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                             15 gevonden resultaten
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
                             15 gevonden resultaten
 
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