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Methods in Molecular Biology (Clifton, N.J.)|March 29, 2012
Exon skipping quantification by real-time PCRAlessandra Ferlini, Paola RimessiBiochemical and Biophysical Research Communications|April 20, 2004
In vivo study of an aberrant dystrophin exon inclusion in X-linked dilated cardiomyopathyNiaz Cohen, Paola Rimessi, Francesca Gualandi, et al.Journal of Molecular Evolution|March 11, 2004
Tempo and mode of evolution of a primate-specific retrotransposon belonging to the LINE 1 familyBarbara Cardazzo, Luca Bargelloni, Luisa Toffolatti, et al.Breast Cancer Research and Treatment|July 16, 2010
Association of CYP1B1 with hypersensitivity induced by taxane therapy in breast cancer patientsRoberta Rizzo, Federica Spaggiari, Monica Indelli, et al.American Journal of Medical Genetics. Part A|January 11, 2005
Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutationPaola Rimessi, Francesca Gualandi, Laurence Duprez, et al.Gene|July 11, 2003
Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: in vitro mimicking and antisense modulation of the splicing abnormalityFrancesca Gualandi, Paola Rimessi, Barbara Cardazzo, et al.Liver International : Official Journal of the International Association for the Study of the Liver|February 2, 2006
Transthyretin RNA profiling in livers from transplanted patients affected by familial amyloidotic polyneuropathy, and identification of a dual transcription start pointPaola Rimessi, Pietro Spitali, Yukio Ando, et al.Human Gene Therapy|May 22, 2010
Antisense modulation of both exonic and intronic splicing motifs induces skipping of a DMD pseudo-exon responsible for x-linked dilated cardiomyopathyPaola Rimessi, Marina Fabris, Matteo Bovolenta, et al.Neuromuscular Disorders : NMD|September 11, 2007
Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the humanMarcella Neri, Silvia Torelli, Sue Brown, et al.Hemoglobin|April 28, 2016
A Family with γ-Thalassemia and High Hb A2 LevelsGiulia Parmeggiani, Francesca Gualandi, Rita Selvatici, et al.Pageof 20