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                             123 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A gender-specific genetic score to predict the risk of autism in siblings Carayol, Jerome
 2011
 11 4 p. 676-
1 p.
 artikel
2 A high throughput screen for effectors of mitochondrial function Sahdeo, Sunil
 2011
 11 4 p. 641-
1 p.
 artikel
3 Allotopic expression for mitochondrial DNA encoded genes in mammals: An achieved goal, an undemonstrated mechanism or an impossible task? Perales-Clemente⁎, Ester
 2011
 11 4 p. 676-677
2 p.
 artikel
4 Altered redox status of coenzyme Q9 reflects mitochondrial electron transport chain defects in C. elegans Vasta, Valeria
 2011
 11 4 p. 672-673
2 p.
 artikel
5 A mouse model of the GRACILE mutation Bsc1l A232G — Clues for another complex III assembly factor during early ontogenesis Kotarsky⁎, Heike
 2011
 11 4 p. 655-
1 p.
 artikel
6 A newly discovered protein is responsible for a progressive mitochondrial encephalomyopathy associated with severe complex III deficiency Ghezzi⁎, Daniele
 2011
 11 4 p. 655-
1 p.
 artikel
7 An new mutation m.3928G>C p.V208L in ND1 causes Leigh disease Van Hove⁎, J.
 2011
 11 4 p. 670-
1 p.
 artikel
8 A novel homozygous deletion in NDUFS4 causes complex I deficient Leigh syndrome Fassone, Elisa
 2011
 11 4 p. 656-
1 p.
 artikel
9 A novel mitochondrial tRNA lysine variant, m.8358A>G, associated with exercise intolerance, muscle weakness, and fatigue Landsverk⁎, Megan
 2011
 11 4 p. 663-
1 p.
 artikel
10 A novel mtDNA mutation determines sensitivity to cisplatin induced cancer cell death Jones, Aleck W.
 2011
 11 4 p. 657-
1 p.
 artikel
11 A Parkinson disease modifier screen identifies dominant suppressors that rescue pink1 associated mitochondrial defects Vos⁎, Melissa
 2011
 11 4 p. 647-648
2 p.
 artikel
12 Are pathogenic mitochondrial DNA missense mutations predictable? Bai⁎, Renkui
 2011
 11 4 p. 661-662
2 p.
 artikel
13 A role for mitochondrial protein phosphorylation in regulating the physiological dynamic range of the heart Phillips⁎, Darci
 2011
 11 4 p. 642-643
2 p.
 artikel
14 A virus-like agent in the mitochondria of bicolor damselfish Schmale⁎, Michael C.
 2011
 11 4 p. 656-
1 p.
 artikel
15 A YARS2 mutation is a novel cause of mitochondrial myopathy lactic acidosis and sideroblastic anemia (MLASA) syndrome Riley, Lisa
 2011
 11 4 p. 670-671
2 p.
 artikel
16 Benign or pathogenic: Using computer based algorithms for POLG mutation prediction Wang⁎, Jing
 2011
 11 4 p. 664-
1 p.
 artikel
17 Biochemical and genetic analysis of Leigh syndrome with complex I deficiency Mehaney⁎, Dina A.
 2011
 11 4 p. 650-651
2 p.
 artikel
18 Characterization of the role of bezafibrate in cancer cell metabolism and tumorigenesis Wang⁎, Xiao
 2011
 11 4 p. 645-646
2 p.
 artikel
19 Chemical inhibition of the Erv1 mitochondrial oxidative folding pathway by a small molecule inhibitor Dabir⁎, Deepa
 2011
 11 4 p. 638-
1 p.
 artikel
20 Cloning a novel mitochondrial protein which regulates tissue-specific mtDNA segregation Jokinen⁎, Riikka
 2011
 11 4 p. 641-642
2 p.
 artikel
21 Coenzyme Q10: A novel therapeutic approach for Fibromyalgia? Case series with 5 patients Cordero, Mario D.
 2011
 11 4 p. 623-625
3 p.
