Zobrazeno 1 - 6
of 6
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
Autor:
Sandra Harjuhaahto, Henna Tyynismaa, Jana Pennonen, Tomi Taira, Hazem Ibrahim, Markus T. Sainio, Svetlana M. Molchanova, Emil Ylikallio, Tiina S Rasila, Jouni Kvist, Timo Otonkoski, Svetlana Konovalova, Rosa Woldegebriel
Mitochondrial intermembrane space proteins CHCHD2 and CHCHD10 have roles in diseases affecting motor neurons such as amyotrophic lateral sclerosis, spinal muscular atrophy and axonal neuropathy and in Parkinson’s disease, and form a complex of unkn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb243d187a42916be1085a7bf5882bf1