonary Endothelial Cells.Engineering oxidative stability in human hemoglobin based on the Hb providence (βK82D) mutation and genetic cross-linking.

P2860

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P2860

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

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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name

Targeting βCys93 in hemoglobin ...... teric and antioxidant effects.

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Targeting βCys93 in hemoglobin ...... teric and antioxidant effects.

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Targeting βCys93 in hemoglobin ...... teric and antioxidant effects.

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Targeting βCys93 in hemoglobin ...... teric and antioxidant effects.

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Targeting βCys93 in hemoglobin ...... teric and antioxidant effects.

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Targeting βCys93 in hemoglobin ...... teric and antioxidant effects.

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P1476

Targeting βCys93 in hemoglobin ...... teric and antioxidant effects.

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P2093

Abdu I Alayash

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Akito Nakagawa

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M B Strader

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Tigist Kassa

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Warren M Zapol

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P2860

Identification of a Small Molecule that Increases Hemoglobin Oxygen Affinity and Reduces SS Erythrocyte Sickling

Kinetics of increased deformability of deoxygenated sickle cells upon oxygenation.

The Molecular Mechanism of Autoxidation for Myoglobin and Hemoglobin: A Venerable Puzzle.

Reconstructing sickle cell disease: a data-based analysis of the "hyperhemolysis paradigm" for pulmonary hypertension from the perspective of evidence-based medicine.

Redox properties of human hemoglobin in complex with fractionated dimeric and polymeric human haptoglobin

Harnessing free radicals: formation and function of the tyrosyl radical in ribonucleotide reductase.

Hemoglobins S and C interfere with actin remodeling in Plasmodium falciparum-infected erythrocytes.

Sickle cell disease vasculopathy: a state of nitric oxide resistance.

Circulating cell membrane microparticles transfer heme to endothelial cells and trigger vasoocclusions in sickle cell disease.

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

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1260-1270

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scholarly article

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10.1039/C7MT00104E

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2017-08-03T00:00:00Z

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28770911

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5607114

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

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P2860

P2860

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

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P932