 artikel
22 Combined treatment with oral metronidazole and N-acetylcysteine is effective in ethylmalonic encephalopathy Viscomi⁎, Carlo
 2011
 11 4 p. 652-
1 p.
 artikel
23 Contribution of polymerase gamma mutations to the Warburg effect and its role in cancer Owens⁎, Kjerstin M.
 2011
 11 4 p. 658-
1 p.
 artikel
24 Cytochrome c oxidase deficiency in Czech and Slovak children Vesela⁎, Katerina
 2011
 11 4 p. 651-
1 p.
 artikel
25 Degeneration of olivo-cerebellar circuitry in patients with mitochondrial disease: A neuropathological study Lax⁎, Nichola Z.
 2011
 11 4 p. 672-
1 p.
 artikel
26 Deoxyguanosine kinase deficiency presenting as neonatal hemochromatosis Hanchard, Neil
 2011
 11 4 p. 661-
1 p.
 artikel
27 Differential diagnosis in pediatrics: Assisting allied health professionals in identifying clinical indicators of mitochondrial disorders Parker⁎, Mary Elizabeth
 2011
 11 4 p. 650-
1 p.
 artikel
28 Discovery of a novel function for human Rad51: Maintenance of the mitochondrial genome Sage⁎, Jay M.
 2011
 11 4 p. 676-
1 p.
 artikel
29 Disrupted somatic stem cell homeostasis in mice with mitochondrial DNA mutagenesis and premature aging Ahlqvist⁎, Kati
 2011
 11 4 p. 641-
1 p.
 artikel
30 DNA packaging proteins Glom and Glom2 coordinately organize the mitochondrial nucleoid of Physarum polycephalum Itoh, Kie
 2011
 11 4 p. 575-586
12 p.
 artikel
31 Dopaminergic neuronal dysfunction in mitochondria leads to Parkinsonism phenotypes in a novel genetic mouse model Pickrell⁎, Alicia M.
 2011
 11 4 p. 644-
1 p.
 artikel
32 Dravet syndrome: Patients with co-morbid SCN1A gene mutations and mitochondrial electron transport chain defects Craig⁎, Alexa K.
 2011
 11 4 p. 639-
1 p.
 artikel
33 Drosophila transgenic RNAi screen of genes implicated in human neurological disease Haddad⁎, Dominik M.
 2011
 11 4 p. 648-
1 p.
 artikel
34 Editorial Board 2011
 11 4 p. IFC-
1 p.
 artikel
35 Effect of bezafibrate on the development and progression of a mitochondrial encephalopathy Wenz⁎, Tina
 2011
 11 4 p. 642-
1 p.
 artikel
36 Effects of acrylamide and glycidamide on the expression levels of hepatic mitochondria-related genes in transgenic Big Blue mice Desai⁎, Varsha G.
 2011
 11 4 p. 653-
1 p.
 artikel
37 Endurance exercise reduces mitochondrial DNA random point mutations and reverses the premature aging transcriptome in PolG mutator mouse: I believe in miracle! Safdar⁎, Adeel
 2011
 11 4 p. 665-666
2 p.
 artikel
38 Energy metabolism in human skeletal muscle mitochondria Hoppel⁎, Charles L.
 2011
 11 4 p. 668-669
2 p.
 artikel
39 Estrogen related receptors (ERRs): A new dawn in transcriptional control of mitochondrial gene networks Eichner, Lillian J.
