| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
51 A common mtDNA control region polymorphism 16519T is associated with migraine without aura and cyclic vomiting
|
Zaki, Essam A.
|
|
2007
|
7 |
6 |
p. 418-419
2 p.
|
artikel
|
| 2 |
56 A de novo nonsense mutation in the DDP1 gene in a patient with Mohr–Tranebjaerg syndrome: New insights into phenotype and molecular findings
|
Blesa, José R.
|
|
2007
|
7 |
6 |
p. 420-
1 p.
|
artikel
|
| 3 |
69 Affected sibpair analysis as a method of identifying nuclear complex I mutations
|
Cameron, Jessie M.
|
|
2007
|
7 |
6 |
p. 424-
1 p.
|
artikel
|
| 4 |
95 A French meta-network against mitochondrial diseases
|
Rossignol, Rodrigue
|
|
2007
|
7 |
6 |
p. 432-
1 p.
|
artikel
|
| 5 |
40 Altered axonal transport of mitochondria in transmitochondrial cybrids from patients with sporadic Parkinson’s disease or a G11778A ND4 gene mutation
|
Trimmer, P.A.
|
|
2007
|
7 |
6 |
p. 415-
1 p.
|
artikel
|
| 6 |
13 Analysis of naturally occurring mutations in pyruvate dehydrogenase complex
|
Lindsay, J.Gordon
|
|
2007
|
7 |
6 |
p. 407-408
2 p.
|
artikel
|
| 7 |
41 Analysis of non-synaptic and synaptic mouse brain mitochondrial lipids and electron transport enzyme activities
|
Kiebish, Michael A.
|
|
2007
|
7 |
6 |
p. 415-416
2 p.
|
artikel
|
| 8 |
73 A new high resolution respirometry assay in platelets
|
Naviaux, Robert K.
|
|
2007
|
7 |
6 |
p. 425-
1 p.
|
artikel
|
| 9 |
A new mtDNA–tRNAGlu mutation (14728T>C) presenting a late-onset mitochondrial encephalomyopathy
|
Nogueira, Célia
|
|
2007
|
7 |
6 |
p. 396-398
3 p.
|
artikel
|
| 10 |
96 A novel heteroplasmic mutation in COXI leads to developmental delay, seizures and stroke-like episodes
|
Robinson, B.H.
|
|
2007
|
7 |
6 |
p. 432-
1 p.
|
artikel
|
| 11 |
98 A novel heteroplasmic mutation in COXI leads to developmental delay, seizures and stroke-like episodes
|
Wiley, Sandra E.
|
|
2007
|
7 |
6 |
p. 433-
1 p.
|
artikel
|
| 12 |
26 A novel mitochondrial ATP 8 (MT-ATP8) gene mutation in a patient with neuropathy and cardiomyopathy
|
Jonckheere, A.I.
|
|
2007
|
7 |
6 |
p. 411-
1 p.
|
artikel
|
| 13 |
10 A novel quantitative denaturing high performance-liquid chromatography assay based on heteroduplex analysis
|
Naviaux, Robert K.
|
|
2007
|
7 |
6 |
p. 407-
1 p.
|
artikel
|
| 14 |
42 Apoptotic and non-apoptotic modes of neuronal death act by distinct mechanisms to induce mitochondrial OPA1 cleavage
|
Loucks, Alexandra
|
|
2007
|
7 |
6 |
p. 416-
1 p.
|
artikel
|
| 15 |
66 A SIRT3/FOXO3a/MnSOD signaling model for mitochondrial superoxide levels
|
Pennington, J. Daniel
|
|
2007
|
7 |
6 |
p. 423-
1 p.
|
artikel
|
| 16 |
Association of mitochondrial disorders with lymphoid malignancies
|
Mende, Susanne
|
|
2007
|
7 |
6 |
p. 401-403
3 p.
|
artikel
|
| 17 |
68 A virus-like agent infecting mitochondria in neurogenic tumors of a tropical marine fish
|
Schmale, Michael C.
|
|
2007
|
7 |
6 |
p. 423-424
2 p.
|
artikel
|
| 18 |
58 Barth syndrome – Mitochondrial phospholipid disorder
|
Acehan, Devrim
|
|
2007
|
7 |
6 |
p. 420-421
2 p.
