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International Journal of Molecular Sciences
|
August 4, 2018
STAT3 in Skeletal Muscle Function and Disorders
Eleonora Guadagnin, Davi Mázala, Yi-Wen Chen
Annals of Clinical and Translational Neurology
|
June 3, 2022
Attribution of original contribution in large datasets in the era of multi-omic studies
Payam Mohassel, Eleonora Guadagnin, Carsten G Bönnemann
Biochemical and Biophysical Research Communications
|
December 12, 2018
Nuclear localized Akt limits skeletal muscle derived fibrotic signaling
Eleonora Guadagnin, Debalina Bagchi, Indranil Sinha, et al.
Biomed Research International
|
September 18, 2015
Tyrosine 705 Phosphorylation of STAT3 Is Associated with Phenotype Severity in TGFβ1 Transgenic Mice
Eleonora Guadagnin, Jigna Narola, Carsten G Bönnemann, et al.
Veterinary Journal (London, England : 1997)
|
April 5, 2014
Minimal residual disease detection by flow cytometry and PARR in lymph node, peripheral blood and bone marrow, following treatment of dogs with diffuse large B-cell lymphoma
Luca Aresu, Arianna Aricò, Serena Ferraresso, et al.
The EMBO Journal
|
April 20, 2010
Mitochondrial fission and remodelling contributes to muscle atrophy
Vanina Romanello, Eleonora Guadagnin, Ligia Gomes, et al.
Annals of Clinical and Translational Neurology
|
November 3, 2021
Transcriptome analysis of collagen VI-related muscular dystrophy muscle biopsies
Eleonora Guadagnin, Payam Mohassel, Kory R Johnson, et al.
Journal of Proteomics
|
April 29, 2014
Conditional independence mapping of DIGE data reveals PDIA3 protein species as key nodes associated with muscle aerobic capacity
Jatin G Burniston, Jenna Kenyani, Donna Gray, et al.
Scientific Reports
|
April 29, 2020
Systemic modified messenger RNA for replacement therapy in alpha 1-antitrypsin deficiency
Ahmad Karadagi, Alex G Cavedon, Helen Zemack, et al.
Molecular Genetics and Metabolism
|
December 29, 2022
Synthetic mRNA rescues very long-chain acyl-CoA dehydrogenase deficiency in patient fibroblasts and a murine model
Xue-Jun Zhao, Ai-Walid Mohsen, Stephanie Mihalik, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 2
International Journal of Molecular Sciences
|
August 4, 2018
STAT3 in Skeletal Muscle Function and Disorders
Eleonora Guadagnin, Davi Mázala, Yi-Wen Chen
Annals of Clinical and Translational Neurology
|
June 3, 2022
Attribution of original contribution in large datasets in the era of multi-omic studies
Payam Mohassel, Eleonora Guadagnin, Carsten G Bönnemann
Biochemical and Biophysical Research Communications
|
December 12, 2018
Nuclear localized Akt limits skeletal muscle derived fibrotic signaling
Eleonora Guadagnin, Debalina Bagchi, Indranil Sinha, et al.
Biomed Research International
|
September 18, 2015
Tyrosine 705 Phosphorylation of STAT3 Is Associated with Phenotype Severity in TGFβ1 Transgenic Mice
Eleonora Guadagnin, Jigna Narola, Carsten G Bönnemann, et al.
Veterinary Journal (London, England : 1997)
|
April 5, 2014
Minimal residual disease detection by flow cytometry and PARR in lymph node, peripheral blood and bone marrow, following treatment of dogs with diffuse large B-cell lymphoma
Luca Aresu, Arianna Aricò, Serena Ferraresso, et al.
The EMBO Journal
|
April 20, 2010
Mitochondrial fission and remodelling contributes to muscle atrophy
Vanina Romanello, Eleonora Guadagnin, Ligia Gomes, et al.
Annals of Clinical and Translational Neurology
|
November 3, 2021
Transcriptome analysis of collagen VI-related muscular dystrophy muscle biopsies
Eleonora Guadagnin, Payam Mohassel, Kory R Johnson, et al.
Journal of Proteomics
|
April 29, 2014
Conditional independence mapping of DIGE data reveals PDIA3 protein species as key nodes associated with muscle aerobic capacity
Jatin G Burniston, Jenna Kenyani, Donna Gray, et al.
Scientific Reports
|
April 29, 2020
Systemic modified messenger RNA for replacement therapy in alpha 1-antitrypsin deficiency
Ahmad Karadagi, Alex G Cavedon, Helen Zemack, et al.
Molecular Genetics and Metabolism
|
December 29, 2022
Synthetic mRNA rescues very long-chain acyl-CoA dehydrogenase deficiency in patient fibroblasts and a murine model
Xue-Jun Zhao, Ai-Walid Mohsen, Stephanie Mihalik, et al.
Page
of 2