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                             154 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 144 Aberrant amino acid signalling and metabolism in the Deletor mouse Carroll, Christopher J.
 2010
 10 2 p. 240-241
2 p.
 artikel
2 110 Abnormal biomarker of energy metabolism in children with autism Frye, Richard E.
 2010
 10 2 p. 231-
1 p.
 artikel
3 72 A common mtDNA polymorphism is associated with complex regional pain syndrome type I Boles, Richard G.
 2010
 10 2 p. 220-
1 p.
 artikel
4 10 Adeno-associated virus-mediated knockdown of pyruvate dehydrogenase E1 α in specific regions of the rat brain Ojano-Dirain, Carolyn
 2010
 10 2 p. 202-203
2 p.
 artikel
5 137 A lipophilic metalloporphyrin antioxidant attenuates behavioral seizures and mitochondrial dysfunction in the B6D2 Sod2-/-mice Patel, Manisha
 2010
 10 2 p. 238-239
2 p.
 artikel
6 43 Altered mitochondria structure in cells undergoing glucose starvation Jeon, Dong Min
 2010
 10 2 p. 211-
1 p.
 artikel
7 95 A mouse model of Parkinson’s Disease based on CoQ deficiency Gasser, David L.
 2010
 10 2 p. 226-
1 p.
 artikel
8 89 Analysis of extensive RNA/DNA hybrids in the replicating mammalian mitochondrial genome Holmes, J. Bradley
 2010
 10 2 p. 225-
1 p.
 artikel
9 127 A new generalized energy transduction rate law for modeling of OXPHOS systems and pathologies Chang, Ivan
 2010
 10 2 p. 235-236
2 p.
 artikel
10 A novel c.592-4_c.592-3delTT mutation in DGUOK gene causes exon skipping Ji, Jack Q.
 2010
 10 2 p. 188-191
4 p.
 artikel
11 51 A novel mouse model exhibiting phenotypical signs of aging and neurodegeneration after induced double-strand breaks in mtDNA Pickrell, Alicia
 2010
 10 2 p. 214-
1 p.
 artikel
12 99 Antibiotic effects on mitochondrial translation and in patients with mitochondrial translational defects Jones, Christie N.
 2010
 10 2 p. 227-
1 p.
 artikel
13 60 A parasite of mitochondria? A virus-like agent in neurogenic tumors of a tropical marine fish Schmale, Michael C.
 2010
 10 2 p. 216-
1 p.
 artikel
14 70 Arrest of mitochondrial RNA polymerase by the malondialdehyde adduct, M1dG Cline, Susan D.
 2010
 10 2 p. 219-
1 p.
 artikel
15 117 Asian mitochondrial DNA (mtDNA) lineage F4 is associated with increased risk of developing metabolic syndrome Lvova, Maria A.
 2010
 10 2 p. 233-
1 p.
 artikel
16 74 A splice-site mutation in C8orf38 causes impaired Complex I assembly due to a defect in translation or integration of ND1 into an early assembly intermediate Tucker, Elena
 2010
 10 2 p. 221-
1 p.
 artikel
17 90 Bcs1L A232G mutant mice: A new model of complex III deficiency and hepatic cirrhosis Levéen, Per
 2010
 10 2 p. 225-
1 p.
 artikel
18 96 Biochemical analysis of POLG2 variants associated with mitochondrial disease Young, Matthew J.
 2010
 10 2 p. 226-227
2 p.
 artikel
19 52 Biochemical characterization of human mitochondrial RNA polymerase reveals differences in formation and fidelity of elongation complexes relative to T7 RNA polymerase Smidansky, Eric D.
 2010
 10 2 p. 214-
1 p.
 artikel
20 33 Biomarkers of mitochondrial dysfunction—Distinct metabolomic profiles differentiate long-lived from short-lived mitochondrial mutants in C. elegans Butler, Jeffrey
 2010
 10 2 p. 209-
1 p.
 artikel
21 26 Biomarkers of redox abnormalities in mitochondrial disorders and organic acidemias Atkuri, Kondala R.
