Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Atefeh Kianian"'
Autor:
Anbin Chen, Cecilie Katrin Kristiansen, Yu Hong, Atefeh Kianian, Evandro Fei Fang, Gareth John Sullivan, Jian Wang, Xingang Li, Laurence A. Bindoff, Kristina Xiao Liang
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Mitophagy specifically recognizes and removes damaged or superfluous mitochondria to maintain mitochondrial homeostasis and proper neuronal function. Defective mitophagy and the resulting accumulation of damaged mitochondria occur in several neurodeg
Externí odkaz:
https://doaj.org/article/2a4dff71cdaf47aab7ed7d5d5242e062
Autor:
Kristina Xiao Liang, Cecilie Katrin Kristiansen, Sepideh Mostafavi, Guro Helén Vatne, Gina Alien Zantingh, Atefeh Kianian, Charalampos Tzoulis, Lena Elise Høyland, Mathias Ziegler, Roberto Megias Perez, Jessica Furriol, Zhuoyuan Zhang, Novin Balafkan, Yu Hong, Richard Siller, Gareth John Sullivan, Laurence A Bindoff
Publikováno v:
EMBO Molecular Medicine, Vol 12, Iss 10, Pp n/a-n/a (2020)
Abstract Mutations in POLG disrupt mtDNA replication and cause devastating diseases often with neurological phenotypes. Defining disease mechanisms has been hampered by limited access to human tissues, particularly neurons. Using patient cells carryi
Externí odkaz:
https://doaj.org/article/dfb26524884144999cd67cac00ad6106
Autor:
Xiao Liang, Atefeh Kianian, Anbin Chen, Cecilie Katrin Kristiansen, Yu Hong, Jessica Furriol, Lena Elise Høyland, Mathias Ziegler, Torbjørn Kråkenes, Charalampos Tzoulis, Gareth John Sullivan, Laurence Albert Bindoff
Publikováno v:
SSRN Electronic Journal.
Autor:
Cecilie Katrin Kristiansen, Kristina Xiao Liang, Jessica Furriol, Anbin Chen, Mathias Ziegler, Atefeh Kianian, Laurence A. Bindoff, Gareth J. Sullivan, Yu Hong, Charalampos Tzoulis, Lena Elise Høyland, Torbjørn Kråkenes
The inability to reliably replicate mitochondrial DNA (mtDNA) by mitochondrial DNA polymerase gamma (POLG) leads to a subset of common mitochondrial diseases associated with neuronal death and depletion of neuronal mtDNA. Defining disease mechanisms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f8b26c2ad8474fc2a729caf204131e0
https://doi.org/10.1101/2020.12.20.423652
https://doi.org/10.1101/2020.12.20.423652
Autor:
Lena Elise Høyland, Gareth J. Sullivan, Roberto Megias Perez, Gina Alien Zantingh, Kristina Xiao Liang, Guro Helén Vatne, Mathias Ziegler, Sepideh Mostafavi, Richard Siller, Laurence A. Bindoff, Novin Balafkan, Atefeh Kianian, Cecilie Katrin Kristiansen, Zhuoyuan Zhang, Jessica Furriol, Yu Hong, Charalampos Tzoulis
Publikováno v:
EMBO Molecular Medicine, Vol 12, Iss 10, Pp n/a-n/a (2020)
e12146
EMBO Molecular Medicine
e12146
EMBO Molecular Medicine
Mutations in POLG disrupt mtDNA replication and cause devastating diseases often with neurological phenotypes. Defining disease mechanisms has been hampered by limited access to human tissues, particularly neurons. Using patient cells carrying POLG m