Oldfors, Anders

Premature ageing in mice expressing defective mitochondrial DNA polymerase

Trifunovic, A., Wredenberg, A., Falkenberg, M., Spelbrink, J. N., Rovio, A. T., Bruder, C. E., Bohlooly-Y, M., Gidlöf, S., Oldfors, A., Wibom, R., et al. (2004) · Nature

Mitochondrial Function and PathologyGenetics, Aging, and Longevity in Model Organisms

Cited by 2,734

Mitochondrial transcription factor A is necessary for mtDNA maintance and embryogenesis in mice

Larsson, N.-G., Wang, J., Wilhelmsson, H., Oldfors, A., Rustin, P., Lewandoski, M., Barsh, G. S., & Clayton, D. A. (1998) · Nature Genetics

Mitochondrial Function and PathologyAutophagy in Disease and Therapy

Cited by 1,594

Parkinsonism, premature menopause, and mitochondrial DNA polymerase γ mutations: clinical and molecular genetic study

Luoma, P., Melberg, A., Rinne, J. O., Kaukonen, J. A., Nupponen, N. N., Chalmers, R. M., Oldfors, A., Rautakorpi, I., Peltonen, L., Majamaa, K., et al. (2004) · The Lancet

Parkinson's Disease Mechanisms and TreatmentsMitochondrial Function and Pathology

Cited by 548

Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression.

Wang, J., Wilhelmsson, H., Graff, C., Li, H., Oldfors, A., Rustin, P., Brüning, J. C., Kahn, C. R., Clayton, D. A., Barsh, G. S., et al. (1999) · Nature Genetics

Mitochondrial Function and PathologyCardiac electrophysiology and arrhythmias

Cited by 435

Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy

Nicot, A.-S., Toussaint, A., Tosch, V., Kretz, C., Wallgren-Pettersson, C., Iwarsson, E., Kingston, H., Garnier, J.-M., Biancalana, V., Oldfors, A., et al. (2007) · Nature Genetics

Muscle Physiology and DisordersGenomics and Rare Diseases

Cited by 434

Impaired insulin secretion and β-cell loss in tissue-specific knockout mice with mitochondrial diabetes

Silva, J. P., Köhler, M., Graff, C., Oldfors, A., Magnuson, M. A., Berggren, P.-O., & Larsson, N.-G. (2000) · Nature Genetics

Pancreatic function and diabetesMitochondrial Function and Pathology

Cited by 433

Progressive Increase of the Mutated Mitochondrial DNA Fraction in Kearns-Sayre Syndrome

Larsson, N.-G., Holme, E., Kristiansson, B., Oldfors, A., & Tulinius, M. (1990) · Pediatric Research

Mitochondrial Function and PathologyMetabolism and Genetic Disorders

Cited by 324

Increased mitochondrial mass in mitochondrial myopathy mice

Wredenberg, A., Wibom, R., Wilhelmsson, H., Graff, C., Wiener, H. H., Burden, S. J., Oldfors, A., Westerblad, H., & Larsson, N.-G. (2002) · Proceedings of the National Academy of Sciences

Mitochondrial Function and PathologyMuscle Physiology and Disorders

Cited by 302

Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial function

Fayet, G., Jansson, M., Sternberg, D., Moslemi, A.-R., Blondy, P., Lombès, A., Fardeau, M., & Oldfors, A. (2002) · Neuromuscular Disorders

Mitochondrial Function and PathologyMuscle Physiology and Disorders

Cited by 206

Mitochondrial myopathies

Larsson, N. ‐., & Oldfors, A. (2001) · Acta Physiologica Scandinavica

Mitochondrial Function and PathologyMetabolism and Genetic Disorders

Cited by 65

Autosomal dominant progressive external ophthalmoplegia: Distribution of multiple mitochondrial DNA deletions

Moslemi, A.-R., Melberg, A., Holme, E., & Oldfors, A. (1999) · Neurology

Mitochondrial Function and PathologyParkinson's Disease Mechanisms and Treatments

Cited by 61

The localization of amyloid precursor protein to ependymal cilia in vertebrates and its role in ciliogenesis and brain development in zebrafish

Chebli, J., Rahmati, M., Lashley, T., Edeman, B., Oldfors, A., Zetterberg, H., & Abramsson, A. (2021) · Scientific Reports

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 17