 2011
 11 4 p. 544-552
9 p.
 artikel
40 Evaluating the broader metabolic effects of mitochondrial diseases Capaldi⁎, R.A.
 2011
 11 4 p. 675-
1 p.
 artikel
41 Evidence for the physical association of mitochondrial fatty acid oxidation and oxidative phosphorylation complexes Wang⁎, Yudong
 2011
 11 4 p. 644-
1 p.
 artikel
42 Exacerbation of vulnerability of short-chain acyl-CoA dehydrogenase deficient (SCADD) fibroblasts to oxidative stress in vitro by risk factors mimicking an infectious crisis in patients and response to rescue with normothermia and glucose Zolkipli⁎, Zarazuela
 2011
 11 4 p. 674-
1 p.
 artikel
43 Fibroblast immuno-diagnosis of cytochrome oxidase (COX) deficiency in mitochondrial disease Du, AiLian
 2011
 11 4 p. 649-650
2 p.
 artikel
44 Germ line selection against point mutations in mitochondrial DNA Stewart⁎, James B.
 2011
 11 4 p. 651-652
2 p.
 artikel
45 Heterozygous deletion of TYMP and SCO2 genes in combination with c.261C>T mutation in TYMP as a cause of MNGIE Tesařová⁎, Markéta
 2011
 11 4 p. 645-
1 p.
 artikel
46 Hsp90 and mitochondrial proteases Yme1 and Yta10/12 participate in ATP synthase assembly in Saccharomyces cerevisiae Francis, Brian R.
 2011
 11 4 p. 587-600
14 p.
 artikel
47 Human polymorphisms in the glutathione transferase zeta 1 maleylacetoacetate isomerase gene predict the kinetics and toxicity of dichloroacetate Shroads, A. Larry
 2011
 11 4 p. 654-
1 p.
 artikel
48 Immune system abnormalities in children with mitochondrial disease are manifested as severe or recurrent infections Pacheco⁎, Susan E.
 2011
 11 4 p. 664-665
2 p.
 artikel
49 Impaired amino acid metabolism in cells affected by the T8993G (NARP) mtDNA mutation: A potential novel therapeutic target D'Aurelio⁎, Marilena
 2011
 11 4 p. 652-
1 p.
 artikel
50 Improving mitochondrial targeting of zinc-finger nucleases Williams⁎, Siôn Ll.
 2011
 11 4 p. 670-
1 p.
 artikel
51 In mtDNA diseases, the reversion of the F1Fo-ATPsynthase is associated to defects in mitochondrial quality control: Evidence for a novel pathogenic mechanism and therapeutic target Holly, Callaghan
 2011
 11 4 p. 668-
1 p.
 artikel
52 Insights in the pathogenesis of impaired glucose tolerance in patients with mitochondrial cytopathy Samjoo⁎, Imtiaz A.
 2011
 11 4 p. 667-
1 p.
 artikel
53 Insulin signaling regulates mitochondrial membrane potential, resistance to oxidative stress and mtDNA copy number Lemire⁎, Bernard D.
 2011
 11 4 p. 644-
1 p.
 artikel
54 Inverse relation of hyperammonemia to serum arginine in children with Mitochondrial Disorders (MD) Bhardwaj⁎, Jatinder
 2011
 11 4 p. 640-
1 p.
 artikel
55 Investigating accuracy of mitochondrial translation at the molecular level Kehrein, Kirsten
 2011
 11 4 p. 647-
1 p.
 artikel
56 Investigation of the interaction between mitochondrial transcription factor A and amyloid beta and implications for Alzheimer's disease Malarkey⁎, Christopher S.
 2011
 11 4 p. 657-658
2 p.
 artikel
57 Large-scale mutation screening in combination with lentiviral complementation of rare variants aid gene identification in mitochondrial disorders Prokisch⁎, H.
 2011
 11 4 p. 660-
1 p.
 artikel
58 Manipulation of the mitochondrial genome to improve bioenergetics in human childhood disease models Iyer⁎, Shilpa
 2011
 11 4 p. 643-
1 p.
 artikel
59 3-Methylglutaconic aciduria type IV due to novel mutation in TMEM70 Shchelochkov⁎, Oleg A.