 2010
 10 2 p. 206-207
2 p.
 artikel
22 116 Bipolar disorder as the presenting clinical feature of the 3243A>G mutation in the mitochondrial tRNALeu(UUR) gene Scaglia, Fernando
 2010
 10 2 p. 232-233
2 p.
 artikel
23 94 Cardiac, hepatic and renal mitochondrial toxicity of doxorubicin in a sub-chronic in vivo model Pereira, Goncalo C.
 2010
 10 2 p. 226-
1 p.
 artikel
24 53 Characterization of mitochondrial transcription using bacterially expressed proteins and oligonucleotide templates reveals promoter melting and dinucleotide synthesis as rate-limiting steps in transcription initiation Lodeiro, Maria Fernanda
 2010
 10 2 p. 214-
1 p.
 artikel
25 135 CMA-244K oligonucleotide array based analysis of 5q31.1 region deletion associated with dysmorphism and sensorineural hearing loss Sheehan, Meghan
 2010
 10 2 p. 238-
1 p.
 artikel
26 147 Compound heterozygosity for mutations in TMEM70 Sperl, W.
 2010
 10 2 p. 241-
1 p.
 artikel
27 Construction and validation of a yeast model system for studying in vivo the susceptibility to nucleoside analogues of DNA polymerase gamma allelic variants Baruffini, Enrico
 2010
 10 2 p. 183-187
5 p.
 artikel
28 Contribution of the FAD and quinone binding sites to the production of reactive oxygen species from Ascaris suum mitochondrial complex II Paranagama, Madhavi P.
 2010
 10 2 p. 158-165
8 p.
 artikel
29 130 Cross-platform expression microarray performance in a mouse model of mitochondrial disease therapy Zhang, Zhe
 2010
 10 2 p. 236-237
2 p.
 artikel
30 Cyclosporine A suppresses keratinocyte cell death through MPTP inhibition in a model for skin cancer in organ transplant recipients Norman, Kimberly G.
 2010
 10 2 p. 94-101
8 p.
 artikel
31 4 Cytochrome c: A recurring nightmare in mitochondrial diagnostic assays Hoppel, Charles
 2010
 10 2 p. 201-
1 p.
 artikel
32 136 Decreased ATP production in skin fibroblasts of children with POLG1 mutations de Vries, Maaike C.
 2010
 10 2 p. 238-
1 p.
 artikel
33 8 Decrease of aerobic mitochondrial energy metabolism in ganglioneuromas Feichtinger, Rene’ G.
 2010
 10 2 p. 202-
1 p.
 artikel
34 123 Defective Complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome de Coo, Irenaeus F.M.
 2010
 10 2 p. 234-
1 p.
 artikel
35 133 Detection of mitochondrial defects in patients with mitochondrial diseases: A case study Lemieux, Hélène
 2010
 10 2 p. 237-238
2 p.
 artikel
36 143 Development of a cell based screening assay for drugs that alter mitochondrial function Schoenfeld, Robert
 2010
 10 2 p. 240-
1 p.
 artikel
37 107 Differential age-related changes in mitochondrial DNA repair activities in mouse brain regions Gredilla, Ricardo
 2010
 10 2 p. 230-
1 p.
 artikel
38 62 Differential translational initiation directs localization of mouse ribonuclease H1 to either mitochondria or nuclei Suzuki, Yutaka
 2010
 10 2 p. 217-
1 p.
 artikel
39 146 Difficulty in the diagnosis of X-linked PDHC deficiency due to a large deletion affecting the PDHA1 gene Sperl, W.
 2010
 10 2 p. 241-
1 p.
 artikel
40 54 Discovery of the mitochondrial cells and its progress Nakano, Kazutoshi
 2010
 10 2 p. 215-
1 p.
 artikel
41 92 Disease mutations in the human mitochondrial DNA polymerase thumb subdomain impart severe defects in mtDNA replication Kasiviswanathan, Rajesh
 2010
 10 2 p. 225-226
2 p.
 artikel
42 138 Double strand break repair in human mitochondrial extracts Hunter, Senyene E.
 2010
 10 2 p. 239-
1 p.
 artikel
43 Dynamic NAD(P)H post-synaptic autofluorescence signals for the assessment of mitochondrial function in a neurodegenerative disease: Monitoring the primary motor cortex of G93A mice, an amyotrophic lateral sclerosis model Loizzo, Stefano
 2010
 10 2 p. 108-114
7 p.
 artikel
44 Editorial Board 2010
 10 2 p. IFC-
1 p.
 artikel
45 58 Effect of diazoxide and Ca2+ on sodium-loaded rat heart mitochondria Korotkov, Sergey M.
