Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sarah M. Halawani"'
Autor:
Hong Lin, Jordi Magrane, Elisia M. Clark, Sarah M. Halawani, Nathan Warren, Amy Rattelle, David R. Lynch
Publikováno v:
Disease Models & Mechanisms, Vol 10, Iss 12, Pp 1529-1538 (2017)
Friedreich ataxia (FRDA) is an autosomal recessive neurodegenerative disorder with progressive ataxia that affects both the peripheral and central nervous system (CNS). While later CNS neuropathology involves loss of large principal neurons and gluta
Externí odkaz:
https://doaj.org/article/940a8e6b41d947a5b3b112e72e8b3419
Autor:
Hong Lin, Jordi Magrane, Amy Rattelle, Anna Stepanova, Alexander Galkin, Elisia M. Clark, Yi Na Dong, Sarah M. Halawani, David R. Lynch
Publikováno v:
Disease Models & Mechanisms, Vol 10, Iss 11, Pp 1343-1352 (2017)
Friedreich ataxia (FRDA), the most common recessive inherited ataxia, results from deficiency of frataxin, a small mitochondrial protein crucial for iron-sulphur cluster formation and ATP production. Frataxin deficiency is associated with mitochondri
Externí odkaz:
https://doaj.org/article/d79fcb553b9b47c5bc781c43cb423749
Autor:
Hong Lin, Jordi Magrane, Amy Rattelle, Anna Stepanova, Alexander Galkin, Elisia M. Clark, Yi Na Dong, Sarah M. Halawani, David R. Lynch
Publikováno v:
Disease Models & Mechanisms, Vol 11, Iss 1 (2018)
Externí odkaz:
https://doaj.org/article/97cbd0599aa94169adb7d5b8df7ca5e5
Autor:
Anna Stepanova, David A. Lynch, Amy Rattelle, Yi Na Dong, Hong Lin, Jordi Magrané, Alexander Galkin, Elisia M. Clark, Sarah M. Halawani
Publikováno v:
Disease Models & Mechanisms, Vol 10, Iss 11, Pp 1343-1352 (2017)
Disease Models & Mechanisms
Disease Models & Mechanisms
Friedreich ataxia (FRDA), the most common recessive inherited ataxia, results from deficiency of frataxin, a small mitochondrial protein crucial for iron-sulphur cluster formation and ATP production. Frataxin deficiency is associated with mitochondri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e14bee8d18cea8ff68d90c194eab6c2
http://dmm.biologists.org/content/10/11/1343
http://dmm.biologists.org/content/10/11/1343
Autor:
Yesica Mercado-Ayon, Sarah M. Halawani, Elizabeth Mercado-Ayon, Lucie V. Ngaba, David A. Lynch, Yi Na Dong, Joseph Johnson
Publikováno v:
Archives of Biochemistry and Biophysics. 702:108698
In addition to ATP synthesis, mitochondria are highly dynamic organelles that modulate apoptosis, ferroptosis, and inflammasome activation. Through executing these varied functions, the mitochondria play critical roles in the development and progress
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d67dcc84f7c406ba72fd3cccabdeff1
https://doi.org/10.1016/j.abb.2020.108698
https://doi.org/10.1016/j.abb.2020.108698
Autor:
Alexander Galkin, David A. Lynch, Yi Na Dong, Anna Stepanova, Amy Rattelle, Hong Lin, Jordi Magrané, Elisia M. Clark, Sarah M. Halawani
Publikováno v:
Disease Models & Mechanisms
Disease Models & Mechanisms, Vol 11, Iss 1 (2018)
Disease Models & Mechanisms, Vol 11, Iss 1 (2018)
Friedreich ataxia (FRDA), the most common recessive inherited ataxia, results from deficiency of frataxin, a small mitochondrial protein crucial for iron-sulphur cluster formation and ATP production. Frataxin deficiency is associated with mitochondri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e6b28548637e99e5c6a41b18e0bb082
http://europepmc.org/articles/PMC5818085
http://europepmc.org/articles/PMC5818085