 2011
 11 4 p. 666-
1 p.
 artikel
60 Mitochondrial abnormalities in the Mecp2tm1Tam mouse model of Rett syndrome Williamson, S.L.
 2011
 11 4 p. 662-663
2 p.
 artikel
61 Mitochondrial and nuclear genomic responses to loss of LRPPRC expression Gohil⁎, Vishal M.
 2011
 11 4 p. 675-
1 p.
 artikel
62 Mitochondrial changes in aged oocytes and improvement of fertility rate through autologous mitochondrial microinjection Li⁎, Fang
 2011
 11 4 p. 660-
1 p.
 artikel
63 Mitochondrial C150T polymorphism increases the risk of cervical cancer and HPV infection Zhai, Kan
 2011
 11 4 p. 559-563
5 p.
 artikel
64 Mitochondrial division in rat cardiomyocytes: An electron microscope study Fujioka, Hisashi
 2011
 11 4 p. 668-
1 p.
 artikel
65 Mitochondrial DNA damage increases in an age-dependent manner in liver from APEX1 haploinsufficient mice Torres-Ortiz⁎, Ceidy
 2011
 11 4 p. 659-660
2 p.
 artikel
66 Mitochondrial DNA mutations in cases of Leigh-like disease Itkis⁎, Yulia S.
 2011
 11 4 p. 647-
1 p.
 artikel
67 Mitochondrial DNA mutations provide selective advantage in hematopoietic stem cell niche Chen, Michael L.
 2011
 11 4 p. 661-
1 p.
 artikel
68 Mitochondrial dysfunction of children with initial mitral valve prolapse Chernozubova⁎, Nelli Y.
 2011
 11 4 p. 643-
1 p.
 artikel
69 Mitochondrial heteroplasmy and the influence of aging Sondheimer⁎, Neal
 2011
 11 4 p. 654-
1 p.
 artikel
70 Mitochondrial metabolism and cancer Kurelac, Ivana
 2011
 11 4 p. 635-637
3 p.
 artikel
71 Mitochondrial viability in mouse and human postmortem brain Barksdale⁎, Keri A.
 2011
 11 4 p. 656-
1 p.
 artikel
72 MitoDx: Massively parallel sequencing of the mitochondrial genome may diagnose mitochondrial disease without invasive biopsies Sommer⁎, Steve S.
 2011
 11 4 p. 664-
1 p.
 artikel
73 Molecular confirmation of VLCAD deficiencies in newborns Landsverk⁎, Megan
 2011
 11 4 p. 667-668
2 p.
 artikel
74 Motor neuron degeneration is linked with defects in mitochondrial dynamics in amyotrophic lateral sclerosis Song⁎, Wenjun
 2011
 11 4 p. 648-649
2 p.
 artikel
75 MtDNA haplogroups M7 and B in southwestern Han Chinese at risk for acute mountain sickness Li, Fu-Xiang
 2011
 11 4 p. 553-558
6 p.
 artikel
76 Mutant Huntington interaction with DRP1 impairs the mitochondrial fission and fusion balance and mediates neuronal injury Petrilli⁎, Alejandra M.
 2011
 11 4 p. 649-
1 p.
 artikel
77 Mutation in the mitochondrial tRNAVal causes mitochondrial encephalopathy, lactic acidosis and stroke-like episodes Glatz, Catherine
 2011
 11 4 p. 615-619
5 p.
 artikel
78 ND3 Mutation 10191T>C causes rapidly progressive infantile Leigh disease Baker, P.R.
 2011
 11 4 p. 669-670
2 p.
 artikel
79 Next generation sequencing as a means to detect low frequency mtDNA variants Williams⁎, Siôn Ll.
 2011
 11 4 p. 653-
1 p.
 artikel
80 Next generation sequencing for mitochondrial disorders Vasta, Valeria
 2011
 11 4 p. 669-
1 p.
 artikel
81 Nitric oxide production in subjects with MELAS syndrome and the effect of arginine and citrulline supplementation: Interim results El-Hattab⁎, Ayman
 2011
 11 4 p. 663-
1 p.
 artikel
82 Non-invasive evaluation of mitochondrial defects in children Goldenthal⁎, Michael J.
 2011
 11 4 p. 659-
1 p.
 artikel
83 Novel approaches toward a one-step comprehensive molecular diagnosis of mitochondrial disorders Zhan⁎, Hongli
 2011
 11 4 p. 673-674
2 p.
 artikel
84 OPAopathies: Widening the spectrum of human diseases associated with mutations in the OPA1 gene Caporali⁎, Leonardo
 2011
 11 4 p. 645-
1 p.
 artikel
85 Organ-specific shifts in mtDNA heteroplasmy following systemic delivery of a mitochondria-targeted restriction endonuclease Bacman⁎, Sandra R.
