A transgenic mouse model expressing exclusively human hemoglobin E: indications of a mild oxidative stress.
about
HbE/β-Thalassemia and Oxidative Stress: The Key to Pathophysiological Mechanisms and Novel Therapeutics.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.Generating S-nitrosothiols from hemoglobin: mechanisms, conformational dependence, and physiological relevance.The G6PD flow-cytometric assay is a reliable tool for diagnosis of G6PD deficiency in women and anaemic subjects.Oxidized Mutant Human Hemoglobins S and E Induce Oxidative Stress and Bioenergetic Dysfunction in Human Pulmonary Endothelial Cells.
P2860
A transgenic mouse model expressing exclusively human hemoglobin E: indications of a mild oxidative stress.
description
2012 nî lūn-bûn
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2012年の論文
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name
A transgenic mouse model expre ...... ns of a mild oxidative stress.
@ast
A transgenic mouse model expre ...... ns of a mild oxidative stress.
@en
type
label
A transgenic mouse model expre ...... ns of a mild oxidative stress.
@ast
A transgenic mouse model expre ...... ns of a mild oxidative stress.
@en
prefLabel
A transgenic mouse model expre ...... ns of a mild oxidative stress.
@ast
A transgenic mouse model expre ...... ns of a mild oxidative stress.
@en
P2093
P2860
P1476
A transgenic mouse model expre ...... ns of a mild oxidative stress.
@en
P2093
Anne C Rybicki
David Lefer
Dhananjay K Kaul
Edna K Akoto
Eric E Bouhassira
Frans A Kuypers
Joseph E Canterino
Kitty de Jong
Mary E Fabry
Qiuying Chen
P2860
P304
P356
10.1016/J.BCMD.2011.12.002
P577
2012-01-18T00:00:00Z