Publications

Found 5 results
Filters: Keyword is Microscopy, Fluorescence  [Clear All Filters]
2009
Orthmann-Murphy JL, Salsano E, Abrams CK, Bizzi A, Uziel G, Freidin MM, Lamantea E, Zeviani M, Scherer SS & Pareyson D (2009) Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations. Brain 132, 426-38
Ricart KC, Bolisetty S, Johnson MS, Perez J, Agarwal A, Murphy MP & Landar A (2009) The permissive role of mitochondria in the induction of haem oxygenase-1 in endothelial cells. Biochem J 419, 427-36
2005
Vogel RO, Janssen RJRJ, Ugalde C, Grovenstein M, Huijbens RJ, Visch H-J, van den Heuvel LP, Willems PH, Zeviani M, Smeitink JAM & Nijtmans LGJ (2005) Human mitochondrial complex I assembly is mediated by NDUFAF1. FEBS J 272, 5317-26
2003
Piwowarski J, Grzechnik P, Dziembowski A, Dmochowska A, Minczuk M & Stepien PP (2003) Human polynucleotide phosphorylase, hPNPase, is localized in mitochondria. J Mol Biol 329, 853-7
1997
Noji H, Yasuda R, Yoshida M & Kinosita K (1997) Direct observation of the rotation of F1-ATPase. Nature 386, 299-302