 2011
 11 4 p. 653-
1 p.
 artikel
86 Oxygen regulation of cytochrome oxidase subunit 4–2 Grossman⁎, Lawrence
 2011
 11 4 p. 675-
1 p.
 artikel
87 Phase 3 trial of Coenzyme Q10 in mitochondrial diseases Kurtz⁎, Tracie L.
 2011
 11 4 p. 642-
1 p.
 artikel
88 Phenotypic differences of animal models of complex III and complex IV deficiencies in neurons Diaz⁎, Francisca
 2011
 11 4 p. 651-
1 p.
 artikel
89 Polar body mutation load analysis in a patient with A3243G tRNALeu(UUR) point mutation Vandewoestyne, Mado
 2011
 11 4 p. 626-629
4 p.
 artikel
90 Primary oligodendropathy in a patient with Kearns Sayre syndrome Lax⁎, Nichola Z.
 2011
 11 4 p. 672-
1 p.
 artikel
91 Proficiency testing for mitochondrial electron transport chain (ETC) enzyme assays using C. elegans Chen, Xiulian
 2011
 11 4 p. 658-
1 p.
 artikel
92 Protein mislocalization and long-term follow-up of a patient with malonyl-CoA decarboxylase deficiency Polinati⁎, Padmini P.
 2011
 11 4 p. 639-
1 p.
 artikel
93 Quantitative assessment of mtDNA damage differentiates long-term and short-term survivors with glioblastoma Han, Ying
 2011
 11 4 p. 675-676
2 p.
 artikel
94 Reconstitution of the mitochondrial inner membrane protein Cox10 by using inteins Marco-Lázaro⁎, R.
 2011
 11 4 p. 677-
1 p.
 artikel
95 Regulation of mtDNA damage by the DNA binding protein TFAM Kolesar, Jill E.
 2011
 11 4 p. 664-
1 p.
 artikel
96 Regulation of oxidative phosphorylation through phosphorylation of cytochrome oxidase Acin-Perez⁎, Rebeca
 2011
 11 4 p. 655-
1 p.
 artikel
97 Relationship between mitochondria and the development of specific lipid droplets in capillary endothelial cells of the respiratory tract in patients with sarcoidosis Mochizuki, Ichiro
 2011
 11 4 p. 601-606
6 p.
 artikel
98 Repair of H2O2-induced mtDNA damage requires the BER enzyme Apn1 Arroyo-Torres⁎, Yaria
 2011
 11 4 p. 649-
1 p.
 artikel
99 Replenishment with Coenzyme Q restores defective complex I–III activity Yang, Yu-Ying
 2011
 11 4 p. 673-
1 p.
 artikel
100 Replication stalling by catalytically impaired Twinkle induces mitochondrial DNA rearrangements in cultured cells Pohjoismäki, Jaakko L.O.
 2011
 11 4 p. 630-634
5 p.
 artikel
101 Respiratory activity of Surf1 knockout mice differs from wild type mice in an arterially perfused brainstem preparation Stettner⁎, Georg M.
