Paola Riva - Dissemin

Papers authored by Paola Riva

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2009 Lidia Larizza, Cristina Gervasini, Federica Natacci, Paola Riva

Developmental Abnormalities and Cancer Predisposition in Neurofibromatosis Type 1

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Alessandro Salvi, Cristiano Sabelli, Silvia Moncini, Marco Venturin

, Bruna Arici, Paola Riva

, Nazario Portolani, Stefano M. Giulini, Giuseppina De Petro, Sergio Barlati

MicroRNA-23b mediates urokinase and c-met downmodulation and a decreased migration of human hepatocellular carcinoma cells

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2008 P. Riva

, I. Magnani, A. M. Fuhrmann Conti, D. Gelli, C. Sala, D. Toniolo, L. Larizza

FISH characterization of the Xq21 breakpoint in a translocation carrier with premature ovarian failure

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Francesca Orzan, Michela Stroppi, Marco Venturin

, M. Carmen Valero, Concepcion Hernández, Paola Riva

Breakpoint characterization of a novel NF1 multiexonic deletion: a case showing expression of the mutated allele

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Mauro Longoni, Francesca Orzan, Michela Stroppi, Nicola Boari, Pietro Mortini, Paola Riva

Evaluation of 1p36 markers and clinical outcome in a skull base chordoma study

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2007 E. Rossi, J. Messa, M. Riegel, S. Gimelli, R. Ciccone, P. Maraschio, P. Riva

, M. Stroppi, T. Mattina

, C. S. Perrotta, L. Memo, A. Baumer, V. Kucinskas, C. Castellan, A. Schinzel and 1 other authors

Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation

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Francesca Orzan, Maria R. Terreni, Mauro Longoni, Nicola Boari, Pietro Mortini, Claudio Doglioni, Paola Riva

Expression study of the target receptor tyrosine kinase of Imatinib mesylate in skull base chordomas

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Silvia Moncini, Annamaria Bevilacqua, Marco Venturin

, Claudia Fallini

, Antonia Ratti, Angelo Nicolin, Paola Riva

The 3' untranslated region of human Cyclin-Dependent Kinase 5 Regulatory subunit 1 contains regulatory elements affecting transcript stability

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Beatrice Bodega

, Maria Francesca Cardone, Cardone Mf, Stefan Müller, Michaela Neusser, Francesca Orzan, Elena Rossi, Elena Battaglioli, Anna Marozzi, Paola Riva

, Mariano Rocchi, Raffaella Meneveri, Enrico Ginelli

Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2)

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2006 Marco Venturin

, Silvia Moncini, Valentina Villa, Silvia Russo

, Maria Teresa Bonati, Lidia Larizza, Paola Riva

Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation

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2005 Giorgio Portera, Marco Venturin

, Antonella Patrizi, Emanuela Martinoli, Paola Riva

, Leda Dalprà

Characterisation of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams–Beuren syndrome region in chromosomal rearrangements

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M. Venturin

, A. Bentivegna, R. Moroni, L. Larizza, P. Riva

Evidence by Expression Analysis of Candidate Genes for Congenital Heart Defects in the NF1 Microdeletion Interval

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Lidia Larizza, Pietro Mortini, Paola Riva

Update on the Cytogenetics and Molecular Genetics of Chordoma

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Cristina Gervasini, Marco Venturin

, Francesca Orzan, Alessandra Friso, Maurizio Clementi, Romano Tenconi, Lidia Larizza, Paola Riva

Uncommon Alu-mediated NF1 microdeletion with a breakpoint inside the NF1 gene

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2004 Cristina Gervasini, Francesca Orzan, Angela Bentivegna, Patrizia Colapietro, Alessandra Friso, Romano Tenconi, Meena Upadhyaya, Lucia Corrado, Lidia Larizza, Marco Venturin

, Paola Riva

Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions

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P. Guarnieri, F. Natacci, M. Stabile, R. Tenconi, M. Clementi, C. Hernandez, P. Thompson, M. Upadhyaya, M. Venturin

, L. Larizza, P. Riva

Mental retardation and cardiovascular malformations in NF1 microdeleted patients point to candidate genes in 17q11.2

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2003 Patrizia Colapietro, Cristina Gervasini, Federica Natacci, Livia Rossi, Paola Riva

, Lidia Larizza

NF1 exon�7 skipping and sequence alterations in exonic splice enhancers (ESEs) in a neurofibromatosis�1 patient

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Paola Riva

, Francesca Crosti, Francesca Orzan, Leda Dalprà, Pietro Mortini, Antonina Parafioriti, Bianca Pollo, Anna Maria Fuhrman Conti, Monica Miozzo, Lidia Larizza

Mapping of candidate region for chordoma development to 1p36.13 by LOH analysis: Mapping of Chordoma Region to 1p36.13

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2002 Paola Riva

, Cristina Gervasini, Lidia Larizza

Genomic evidence versus characterisation of a single (17;22) translocation on NF1 gene duplication: lessons from deletions in "balanced" chromosomal rearrangements. Reply

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N. Villa, T. Varisco, P. Riva

, E. Sala, L. Larizza, L. Dalpra

Interstitial telomeres of an inv(9)(p11.2;q34) involved in a jumping translocation found in a woman through a stable unbalanced translocation in her malformed child

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Papers authored by Paola Riva