 2010
 10 2 p. 215-216
2 p.
 artikel
46 101 Effects of dideoxycytidine treatment on mitochondrial gene expression and proliferation of human neural progenitors Iyer, Shilpa
 2010
 10 2 p. 228-
1 p.
 artikel
47 Effects of α-mangostin on mitochondrial energetic metabolism Martínez-Abundis, E.
 2010
 10 2 p. 151-157
7 p.
 artikel
48 63 Electron transport chain abnormalities in lymphoblasts from autistic children Holtzman, David
 2010
 10 2 p. 217-
1 p.
 artikel
49 Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity Guillet, Virginie
 2010
 10 2 p. 115-124
10 p.
 artikel
50 114 Expanding clinical spectrum of RRM2B mutations to include MNGIE Wong, Lee-Jun
 2010
 10 2 p. 232-
1 p.
 artikel
51 46 Functional characterization of energy deficient myoblasts and myotubes Huigsloot, M.
 2010
 10 2 p. 212-
1 p.
 artikel
52 115 Functional consequences of mtDNA variation in wild C. elegans isolates Falk, Marni J.
 2010
 10 2 p. 232-
1 p.
 artikel
53 68 Functional link between the neurogenic transcription factor NeuroD6 and mitochondrial bioenergetics: Clinical implications for mitochondrial encephalopathies Yoon, Jeongae
 2010
 10 2 p. 219-
1 p.
 artikel
54 Gases in the mitochondria Pun, Pamela B.L.
 2010
 10 2 p. 83-93
11 p.
 artikel
55 29 Genetic suppressors of Barth syndrome as potential targets for therapeutic intervention Malhotra, Ashim
 2010
 10 2 p. 207-208
2 p.
 artikel
56 77 Healthy baby girl born following PGD for the mitochondrial DNA mutation m.8993T>G Thorburn, David
 2010
 10 2 p. 222-
1 p.
 artikel
57 59 Heterozygous mutation of Drosophila Opa1 causes the development of multiple organ abnormalities in an age-dependent and organ-specific manner Shahrestani, Parvin
 2010
 10 2 p. 216-
1 p.
 artikel
58 11 HIV and antiretroviral-mediated mitochondrial dna depletion in children Morén, Constanza
 2010
 10 2 p. 203-
1 p.
 artikel
59 Human mitochondrial haplogroup H: The highest VO2max consumer – Is it a paradox? Martínez-Redondo, Diana
 2010
 10 2 p. 102-107
6 p.
 artikel
60 28 Hyperammonemic crises in patients with F1FO-ATP synthase deficiency due to mutation in TMEM70 Tesařová, Markéta
 2010
 10 2 p. 207-
1 p.
 artikel
61 80 Impaired function of mitochondria in tissues from mice expressing defective mitochondrial DNA polymerase Shabalina, I.G.
 2010
 10 2 p. 222-223
2 p.
 artikel
62 129 Implications of mtDNA somatic mutation on aging and neurodegenerative diseases Marciniak, Christine
 2010
 10 2 p. 236-
1 p.
 artikel
63 35 Increased mitochondrial biogenesis as therapy for mitochondrial myopathies Wenz, Tina
 2010
 10 2 p. 209-
1 p.
 artikel
64 12 Increase in mitochondrial DNA amount in perinatally HIV-infected children caused by treatment interruption Nunez, Constanza Morén
 2010
 10 2 p. 203-
1 p.
 artikel
65 38 Investigator mediated Phase III open labeled l-arginine clinical trial to cure and prevent the stroke-like episodes in MELAS: Study design and outcome Koga, Y.
 2010
 10 2 p. 210-
1 p.
 artikel
66 112 In vivo measurement of heterogeneous mitochondrial metabolic fluxes in small myocardial regions van Beek, Johannes H.G.M.
