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                             26 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A case of Kearns–Sayre syndrome with two novel deletions (9.768 and 7.253kb) of the mtDNA associated with the common deletion in blood leukocytes, buccal mucosa and hair follicles Mkaouar-Rebai, Emna
2010
10 5 p. 449-455
7 p.
artikel
2 Announcement: Targeting Mitochondria 2010 2010
10 5 p. V-
1 p.
artikel
3 Apparent longevity-related adaptation of mitochondrial amino acid content is due to nucleotide compositional shifts Jobson, Richard W.
2010
10 5 p. 540-547
8 p.
artikel
4 A quantitative assay for mitochondrial fusion using Renilla luciferase complementation Huang, Huiyan
2010
10 5 p. 559-566
8 p.
artikel
5 Bupivacaine uncouples the mitochondrial oxidative phosphorylation, inhibits respiratory chain complexes I and III and enhances ROS production: Results of a study on cell cultures Cela, Olga
2010
10 5 p. 487-496
10 p.
artikel
6 Calendar of Events 2010
10 5 p. I-II
nvt p.
artikel
7 Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutation Kotarsky, Heike
2010
10 5 p. 497-509
13 p.
artikel
8 Coexistence of mitochondrial and nuclear DNA mutations in a woman with mitochondrial encephalomyopathy and double cortex Scuderi, Carmela
2010
10 5 p. 548-554
7 p.
artikel
9 Depressive behaviour in children diagnosed with a mitochondrial disorder Morava, E.
2010
10 5 p. 528-533
6 p.
artikel
10 3-D structure of mitochondrial cristae in rat adrenal cortex varies after acute stimulation with ACTH and CRH Isola, Raffaella
2010
10 5 p. 472-478
7 p.
artikel
11 Editorial Board 2010
10 5 p. IFC-
1 p.
artikel
12 Fish as a model in investigations about the relationship between oxygen consumption and hydroxyl radical production in permeabilized muscle fibers Mortelette, H.
2010
10 5 p. 555-558
4 p.
artikel
13 Genetic, functional and evolutionary characterization of scox, the Drosophila melanogaster ortholog of the human SCO1 gene Porcelli, Damiano
2010
10 5 p. 433-448
16 p.
artikel
14 Illness-induced exacerbation of Leigh syndrome in a patient with the MTATP6 mutation, m. 9185 T>C Saneto, Russell P.
2010
10 5 p. 567-572
6 p.
artikel
15 Indirubin-3′-oxime prevents hepatic I/R damage by inhibiting GSK-3β and mitochondrial permeability transition Varela, Ana T.
2010
10 5 p. 456-463
8 p.
artikel
16 Kearns-Sayre syndrome: Cerebral folate deficiency, MRI findings and new cerebrospinal fluid biochemical features Serrano, Mercedes
2010
10 5 p. 429-432
4 p.
artikel
17 Maternal diabetes and oocyte quality Wang, Qiang
2010
10 5 p. 403-410
8 p.
artikel
18 Meeting report: Identification of biomarkers for early detection of mitochondrial dysfunction Shaughnessy, Daniel T.
2010
10 5 p. 579-581
3 p.
artikel
19 Mitochondrial DNA sequences are present inside nuclear DNA in rat tissues and increase with age Caro, Pilar
2010
10 5 p. 479-486
8 p.
artikel
20 Mitochondrial dysfunction: A potential link between neuroinflammation and neurodegeneration? Witte, Maarten E.
2010
10 5 p. 411-418
8 p.
artikel
21 Mitochondrial dysfunction in CD4+lymphocytes from stavudine-treated HIV patients Einsiedel, Lloyd
2010
10 5 p. 534-539
6 p.
artikel
22 Mitochondria, spermatogenesis and male infertility Rajender, Singh
2010
10 5 p. 419-428
10 p.
artikel
23 Nonsense mutations in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophy Gerards, Mike
2010
10 5 p. 510-515
6 p.
artikel
24 PGC-1β-Regulated mitochondrial biogenesis and function in myotubes is mediated by NRF-1 and ERRα Shao, Di
2010
10 5 p. 516-527
12 p.
artikel
25 Phosphorylation pattern of the NDUFS4 subunit of complex I of the mammalian respiratory chain Rasmo, Domenico De
2010
10 5 p. 464-471
8 p.
artikel
26 S-Nitrosylation of Drp1 links excessive mitochondrial fission to neuronal injury in neurodegeneration Nakamura, Tomohiro
2010
10 5 p. 573-578
6 p.
artikel
                             26 gevonden resultaten
 
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