|
artikel
|
| 19 |
39 Bcl-2 regulates mitochondrial oxidative stress via glutathione binding to the BH3 groove
|
Loucks, Alexandra
|
|
2007
|
7 |
6 |
p. 415-
1 p.
|
artikel
|
| 20 |
62 Biochemical consequences of pyruvate dehydrogenase complex deficiency in human fibroblasts
|
Pourang, Deena
|
|
2007
|
7 |
6 |
p. 422-
1 p.
|
artikel
|
| 21 |
76 Biochemical study of complex i deficient patient cell lines
|
Potluri, Prasanth
|
|
2007
|
7 |
6 |
p. 426-
1 p.
|
artikel
|
| 22 |
53 Bioenergetics of tumors: Investigation of mitochondrial function, structure and composition in human lung cancer
|
Bellance, N.
|
|
2007
|
7 |
6 |
p. 419-
1 p.
|
artikel
|
| 23 |
90 Biophysical probes of iron metabolism in mitochondria
|
Garber-Morales, Jessica
|
|
2007
|
7 |
6 |
p. 430-
1 p.
|
artikel
|
| 24 |
Calendar of Events
|
|
|
2007
|
7 |
6 |
p. I-
1 p.
|
artikel
|
| 25 |
44 Cardiomyocyte Ca2+ handling is altered in mTerf3 knock out mice, a model of mitochondrial dysfunction
|
Andersson, Daniel C.
|
|
2007
|
7 |
6 |
p. 416-417
2 p.
|
artikel
|
| 26 |
82 Clinical case histories suggest intracellular mitochondrial up regulation reverses genomic instability
|
Nagel, Mike
|
|
2007
|
7 |
6 |
p. 428-
1 p.
|
artikel
|
| 27 |
45 Complex IV defects alter supercomplex formation in C. elegans
|
Suthammarak, Wichit
|
|
2007
|
7 |
6 |
p. 417-
1 p.
|
artikel
|
| 28 |
27 Confirmation of mitochondrial proliferation as an adaptation mechanism in structural myopathy
|
Sukhorukov, Vladimir
|
|
2007
|
7 |
6 |
p. 411-412
2 p.
|
artikel
|
| 29 |
Contents
|
|
|
2007
|
7 |
6 |
p. v-
1 p.
|
artikel
|
| 30 |
Convergence of multiple signaling pathways is required to coordinately up-regulate mtDNA and mitochondrial biogenesis during T cell activation
|
D’Souza, Anthony D.
|
|
2007
|
7 |
6 |
p. 374-385
12 p.
|
artikel
|
| 31 |
31 Correlated three-dimensional light and electron microscopy reveals the mechanisms of cytochrome c release during apoptosis
|
Sun, Mei G.
|
|
2007
|
7 |
6 |
p. 412-413
2 p.
|
artikel
|
| 32 |
21 Cross talk between reactive oxygen species producing mitochondria and NADPH oxidase
|
Kulawiec, Mariola
|
|
2007
|
7 |
6 |
p. 410-
1 p.
|
artikel
|
| 33 |
50 Determination of the transcriptional responses that affect C. elegans lifespan upon impaired mitochondrial respiratory chain
|
Lee, Siu Sylvia
|
|
2007
|
7 |
6 |
p. 418-
1 p.
|
artikel
|
| 34 |
81 Differential gene expression response to point mutations, A3243G and A3260G, in mitochondrial DNA of human skeletal muscle
|
Raha, Sandeep
|
|
2007
|
7 |
6 |
p. 427-428
2 p.
|
artikel
|
| 35 |
15 Differential susceptibility of rod photoreceptor synaptic and non-synaptic mitochondria to divalent cation exposure: Neuroprotection by Bcl-xL overexpression
|
Fox, Donald A.
|
|
2007
|
7 |
6 |
p. 408-
1 p.
|
artikel
|
| 36 |
67 Discovery of a mitochondria rich apocrine secretion in the gastrointestinal tract
|
Donndelinger, Tom
|
|
2007
|
7 |
6 |
p. 423-
1 p.