 2010
 10 2 p. 231-
1 p.
 artikel
67 76 In vivo metabolic flux profiling using stable isotopes discriminates mitochondrial dysfunction in C. elegans Rao, Meera
 2010
 10 2 p. 221-
1 p.
 artikel
68 69 In vivo methylation of mtDNA in living cells shows the strength and dynamics of protein factors–mtDNA interactions Rebelo, Adriana
 2010
 10 2 p. 219-
1 p.
 artikel
69 44 Knockdown of Cox6a subunit leads to decreased affinity for oxygen of cytochrome c oxidase Wenchich, L.
 2010
 10 2 p. 211-
1 p.
 artikel
70 97 Light therapy—A promising new treatment for Parkinson’s disease and other mitochondrial diseases Trimmer, P.A.
 2010
 10 2 p. 227-
1 p.
 artikel
71 106 LRPPRC, a human PPR motif protein, binds to mitochondrially-encoded mRNAs and is essential for their accumulation Bangeranye, Catherine
 2010
 10 2 p. 229-230
2 p.
 artikel
72 82 Measurement of mitochondrial DNA damage in human cells adjusted for copy number by the combined use of real-time and quantitative Han, Ying
 2010
 10 2 p. 223-
1 p.
 artikel
73 47 Measurement of mitochondrial oxygen consumption using a fluorescence-based oxygen-sensitive probe: Application to mitochondrial medicine Jonckheere, A.I.
 2010
 10 2 p. 212-
1 p.
 artikel
74 139 Mechanisms of berberine [Natural Yellow 18, 5,6-dihydro-9,10-dimethoxybenzo(g)-1,3-benzodioxolo (5,6-a)quinolizinium]-induced mitochondrial dysfunction role of the adenine nucleotide translocator Pereira, Cláudia V.
 2010
 10 2 p. 239-
1 p.
 artikel
75 126 Melanopsin-containing retinal ganglion cells resist degeneration in mitochondrial optic neuropathies Morgia, Chiara La
 2010
 10 2 p. 235-
1 p.
 artikel
76 113 MELAS: Molecular, pathological and radiological correlates Narayan, B.
 2010
 10 2 p. 231-232
2 p.
 artikel
77 20 Methylene blue enhances specific mitochondrial functions in vitro and in vivo Atamna, Hani
 2010
 10 2 p. 205-
1 p.
 artikel
78 18 Methylene chloride effects on mitochondria Garrabou, G.
 2010
 10 2 p. 205-
1 p.
 artikel
79 Microinjection of serum-starved mitochondria derived from somatic cells affects parthenogenetic development of bovine and murine oocytes Takeda, Kumiko
 2010
 10 2 p. 137-142
6 p.
 artikel
80 81 Mitochondrial abnormalities in lymphoblasts from autism Chauhan, Abha
 2010
 10 2 p. 223-
1 p.
 artikel
81 121 Mitochondrial aging countermeasure—Endurance exercise confers complete phenotypic protection in PolG mutator mouse Safdar, Adeel
 2010
 10 2 p. 233-234
2 p.
 artikel
82 105 Mitochondrial alterations in pulmonary arterial smooth muscle cells in pulmonary arterial hypertension Sommer, Natascha
 2010
 10 2 p. 229-
1 p.
 artikel
83 79 “Mitochondrial cells (Mito Cells)” can live without nucleus, and have proteins encoded by both nuclear and mitochondrial DNA Nakayama, Tomohiro
 2010
 10 2 p. 222-
1 p.
 artikel
84 16 Mitochondrial damage in acute carbon monoxide poisoning: The effect of oxygen treatment Garrabou, G.
 2010
 10 2 p. 204-
1 p.
 artikel
85 64 Mitochondrial depletion syndrome associated with pyruvate dehydrogenase deficiency Wolfe, Lynne A.
 2010
 10 2 p. 217-218
2 p.
 artikel
86 Mitochondrial DNA haplogroup ‘R’ is associated with Noonan syndrome of South India Rani, Deepa Selvi
 2010
 10 2 p. 166-173
8 p.
 artikel
87 119 Mitochondrial DNA mutations found in native Central and South American samples provide evidence for mitochondrial adaptation to new environments Derbeneva, O.
 2010
 10 2 p. 233-
1 p.
 artikel
88 37 Mitochondrial dynamics and function Koopman, Werner J.H.
