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The Journal of Cell Biology
|
January 11, 2007
The AAA+ protein ATAD3 has displacement loop binding properties and is involved in mitochondrial nucleoid organization
Jiuya He, Chih-Chieh Mao, Aurelio Reyes, et al.
EMBO Molecular Medicine
|
February 29, 2020
Metabolic effects of bezafibrate in mitochondrial disease
Hannah Steele, Aurora Gomez-Duran, Angela Pyle, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 9, 2018
Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease
Veronika Boczonadi, Martin S King, Anthony C Smith, et al.
Journal of Medical Genetics
|
May 23, 2020
Mutation in the MICOS subunit gene <i>APOO</i> (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features
Cristiane Benincá, Vanessa Zanette, Michele Brischigliaro, et al.
Nature Medicine
|
May 28, 2013
Cardioprotection by S-nitrosation of a cysteine switch on mitochondrial complex I
Edward T Chouchani, Carmen Methner, Sergiy M Nadtochiy, et al.
Nature Metabolism
|
May 13, 2020
Succinate accumulation drives ischaemia-reperfusion injury during organ transplantation
Jack L Martin, Ana S H Costa, Anja V Gruszczyk, et al.
Nature
|
November 11, 2014
Ischaemic accumulation of succinate controls reperfusion injury through mitochondrial ROS
Edward T Chouchani, Victoria R Pell, Edoardo Gaude, et al.
Cell Metabolism
|
March 13, 2012
Fumarate is cardioprotective via activation of the Nrf2 antioxidant pathway
Houman Ashrafian, Gabor Czibik, Mohamed Bellahcene, et al.
American Journal of Human Genetics
|
September 3, 2013
Mutations in FBXL4, encoding a mitochondrial protein, cause early-onset mitochondrial encephalomyopathy
Xiaowu Gai, Daniele Ghezzi, Mark A Johnson, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 49 results.
The Journal of Cell Biology
|
January 11, 2007
The AAA+ protein ATAD3 has displacement loop binding properties and is involved in mitochondrial nucleoid organization
Jiuya He, Chih-Chieh Mao, Aurelio Reyes, et al.
EMBO Molecular Medicine
|
February 29, 2020
Metabolic effects of bezafibrate in mitochondrial disease
Hannah Steele, Aurora Gomez-Duran, Angela Pyle, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 9, 2018
Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease
Veronika Boczonadi, Martin S King, Anthony C Smith, et al.
Journal of Medical Genetics
|
May 23, 2020
Mutation in the MICOS subunit gene <i>APOO</i> (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features
Cristiane Benincá, Vanessa Zanette, Michele Brischigliaro, et al.
Nature Medicine
|
May 28, 2013
Cardioprotection by S-nitrosation of a cysteine switch on mitochondrial complex I
Edward T Chouchani, Carmen Methner, Sergiy M Nadtochiy, et al.
Nature Metabolism
|
May 13, 2020
Succinate accumulation drives ischaemia-reperfusion injury during organ transplantation
Jack L Martin, Ana S H Costa, Anja V Gruszczyk, et al.
Nature
|
November 11, 2014
Ischaemic accumulation of succinate controls reperfusion injury through mitochondrial ROS
Edward T Chouchani, Victoria R Pell, Edoardo Gaude, et al.
Cell Metabolism
|
March 13, 2012
Fumarate is cardioprotective via activation of the Nrf2 antioxidant pathway
Houman Ashrafian, Gabor Czibik, Mohamed Bellahcene, et al.
American Journal of Human Genetics
|
September 3, 2013
Mutations in FBXL4, encoding a mitochondrial protein, cause early-onset mitochondrial encephalomyopathy
Xiaowu Gai, Daniele Ghezzi, Mark A Johnson, et al.
Page
of 5