| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acquired coenzyme Q10 deficiency in children with recurrent food intolerance and allergies
|
Miles, Michael V.
|
|
2011
|
11 |
1 |
p. 127-135
9 p.
|
artikel
|
| 2 |
Altered redox status of coenzyme Q9 reflects mitochondrial electron transport chain deficiencies in Caenorhabditis elegans
|
Vasta, V.
|
|
2011
|
11 |
1 |
p. 136-138
3 p.
|
artikel
|
| 3 |
Alzheimer's disease: Effects of β-amyloid on mitochondria
|
Tillement, Laurent
|
|
2011
|
11 |
1 |
p. 13-21
9 p.
|
artikel
|
| 4 |
A mitochondrial ubiquitin ligase MITOL controls cell toxicity of polyglutamine-expanded protein
|
Sugiura, Ayumu
|
|
2011
|
11 |
1 |
p. 139-146
8 p.
|
artikel
|
| 5 |
A novel mutation in the mitochondrial tRNAAla gene (m.5636T>C) in a patient with progressive external ophthalmoplegia
|
Pinós, Tomàs
|
|
2011
|
11 |
1 |
p. 228-233
6 p.
|
artikel
|
| 6 |
Application of oligonucleotide array CGH in the detection of a large intragenic deletion in POLG associated with Alpers Syndrome
|
Compton, Alison G.
|
|
2011
|
11 |
1 |
p. 104-107
4 p.
|
artikel
|
| 7 |
Association of mitochondrial haplogroup D and risk of esophageal cancer in Taihang Mountain and Chaoshan areas in China
|
Li, Xiao-Yun
|
|
2011
|
11 |
1 |
p. 27-32
6 p.
|
artikel
|
| 8 |
Calendar of Events
|
|
|
2011
|
11 |
1 |
p. III-
1 p.
|
artikel
|
| 9 |
Complete mitochondrial DNA sequence analysis of Bison bison and bison–cattle hybrids: Function and phylogeny
|
Douglas, Kory C.
|
|
2011
|
11 |
1 |
p. 166-175
10 p.
|
artikel
|
| 10 |
Complex V TMEM70 deficiency results in mitochondrial nucleoid disorganization
|
Cameron, Jessie M.
|
|
2011
|
11 |
1 |
p. 191-199
9 p.
|
artikel
|
| 11 |
Contents cont'd
|
|
|
2011
|
11 |
1 |
p. V-VI
nvt p.
|
artikel
|
| 12 |
Dietary fatty acids and oxidative stress in the heart mitochondria
|
Lemieux, Hélène
|
|
2011
|
11 |
1 |
p. 97-103
7 p.
|
artikel
|
| 13 |
Doxorubicin induces mitochondrial permeability transition and contractile dysfunction in the human myocardium
|
Montaigne, David
|
|
2011
|
11 |
1 |
p. 22-26
5 p.
|
artikel
|
| 14 |
Endurance training reverts heart mitochondrial dysfunction, permeability transition and apoptotic signaling in long-term severe hyperglycemia
|
Lumini-Oliveira, José
|
|
2011
|
11 |
1 |
p. 54-63
10 p.
|
artikel
|
| 15 |
Functional characterization of the promoter of the human Lon protease gene
|
Pinti, Marcello
|
|
2011
|
11 |
1 |
p. 200-206
7 p.
|
artikel
|
| 16 |
Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation
|
Verny, Christophe
|
|
2011
|
11 |
1 |
p. 70-75
6 p.
|
artikel
|
| 17 |
Improvement of mitochondrial energy and oxidative balance during intestinal differentiation
|
Santandreu, Francisca M.
|
|
2011
|
11 |
1 |
p. 89-96
8 p.
|
artikel
|
| 18 |
Mitochondria and viruses
|
Ohta, Akane
|
|
2011
|
11 |
1 |
p. 1-12
12 p.
|
artikel
|
| 19 |
Mitochondrial biogenesis related endurance genotype score and sports performance in athletes
|
Eynon, Nir
|
|
2011
|
11 |
1 |
p. 64-69
6 p.