 2010
 10 2 p. 210-
1 p.
 artikel
89 132 Mitochondrial dysfunction preceeds insulin resistance in skeletal muscle of mice fed high fat diet Boudina, Sihem
 2010
 10 2 p. 237-
1 p.
 artikel
90 45 Mitochondrial energy system in liver and muscle tissue during foetal development Hansikova, Hana
 2010
 10 2 p. 212-
1 p.
 artikel
91 61 Mitochondrial fusion protects mtDNA stability Chen, Hsiuchen
 2010
 10 2 p. 216-
1 p.
 artikel
92 7 Mitochondrial haplogroups and control region polymorphisms are not associated with prostate cancer in Middle European caucasians Mueller, Edith E.
 2010
 10 2 p. 201-202
2 p.
 artikel
93 21 Mitochondrial outer membrane associated cholesterol transport is essential for steroidogenesis Debnath, Dilip
 2010
 10 2 p. 205-206
2 p.
 artikel
94 41 Mitochondrial quality enhancement by a metabolic approach Jang, So-Young
 2010
 10 2 p. 211-
1 p.
 artikel
95 83 Mitochondrial respiratory chain dysfunction as a critical event in heavy metal-induced neurotoxicity Belyaeva, Elena A.
 2010
 10 2 p. 223-224
2 p.
 artikel
96 49 Mitochondrial respiratory chain dysfunction variably increases in vivo oxidant stress in C. elegans Dingley, Stephen
 2010
 10 2 p. 213-
1 p.
 artikel
97 Mitochondrial respiratory chain dysfunction variably increases oxidant stress in Caenorhabditis elegans Dingley, Stephen
 2010
 10 2 p. 125-136
12 p.
 artikel
98 145 Mitochondrial thioredoxin-2 blocks pro-inflammatory signaling by plasma cysteine redox potential Go, Young-Mi
 2010
 10 2 p. 241-
1 p.
 artikel
99 141 Mitochondrial transcription factor a mitochondrial DNA repair Croteau, Deborah L.
 2010
 10 2 p. 240-
1 p.
 artikel
100 MitoZoa: A curated mitochondrial genome database of metazoans for comparative genomics studies Lupi, Renato
 2010
 10 2 p. 192-199
8 p.
 artikel
101 36 Modeling metabolism in pancreatic beta-cell mitochondria Heuett, William J.
 2010
 10 2 p. 210-
1 p.
 artikel
102 57 Modelling ND subunits of complex I: Leber’s hereditary optic neuropathy (LHON) pathogenic mutations and non-synonymous population variants in genotype–phenotype correlation Iommarini, Luisa
 2010
 10 2 p. 215-
1 p.
 artikel
103 87 Modulation of mitochondrial function in C. elegans by modification of supercomplexes—Two wrongs almost make a right Suthammarak, Wichit
 2010
 10 2 p. 224-
1 p.
 artikel
104 9 Molecular characterization of mitochondrial diseases with cardiac dysfunction Bornstein, Belen
 2010
 10 2 p. 202-
1 p.
 artikel
105 78 MPV17—Associated hepatocerebral mitochondrial DNA depletion syndrome: New patients and novel mutations El-Hattab, Ayman W.
 2010
 10 2 p. 222-
1 p.
 artikel
106 103 MtDNA content in the progression of endometrial pathology from normal endometrium to hyperplasia to type I endometrial carcinoma Cormio, A.
 2010
 10 2 p. 228-229
2 p.
 artikel
107 67 mtDNA haplogroup A is associated with gestational diabetes in hispanics Gutierrez, Sonia
 2010
 10 2 p. 218-219
2 p.
 artikel
108 98 Mutant huntingtin leads to increased levels of mitochondrial DNA damage and mitochondrial dysfunction in mouse striatal cells Ayala-Torres, Sylvette
 2010
 10 2 p. 227-
1 p.
 artikel
109 22 NAD+-dependent deacetylase SIRT3 regulates mitochondrial protein synthesis by deacetylation of the ribosomal protein MRPL10 Cimen, Huseyin
 2010
 10 2 p. 206-
1 p.
 artikel
110 13 NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvement Leshinsky, Esther
 2010
 10 2 p. 203-
1 p.
