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Oncogene
|
May 31, 2002
Activation of MyoD-dependent transcription by cdk9/cyclin T2
Cristiano Simone, Peter Stiegler, Luigi Bagella, et al.
Cell & Bioscience
|
December 2, 2023
Uncoupling p38α nuclear and cytoplasmic functions and identification of two p38α phosphorylation sites on β-catenin: implications for the Wnt signaling pathway in CRC models
Martina Lepore Signorile, Candida Fasano, Giovanna Forte, et al.
Computational and Structural Biotechnology Journal
|
November 13, 2023
The chromatin remodeling factors EP300 and TRRAP are novel SMYD3 interactors involved in the emerging 'nonmutational epigenetic reprogramming' cancer hallmark
Candida Fasano, Martina Lepore Signorile, Elisabetta Di Nicola, et al.
Cancers
|
January 11, 2024
Understanding the Genetic Landscape of Pancreatic Ductal Adenocarcinoma to Support Personalized Medicine: A Systematic Review
Antonino Pantaleo, Giovanna Forte, Candida Fasano, et al.
Journal of Medical Genetics
|
October 9, 2019
Gastric polyposis and desmoid tumours as a new familial adenomatous polyposis clinical variant associated with <i>APC</i> mutation at the extreme 3'-end
Vittoria Disciglio, Candida Fasano, Filomena Cariola, et al.
Developmental Cell
|
May 8, 2004
Deacetylase inhibitors increase muscle cell size by promoting myoblast recruitment and fusion through induction of follistatin
Simona Iezzi, Monica Di Padova, Carlo Serra, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
February 17, 2022
CD90 is regulated by notch1 and hallmarks a more aggressive intrahepatic cholangiocarcinoma phenotype
Serena Mancarella, Grazia Serino, Isabella Gigante, et al.
Cancers
|
November 9, 2024
Clinical Assessment and Genetic Testing for Hereditary Polyposis Syndromes in an Italian Cohort of Patients with Colorectal Polyps
Candida Fasano, Filomena Cariola, Giovanna Forte, et al.
Molecular Cell
|
October 30, 2007
Functional interdependence at the chromatin level between the MKK6/p38 and IGF1/PI3K/AKT pathways during muscle differentiation
Carlo Serra, Daniela Palacios, Chiara Mozzetta, et al.
Human Pathology
|
August 10, 2014
A rare MSH2 mutation causes defective binding to hMSH6, normal hMSH2 staining, and loss of hMSH6 at advanced cancer stage
Daria Carmela Loconte, Margherita Patruno, Patrizia Lastella, et al.
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of 9
Search research articles
Search
Showing results (41-50 of 87) with videos related to
Sort By:
Page
of 9
Oncogene
|
May 31, 2002
Activation of MyoD-dependent transcription by cdk9/cyclin T2
Cristiano Simone, Peter Stiegler, Luigi Bagella, et al.
Cell & Bioscience
|
December 2, 2023
Uncoupling p38α nuclear and cytoplasmic functions and identification of two p38α phosphorylation sites on β-catenin: implications for the Wnt signaling pathway in CRC models
Martina Lepore Signorile, Candida Fasano, Giovanna Forte, et al.
Computational and Structural Biotechnology Journal
|
November 13, 2023
The chromatin remodeling factors EP300 and TRRAP are novel SMYD3 interactors involved in the emerging 'nonmutational epigenetic reprogramming' cancer hallmark
Candida Fasano, Martina Lepore Signorile, Elisabetta Di Nicola, et al.
Cancers
|
January 11, 2024
Understanding the Genetic Landscape of Pancreatic Ductal Adenocarcinoma to Support Personalized Medicine: A Systematic Review
Antonino Pantaleo, Giovanna Forte, Candida Fasano, et al.
Journal of Medical Genetics
|
October 9, 2019
Gastric polyposis and desmoid tumours as a new familial adenomatous polyposis clinical variant associated with <i>APC</i> mutation at the extreme 3'-end
Vittoria Disciglio, Candida Fasano, Filomena Cariola, et al.
Developmental Cell
|
May 8, 2004
Deacetylase inhibitors increase muscle cell size by promoting myoblast recruitment and fusion through induction of follistatin
Simona Iezzi, Monica Di Padova, Carlo Serra, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
February 17, 2022
CD90 is regulated by notch1 and hallmarks a more aggressive intrahepatic cholangiocarcinoma phenotype
Serena Mancarella, Grazia Serino, Isabella Gigante, et al.
Cancers
|
November 9, 2024
Clinical Assessment and Genetic Testing for Hereditary Polyposis Syndromes in an Italian Cohort of Patients with Colorectal Polyps
Candida Fasano, Filomena Cariola, Giovanna Forte, et al.
Molecular Cell
|
October 30, 2007
Functional interdependence at the chromatin level between the MKK6/p38 and IGF1/PI3K/AKT pathways during muscle differentiation
Carlo Serra, Daniela Palacios, Chiara Mozzetta, et al.
Human Pathology
|
August 10, 2014
A rare MSH2 mutation causes defective binding to hMSH6, normal hMSH2 staining, and loss of hMSH6 at advanced cancer stage
Daria Carmela Loconte, Margherita Patruno, Patrizia Lastella, et al.
Page
of 9