| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A genome-wide association study in the genetic analysis of idiopathic thrombophilia project suggests sex-specific regulation of mitochondrial DNA levels
|
López, Sonia
|
|
2014
|
18 |
C |
p. 34-40
7 p.
|
artikel
|
| 2 |
Assessment of nuclear transfer techniques to prevent the transmission of heritable mitochondrial disorders without compromising embryonic development competence in mice
|
Neupane, Jitesh
|
|
2014
|
18 |
C |
p. 27-33
7 p.
|
artikel
|
| 3 |
Comparative analysis of human mitochondrial methylomes shows distinct patterns of epigenetic regulation in mitochondria
|
Ghosh, Sourav
|
|
2014
|
18 |
C |
p. 58-62
5 p.
|
artikel
|
| 4 |
Editorial Board
|
|
|
2014
|
18 |
C |
p. IFC-
1 p.
|
artikel
|
| 5 |
Glucose metabolism derangements in adults with the MELAS m.3243A>G mutation
|
El-Hattab, Ayman W.
|
|
2014
|
18 |
C |
p. 63-69
7 p.
|
artikel
|
| 6 |
Leber's hereditary optic neuropathy caused by the homoplasmic ND1 m.3635G>A mutation in nine Han Chinese families
|
Zhang, Juanjuan
|
|
2014
|
18 |
C |
p. 18-26
9 p.
|
artikel
|
| 7 |
Mitochondrial macro-haplogroup JT may play a protective role in ovarian ageing
|
May-Panloup, P.
|
|
2014
|
18 |
C |
p. 1-6
6 p.
|
artikel
|
| 8 |
Mitogenomic analyses propose positive selection in mitochondrial genes for high-altitude adaptation in galliform birds
|
Zhou, Taicheng
|
|
2014
|
18 |
C |
p. 70-75
6 p.
|
artikel
|
| 9 |
Mutation-free baby born from a mitochondrial encephalopathy, lactic acidosis and stroke-like syndrome carrier after blastocyst trophectoderm preimplantation genetic diagnosis
|
Heindryckx, Björn
|
|
2014
|
18 |
C |
p. 12-17
6 p.
|
artikel
|
| 10 |
Mutation of the mitochondrial large ribosomal RNA can provide pentamidine resistance to Saccharomyces cerevisiae
|
Örs, Ş. Tomris
|
|
2014
|
18 |
C |
p. 7-11
5 p.
|
artikel
|
| 11 |
Potential roles of PINK1 for increased PGC-1α-mediated mitochondrial fatty acid oxidation and their associations with Alzheimer disease and diabetes
|
Choi, Joungil
|
|
2014
|
18 |
C |
p. 41-48
8 p.
|
artikel
|
| 12 |
Riboflavin responsive mitochondrial myopathy is a new phenotype of dihydrolipoamide dehydrogenase deficiency. The chaperon-like effect of vitamin B2
|
Carrozzo, Rosalba
|
|
2014
|
18 |
C |
p. 49-57
9 p.
|
artikel
|
| 13 |
Sirtuin 3 interacts with Lon protease and regulates its acetylation status
|
Gibellini, Lara
|
|
2014
|
18 |
C |
p. 76-81
6 p.
|
artikel
|
Tijdschrift beschrijving