Torthaí cuardaigh - Francesca Torricelli
- 1 - 13 toradh as 13 á dtaispeáint
-
1
Read count approach for DNA copy number variants detection de réir Alberto Magi, Lorenzo Tattini, Tommaso Pippucci, Francesca Torricelli, Matteo Benelli
Foilsithe / Cruthaithe 2011Artigo -
2
Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm de réir Alberto Magi, Matteo Benelli, Seungtai Yoon, Franco Roviello, Francesca Torricelli
Foilsithe / Cruthaithe 2011Artigo -
3
Discovering chimeric transcripts in paired-end RNA-seq data by using EricScript de réir Matteo Benelli, Chiara Pescucci, Giuseppina Marseglia, Marco Severgnini, Francesca Torricelli, Alberto Magi
Foilsithe / Cruthaithe 2012Artigo -
4
Bioinformatics for Next Generation Sequencing Data de réir Alberto Magi, Matteo Benelli, Alessia Gozzini, Francesca Girolami, Francesca Torricelli, Maria Luisa Brandi
Foilsithe / Cruthaithe 2010Artigo -
5
Coronary microvascular dysfunction is an early feature of cardiac involvement in patients with Anderson–Fabry disease de réir Benedetta Tomberli, Franco Cecchi, Roberto Sciagrà, Valentina Berti, Francesca Lisi, Francesca Torricelli, Amelia Morrone, Gabriele Castelli, Magdi H. Yacoub, Iacopo Olivotto
Foilsithe / Cruthaithe 2013Artigo -
6
Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations de réir Francesca Girolami, Carolyn Y. Ho, Christopher Semsarian, Massimo Baldi, Melissa L. Will, Katia Baldini, Francesca Torricelli, Laura Yeates, Franco Cecchi, Michael J. Ackerman, Iacopo Olivotto
Foilsithe / Cruthaithe 2010Artigo -
7
Microvascular Function Is Selectively Impaired in Patients With Hypertrophic Cardiomyopathy and Sarcomere Myofilament Gene Mutations de réir Iacopo Olivotto, Francesca Girolami, Roberto Sciagrà, Michael J. Ackerman, Barbara Sotgia, J. Martijn Bos, Stefano Nistri, A Sgalambro, Camilla Grifoni, Francesca Torricelli, Paolo G. Camici, Franco Cecchi
Foilsithe / Cruthaithe 2011Artigo -
8
Use of donor bone marrow mesenchymal stem cells for treatment of skin allograft rejection in a preclinical rat model de réir Paolo Sbano, Aldo Cuccia, Benedetta Mazzanti, Serena Urbani, Betti Giusti, Ilaria Lapini, Luciana Rossi, Rosanna Abbate, Giuseppina Marseglia, Genni Nannetti, Francesca Torricelli, Clelia Miracco, Alberto Bosi, Michele Fimiani, Riccardo Saccardi
Foilsithe / Cruthaithe 2008Artigo -
9
Clinical Phenotype and Outcome of Hypertrophic Cardiomyopathy Associated With Thin-Filament Gene Mutations de réir Raffaele Coppini, Carolyn Y. Ho, Euan A. Ashley, Sharlene M. Day, Cecilia Ferrantini, Francesca Girolami, Benedetta Tomberli, Sara Bardi, Francesca Torricelli, Franco Cecchi, Alessandro Mugelli, Corrado Poggesi, Jil C. Tardiff, Iacopo Olivotto
Foilsithe / Cruthaithe 2014Artigo -
10
Novel α-Actinin 2 Variant Associated With Familial Hypertrophic Cardiomyopathy and Juvenile Atrial Arrhythmias de réir Francesca Girolami, Maria Iascone, Benedetta Tomberli, Sara Bardi, Matteo Benelli, Giuseppina Marseglia, Chiara Pescucci, Laura Pezzoli, Maria Elena Sana, Cristina Basso, Nicola Marziliano, Piera Angelica Merlini, Alessandra Fornaro, Franco Cecchi, Francesca Torricelli, Iacopo Olivotto
Foilsithe / Cruthaithe 2014Artigo -
11
Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center de réir Francesco Mazzarotto, Francesca Girolami, Beatrice Boschi, Fausto Barlocco, Alessia Tomberli, Katia Baldini, Raffaele Coppini, Ilaria Tanini, Sara Bardi, Elisa Contini, Franco Cecchi, Elisabetta Pelo, Stuart A. Cook, Elisabetta Cerbai, Corrado Poggesi, Francesca Torricelli, Roddy Walsh, Iacopo Olivotto
Foilsithe / Cruthaithe 2018Artigo -
12
Gross genomic rearrangements involving deletions in the CFTR gene: characterization of six new events from a large cohort of hitherto unidentified cystic fibrosis chromosomes and m... de réir Claude Férec, Teresa Casals, Nadia Chuzhanova, Milan Maçek, Thierry Bienvenu, A. Holubová, Caitriona King, Trudi McDevitt, Carlo Castellani, Philip M. Farrell, Molly B. Sheridan, Sarah‐Jane Pantaleo, Ourida Loumi, Taïeb Messaoud, Harry Cuppens, Francesca Torricelli, Garry R. Cutting, Robert Williamson, Maria Jesus Alonso Ramos, Pier Franco Pignatti, Odile Raguénès, D.N. Cooper, Marie‐Pierre Audrézet, Jian‐Min Chen
Foilsithe / Cruthaithe 2006Artigo -
13
<i>De novo</i> balanced chromosome rearrangements in prenatal diagnosis de réir Daniela Giardino, Cecilia Corti, Lucia Ballarati, Daniela Colombo, Elena Sala, Nicoletta Villa, Giuseppe Piombo, Mauro Pierluigi, Francesca Faravelli, Silvana Guerneri, Domenico Coviello, Faustina Lalatta, Ugo Cavallari, Daniela Bellotti, Sergio Barlati, Gianfranco Croci, Fabrizia Franchi, Elisa Savin, G. Nocera, Francesco Amico, Paola Granata, Rosario Casalone, Lucia Nutini, Ermanna Lisi, Francesca Torricelli, Ursula Giussani, Barbara Facchinetti, Ginevra Guanti, Marilena Di Giacomo, Francesco Paolo Susca, Vanna Pecile, Lorenza Romitti, Laura Cardarelli, Erika Racalbuto, Maria Adalgisa Police, Francamaria Chiodo, Ornella Rodeschini, Patrizia Falcone, Emilio Donti, Maria Grazia Grimoldi, Emanuela Martinoli, Sabine Stioui, Daniele Caufin, S. Lauricella, Salvatrice Antonella Tanzariello, Gianfranco Voglino, Elisabetta Lenzini, M Besozzi, Lidia Larizza, Leda Dalprà
Foilsithe / Cruthaithe 2009Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Genetics
Gene
Medicine
Internal medicine
Cardiology
Computational biology
Hypertrophic cardiomyopathy
Computer science
Mutation
Cardiomyopathy
DNA sequencing
Heart failure
Blood pressure
Chromosome
Copy-number variation
Gene expression
Gene mutation
Genome
Left ventricular hypertrophy
Myocardial infarction
Myocyte
Pathology
Proband
Sanger sequencing
Sarcomere
Transcriptome
Troponin
Actin
Amniotic fluid