IRP1-independent alterations of cardiac iron metabolism in doxorubicin-treated mice.
about
Regulation of cellular iron metabolismDual Role of ROS as Signal and Stress Agents: Iron Tips the Balance in favor of Toxic EffectsIron-regulatory proteins: molecular biology and pathophysiological implicationsMice lacking mitochondrial ferritin are more sensitive to doxorubicin-mediated cardiotoxicity.Iron regulatory protein 1 outcompetes iron regulatory protein 2 in regulating cellular iron homeostasis in response to nitric oxide.Cysteine oxidation regulates the RNA-binding activity of iron regulatory protein 2The role of iron in anthracycline cardiotoxicity.Redox control of iron regulatory protein 2 stability.Protective effect of mitochondrial ferritin on cytosolic iron dysregulation induced by doxorubicin in HeLa cells.H-Chain Ferritin: A Natural Nuclei Targeting and Bioactive Delivery Nanovector.
P2860
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P2860
IRP1-independent alterations of cardiac iron metabolism in doxorubicin-treated mice.
description
2006 nî lūn-bûn
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name
IRP1-independent alterations of cardiac iron metabolism in doxorubicin-treated mice.
@en
IRP1-independent alterations of cardiac iron metabolism in doxorubicin-treated mice.
@nl
type
label
IRP1-independent alterations of cardiac iron metabolism in doxorubicin-treated mice.
@en
IRP1-independent alterations of cardiac iron metabolism in doxorubicin-treated mice.
@nl
prefLabel
IRP1-independent alterations of cardiac iron metabolism in doxorubicin-treated mice.
@en
IRP1-independent alterations of cardiac iron metabolism in doxorubicin-treated mice.
@nl
P1476
IRP1-independent alterations of cardiac iron metabolism in doxorubicin-treated mice.
@en
P2093
Bruno Galy
Gianfranca Corna
P2888
P304
P356
10.1007/S00109-006-0068-Y
P577
2006-06-13T00:00:00Z