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The American Journal of Pathology
|
February 11, 2012
The Gne M712T mouse as a model for human glomerulopathy
Sravan Kakani, Tal Yardeni, Justin Poling, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 2, 2022
Combination of common mtDNA variants results in mitochondrial dysfunction and a connective tissue dysregulation
Patrick M Schaefer, Leonardo Scherer Alves, Maria Lvova, et al.
Human Gene Therapy
|
April 27, 2011
Hereditary inclusion body myopathy: single patient response to intravenous dosing of GNE gene lipoplex
Gregory Nemunaitis, Chris M Jay, Phillip B Maples, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 3, 2025
Mitochondrial DNA lineages determine tumor progression through T cell reactive oxygen signaling
Tal Yardeni, Arnold Z Olali, Hsiao-Wen Chen, et al.
Human Mutation
|
October 19, 2017
A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C-methyltransferase deficiency
May Christine V Malicdan, Thierry Vilboux, Bruria Ben-Zeev, et al.
Brain : a Journal of Neurology
|
April 2, 2017
Deleterious variants in TRAK1 disrupt mitochondrial movement and cause fatal encephalopathy
Ortal Barel, May Christine V Malicdan, Bruria Ben-Zeev, et al.
Cell
|
December 16, 2025
HLA export by melanoma cells decoys cytotoxic T cells to promote immune evasion
Yoav Chemla, Orit Itzhaki, Stav Melamed, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 27) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 27 results.
The American Journal of Pathology
|
February 11, 2012
The Gne M712T mouse as a model for human glomerulopathy
Sravan Kakani, Tal Yardeni, Justin Poling, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 2, 2022
Combination of common mtDNA variants results in mitochondrial dysfunction and a connective tissue dysregulation
Patrick M Schaefer, Leonardo Scherer Alves, Maria Lvova, et al.
Human Gene Therapy
|
April 27, 2011
Hereditary inclusion body myopathy: single patient response to intravenous dosing of GNE gene lipoplex
Gregory Nemunaitis, Chris M Jay, Phillip B Maples, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 3, 2025
Mitochondrial DNA lineages determine tumor progression through T cell reactive oxygen signaling
Tal Yardeni, Arnold Z Olali, Hsiao-Wen Chen, et al.
Human Mutation
|
October 19, 2017
A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C-methyltransferase deficiency
May Christine V Malicdan, Thierry Vilboux, Bruria Ben-Zeev, et al.
Brain : a Journal of Neurology
|
April 2, 2017
Deleterious variants in TRAK1 disrupt mitochondrial movement and cause fatal encephalopathy
Ortal Barel, May Christine V Malicdan, Bruria Ben-Zeev, et al.
Cell
|
December 16, 2025
HLA export by melanoma cells decoys cytotoxic T cells to promote immune evasion
Yoav Chemla, Orit Itzhaki, Stav Melamed, et al.
Page
of 3