 artikel
111 148 Nonylphenol ethoxylate present in plastic labware inhibit mitochondrial respiratory chain complex I Saada, Ann
 2010
 10 2 p. 242-
1 p.
 artikel
112 Oligodendroglial differentiation induces mitochondrial genes and inhibition of mitochondrial function represses oligodendroglial differentiation Schoenfeld, Robert
 2010
 10 2 p. 143-150
8 p.
 artikel
113 50 Oxidative damage in cells with altered mitochondrial content Crammer, Cody
 2010
 10 2 p. 213-
1 p.
 artikel
114 134 Permeabilized fibers or isolated mitochondria for the detection of oxidative phosphorylation defects in patients with mitochondrial diseases Lemieux, Hélène
 2010
 10 2 p. 238-
1 p.
 artikel
115 111 Phase 3 trial of coenzyme Q10 in mitochondrial diseases Kurtz, Tracie L.
 2010
 10 2 p. 231-
1 p.
 artikel
116 65 Phenotypic differences of animal models of complex III and complex IV deficiencies in neurons Diaz, Francisca
 2010
 10 2 p. 218-
1 p.
 artikel
117 27 Polymer blend nanoparticulate carriers for combination paclitaxel/lonidamine therapy in overcoming multidrug resistance in breast and ovarian cancer via exploitation of the Warburg effect Milane, Lara Scheherazade
 2010
 10 2 p. 207-
1 p.
 artikel
118 48 PPAR signaling modulates metabolic consequences of coenzyme Q deficiency in Pdss2 mutant mice and is normalized by Probucol therapy Falk, Marni J.
 2010
 10 2 p. 213-
1 p.
 artikel
119 131 Prevalence of autistic features in patients with definite diagnosis of mitochondrial disorder Scaglia, Fernando
 2010
 10 2 p. 237-
1 p.
 artikel
120 75 Protective effect of mitochondrial catalase on AZT mitochondrial toxicity Marcinek, David J.
 2010
 10 2 p. 221-
1 p.
 artikel
121 31 Pyrroloquinoline quinone and mitochondriogenesis Rucker, Robert B.
 2010
 10 2 p. 208-
1 p.
 artikel
122 85 Pyruvate therapy for Leigh syndrome with hypertrophic cardiomyopathy Tanaka, Masashi
 2010
 10 2 p. 224-
1 p.
 artikel
123 124 Rapid immunoassays for diagnosis and characterization of mitochondrial disease and dysfunction Marusich, Michael F.
 2010
 10 2 p. 234-235
2 p.
 artikel
124 2 Reactive oxygen species mediated regulation of mitochondrial biogenesis in the yeast Saccharomyces cerevisiae Devin, Anne
 2010
 10 2 p. 200-
1 p.
 artikel
125 108 Recurrent sinopulmonary infections, bacteremia and sepsis in children with mitochondrial complexes I–III deficiency: Immunological abnormalities Pacheco, S.E.
 2010
 10 2 p. 230-
1 p.
 artikel
126 15 Regulation of mitochondria by extramitochondrial calcium is impaired in transgenic models of HD Gellerich, Frank N.
 2010
 10 2 p. 204-
1 p.
 artikel
127 128 Regulation of mitochondrial gene expression by LRPPRC Sondheimer, Neal
 2010
 10 2 p. 236-
1 p.
 artikel
128 6 Respiratory chain complex I deficiency in oncocytic tumours Zimmermann, Franz A.
 2010
 10 2 p. 201-
1 p.
 artikel
129 91 Role of MRPL10 acetylation on mitochondrial translation Han, Min-Joon
 2010
 10 2 p. 225-
1 p.
 artikel
130 100 Role of oxidative phosphorylation in breast tumorigenesis Owens, Kjerstin M.
 2010
 10 2 p. 228-
1 p.
 artikel
131 19 Role of three different variants of mitochondrial ribosomal S18s in mitochondrial translation Akpinar, Gurler
 2010
 10 2 p. 205-
1 p.
 artikel
132 1 Screening of candidate nuclear genes for modifying role in Leber’s hereditary optic neuropathy penetrance: A signal from manganese superoxide dismutase Maresca, Alessandra
 2010
 10 2 p. 200-
1 p.
 artikel
133 30 Searching for early biomarkers exploitable to prevent or delay human mitochondrial-associated diseases onset: C. elegans models as a screening tool Kell, Alison
 2010
 10 2 p. 208-
1 p.
 artikel
134 17 Sepsis effects on mitochondria Garrabou, G.
