Ylikallio, Emil

Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice

Tyynismaa, H., Mjosund, K. P., Wanrooij, S., Lappalainen, I., Ylikallio, E., Jalanko, A., Spelbrink, J. N., Paetau, A., & Suomalainen, A. (2005) · Proceedings of the National Academy of Sciences

Mitochondrial Function and PathologyMetabolism and Genetic Disorders

Cited by 342

The overexpression of twinkle helicase ameliorates the progression of cardiac fibrosis and heart failure in pressure overload model in mice

Tanaka, A., Ide, T., Fujino, T., Onitsuka, K., Ikeda, M., Takehara, T., Hata, Y., Ylikallio, E., Tyynismaa, H., Suomalainen, A., et al. (2013) · PLoS ONE

Cardiac Fibrosis and RemodelingMitochondrial Function and Pathology

Cited by 23

Structural insights into Charcot-Marie-Tooth disease-linked mutations in human GDAP1

Sutinen, A., Nguyen, G. T. T., Raasakka, A., Muruganandam, G., Loris, R., Ylikallio, E., Tyynismaa, H., Bartesaghi, L., Ruskamo, S., & Kursula, P. (2022) · FEBS Open Bio

Hereditary Neurological DisordersPeripheral Neuropathies and Disorders

Cited by 13

Structural insights into Charcot–Marie–Tooth disease‐linked mutations in human GDAP1

Sutinen, A., Nguyen, G. T. T., Raasakka, A., Muruganandam, G., Loris, R., Ylikallio, E., Tyynismaa, H., Bartesaghi, L., Ruskamo, S., & Kursula, P. (2022) · FEBS Open Bio

Hereditary Neurological DisordersPeripheral Neuropathies and Disorders

Cited by 13