|
artikel
|
| 37 |
91 Drug-induced mitochondrial toxicity: Drug safety considerations
|
Dykens, J.A.
|
|
2007
|
7 |
6 |
p. 430-431
2 p.
|
artikel
|
| 38 |
Editorial Board
|
|
|
2007
|
7 |
6 |
p. IFC-
1 p.
|
artikel
|
| 39 |
36 Effect of auxotrophic markers on mitochondrial DNA maintenance
|
Young, Matthew J.
|
|
2007
|
7 |
6 |
p. 414-
1 p.
|
artikel
|
| 40 |
18 Effect of neonatal exposure of 3′-azido-3′-deoxythymidine on the expression level of mitochondrial genes in the skeletal muscle of mouse as measured by mitochondria-specific microarray
|
Lee, Taewon
|
|
2007
|
7 |
6 |
p. 409-
1 p.
|
artikel
|
| 41 |
79 Effects of common mtDNA variants on mitochondrial function
|
Poole, Jason C.
|
|
2007
|
7 |
6 |
p. 427-
1 p.
|
artikel
|
| 42 |
29 Enzymology of mammalian mitochondrial one-carbon metabolism
|
Tibbetts, Anne S.
|
|
2007
|
7 |
6 |
p. 412-
1 p.
|
artikel
|
| 43 |
65 Fatty acid oxidation in human skeletal muscle mitochondria determined by oxidative phosphorylation as a function of age
|
Kypriotakis, George
|
|
2007
|
7 |
6 |
p. 422-423
2 p.
|
artikel
|
| 44 |
57 General anesthesia does not alter adenosine nucleotide levels of Caenorhabditis elegans
|
Morgan, Phil G.
|
|
2007
|
7 |
6 |
p. 420-
1 p.
|
artikel
|
| 45 |
63 Gene transcript profile of mitochondrial energetic pathways in the aging heart
|
Cabrera Aguilera, Claudia C.
|
|
2007
|
7 |
6 |
p. 422-
1 p.
|
artikel
|
| 46 |
1 Heart mitochondria nitric oxide synthase
|
Ghafourifar, Pedram
|
|
2007
|
7 |
6 |
p. 404-
1 p.
|
artikel
|
| 47 |
37 Heterozygous mutations in BCS1L gene: A clinical case of Bjornstad syndrome
|
Foster, D.
|
|
2007
|
7 |
6 |
p. 414-
1 p.
|
artikel
|
| 48 |
Hydrogen peroxide induces apoptosis in HeLa cells through mitochondrial pathway
|
Singh, Mayank
|
|
2007
|
7 |
6 |
p. 367-373
7 p.
|
artikel
|
| 49 |
6 ICA stenosis associated with G617A mutation in the mitochondrial tRNA phenylalanine gene: A possible new phenotype
|
Miyakawa, Saori
|
|
2007
|
7 |
6 |
p. 405-
1 p.
|
artikel
|
| 50 |
54 Improved subcellular fractionation of the heavy mitochondria pellet using Free Flow Electrophoresis system
|
Aboldzade-Bavil, A.
|
|
2007
|
7 |
6 |
p. 419-420
2 p.
|
artikel
|
| 51 |
83 Increased risk of type 2 diabetes in patients with mitochondrial cytopathy and the relationship with obesity
|
D’Sa, Heathcliff
|
|
2007
|
7 |
6 |
p. 428-
1 p.
|
artikel
|
| 52 |
48 Integrative research and evaluation: Beyond metabolism
|
Nixon, Sara Jo
|
|
2007
|
7 |
6 |
p. 418-
1 p.
|
artikel
|
| 53 |
8 Internalization of isolated mitochondria by mammalian cells
|
Weissig, Volkmar
|
|
2007
|
7 |
6 |
p. 406-
1 p.
|
artikel
|
| 54 |
71 Ischemic damage to the electron transport chain increases the production of reactive oxygen species from isolated rat heart mitochondria
|
Chen, Qun
|
|
2007
|
7 |
6 |
p. 424-425
2 p.
|
artikel
|
| 55 |
52 Ketogenic diet as a therapy for late-onset mitochondrial myopathy
|
Mjøsund, Katja Peltola
|
|
2007
|
7 |
6 |
p. 419-
1 p.
