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Maria Elena Sana

Showing results (1-10 of 14) with videos related to

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Circulation. Cardiovascular Genetics|December 20, 2012
Letter by Iascone et al regarding article, "Population-based variation in cardiomyopathy genes"Maria Iascone, Maria Elena Sana, Paolo Ferrazzi
Genome Medicine|March 19, 2010
Non-coding RNAs: a key to future personalized molecular therapy?Marco Galasso, Maria Elena Sana, Stefano Volinia
Gene|July 24, 2012
A new mutational mechanism for hypertrophic cardiomyopathyLaura Pezzoli, Maria Elena Sana, Paolo Ferrazzi, et al.
Bioinformatics (Oxford, England)|October 26, 2010
GAMES identifies and annotates mutations in next-generation sequencing projectsMaria Elena Sana, Maria Iascone, Daniela Marchetti, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 9, 2012
Breast cancer signatures for invasiveness and prognosis defined by deep sequencing of microRNAStefano Volinia, Marco Galasso, Maria Elena Sana, et al.
American Journal of Medical Genetics. Part A|February 25, 2015
Microcephaly, ectodermal dysplasia, multiple skeletal anomalies and distinctive facial appearance: delineation of cerebro-dermato-osseous-dysplasiaMarco Castori, Giulia Pascolini, Valentina Parisi, et al.
American Journal of Medical Genetics. Part A|May 1, 2014
Identification of a novel de novo deletion in RAF1 associated with biventricular hypertrophy in Noonan syndromeMaria Elena Sana, Andrea Spitaleri, Dimitrios Spiliotopoulos, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 4, 2011
miR-34a induces the downregulation of both E2F1 and B-Myb oncogenes in leukemic cellsGiorgio Zauli, Rebecca Voltan, Maria Grazia di Iasio, et al.
Circulation|December 6, 2012
Extensive arterial tortuosity and severe aortic dilation in a newborn with an EFEMP2 mutationMaria Iascone, Maria Elena Sana, Laura Pezzoli, et al.
Plos One|December 22, 2016
A Novel HRAS Mutation Independently Contributes to Left Ventricular Hypertrophy in a Family with a Known MYH7 MutationMaria Elena Sana, Lawrence A Quilliam, Andrea Spitaleri, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Circulation. Cardiovascular Genetics|December 20, 2012
Letter by Iascone et al regarding article, "Population-based variation in cardiomyopathy genes"Maria Iascone, Maria Elena Sana, Paolo Ferrazzi
Genome Medicine|March 19, 2010
Non-coding RNAs: a key to future personalized molecular therapy?Marco Galasso, Maria Elena Sana, Stefano Volinia
Gene|July 24, 2012
A new mutational mechanism for hypertrophic cardiomyopathyLaura Pezzoli, Maria Elena Sana, Paolo Ferrazzi, et al.
Bioinformatics (Oxford, England)|October 26, 2010
GAMES identifies and annotates mutations in next-generation sequencing projectsMaria Elena Sana, Maria Iascone, Daniela Marchetti, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 9, 2012
Breast cancer signatures for invasiveness and prognosis defined by deep sequencing of microRNAStefano Volinia, Marco Galasso, Maria Elena Sana, et al.
American Journal of Medical Genetics. Part A|February 25, 2015
Microcephaly, ectodermal dysplasia, multiple skeletal anomalies and distinctive facial appearance: delineation of cerebro-dermato-osseous-dysplasiaMarco Castori, Giulia Pascolini, Valentina Parisi, et al.
American Journal of Medical Genetics. Part A|May 1, 2014
Identification of a novel de novo deletion in RAF1 associated with biventricular hypertrophy in Noonan syndromeMaria Elena Sana, Andrea Spitaleri, Dimitrios Spiliotopoulos, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 4, 2011
miR-34a induces the downregulation of both E2F1 and B-Myb oncogenes in leukemic cellsGiorgio Zauli, Rebecca Voltan, Maria Grazia di Iasio, et al.
Circulation|December 6, 2012
Extensive arterial tortuosity and severe aortic dilation in a newborn with an EFEMP2 mutationMaria Iascone, Maria Elena Sana, Laura Pezzoli, et al.
Plos One|December 22, 2016
A Novel HRAS Mutation Independently Contributes to Left Ventricular Hypertrophy in a Family with a Known MYH7 MutationMaria Elena Sana, Lawrence A Quilliam, Andrea Spitaleri, et al.
Pageof 2