Search research articles
Contact Us
Filters
Showing results (1-10 of 14) with videos related to
Page
of 2
Sort By:
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 cardiomyopathy
Laura Pezzoli, Maria Elena Sana, Paolo Ferrazzi, et al.
Bioinformatics (Oxford, England)
|
October 26, 2010
GAMES identifies and annotates mutations in next-generation sequencing projects
Maria 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 microRNA
Stefano 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-dysplasia
Marco 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 syndrome
Maria 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 cells
Giorgio 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 mutation
Maria 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 Mutation
Maria Elena Sana, Lawrence A Quilliam, Andrea Spitaleri, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 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 cardiomyopathy
Laura Pezzoli, Maria Elena Sana, Paolo Ferrazzi, et al.
Bioinformatics (Oxford, England)
|
October 26, 2010
GAMES identifies and annotates mutations in next-generation sequencing projects
Maria 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 microRNA
Stefano 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-dysplasia
Marco 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 syndrome
Maria 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 cells
Giorgio 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 mutation
Maria 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 Mutation
Maria Elena Sana, Lawrence A Quilliam, Andrea Spitaleri, et al.
Page
of 2