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Frontiers in Cardiovascular Medicine
|
December 6, 2019
SS-31 Peptide Reverses the Mitochondrial Fragmentation Present in Fibroblasts From Patients With DCMA, a Mitochondrial Cardiomyopathy
Pranav Machiraju, Xuemei Wang, Rasha Sabouny, et al.
Antioxidants & Redox Signaling
|
May 8, 2023
Potentiation of Adipogenesis by Reactive Oxygen Species Is a Unifying Mechanism in the Proadipogenic Properties of Bisphenol A and Its New Structural Analogues
Radha D Singh, Jessica L Wager, Taylor B Scheidl, et al.
Life Science Alliance
|
March 13, 2019
<i>PISD</i> is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes
Tian Zhao, Caitlin M Goedhart, Pingdewinde N Sam, et al.
Ebiomedicine
|
June 25, 2019
The R941L mutation in MYH14 disrupts mitochondrial fission and associates with peripheral neuropathy
Walaa Almutawa, Christopher Smith, Rasha Sabouny, et al.
Human Molecular Genetics
|
May 2, 2023
Activation of the cGAS-STING innate immune response in cells with deficient mitochondrial topoisomerase TOP1MT
Iman Al Khatib, Jingti Deng, Yuanjiu Lei, et al.
Cell
|
June 23, 2023
Cooperative sensing of mitochondrial DNA by ZBP1 and cGAS promotes cardiotoxicity
Yuanjiu Lei, Jordyn J VanPortfliet, Yi-Fan Chen, et al.
Autophagy
|
February 26, 2021
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)<sup>1</sup>
Daniel J Klionsky, Amal Kamal Abdel-Aziz, Sara Abdelfatah, et al.
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Search research articles
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Showing results (51-60 of 57) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 57 results.
Frontiers in Cardiovascular Medicine
|
December 6, 2019
SS-31 Peptide Reverses the Mitochondrial Fragmentation Present in Fibroblasts From Patients With DCMA, a Mitochondrial Cardiomyopathy
Pranav Machiraju, Xuemei Wang, Rasha Sabouny, et al.
Antioxidants & Redox Signaling
|
May 8, 2023
Potentiation of Adipogenesis by Reactive Oxygen Species Is a Unifying Mechanism in the Proadipogenic Properties of Bisphenol A and Its New Structural Analogues
Radha D Singh, Jessica L Wager, Taylor B Scheidl, et al.
Life Science Alliance
|
March 13, 2019
<i>PISD</i> is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes
Tian Zhao, Caitlin M Goedhart, Pingdewinde N Sam, et al.
Ebiomedicine
|
June 25, 2019
The R941L mutation in MYH14 disrupts mitochondrial fission and associates with peripheral neuropathy
Walaa Almutawa, Christopher Smith, Rasha Sabouny, et al.
Human Molecular Genetics
|
May 2, 2023
Activation of the cGAS-STING innate immune response in cells with deficient mitochondrial topoisomerase TOP1MT
Iman Al Khatib, Jingti Deng, Yuanjiu Lei, et al.
Cell
|
June 23, 2023
Cooperative sensing of mitochondrial DNA by ZBP1 and cGAS promotes cardiotoxicity
Yuanjiu Lei, Jordyn J VanPortfliet, Yi-Fan Chen, et al.
Autophagy
|
February 26, 2021
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)<sup>1</sup>
Daniel J Klionsky, Amal Kamal Abdel-Aziz, Sara Abdelfatah, et al.
Page
of 6