|
artikel
|
| 56 |
34 Lack of immune response associated with expression of the yeast Ndi1 enzyme in rodents
|
Seo, Byoung Boo
|
|
2007
|
7 |
6 |
p. 413-414
2 p.
|
artikel
|
| 57 |
23 Lambda profiling and biocavity laser spectroscopy – Testing a new technology for mitochondrial disease diagnosis
|
Naviaux, Robert K.
|
|
2007
|
7 |
6 |
p. 410-
1 p.
|
artikel
|
| 58 |
80 Lateral-flow “dipstick” immunoassays rapidly identify and quantitate mitochondrial Complex I and Complex IV deficiencies
|
Willis, J.
|
|
2007
|
7 |
6 |
p. 427-
1 p.
|
artikel
|
| 59 |
Liver mtDNA content increases during development: A comparison of methods and the importance of age- and tissue-specific controls for the diagnosis of mtDNA depletion
|
Morten, Karl J.
|
|
2007
|
7 |
6 |
p. 386-395
10 p.
|
artikel
|
| 60 |
61 Long-term treatment of children with congenital lactic acidosis with dichloroacetate
|
Stacpoole, P.W.
|
|
2007
|
7 |
6 |
p. 421-422
2 p.
|
artikel
|
| 61 |
93 Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma
|
Stanger, Olaf
|
|
2007
|
7 |
6 |
p. 431-
1 p.
|
artikel
|
| 62 |
25 Mechanism of cell death caused by complex 1 defects in a rat dopaminergic cell line
|
Marella, M.
|
|
2007
|
7 |
6 |
p. 411-
1 p.
|
artikel
|
| 63 |
35 Mechanism of MnSOD posttranslational structural adaptation
|
Glumac, Ashley
|
|
2007
|
7 |
6 |
p. 414-
1 p.
|
artikel
|
| 64 |
2 Mitochondrial and nuclear encoded subunit assembly into Complex I and assembly defects in mitochondrial disease
|
McKenzie, Matthew
|
|
2007
|
7 |
6 |
p. 404-
1 p.
|
artikel
|
| 65 |
46 Mitochondrial DNA haplogroup distribution in patients with and without diabetic retinopathy
|
Maier, Richard
|
|
2007
|
7 |
6 |
p. 417-
1 p.
|
artikel
|
| 66 |
84 Mitochondrial gene shifting and aging: Resistance is not futile
|
Safdar, Adeel
|
|
2007
|
7 |
6 |
p. 428-429
2 p.
|
artikel
|
| 67 |
30 Mitochondrial haplogroup T is associated with coronary artery disease
|
Stanger, Olaf
|
|
2007
|
7 |
6 |
p. 412-
1 p.
|
artikel
|
| 68 |
94 Mitochondrial lipid and electron transport chain abnormalities in mouse brain tumors
|
Kiebish, Michael A.
|
|
2007
|
7 |
6 |
p. 431-432
2 p.
|
artikel
|
| 69 |
22 Mitochondrial ND5: A candidate gene for neuromuscular diseases in India
|
Vanniarajan, A.
|
|
2007
|
7 |
6 |
p. 410-
1 p.
|
artikel
|
| 70 |
74 Mitomaster – Analytical tool for clinical mitochondrial sequence data
|
Brandon, Martin
|
|
2007
|
7 |
6 |
p. 425-
1 p.
|
artikel
|
| 71 |
59 Modulation of the W748S mutation in DNA polymerase gamma by the E1143G polymorphism in mitochondrial disorders
|
Longley, Matthew J.
|
|
2007
|
7 |
6 |
p. 421-
1 p.
|
artikel
|
| 72 |
20 Mutual control of mitochondrial bioenergetics
|
Bernard, G.
|
|
2007
|
7 |
6 |
p. 409-
1 p.
|
artikel
|
| 73 |
72 Myocardial ischemia does not alter electron transport chain supercomplexes
|
Moghaddas, Shadi
|
|
2007
|
7 |
6 |
p. 425-
1 p.
|
artikel
|
| 74 |
19 New downstream compatible approach to membrane protein separation via free-flow electrophoresis
|
Hartmann, K.
