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NADH oxidation
Known as:
reduced nicotinamide adenine dinucleotide oxidation
, reduced nicotinamide adenine dinucleotide dehydrogenation
, NAD (reduced) dehydrogenation
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A metabolic process that results in the oxidation of reduced nicotinamide adenine dinucleotide, NADH, to the oxidized form, NAD. [GOC:ai]
National Institutes of Health
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Highly Cited
2018
Highly Cited
2018
Hydroxyl-Mediated Non-oxidative Propane Dehydrogenation over VOx /γ-Al2 O3 Catalysts with Improved Stability.
Zhijian Zhao
,
Tengfang Wu
,
+4 authors
Jinlong Gong
Angewandte Chemie
2018
Corpus ID: 3822734
Supported vanadium oxides are one of the most promising alternative catalysts for propane dehydrogenation (PDH) and efforts have…
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Highly Cited
2009
Highly Cited
2009
Lignosulfonate-modified electrodes: electrochemical properties and electrocatalysis of NADH oxidation.
G. Milczarek
Langmuir
2009
Corpus ID: 6074874
Lignosulfonic acid (LS1) and partially desulfonated lignosulfonic acid (LS2) were oxidatively deposited on a preactivated glassy…
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Highly Cited
2009
Highly Cited
2009
1,1,8,8-Tetramethyl[8](2,11)teropyrenophane: half of an aromatic belt and a segment of an (8,8) single-walled carbon nanotube.
B. Merner
,
Louise N. Dawe
,
G. Bodwell
Angewandte Chemie
2009
Corpus ID: 24614769
and single-walled carbon nanotubes (SWCNTs). Indeed, they can be viewed as the shortest possible open-ended (uncapped) zig-zag…
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Highly Cited
2007
Highly Cited
2007
Production of l-alanine by metabolically engineered Escherichia coli
Xueli Zhang
,
Kaemwich Jantama
,
Jonathan C. Moore
,
K. T. Shanmugam
,
L. O. Ingram
Applied Microbiology and Biotechnology
2007
Corpus ID: 9161551
Escherichia coli W was genetically engineered to produce l-alanine as the primary fermentation product from sugars by replacing…
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Highly Cited
2002
Highly Cited
2002
Halothane, isoflurane and sevoflurane inhibit NADH: ubiquinone oxidoreductase (complex I) of cardiac mitochondria
P. Hanley
,
J. Ray
,
U. Brandt
,
J. Daut
Journal of Physiology
2002
Corpus ID: 12615603
We have investigated the effects of volatile anaesthetics on electron transport chain activity in the mammalian heart. Halothane…
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Highly Cited
2002
Highly Cited
2002
KATP channel‐independent targets of diazoxide and 5‐hydroxydecanoate in the heart
P. Hanley
,
M. Mickel
,
M. Löffler
,
U. Brandt
,
J. Daut
Journal of Physiology
2002
Corpus ID: 20963078
Diazoxide and 5‐hydroxydecanoate (5‐HD; C10:0) are reputed to target specifically mitochondrial ATP‐sensitive K+ (KATP) channels…
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Highly Cited
2002
Highly Cited
2002
On the mechanism of (PCP)Ir-catalyzed acceptorless dehydrogenation of alkanes: a combined computational and experimental study.
K. Krogh-Jespersen
,
Margaret Czerw
,
Nadine Summa
,
K. B. Renkema
,
Patrick D Achord
,
A. Goldman
Journal of the American Chemical Society
2002
Corpus ID: 41713458
Pincer complexes of the type ((R)PCP)IrH(2), where ((R)PCP)Ir is [eta(3)-2,6-(R(2)PCH(2))(2)C(6)H(3)]Ir, are the most effective…
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Highly Cited
2000
Highly Cited
2000
In Vivo Analysis of the Mechanisms for Oxidation of Cytosolic NADH by Saccharomyces cerevisiaeMitochondria
K. Overkamp
,
Barbara M. Bakker
,
+4 authors
J. Pronk
Journal of Bacteriology
2000
Corpus ID: 12536869
ABSTRACT During respiratory glucose dissimilation, eukaryotes produce cytosolic NADH via glycolysis. This NADH has to be…
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Highly Cited
1995
Highly Cited
1995
Evidence for free radical generation due to NADH oxidation by aldehyde oxidase during ethanol metabolism.
L. Mira
,
L. Maia
,
L. Barreira
,
C. Manso
Archives of Biochemistry and Biophysics
1995
Corpus ID: 33368804
Several studies associate ethanol hepatic toxicity to the generation of reactive oxygen species. Ethanol metabolism by alcohol…
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Highly Cited
1973
Highly Cited
1973
Mechanism of action of the hypoglycemic agent diphenyleneiodonium.
P. Holland
,
M. Clark
,
D. Bloxham
,
H. Lardy
Journal of Biological Chemistry
1973
Corpus ID: 31186569
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