 2011
 11 4 p. 640-
1 p.
 artikel
102 RNA-mediated restoration of mitochondrial function in cells harboring a Kearns Sayre Syndrome mutation Mahato, Biraj
 2011
 11 4 p. 564-574
11 p.
 artikel
103 Sensory nerve cell dysfunction contributes to peripheral neuropathy in mitochondrial disease Lax⁎, Nichola Z.
 2011
 11 4 p. 671-672
2 p.
 artikel
104 Severe CI and CIV deficiency in infantile cardiomyopathies Götz⁎, Alexandra
 2011
 11 4 p. 643-
1 p.
 artikel
105 Severe X-linked mitochondrial encephalomyopathy associated with a mutation in Apoptosis Inducing Factor 1 Ghezzi⁎, Daniele
 2011
 11 4 p. 671-
1 p.
 artikel
106 Skeletal muscle mitochondrial dysfunction is secondary to type 2 diabetes and can be improved by prolonged exercise training van Tienen⁎, F.H.J.
 2011
 11 4 p. 659-
1 p.
 artikel
107 Somatic AgC/TgG mitochondrial DNA mutations in HIV-infected pregnant women and their infants exposed to HIV antiretroviral therapy during pregnancy Jitratkosol, Marissa
 2011
 11 4 p. 662-
1 p.
 artikel
108 Specialized ribosomes in mammalian mitochondria Wang, Rejean L.
 2011
 11 4 p. 673-
1 p.
 artikel
109 Suppression of reactive oxygen species in cells with multiple mitochondrial DNA deletions by exogenous protein-coding RNAs Jash, Sukanta
 2011
 11 4 p. 607-614
8 p.
 artikel
110 Tardive dyskinesia, a common acquired complex 1 disorder, correlates with growth arrest of lymphocytes exposed to calcium-deficient medium Berner⁎, Jon
 2011
 11 4 p. 646-
1 p.
 artikel
111 The anoxic plant mitochondrion as a nitrite: NO reductase Gupta, Kapuganti J.
 2011
 11 4 p. 537-543
7 p.
 artikel
112 The effect of increased mitochondrial biogenesis on premature aging Dillon⁎, Lloye M.
 2011
 11 4 p. 646-
1 p.
 artikel
113 The overlap of metabolic/mitochondrial disease and Munchausen-by-proxy syndrome (MBPS) Rajagopal⁎, Soumitra
 2011
 11 4 p. 665-
1 p.
 artikel
114 The psychiatric manifestations of mitochondrial cytopathies: A clinical and MR spectroscopy investigation Anglin⁎, Rebecca
 2011
 11 4 p. 639-640
2 p.
 artikel
115 The role of cardiolipin in molecular assemblies of tafazzin Malhotra⁎, Ashim
 2011
 11 4 p. 648-
1 p.
 artikel
116 The utility of exon targeted array CGH in the diagnosis of mitochondrial related disorders Zhan⁎, Hongli
 2011
 11 4 p. 666-
1 p.
 artikel
117 Three-dimensional localization of the GTP-binding protein within the mammalian mitochondrial ribosome Sharma, M.R.
 2011
 11 4 p. 657-
1 p.
 artikel
118 Variation in MAPT is not a contributing factor to the incomplete penetrance in LHON Hudson, Gavin
 2011
 11 4 p. 620-622
3 p.
 artikel
119 Vascular pathology in mitochondrial disease Lax⁎, Nichola Z.
 2011
 11 4 p. 654-655
2 p.
 artikel
120 Vulnerability to oxidative stress in vitro in short-, medium- and long-chain fatty acid oxidation disorders (FAODs): Response to pathophysiology-based interventions Zolkipli⁎, Zarazuela
 2011
 11 4 p. 666-667
2 p.
 artikel
121 Vulnerability to oxidative stress may contribute to pathophysiology of short-chain acyl-CoA dehydrogenase deficient (SCADD) patients and is independent of the genotypic severity Zolkipli⁎, Zarazuela
 2011
 11 4 p. 674-
1 p.
 artikel
122 Water dispersible and highly bioavailable prodrugs of astaxanthin for inflammation-mediated metabolic syndrome Rishton⁎, Gilbert M.
 2011
 11 4 p. 638-
1 p.
 artikel
123 When mitochondrial supercomplexes lose integrity: Two wrongs do not quite make a right Suthammarak⁎, Wichit
 2011
 11 4 p. 646-647
2 p.
 artikel
                             123 gevonden resultaten
 
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