|
|
2007
|
7 |
6 |
p. 409-
1 p.
|
artikel
|
| 75 |
4 New evidence showing neuronal hyperexcitability and trigeminovascular activation during acute stage of stroke-like episodes in MELAS
|
Iizuka, Takahiro
|
|
2007
|
7 |
6 |
p. 405-
1 p.
|
artikel
|
| 76 |
92 Normal biochemical analysis of the oxidative phosphorylation (OXPHOS) system in a child with POLG mutations: A cautionary note!
|
de Vries, Maaike C.
|
|
2007
|
7 |
6 |
p. 431-
1 p.
|
artikel
|
| 77 |
Nuclear–mitochondrial interaction
|
Cannino, G.
|
|
2007
|
7 |
6 |
p. 359-366
8 p.
|
artikel
|
| 78 |
11 Nuclear mitochondrial pseudogenes are amplified by tRNA Leu (UUR) primers but do not interfere with PCR-DHPLC analysis of mitochondrial DNA mutation
|
Lim, Kok Seong
|
|
2007
|
7 |
6 |
p. 407-
1 p.
|
artikel
|
| 79 |
87 Overexpression of mitochondrial Leucyl-tRNA synthetase restore the mitochondrial dysfunctions caused by the MELAS-associated tRNALeu(UUR) A3243G mutation
|
Li, Ronghua
|
|
2007
|
7 |
6 |
p. 429-
1 p.
|
artikel
|
| 80 |
49 Phase 3 trial of coenzyme Q10 in mitochondrial diseases
|
Stacpoole, Peter W.
|
|
2007
|
7 |
6 |
p. 418-
1 p.
|
artikel
|
| 81 |
89 Polymorphisms or pathogenic mutations? Re-evaluation of several PDHA1 mutations by protein structural modeling
|
Okajima, Kazuki
|
|
2007
|
7 |
6 |
p. 430-
1 p.
|
artikel
|
| 82 |
14 Potential of existing drugs in the treatment of respiratory chain disorders: Fibrates can stimulate residual capacities in RC-deficient cells
|
Bastin, J.
|
|
2007
|
7 |
6 |
p. 408-
1 p.
|
artikel
|
| 83 |
75 Prevalence of mitochondrial gene defects in maternally inherited diabetes and deafness and in neuromuscular presentations suggesting respiratory chain dysfunction: Screening of the entire mitochondrial genome in 100 patients
|
Procaccio, V.
|
|
2007
|
7 |
6 |
p. 426-
1 p.
|
artikel
|
| 84 |
78 Protection by the yeast Ndi1 enzyme against neurodegeneration in a chronic rat model of Parkinson’s disease
|
Marella, Mathieu
|
|
2007
|
7 |
6 |
p. 426-427
2 p.
|
artikel
|
| 85 |
33 Protective role of NDI1 in a mouse Parkinson’s model
|
Barber-Singh, Jennifer
|
|
2007
|
7 |
6 |
p. 413-
1 p.
|
artikel
|
| 86 |
70 Quinol type compound in cytochrome c preparations leads to non-enzymatic reduction of cytochrome c during the measurement of complex III activity
|
Moghaddas, Shadi
|
|
2007
|
7 |
6 |
p. 424-
1 p.
|
artikel
|
| 87 |
55 Reactive oxygen species mediated regulation of mitochondrial biogenesis in the yeast Saccharomyces cerevisiae
|
Chevtzoff, Cyrille
|
|
2007
|
7 |
6 |
p. 420-
1 p.
|
artikel
|
| 88 |
24 Reconstructing the tempestuous evolution of the mitochondrial ribosomal proteome
|
Smits, Paulien
|
|
2007
|
7 |
6 |
p. 410-411
2 p.
|
artikel
|
| 89 |
97 Redox chemistry in the mitochondrial intermembrane space: A novel flavoprotein involved in cytochrome c maturation
|
Bernard, Delphine
|
|
2007
|
7 |
6 |
p. 432-433
2 p.
|
artikel
|
| 90 |
28 Relevance of functional investigations of intact mitochondria in the diagnosis of mitochondrial disorders
|
Sperl, Wolfgang
|
|
2007
|
7 |
6 |
p. 412-
1 p.
