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1              Atp5g1 encodes a subunit of the mitochondrial ATP synthase.
2 mPTP in HAP1 cell lines lacking an assembled mitochondrial ATP synthase.
3  microtubules, clathrin, photosystem II, and mitochondrial ATP synthase.
4 pening is markedly sensitized by loss of the mitochondrial ATP synthase.
5 ther (blw) gene encodes the alpha subunit of mitochondrial ATP synthase.
6 omicroscopy (cryo-EM) analysis of the bovine mitochondrial ATP synthase.
7 hesized in eukaryotic cells primarily by the mitochondrial ATP synthase.
8  is one of several assembly modules of yeast mitochondrial ATP synthase.
9 y related to the single b subunit present in mitochondrial ATP synthase.
10 bound to the subunit c(10) ring of the yeast mitochondrial ATP synthase.
11 ediates during the assembly process of plant mitochondrial ATP synthase.
12 present study of the oxidative regulation of mitochondrial ATP synthase.
13  shown to uncouple this process in the yeast mitochondrial ATP synthase.
14 es during assembly of the F(1) moiety of the mitochondrial ATP synthase.
15 inorganic phosphate from cellular ATPases to mitochondrial ATP synthase.
16 utations in the alpha- and gamma-subunits of mitochondrial ATP synthase.
17 equired for assembly of the F1 moiety of the mitochondrial ATP synthase.
18 r proper assembly of the F1 component of the mitochondrial ATP synthase.
19 strates other than subunits in the assembled mitochondrial ATP synthase.
20 on, tendency of amelioration of subunit c of mitochondrial ATP synthase accumulation and glial fibril
21 allmarks include lipofuscin and subunit c of mitochondrial ATP synthase accumulation, mitochondrial d
22 eural dysfunction, and a marked reduction in mitochondrial ATP synthase activity associated with this
23                           This increased the mitochondrial ATP synthase activity to the extent that g
24  FP patient ADEV level but not NDEV level of mitochondrial ATP synthase activity was significantly lo
25 en the cytosol and matrix, [MgADP]-dependent mitochondrial ATP synthase activity, and cytosolic free
26 um handling, beta-adrenergic responsiveness, mitochondrial ATP synthase activity, cell survival signa
27  muscle cells we engineered deficient in the mitochondrial ATP synthase also demonstrate sensitizatio
28 n ATP5F1B, which encodes the beta subunit of mitochondrial ATP synthase (also called complex V).
29 expressed 20-35%, including the f-subunit of mitochondrial ATP synthase and a retrovirus-related DNA.
30  of transcripts encoding the Fo-f subunit of mitochondrial ATP synthase and manganese superoxide dism
31 hat CCCP lowered ATP levels by reversing the mitochondrial ATP synthase and so reducing SR Ca2+ refil
32 rring protein, an essential component of the mitochondrial ATP synthase, and is ubiquitously expresse
33 block the formation of the F(1) component of mitochondrial ATP synthase are also petite-negative.
34                        We identified ectopic mitochondrial ATP synthase as a factor that mediates HIV
35 ptolidins to identify the F(1) subcomplex of mitochondrial ATP synthase as the target of apoptolidin
36 e, we present the structure of intact bovine mitochondrial ATP synthase at approximately 18 A resolut
37  W-chromosomal gene for the alpha subunit of mitochondrial ATP synthase (ATP5A1W).
38 rectly interact with the beta subunit of the mitochondrial ATP-synthase (ATP5B), which may therefore
39 transferase (KMT) targeting the c-subunit of mitochondrial ATP synthase (ATPSc), and was therefore re
40                           We knocked out the mitochondrial ATP synthase beta subunit gene in the rode
41 membrane potential and having identified the mitochondrial ATP synthase beta subunit in a screen for
42 length epitope-tagged ROMK2 colocalizes with mitochondrial ATP synthase beta.
43 el conductance was unaffected by loss of the mitochondrial ATP synthase but still blocked by cyclophi
44 fferent ion channels, and the suppression of mitochondrial ATP synthase by alpha-ketoglutarate, which
45 ior genetic studies indicated that the yeast mitochondrial ATP synthase can be assembled into enzyme
46                                              Mitochondrial ATP synthase catalyzes the coupling of oxi
47 known, is that the beta-subunit of the human mitochondrial ATP synthase co-immunoprecipitates with hs
48                     Our data reveal that the mitochondrial ATP synthase complex functions in the bloo
49 ction between protein C7orf55 (FMC1) and the mitochondrial ATP synthase complex that we have experime
50 Pase 6, a component of the F0 portion of the mitochondrial ATP synthase complex.
51 th the myofibrils: GAPDH and proteins of the mitochondrial ATP synthase complex.
52  downregulation impairs only subunits of the mitochondrial ATP synthase (complex V).
