nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Analysis of mitochondrial genome revealed a rare 50bp deletion and substitutions in a family with hypertension
|
Elango, Santhini |
|
2011 |
11 |
6 |
p. 878-885 8 p. |
artikel |
2 |
A novel mitotropic oligolysine nanocarrier: Targeted delivery of covalently bound D-Luciferin to cell mitochondria
|
Theodossiou, Theodossis A. |
|
2011 |
11 |
6 |
p. 982-986 5 p. |
artikel |
3 |
Are mitochondrial haplogroups associated with elite athletic status? A study on a Spanish cohort
|
Nogales-Gadea, Gisela |
|
2011 |
11 |
6 |
p. 905-908 4 p. |
artikel |
4 |
Biochemical analysis of the G517V POLG variant reveals wild-type like activity
|
Kasiviswanathan, Rajesh |
|
2011 |
11 |
6 |
p. 929-934 6 p. |
artikel |
5 |
Biochemical parameters to assess choroid plexus dysfunction in Kearns–Sayre syndrome patients
|
Tondo, Mireia |
|
2011 |
11 |
6 |
p. 867-870 4 p. |
artikel |
6 |
Calcium-dependent mitochondrial extrusion in ciliated protozoa
|
Bisharyan, Yelena |
|
2011 |
11 |
6 |
p. 909-918 10 p. |
artikel |
7 |
Contents cont'd
|
|
|
2011 |
11 |
6 |
p. III- 1 p. |
artikel |
8 |
Control of mitochondrial volume by mitochondrial metabolic water
|
Casteilla, Louis |
|
2011 |
11 |
6 |
p. 862-866 5 p. |
artikel |
9 |
Corrigendum to “Mitochondrially targeted anti-cancer agents” [Mitochondrion 10 (2010) 670–681]
|
Biasutto, Lucia |
|
2011 |
11 |
6 |
p. 996- 1 p. |
artikel |
10 |
Cytochrome c Trp65Ser substitution results in inhibition of acetic acid-induced programmed cell death in Saccharomyces cerevisiae
|
Guaragnella, Nicoletta |
|
2011 |
11 |
6 |
p. 987-991 5 p. |
artikel |
11 |
Editorial Board
|
|
|
2011 |
11 |
6 |
p. IFC- 1 p. |
artikel |
12 |
Effects of X-irradiation on mitochondrial DNA damage and its supercoiling formation change
|
Zhou, Xin |
|
2011 |
11 |
6 |
p. 886-892 7 p. |
artikel |
13 |
Human cytomegalovirus infection increases mitochondrial biogenesis
|
Kaarbø, Mari |
|
2011 |
11 |
6 |
p. 935-945 11 p. |
artikel |
14 |
Large scale mtDNA sequencing reveals sequence and functional conservation as major determinants of homoplasmic mtDNA variant distribution
|
Voets, A.M. |
|
2011 |
11 |
6 |
p. 964-972 9 p. |
artikel |
15 |
MitoBamAnnotator: A web-based tool for detecting and annotating heteroplasmy in human mitochondrial DNA sequences
|
Zhidkov, Ilia |
|
2011 |
11 |
6 |
p. 924-928 5 p. |
artikel |
16 |
Mitochondrial DNA variation in human metabolic rate and energy expenditure
|
Tranah, Gregory J. |
|
2011 |
11 |
6 |
p. 855-861 7 p. |
artikel |
17 |
Mitochondrial gene therapy: The tortuous path from bench to bedside
|
Adhya, Samit |
|
2011 |
11 |
6 |
p. 839-844 6 p. |
artikel |
18 |
Mitochondrial small RNAs that are up-regulated in hippocampus during olfactory discrimination training in mice
|
Smalheiser, Neil R. |
|
2011 |
11 |
6 |
p. 994-995 2 p. |
artikel |
19 |
Mitochondrial targeting of peroxiredoxin 5 is preserved from annelids to mammals but is absent in pig Sus scrofa domesticus
|
Van der Eecken, Valérie |
|
2011 |
11 |
6 |
p. 973-981 9 p. |
artikel |
20 |
Nuclear insertions of mitochondrial origin: Database updating and usefulness in cancer studies
|
Ramos, Amanda |
|
2011 |
11 |
6 |
p. 946-953 8 p. |
artikel |
21 |
Nutrient excess and altered mitochondrial proteome and function contribute to neurodegeneration in diabetes
|
Chowdhury, Subir K. Roy |
|
2011 |
11 |
6 |
p. 845-854 10 p. |
artikel |
22 |
Optimization of respiratory chain enzymatic assays in muscle for the diagnosis of mitochondrial disorders
|
Spinazzi, Marco |
|
2011 |
11 |
6 |
p. 893-904 12 p. |
artikel |
23 |
Peptides from aminoacyl-tRNA synthetases can cure the defects due to mutations in mt tRNA genes
|
Francisci, Silvia |
|
2011 |
11 |
6 |
p. 919-923 5 p. |
artikel |
24 |
Rapid-onset, linezolid-induced lactic acidosis in MELAS
|
Cope, Thomas E. |
|
2011 |
11 |
6 |
p. 992-993 2 p. |
artikel |
25 |
Restoration of complex V deficiency caused by a novel deletion in the human TMEM70 gene normalizes mitochondrial morphology
|
Jonckheere, An I. |
|
2011 |
11 |
6 |
p. 954-963 10 p. |
artikel |
26 |
The altered activity of complex III may contribute to the high penetrance of Leber's hereditary optic neuropathy in a Chinese family carrying the ND4 G11778A mutation
|
Qian, Yaping |
|
2011 |
11 |
6 |
p. 871-877 7 p. |
artikel |