Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ilse Lappalainen"'
Autor:
Anu Jalanko, Emil Ylikallio, Anu Suomalainen, Ilse Lappalainen, Katja Peltola Mjosund, Anders Paetau, Johannes N. Spelbrink, Henna Tyynismaa, Sjoerd Wanrooij
Publikováno v:
Proceedings of the National Academy of Sciences. 102:17687-17692
Defects of mitochondrial DNA (mtDNA) maintenance have recently been associated with inherited neurodegenerative and muscle diseases and the aging process. Twinkle is a nuclear-encoded mtDNA helicase, dominant mutations of which cause adult-onset prog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::357cb8314436b47f8c2f3830aa9433b9
https://doi.org/10.1073/pnas.0505551102
https://doi.org/10.1073/pnas.0505551102
Autor:
Peter Hackman, Helena Kääriäinen, Teppo Varilo, Laurence A. Bindoff, Ann Löfgren, Petri Luoma, Anu Suomalainen, Seppo Kaakkola, Gert Van Goethem, Kari Majamaa, Silja Heiskanen, Bjarne Udd, Anders Paetau, Ilse Lappalainen, Maria Rantamäki, Vesa Juvonen, Anna H. Hakonen
Publikováno v:
The American journal of human genetics
Mutations in the catalytic subunit of the mitochondrial DNA polymerase g ( POLG) have been found to be an important cause of neurological disease. Recently, we and collaborators reported a new neurodegenerative disorder with autosomal recessive ataxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec5f93a21f1f8f10bdd02f1cf23176f1
https://doi.org/10.1086/444548
https://doi.org/10.1086/444548
Publikováno v:
Mitochondrion. 7:419
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::060b564afc05c50d0c9a17ec35514d07
https://doi.org/10.1016/j.mito.2007.08.056
https://doi.org/10.1016/j.mito.2007.08.056
Publikováno v:
Medicine & Science in Sports & Exercise. 39:S292
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3084dfd081c08a3e0bdfea4804dd1a94
https://doi.org/10.1249/01.mss.0000274128.23981.55
https://doi.org/10.1249/01.mss.0000274128.23981.55