Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jana, Pennonen"'
Autor:
Markus T. Sainio, Tiina Rasila, Svetlana M. Molchanova, Julius Järvilehto, Rubén Torregrosa-Muñumer, Sandra Harjuhaahto, Jana Pennonen, Nadine Huber, Sanna-Kaisa Herukka, Annakaisa Haapasalo, Henrik Zetterberg, Tomi Taira, Johanna Palmio, Emil Ylikallio, Henna Tyynismaa
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2022)
Neurofilament light (NFL) is one of the proteins forming multimeric neuron-specific intermediate filaments, neurofilaments, which fill the axonal cytoplasm, establish caliber growth, and provide structural support. Dominant missense mutations and rec
Externí odkaz:
https://doaj.org/article/f4541e595e534acebc0b20319f10d18f
Autor:
Sandra Harjuhaahto, Tiina S. Rasila, Svetlana M. Molchanova, Rosa Woldegebriel, Jouni Kvist, Svetlana Konovalova, Markus T. Sainio, Jana Pennonen, Rubén Torregrosa-Muñumer, Hazem Ibrahim, Timo Otonkoski, Tomi Taira, Emil Ylikallio, Henna Tyynismaa
Publikováno v:
Neurobiology of Disease, Vol 141, Iss , Pp 104940- (2020)
Mitochondrial intermembrane space proteins CHCHD2 and CHCHD10 have roles in motor neuron diseases such as amyotrophic lateral sclerosis, spinal muscular atrophy and axonal neuropathy and in Parkinson's disease. They form a complex of unknown function
Externí odkaz:
https://doaj.org/article/7dd3bc2f74c846f5b352a344121de51b
Autor:
Jeremi J Turkia, Jouni Kvist, Nadine Huber, Ras Trokovic, Vivek Sharma, Markus T. Sainio, Annakaisa Haapasalo, Jana Pennonen, Henna Tyynismaa, Emil Ylikallio, Sanna-Kaisa Herukka, Mari Auranen, Erika Rannila, Marco Reidelbach, Rubén Torregrosa-Muñumer, Sebastian Kenvin
Mutations in mitochondrial DNA encoded subunit of ATP synthase, MT-ATP6, are frequent causes of neurological mitochondrial diseases with a range of phenotypes from Leigh syndrome and NARP to ataxias and neuropathies. Here we investigated the function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2f50f541aa9661cc3bf7d89a952c14d
http://hdl.handle.net/10138/345126
http://hdl.handle.net/10138/345126
Autor:
Markus T, Sainio, Tiina, Rasila, Svetlana M, Molchanova, Julius, Järvilehto, Rubén, Torregrosa-Muñumer, Sandra, Harjuhaahto, Jana, Pennonen, Nadine, Huber, Sanna-Kaisa, Herukka, Annakaisa, Haapasalo, Henrik, Zetterberg, Tomi, Taira, Johanna, Palmio, Emil, Ylikallio, Henna, Tyynismaa
Publikováno v:
Frontiers in cell and developmental biology. 9
Neurofilament light (NFL) is one of the proteins forming multimeric neuron-specific intermediate filaments, neurofilaments, which fill the axonal cytoplasm, establish caliber growth, and provide structural support. Dominant missense mutations and rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4e467564e71bf755d01fe6739005a578
https://pubmed.ncbi.nlm.nih.gov/35237613
https://pubmed.ncbi.nlm.nih.gov/35237613
Autor:
Jana Pennonen, Markus T. Sainio, Svetlana M. Molchanova, Sandra Harjuhaahto, Jouni Kvist, Henna Tyynismaa, Tomi Taira, Emil Ylikallio, Hazem Ibrahim, Tiina S Rasila, Timo Otonkoski, Rubén Torregrosa-Muñumer, Svetlana Konovalova, Rosa Woldegebriel
Publikováno v:
Neurobiology of Disease, Vol 141, Iss, Pp 104940-(2020)
Mitochondrial intermembrane space proteins CHCHD2 and CHCHD10 have roles in motor neuron diseases such as amyotrophic lateral sclerosis, spinal muscular atrophy and axonal neuropathy and in Parkinson's disease. They form a complex of unknown function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::191057f2ef982386dd6e451124a5528c
http://hdl.handle.net/10138/317778
http://hdl.handle.net/10138/317778