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1 This was due to an increase in the amount of adenine nucleotide translocase.
2  source, ATP depletion, or inhibition of the adenine nucleotide translocase.
3 tage-dependent anion channel (porin) and the adenine nucleotide translocase.
4 of porin, mitochondrial creatine kinase, and adenine nucleotide translocase.
5 hondria is known to be cardioprotective, and adenine nucleotide translocase 1 (ANT1) is a key mediato
6                                              Adenine nucleotide translocase 1 (Ant1) is a mitochondri
7 ondria, to interact with and dephosphorylate adenine nucleotide translocase 1 (ANT1), a central molec
8               For mice deficient in the nDNA adenine nucleotide translocase 1 (Ant1), endurance exerc
9 nd several mitochondrial proteins, including adenine nucleotide translocase 1 (ANT1), were more oxidi
10 xhibit strong deacetylation of mitochondrial adenine nucleotide translocases 1 and 2 (ANT1/2).
11 eviously cloned cDNAs derived from the mouse adenine nucleotide translocase-1 and -2 genes (Ant1 and
12 els of cytochrome oxidase, cytochrome c, and adenine nucleotide translocase-1.
13 his study sheds light on the central role of adenine nucleotide translocase 2 (ANT2) in the pathogene
14 olve saturated fatty acid stimulation of the adenine nucleotide translocase 2 (ANT2), an inner mitoch
15              Proteomics screening identified adenine nucleotide translocase 3 (ANT3) as a previously
16 us-purified voltage-dependent anion channel, adenine nucleotide translocase and the fusion protein we
17 bility transition pore that is formed by the adenine nucleotide translocase and the voltage-dependent
18  increased oxygen consumption independent of adenine nucleotide translocase and uncoupling proteins,
19 ctivity was insensitive to inhibitors of the adenine nucleotide translocase (ANT) and of the voltage-
20 ease of the apparent molecular weight of the adenine nucleotide translocase (ANT) by up to 1.2 kDa.
21 een mitochondrial creatine kinase (MtCK) and adenine nucleotide translocase (ANT) can play an importa
22                                              Adenine nucleotide translocase (Ant) catalyzes ADP/ATP e
23                                              Adenine nucleotide translocase (ANT) exchanges ADP/ATP t
24                               Members of the adenine nucleotide translocase (ANT) family exchange ADP
25 t the MPTP has two molecular components, the adenine nucleotide translocase (ANT) family of proteins
26  regulators are cyclophilin D (CypD) and the adenine nucleotide translocase (ANT) family.
27 n maleimide is known to attack Cys159 of the adenine nucleotide translocase (ANT) in a CAT-sensitive
28 nding puzzle is that in permeabilized cells, adenine nucleotide translocase (ANT) is less accessible
29                                              Adenine nucleotide translocase (Ant) is the most abundan
30                     Only two isoforms of the adenine nucleotide translocase (Ant) protein have been i
31 oside and bongkrekic acid, inhibitors of the adenine nucleotide translocase (ANT) that lock the trans
32                                              Adenine nucleotide translocase (ANT) was found to be the
33 mely voltage-dependent anion channel (VDAC), adenine nucleotide translocase (ANT), and hexokinase II
34 was attenuated by knockdown or inhibition of adenine nucleotide translocase (ANT), cyclophilin D (Cyp
35 trometry analysis identified this protein as adenine nucleotide translocase (ANT), represented by two
36 or alpha induced RIP-dependent inhibition of adenine nucleotide translocase (ANT)-conducted transport
37 ibits all ADP-ATP-using reactions except the adenine nucleotide translocase (ANT)-mediated mitochondr
38 by carboxyatractyloside, an inhibitor of the adenine nucleotide translocase (ANT).
39 oupling proteins UCP1, UCP2 and UCP3 and the adenine nucleotide translocase (ANT).
40                                          The adenine nucleotide translocases (Ant) facilitate the tra
41                 The ADP/ATP translocator (or adenine nucleotide translocase; ANT) is thought to play
42 rebellar glucocorticoid hormone receptor and adenine nucleotide translocase (ANT1) were downregulated
43                                              Adenine nucleotide translocases are mitochondrial membra
44 ds, these mitochondria also showed a greater adenine nucleotide translocase-catalysed proton conducta
45                               Suppression of adenine nucleotide translocase content may be a key fact
46 n pore (ie, voltage-dependent anion channel, adenine nucleotide translocase, cyclophilin D).
47 d increased proton transport activity of the adenine nucleotide translocase (dependent on fatty acids
48 cle depended on electron transport chain and adenine nucleotide translocase functionality, but it was
49   This study provides evidence for a role of adenine nucleotide translocase in the mechanism underlyi
50                                          The adenine nucleotide translocase inhibitor bongkrekic acid
51 ependent anion channel (outer membrane), the adenine nucleotide translocase (inner membrane) and cycl
52 ge-dependent anion channel (outer membrane), adenine nucleotide translocase (inner membrane) and cycl
53 ation, increased levels of the mitochondrial adenine nucleotide translocase stress-sensitive B (SesB)
54  the voltage-dependent anion channel and the adenine nucleotide translocase were similar in the two m
55 ction of both the F(1)F(O)-ATPase and of the adenine nucleotide translocase, which delivers nucleotid
56 ation/knockdown-induced dysregulation in the adenine nucleotide translocase, which results in a slowe