 2010
 10 2 p. 204-
1 p.
 artikel
135 Somatic mutations of mitochondrial genome in hepatocellular carcinoma Yin, Pen-Hui
 2010
 10 2 p. 174-182
9 p.
 artikel
136 40 Spectrum of gastrointestinal problems in children with established ETC mitochondrial disorders Bhardwaj, Jatinder
 2010
 10 2 p. 210-211
2 p.
 artikel
137 120 Successful orthotopic liver transplantation in a patient with complex IV deficiency Kallish, S.
 2010
 10 2 p. 233-
1 p.
 artikel
138 25 Surf-1 gene mutation associated with leukoencephalopathy at presentation Timothy, Jeremy
 2010
 10 2 p. 206-
1 p.
 artikel
139 32 Systemic delivery of mitochondria-targeted restriction endonucleases to alter mtDNA heteroplasmy in specific tissue Bacman, Sandra R.
 2010
 10 2 p. 208-209
2 p.
 artikel
140 23 The human mitochondrial RNA polymerase as an off target for antiviral ribonucleosides Arnold, Jamie J.
 2010
 10 2 p. 206-
1 p.
 artikel
141 140 The locus ceruleus contains mitochondrial DNA deletions in Alzheimer’s Disease Miller, Bradley
 2010
 10 2 p. 239-240
2 p.
 artikel
142 56 The mitochondrial and β -amyloid relationship in Alzheimer’s disease Young, Kisha
 2010
 10 2 p. 215-
1 p.
 artikel
143 125 The role of mitochondria during differentiation of preadipocytes and insulin insensitivity of adipocytes with mitochondrial dysfunction Wang, Chih-Hao
 2010
 10 2 p. 235-
1 p.
 artikel
144 104 The role of mitochondrial dysregulation in death resistance and survival signaling Wright, Kristen P.
 2010
 10 2 p. 229-
1 p.
 artikel
145 3 The unexpected capacity of melanin to dissociate water molecule is a new way to improve mitochondrial cytopathies Herrera, Arturo Solı´s
 2010
 10 2 p. 200-201
2 p.
 artikel
146 86 Tissue-specific control of mitochondrial DNA genetics Battersby, Brendan J.
 2010
 10 2 p. 224-
1 p.
 artikel
147 73 Transcriptional coordination of mitochondrial biogenesis with cytoskeletal remodeling upon neuronal differentiation Baxter, Kristin K.
 2010
 10 2 p. 220-
1 p.
 artikel
148 66 Two common mtDNA polymorphisms are associated with pervasive developmental disorder NOS, also known as “Atypical Autism” Boles, Richard G.
 2010
 10 2 p. 218-
1 p.
 artikel
149 71 Two common mtDNA polymorphisms are associated with sudden infant death syndrome (SIDS) Boles, Richard G.
 2010
 10 2 p. 219-220
2 p.
 artikel
150 142 Unraveling the potential role of human Suv3 in genome maintenance Venoe, Susanne T.
 2010
 10 2 p. 240-
1 p.
 artikel
151 109 Use of MitoChip to understand the mechanism of mitochondrial dysfunction in mice exposed to anti-HIV Desai, Varsha G.
 2010
 10 2 p. 230-231
2 p.
 artikel
152 122 Use of templates that bypass the need for mitochondrial promoter melting reveal distinct functions for human mitochondrial transcription factors in polymerase recruitment to and function at the mitochondrial promoters and identify promoter clearance as another rate-limiting step Uchida, Akira
 2010
 10 2 p. 234-
1 p.
 artikel
153 102 Yeast homologues of disease mutations in DNA polymerase gamma cause mtDNA depletion and mutagenesis Stumpf, Jeffrey D.
 2010
 10 2 p. 228-
1 p.
 artikel
154 34 Zinc finger nucleases targeted to the m.3243A>G mutation in mitochondrial encephalomyopathy (MELAS) Williams, Siôn
 2010
 10 2 p. 209-
1 p.
 artikel
                             154 gevonden resultaten
 
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