53 rial inner membrane and the interaction with mitochondrial ATP synthase, contributing to the maintena
54                                          The mitochondrial ATP synthase couples the flow of protons w
55 ologous to the 5'UTR of mouse, rat and human mitochondrial ATP synthase coupling factor 6 (ATPsynCF6)
56                            ATP hydrolysis by mitochondrial ATP Synthase (CV) is induced by loss of pr
57     We determined the structure of an intact mitochondrial ATP synthase dimer by electron cryo-micros
58 he in situ structure and organization of the mitochondrial ATP synthase dimer of the ciliate Parameci
59          We reconstituted detergent-purified mitochondrial ATP synthase dimers from the green algae P
60 aging to determine the in situ structures of mitochondrial ATP synthase dimers from two organisms bel
61                                Structures of mitochondrial ATP synthase dimers indicate how they shap
62                        Using yeast models of mitochondrial ATP synthase disorders, we screened a drug
63                         We conclude that the mitochondrial ATP synthase does not function as mPTP and
64                                          The mitochondrial ATP synthase emerges as key hub of cellula
65 ecular insight into the complex structure of mitochondrial ATP synthase (F(0)F(1)) and its relationsh
66                                          The mitochondrial ATP synthase (F(1)-F(0) complex) of Saccha
67                                          The mitochondrial ATP synthase (F(1)F(o) complex) is an evol
68 ansduction and stress responses, whereas the mitochondrial ATP synthase F0 subunit component is a vas
69 rotein (OSCP) is an essential subunit of the mitochondrial ATP synthase (F0F1) long regarded as being
70 sitivity conferring protein (OSCP) of bovine mitochondrial ATP synthase (F1Fo) indicated that a delet
71 er anaplerotic, tricarboxylic acid cycle and mitochondrial ATP synthase fluxes predicted in the forme
72 e C-terminus within the gamma subunit of the mitochondrial ATP synthase form a "catch" with an anioni
73                                              Mitochondrial ATP synthases form dimers, which assemble
74                                          The mitochondrial ATP synthase fuels eukaryotic cells with c
75 he hydrolysis of ATP within the F1 moiety of mitochondrial ATP synthase function in a kinetically equ
76  in Arabidopsis thaliana of the d subunit of mitochondrial ATP synthase (gene name: ATPQ, AT3G52300,
77 ted membrane protein 1), SCMAS (subunit c of mitochondrial ATP synthase), glypican 5, beta-amyloid, P
78                                     Purified mitochondrial ATP synthase has been shown to form Ca(2+)
79 ays a crucial role in proper function of the mitochondrial ATP synthase holoenzyme, which, when reduc
80 nt zebrafish display storage of subunit c of mitochondrial ATP-synthase, hypertrophic lysosomes as we
81 ed for assembly of the F(1) component of the mitochondrial ATP synthase in Saccharomyces cerevisiae.
82   These data reveal the fuel-sensing role of mitochondrial ATP synthase in the control of ATP product
83 ut not lefleuganan, specifically targets the mitochondrial ATP synthase, inhibiting ATP synthesis by
84                                          The mitochondrial ATP synthase inhibitor oligomycin protecte
85  mimicked by treating MDM with oligomycin (a mitochondrial ATP synthase inhibitor), both 2-DG and glu
86                   In contrast, oligomycin, a mitochondrial ATP synthase inhibitor, had minimal effect
87                                          The mitochondrial ATP synthase inhibitor, oligomycin, signif
88 ect is prevented by NMMA and mimicked by the mitochondrial ATP-synthase inhibitor oligomycin.
89 uscularis preparations were treated with the mitochondrial ATP synthase inhibitors oligomycin or dicy
90 dence that, rather than serving as mPTP, the mitochondrial ATP synthase inhibits this pore.
91                                        Human mitochondrial ATP synthase is a molecular machine with a
92                                          The mitochondrial ATP synthase is a molecular motor, which c
93                                              Mitochondrial ATP synthase is a reversible nanomotor syn
94 r machinery required for the assembly of the mitochondrial ATP synthase is conserved from bovine and
95            Proton-powered c-ring rotation in mitochondrial ATP synthase is crucial to convert the tra
96   Further, mPTP opening in cells lacking the mitochondrial ATP synthase is desensitized by pharmacolo
97                                              Mitochondrial ATP synthase is driven by chemiosmotic oxi
98 sts and sporozoites, which demonstrates that mitochondrial ATP synthase is essential for ongoing viab
99 neration, which begs the question of whether mitochondrial ATP synthase is necessary during the blood
100                                              Mitochondrial ATP synthase is responsible for the synthe
101                                Inhibition of mitochondrial ATP synthase markedly reduces macrophage c
102 s variants in genes encoding subunits of the mitochondrial ATP synthase may cause autosomal dominant
103                  ATP5F1B is a subunit of the mitochondrial ATP synthase or complex V of the mitochond
104                                              Mitochondrial ATP synthase plays a key role in inducing
105                                  Monomers of mitochondrial ATP synthase reconstituted into liposomes
106 ion and nucleotide clamping or inhibition of mitochondrial ATP synthase, regulate NO signaling by sGC
107                    These features, absent in mitochondrial ATP synthases, represent attractive target
108 ent storage material containing subunit c of mitochondrial ATP synthase (SCMAS), ultimately resulting
109 e of catabolites, including the subunit c of mitochondrial ATP synthase (SCMAS).
110 ained from crystals of a subcomplex of yeast mitochondrial ATP synthase shows a ring of 10 c subunits
111  An X-ray structure of the F1 portion of the mitochondrial ATP synthase shows asymmetry and differenc
112 uld not be explained by the reversed mode of mitochondrial ATP-synthase, since oligomycin was not eff
113 e Drosophila gene for the epsilon-subunit of mitochondrial ATP synthase, stunted (sun).
114  and interacts with the alpha-subunit of the mitochondrial ATP synthase to promote mitochondrial biog
115                                    Extracted mitochondrial ATP synthase was specifically immunofixed
116 sitivity conferring protein (OSCP) of bovine mitochondrial ATP synthase were studied by nested deleti
117                One proposed candidate is the mitochondrial ATP synthase, whose canonical function is

 
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