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1 he outside of mitochondria, SH1 and SUS1 are intramitochondrial.
2 type inborn errors of metabolism because the intramitochondrial accumulation of P-CoA, M-CoA, and oth
3       This is associated with a reduction in intramitochondrial accumulation of the Mia40 substrate,
4   In conclusion, unlike fungi, which have an intramitochondrial acetyl-CoA carboxylase, animals requi
5 ated in neurons after ischemia and to cleave intramitochondrial AIF near its N terminus.
6 The results substantiate the hypothesis that intramitochondrial arginase, presumably the arginase-II
7 re known to bind to VDAC and directly couple intramitochondrial ATP synthesis to glucose metabolism.
8 ricular mitochondria demonstrated negligible intramitochondrial CA activity.
9 e sites, possibly reflecting a high-capacity intramitochondrial Ca storage mechanism.
10 y the activity of the complete MAS, and that intramitochondrial Ca(2+) accounts for the remaining 15%
11 Ca(2+) that entered mitochondria is bound by intramitochondrial Ca(2+) buffering systems.
12 ctivation of mitochondrial dehydrogenases by intramitochondrial Ca(2+) cannot be the exclusive mechan
13              We hypothesized that changes in intramitochondrial Ca(2+) concentration ([Ca(2+)](m)) de
14 a are also Ca(2+)-dependent, suggesting that intramitochondrial Ca(2+) concentration is important for
15            The elevations of cytoplasmic and intramitochondrial Ca(2+) concentrations and mitochondri
16 a(2+) affinities are engineered to match the intramitochondrial Ca(2+) concentrations.
17 study is the first to show that NLF inhibits intramitochondrial Ca(2+) flux and protects developing b
18 ermine in a quantitative manner if extra- or intramitochondrial Ca(2+) modulates oxidative phosphoryl
19 ental mechanism of post-ischemic cell death: intramitochondrial Ca(2+) overload --> mitochondrial mem
20 ) currents via PTP opening and a decrease in intramitochondrial [Ca(2+)].
21 iew, we critically evaluate the evidence for intramitochondrial Ca2+ ([Ca2+](m)) sensitivity in key e
22                                              Intramitochondrial Ca2+ concentration, measured using rh
23 ochondrial Ca2+ ([Ca2+]m) increase regulates intramitochondrial Ca2+-sensitive targets.
24                   MCUC dysfunction decreases intramitochondrial calcium ([Ca(2+)]mito), inhibiting py
25  exocytosis but also, via an increase in the intramitochondrial calcium ion concentration, stimulate
26 ix-bound soluble adenylyl cyclase) increased intramitochondrial cAMP, but along with membrane-permean
27            Glucocorticoid synthesis requires intramitochondrial cholesterol transport mediated by the
28 ick-triggered activation of a caged prodrug, intramitochondrial cleavage of a fluorogenic probe (turn
29                       In mammalian cells, an intramitochondrial CO2-adenylyl cyclase (AC)-cyclic AMP
30 c mice and that SOD1 displays a very complex intramitochondrial compartmentalization.
31 in vivo could be modulated by changes in the intramitochondrial concentrations of Ca2+ or Mg2+.
32 gnificance of interorganellar communication, intramitochondrial contact sites, and lipid transfer pro
33           Overall, the pathway is subject to intramitochondrial control at multiple sites.
34                                              Intramitochondrial cristae density of synGLT-1 KO mice w
35 the redistribution of cytochrome c stored in intramitochondrial cristae.
36 sion are regulated and to what extent direct intramitochondrial cross talk between different processe
37                                              Intramitochondrial crystals (IMCs) are a well-documented
38              These results indicate that the intramitochondrial crystals characteristic of NASH are h
39 ial quality control prevents accumulation of intramitochondrial-derived reactive oxygen species (mtRO
40                           We postulated that intramitochondrial disturbances in NASH are sufficient t
41 e consistent with the hypothesis that normal intramitochondrial dNTP pool asymmetries may contribute
42  the cell nucleus can compensate for loss of intramitochondrial dTMP synthesis in differentiated tiss
43 ial (DeltaPsim), but Ca(2)(+) binding of the intramitochondrial enzymes accelerates oxidative phospho
44                  We now show that these same intramitochondrial events that generate signals for leuc
45 and mitochondrial integrity during ischemia, intramitochondrial F(0)F(1) adenosine triphosphate (ATP)
46 ogeneity of DeltaPsim is mainly modulated by intramitochondrial factors, it is independent of the Del
47 r heterogeneity of Wm is mainly modulated by intramitochondrial factors, it is independent of the Wm
48 ADP(H)-binding 39-kDa subunit is involved in intramitochondrial fatty acid synthesis.
49    We also describe a hitherto unrecognized, intramitochondrial, filamentous structure rich in basic
50 itochondrial superoxide anion (O(2)(.-)) and intramitochondrial free iron released as a result of MOS
51                                              Intramitochondrial free radicals generated by paraquat o
52               We conclude that an endogenous intramitochondrial H(2)S-producing pathway, governed by
53 S-complex components or Opa1 diminished this intramitochondrial heterogeneity of DeltaPsi(m) .
54     Isovaleryl-CoA dehydrogenase (IVD) is an intramitochondrial homotetrameric flavoenzyme that catal
55                                          The intramitochondrial indo-1 concentration was 0.5-2 mM.
56 resent report shows that tamoxifen increases intramitochondrial ionized Ca(2+) concentration and stim
57  neonatal anemia characterized by pathologic intramitochondrial iron deposits in erythrocytes.
