Anders Oldfors
Anders Oldfors
Department of Pathology and Genetics, Sahlgrenska Academy, University of Gothenburg, Sweden
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Cited by
Cited by
Premature ageing in mice expressing defective mitochondrial DNA polymerase
A Trifunovic, A Wredenberg, M Falkenberg, JN Spelbrink, AT Rovio, ...
Nature 429 (6990), 417-423, 2004
Muscle Biopsy E-Book: A Practical Approach
V Dubowitz, A Oldfors, CA Sewry
Elsevier Health Sciences, 2013
Mitochondrial transcription factor A is necessary for mtDNA maintance and embryogenesis in mice
NG Larsson, J Wang, H Wilhelmsson, A Oldfors, P Rustin, M Lewandoski, ...
Nature genetics 18 (3), 231-236, 1998
Parkinsonism, premature menopause, and mitochondrial DNA polymerase γ mutations: clinical and molecular genetic study
P Luoma, A Melberg, JO Rinne, JA Kaukonen, NN Nupponen, ...
The Lancet 364 (9437), 875-882, 2004
Impaired insulin secretion and β-cell loss in tissue-specific knockout mice with mitochondrial diabetes
JP Silva, M Köhler, C Graff, A Oldfors, MA Magnuson, PO Berggren, ...
Nature genetics 26 (3), 336-340, 2000
Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression
J Wang, H Wilhelmsson, C Graff, H Li, A Oldfors, P Rustin, JC Brüning, ...
Nature genetics 21 (1), 133-137, 1999
The incidence of mitochondrial encephalomyopathies in childhood: clinical features and morphological, biochemical, and DNA abnormalities
N Darin, A Oldfors, AR Moslemi, E Holme, M Tulinius
Annals of neurology 49 (3), 377-383, 2001
Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy
AS Nicot, A Toussaint, V Tosch, C Kretz, C Wallgren-Pettersson, ...
Nature genetics 39 (9), 1134-1139, 2007
Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome
N Larsson, E Holme, B Kristiansson, A Oldfors, M Tulinius
Pediatric research 28 (2), 131-136, 1990
ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency
RKJ Olsen, SE Olpin, BS Andresen, ZH Miedzybrodzka, M Pourfarzam, ...
Brain 130 (8), 2045-2054, 2007
Increased mitochondrial mass in mitochondrial myopathy mice
A Wredenberg, R Wibom, H Wilhelmsson, C Graff, HH Wiener, SJ Burden, ...
Proceedings of the National Academy of Sciences 99 (23), 15066-15071, 2002
Cardiomyopathy in children with mitochondrial disease: clinical course and cardiological findings
D Holmgren, H Wahlander, BO Eriksson, A Oldfors, E Holme, M Tulinius
European heart journal 24 (3), 280-288, 2003
Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents.
PV Belichenko, A Oldfors, B Hagberg, A Dahlström
Neuroreport 5 (12), 1509-1513, 1994
Low levels of mitochondrial transcription factor A in mitochondrial DNA depletion
NG Larsson, A Oldfors, E Holme, DA Clayton
Biochemical and biophysical research communications 200 (3), 1374-1381, 1994
Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function
G Fayet, M Jansson, D Sternberg, AR Moslemi, P Blondy, A Lombès, ...
Neuromuscular Disorders 12 (5), 484-493, 2002
Segregation and manifestations of the mtDNA tRNA (Lys) A--> G (8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome.
NG Larsson, MH Tulinius, E Holme, A Oldfors, O Andersen, J Wahlström, ...
American journal of human genetics 51 (6), 1201, 1992
Myosinopathies: pathology and mechanisms
H Tajsharghi, A Oldfors
Acta neuropathologica 125, 3-18, 2013
Autosomal dominant myopathy: missense mutation (Glu-706→ Lys) in the myosin heavy chain IIa gene
T Martinsson, A Oldfors, N Darin, K Berg, H Tajsharghi, M Kyllerman, ...
Proceedings of the National Academy of Sciences 97 (26), 14614-14619, 2000
Leber's hereditary optic neuropathy and complex I deficiency in muscle
NG Larsson, O Andersen, E Holme, A Oldfors, J Wahlström
Annals of Neurology: Official Journal of the American Neurological …, 1991
Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect
J Senderek, JS Müller, M Dusl, TM Strom, V Guergueltcheva, I Diepolder, ...
The American Journal of Human Genetics 88 (2), 162-172, 2011
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