|
artikel
|
| 20 |
Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: Evidence for an association to haplogroup H
|
Palacín, María
|
|
2011
|
11 |
1 |
p. 176-181
6 p.
|
artikel
|
| 21 |
Mitochondrial DNA depletion and its correlation with TFAM, TFB1M, TFB2M and POLG in human diffusely infiltrating astrocytomas
|
Correia, R.L.
|
|
2011
|
11 |
1 |
p. 48-53
6 p.
|
artikel
|
| 22 |
Mitochondrial DNA does not contribute to the heritability of non-alcoholic fatty liver disease
|
de Alwis, Nimantha
|
|
2011
|
11 |
1 |
p. 234-235
2 p.
|
artikel
|
| 23 |
Mitochondrial reactive oxygen species generation by the SDHC V69E mutation causes low birth weight and neonatal growth retardation
|
Ishii, Takamasa
|
|
2011
|
11 |
1 |
p. 155-165
11 p.
|
artikel
|
| 24 |
Nuclear coded mitochondrial protein prohibitin is an iron regulated iron binding protein
|
Ande, Sudharsana R.
|
|
2011
|
11 |
1 |
p. 40-47
8 p.
|
artikel
|
| 25 |
POLG exon 22 skipping induced by different mechanisms in two unrelated cases of Alpers syndrome
|
Mousson de Camaret, Bénédicte
|
|
2011
|
11 |
1 |
p. 223-227
5 p.
|
artikel
|
| 26 |
Predicting the contribution of novel POLG mutations to human disease through analysis in yeast model
|
Baruffini, Enrico
|
|
2011
|
11 |
1 |
p. 182-190
9 p.
|
artikel
|
| 27 |
Protective effect of N-acetylcysteine supplementation on mitochondrial oxidative stress and mitochondrial enzymes in cerebral cortex of streptozotocin-treated diabetic rats
|
Kamboj, Sukhdev S.
|
|
2011
|
11 |
1 |
p. 214-222
9 p.
|
artikel
|
| 28 |
Recombinant human mitochondrial transcription factor A stimulates mitochondrial biogenesis and ATP synthesis, improves motor function after MPTP, reduces oxidative stress and increases survival after endotoxin
|
Thomas, Ravindar R.
|
|
2011
|
11 |
1 |
p. 108-118
11 p.
|
artikel
|
| 29 |
Tissue-specific differences in mitochondrial activity and biogenesis
|
Fernández-Vizarra, Erika
|
|
2011
|
11 |
1 |
p. 207-213
7 p.
|
artikel
|
| 30 |
Title page (with logo)
|
|
|
2011
|
11 |
1 |
p. iii-
1 p.
|
artikel
|
| 31 |
Toll-like receptor-3-induced mitochondrial dysfunction in cultured human hepatocytes
|
Djafarzadeh, Siamak
|
|
2011
|
11 |
1 |
p. 83-88
6 p.
|
artikel
|
| 32 |
Upregulation of human selenoprotein H in murine hippocampal neuronal cells promotes mitochondrial biogenesis and functional performance
|
Mendelev, Natalia
|
|
2011
|
11 |
1 |
p. 76-82
7 p.
|
artikel
|
| 33 |
What limits the allotopic expression of nucleus-encoded mitochondrial genes? The case of the chimeric Cox3 and Atp6 genes
|
Figueroa-Martínez, Francisco
|
|
2011
|
11 |
1 |
p. 147-154
8 p.
|
artikel
|
| 34 |
Xenomitochondrial mice: Investigation into mitochondrial compensatory mechanisms
|
Cannon, M.V.
|
|
2011
|
11 |
1 |
p. 33-39
7 p.
|
artikel
|
| 35 |
Yeast mitochondrial DNA polymerase is a highly processive single-subunit enzyme
|
Viikov, Katrin
|
|
2011
|
11 |
1 |
p. 119-126
8 p.
|
artikel
|
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