|
artikel
|
| 91 |
60 Renal disease associated with coenzyme Q deficiency
|
Lunceford, A.L.
|
|
2007
|
7 |
6 |
p. 421-
1 p.
|
artikel
|
| 92 |
9 Single fibers from myopathic Tfam−/− mice display alterations in Ca2+ handling
|
Aydin, Jan
|
|
2007
|
7 |
6 |
p. 406-407
2 p.
|
artikel
|
| 93 |
77 Somatic mtDNA control region mutations and their effects in down syndrome with Alzheimer dementia
|
Coskun, Pinar E.
|
|
2007
|
7 |
6 |
p. 426-
1 p.
|
artikel
|
| 94 |
16 Sperm motility defects in chronic pain and fatigue syndromes
|
Berner, Jon
|
|
2007
|
7 |
6 |
p. 408-
1 p.
|
artikel
|
| 95 |
17 Studies on the molecular mechanism of Barth syndrome
|
Acehan, Devrim
|
|
2007
|
7 |
6 |
p. 409-
1 p.
|
artikel
|
| 96 |
64 Systematic identification of human mitochondrial disease genes through integrative genomics
|
Calvo, Sarah
|
|
2007
|
7 |
6 |
p. 422-
1 p.
|
artikel
|
| 97 |
32 The detection of low-level heteroplasmic DNA mutation by DHPLC and DNA sequencing
|
Lim, Kok Seong
|
|
2007
|
7 |
6 |
p. 413-
1 p.
|
artikel
|
| 98 |
85 The mitochondrial tRNAIle A4295G mutation is associated with hypertension in two Han Chinese subjects
|
Zhu, Haiyan
|
|
2007
|
7 |
6 |
p. 429-
1 p.
|
artikel
|
| 99 |
43 The molecular findings in a series of Leigh syndrome patients with Surf1 gene mutations in Russia
|
Zakharova, Y.
|
|
2007
|
7 |
6 |
p. 416-
1 p.
|
artikel
|
| 100 |
86 The novel mitochondrial DNA A4401G mutation is involved in left ventricular hypertrophy in two Han Chinese pedigrees
|
Wang, Shiwen
|
|
2007
|
7 |
6 |
p. 429-
1 p.
|
artikel
|
| 101 |
Therapeutic potential of pyruvate therapy for mitochondrial diseases
|
Tanaka, Masashi
|
|
2007
|
7 |
6 |
p. 399-401
3 p.
|
artikel
|
| 102 |
47 Thinking green: A scheme to discover stimulators of cytochrome c oxidase activity
|
Maj, Mary C.
|
|
2007
|
7 |
6 |
p. 417-418
2 p.
|
artikel
|
| 103 |
12 Tissue-distribution and possible functional roles of AK4
|
Noma, Takafumi
|
|
2007
|
7 |
6 |
p. 407-
1 p.
|
artikel
|
| 104 |
Title page (with logo)
|
|
|
2007
|
7 |
6 |
p. iii-
1 p.
|
artikel
|
| 105 |
38 Transcription initiation by yeast mitochondrial RNA polymerase
|
Anikin, Michael
|
|
2007
|
7 |
6 |
p. 415-
1 p.
|
artikel
|
| 106 |
7 Translocator protein 18kDa (TSPO) endogenous ligand affect metabolic activity and cell cycle of human osteoblast-like cell
|
Nahum, Rosenberg
|
|
2007
|
7 |
6 |
p. 406-
1 p.
|
artikel
|
| 107 |
88 Variants in mitochondrial tRNAs may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G and C1494T mutations in Chinese families with hearing loss
|
Guan, Min-Xin
|
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2007
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7 |
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5 What is(are) the primary source(s) of the mitochondrial superoxide/hydrogen peroxide production?
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Grivennikova, Vera G.
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2007
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7 |
6 |
p. 405-
1 p.
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| 109 |
3 Yeast NDI1 improve oxidative phosphorylation capacity and increases protection against oxidative stress and cell death in cells carrying a Leber’s Hereditary Optic Neuropathy Mutation
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Park, Jeong Soon
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2007
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7 |
6 |
p. 404-
1 p.
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artikel
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