nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A mutation in MT-TW causes a tRNA processing defect and reduced mitochondrial function in a family with Leigh syndrome
|
Duff, Rachael M. |
|
2015 |
25 |
C |
p. 113-119 7 p. |
artikel |
2 |
Differences in mitochondrial function in homogenated samples from healthy and epileptic specific brain tissues revealed by high-resolution respirometry
|
Burtscher, Johannes |
|
2015 |
25 |
C |
p. 104-112 9 p. |
artikel |
3 |
Editorial Board
|
|
|
2015 |
25 |
C |
p. IFC- 1 p. |
artikel |
4 |
IL-15Rα deficiency in skeletal muscle alters respiratory function and the proteome of mitochondrial subpopulations independent of changes to the mitochondrial genome
|
O'Connell, Grant C. |
|
2015 |
25 |
C |
p. 87-97 11 p. |
artikel |
5 |
Increased deoxythymidine triphosphate levels is a feature of relative cognitive decline
|
Desler, Claus |
|
2015 |
25 |
C |
p. 34-37 4 p. |
artikel |
6 |
Investigation of mitochondrial DNA variations among Indian Friedreich's ataxia (FRDA) patients
|
Singh, Inder |
|
2015 |
25 |
C |
p. 1-5 5 p. |
artikel |
7 |
Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: A study from south India
|
Bindu, Parayil Sankaran |
|
2015 |
25 |
C |
p. 6-16 11 p. |
artikel |
8 |
Mitoepigenetics: The different shades of grey
|
Ghosh, Sourav |
|
2015 |
25 |
C |
p. 60-66 7 p. |
artikel |
9 |
Novel computer vision algorithm for the reliable analysis of organelle morphology in whole cell 3D images — A pilot study for the quantitative evaluation of mitochondrial fragmentation in amyotrophic lateral sclerosis
|
Lautenschläger, Janin |
|
2015 |
25 |
C |
p. 49-59 11 p. |
artikel |
10 |
Obstetric complications in carriers of the m.3243A>G mutation, a retrospective cohort study on maternal and fetal outcome
|
de Laat, Paul |
|
2015 |
25 |
C |
p. 98-103 6 p. |
artikel |
11 |
Regulation of mitochondrial biogenesis through TFAM–mitochondrial DNA interactions
|
Picca, Anna |
|
2015 |
25 |
C |
p. 67-75 9 p. |
artikel |
12 |
Sequence and expression variations in 23 genes involved in mitochondrial and non-mitochondrial apoptotic pathways and risk of oral leukoplakia and cancer
|
Datta, Sayantan |
|
2015 |
25 |
C |
p. 28-33 6 p. |
artikel |
13 |
The presence of highly disruptive 16S rRNA mutations in clinical samples indicates a wider role for mutations of the mitochondrial ribosome in human disease
|
Elson, Joanna L. |
|
2015 |
25 |
C |
p. 17-27 11 p. |
artikel |
14 |
U-insertion/deletion RNA editing multiprotein complexes and mitochondrial ribosomes in Leishmania tarentolae are located in antipodal nodes adjacent to the kinetoplast DNA
|
Wong, Richard G. |
|
2015 |
25 |
C |
p. 76-86 11 p. |
artikel |
15 |
Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy
|
Nolli, Cecilia |
|
2015 |
25 |
C |
p. 38-48 11 p. |
artikel |