RIVA, PAOLA VANDA

RIVA, PAOLA VANDA  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

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Titolo Data di pubblicazione Autore(i) Tipo File Abstract
19p deletion in recurring leiomyosarcoma lesions from the same patient 1-giu-2000 P. RivaV. GualandriM. VolontèM. MiozzoA. F. ContiL. Larizza + Article (author) -
1p36 LOH and expression study of apoptotic genes in a selected group of chordomas 1-gen-2006 M. StroppiP. Riva + Article (author) -
The 3' untranslated region of human cyclin-dependent kinase 5 regulatory subunit 1 contains regulatory elements affecting transcript stability 3-dic-2007 S. MonciniA. BevilacquaM. VenturinA. RattiA. NicolinP. Riva + Article (author) -
A 12-bp deletion (7818del12) in the c-kit protooncogene in a large Italian kindred with piebaldism 1-gen-1995 P. RivaL. Larizza + Article (author) -
A novel potentially diagnostic polymorphism (4894 A/C) in exon 10 of the human c-kit proto-oncogene 1-ott-1996 P. RivaL. Larizza Article (author) -
A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome 1-apr-2010 E. MartinoliG.V. ZuccottiM. VolontèM. VenturinP.V. Riva + Article (author) -
ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome 1-gen-2014 M. VenturinS. CarraG. GaudenziG.R. GalloS. MonciniF. CotelliP. Riva + Article (author) -
Breakpoint characterization of a novel NF1 multiexonic deletion : a case showing expression of the mutated allele 1-mag-2008 F. OrzanM. StroppiM. VenturinP. Riva + Article (author) -
Centa2 è espresso durante lo sviluppo del cuore ed è un gene candidato per le malformazioni cardiovascolari 1-nov-2008 M. VenturinM. StroppiG. GaudenziF. CotelliP. Riva + Conference Object -
Centa2 is expressed during heart development and is a candidate gene for CVMs 1-set-2008 M. VenturinG. GaudenziM. StroppiM. CrippaF. CotelliP. Riva + Conference Object -
Centaurin-α2 and tubulin interaction increases microtubule stability 1-gen-2010 M. StroppiD. CartelliG. CappellettiM. VenturinE. BattaglioliP. Riva + Article (author) -
Centaurin-α2 Interacts with β-Tubulin and Stabilizes Microtubules 1-dic-2012 P. ZuccottiD. CartelliV. PandiniM. VenturinA. AlivertiE. BattaglioliG. CappellettiP.V. Riva + Article (author) -
Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome 1-dic-1996 P. RivaL. DonedaL. Larizza + Article (author) -
Characterization 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 1-gen-2006 M. VenturinA. PatriziMARTINOLI, EMANUELAP. Riva + Article (author) -
Characterization of breakpoint boundaries in 19 Neurofibromatosis type 1 microdeletions 1-mag-2005 C. GervasiniM.VenturinP.RivaL. Larizza + Article (author) -
Chromosomal instability in Cancer : a genomic condition reflecting alterations of different cellular mechanisms 1-gen-2008 P. RivaLONGONI, MAURO Book Part (author) -
Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome 12-ago-1998 M. MiozzoP. RivaA. M. Fuhrman ContiL. VolpiL. Larizza + Article (author) -
Cromosomi umani 1-gen-2013 P.V. Riva Book Part (author) -
Current therapeutic options and novel molecular markers in skull base chordomas 1-gen-2012 P. Riva + Article (author) -
Developmental abnormalities and cancer predisposition in neurofibromatosis type 1 1-gen-2009 L. LarizzaC.C.G. GervasiniP.V. Riva + Article (author) -