58 brane potential was significantly increased, intramitochondrial levels of reactive oxygen species and
59 ane-bound TIM23-imported proteins have lower intramitochondrial levels, whereas inner membrane multis
60 6 for respiratory complex IV biogenesis, its intramitochondrial localization and the presence of the
61  interaction we evaluated the presence of an intramitochondrial localization for three Midichloria in
62 ve of this study was to identify a source of intramitochondrial malonyl-CoA that could be used for de
63 rial NAD-capped RNA levels and may influence intramitochondrial NAD levels.
64 port for the alternative possibility, namely intramitochondrial NAD(+) synthesis, by demonstrating th
65  for moving reducing equivalents between the intramitochondrial [NAD(+) ]/[NADH] pool to molecular ox
66 shold, which can be modulated by the PO2 and intramitochondrial [NAD(+) ]/[NADH].
67 ivity of the PDC in the face of the elevated intramitochondrial NADH/NAD+ ratios associated with anae
68 activity being markedly enhanced by elevated intramitochondrial NADH:NAD+ and acetyl-CoA:CoA ratios.
69 s are known to be mutagenic, we suggest that intramitochondrial nucleotide imbalance could underlie t
70                           Last, H2O2 induced intramitochondrial O2-, whereas paraquat produced O2- ou
71 d with Fura-2, and a significant increase in intramitochondrial oxidation of dihydrorhodamine 123, pr
72 ctly couple extramitochondrial glycolysis to intramitochondrial oxidative phosphorylation, and are th
73     Instead, deficits of complex I stimulate intramitochondrial oxidative stress, which, in turn, inc
74 ar PA and YME1L-dependent degradation of the intramitochondrial PA transporter PRELID1.
75                        We then elucidated an intramitochondrial pathway in which interaction of JNK a
76   In brief, we found that UCP4 regulates the intramitochondrial pH of astrocytes, which acidifies as
77 ster, and a membrane-permeable base to raise intramitochondrial pH.
78 f BCKD kinase and the activity of an unknown intramitochondrial phosphatase.
79 tes osteogenic differentiation by decreasing intramitochondrial phosphate and ATP synthesis.
80 esult is consistent with a deficiency in the intramitochondrial pool of dTTP relative to dCTP in cell
81 a(2+) uptake by compounds that dissipate the intramitochondrial potential unmasks Ca(2+)-dependent in
82              We found that interference with intramitochondrial proteases, such as HtrA2 and Lon prot
83     Emerging evidence has suggested that the intramitochondrial protein apoptosis-inducing factor (AI
84  and biochemical assays, we report here that intramitochondrial protein homeostasis plays a major rol
85 a specific organellar deposit site we termed intramitochondrial protein quality control compartment (
86 inding protein previously implicated in both intramitochondrial protein synthesis and apoptosis.
87 ber of nuclear genes potentially involved in intramitochondrial protein synthesis, with many not yet
88  embryos, consistent with a role for DAP3 in intramitochondrial protein synthesis.
89  reactive oxygen species production, reduced intramitochondrial protein translation, and increased ce
90                              One mechanism - intramitochondrial quality control (IMQC) - is represent
91  network of conserved proteases known as the intramitochondrial quality control (IMQC) system is cent
92 nd integrity by acting in concert with other intramitochondrial quality control components.
93 f conserved mitochondrial proteases known as intramitochondrial quality control represents one of the
94           Our findings show a new pathway of intramitochondrial quality control.
95 ate synthetase 1 (CPS1) is a liver-specific, intramitochondrial, rate-limiting enzyme in the urea cyc
96 SA-deficient cells, have increased levels of intramitochondrial reactive oxygen species (ROS), especi
97            Comparative analyses suggest that intramitochondrial recombination and errors in replicati
98             Relative changes in the cortical intramitochondrial redox state of cytochrome aa3 (CYT) a
99 nal types of conversional chimerism, namely, intramitochondrial retroprocessing and interorganellar g
100 bserved, suggesting that the fluorescence of intramitochondrial rhod-2 was responding in a Ca(2+)-sen
101 suggested that LRPPRC may have an additional intramitochondrial role by directly interacting with the
102  In this study, we have further examined the intramitochondrial roles for LRPPRC by creating bacteria
103 or mitochondrial CYP2E1 in the generation of intramitochondrial ROS.
104           These findings suggest a conserved intramitochondrial signaling loop regulating epithelial
105  the possibility of eNOS association with an intramitochondrial site or inverted mitochondrial partic
106                                    Moreover, intramitochondrial Smac degradation by XIAP occurs indep
107 ing, membrane depolarization, and release of intramitochondrial solutes.
108 rameric flavoenzyme that catalyzes the first intramitochondrial step in the beta-oxidation of fatty a
109     In addition, CnHsf3 responds to multiple intramitochondrial stresses; this response is mediated b
110 tabolites that anaerobically generate ATP by intramitochondrial substrate-level phosphorylation and m
111 ndrial membrane ATP synthase subunit O is an intramitochondrial target.
112 er compared to controls (p = 0.001), whereas intramitochondrial TFAM abundance was approximate 80% le
113 expression does not translate into increased intramitochondrial TFAM abundance.
114 rements of depolarization-induced changes in intramitochondrial total Ca concentration ([Ca](mito)) o
115     To mimic mt-mRNA species and to optimise intramitochondrial translation, further engineering has
116 teroid hormone biosynthesis by enhancing the intramitochondrial translocation of cholesterol to the c
117             Here, we show that the disturbed intramitochondrial transport of PA in ups1 cells leads t
118 I assembly is principally due to compromised intramitochondrial transport of the MICOS complex.
119  midpiece alterations (swollen mitochondria, intramitochondrial vacuoles, disordered mitochondrial ca

 
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