FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Marco Venturin

Research Profile

Genes & Molecular Sequences

Genes, Neurofibromatosis 1

Anatomy

Chromosomes, Human, Pair 17

Procedures

Disorders

Chemicals & Drugs

Co-author Network

Publications

TOP 3
Paola Zuccotti; Michela Stroppi; Marco Venturin; Alessandro Aliverti; Elena Battaglioli; Graziella Cappelletti; Daniele Cartelli; Vittorio Pandini; Paola Riva
Centaurin-α₂ interacts with β-tubulin and stabilizes microtubules.
Silvia Moncini; Alessandro Salvi; Paola Zuccotti; Gabriella Viero; Alessandro Quattrone; Sergio Barlati; Giuseppina De Petro; Marco Venturin; Paola Riva
The role of miR-103 and miR-107 in regulation of CDK5R1 expression and in cellular migration.
Mauro Longoni; Silvia Moncini; Mariangela Cisternino; Ilaria M Morella; Serena Ferraiuolo; Silvia Russo; Savina Mannarino; Valeria Brazzelli; Paola Coi; Renata Zippel; Marco Venturin; Paola Riva
Noonan syndrome associated with both a new Jnk-activating familial SOS1 and a de novo RAF1 mutations.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Marco Venturin (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: Paola Zuccotti; Michela Stroppi; Marco Venturin; Alessandro Aliverti; Elena Battaglioli; Graziella Cappelletti; Daniele Cartelli; Vittorio Pandini; Paola Riva
Centaurin-α₂ interacts with β-tubulin and stabilizes microtubules.
PloS one 2012;7(12):e52867.
2011: Silvia Moncini; Alessandro Salvi; Paola Zuccotti; Gabriella Viero; Alessandro Quattrone; Sergio Barlati; Giuseppina De Petro; Marco Venturin; Paola Riva
The role of miR-103 and miR-107 in regulation of CDK5R1 expression and in cellular migration.
PloS one 2011;6(5):e20038.
2010: Mauro Longoni; Silvia Moncini; Mariangela Cisternino; Ilaria M Morella; Serena Ferraiuolo; Silvia Russo; Savina Mannarino; Valeria Brazzelli; Paola Coi; Renata Zippel; Marco Venturin; Paola Riva
Noonan syndrome associated with both a new Jnk-activating familial SOS1 and a de novo RAF1 mutations.
American journal of medical genetics. Part A 2010;152A(9):2176-84.
2010: Emanuela Martinoli; Gian Vincenzo Zuccotti; Laura Pogliani; Marinella Volontè; Marco Venturin; Paolo Fortina; Adam Ertel; Serena Redaelli; Paola Riva; Leda Dalprà
A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome.
American journal of medical genetics. Part A 2010;152A(4):1043-5.
2008: Francesca Orzan; Michela Stroppi; Marco Venturin; Maria Carmen Valero; Concepcion Hernández; Paola Riva
Breakpoint characterization of a novel NF1 multiexonic deletion: a case showing expression of the mutated allele.
Neurogenetics 2008;9(2):95-100.
2007: 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.
BMC molecular biology 2007;8():111.
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.
Neurogenetics 2006;7(1):59-66.
2006: 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.
Journal of human genetics 2006;51(1):68-75.
2005: Marco Venturin; Angela Bentivegna; Ramona Frida Moroni; Lidia Larizza; Paola Riva
Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval.
Annals of human genetics 2005;69(Pt 5):508-16.
2005: 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.
Genomics 2005;85(2):273-9.
2004: Marco Venturin; Cristina Gervasini; Francesca Orzan; Angela Bentivegna; Lucia Corrado; Patrizia Colapietro; Alessandra Friso; Romano Tenconi; Meena Upadhyaya; Lidia Larizza; Paola Riva
Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions.
Human genetics 2004;115(1):69-80.
2004: Marco Venturin; P Guarnieri; Federica Natacci; M Stabile; Romano Tenconi; Maurizio Clementi; C Hernandez; P Thompson; M Upadhyaya; Lidia Larizza; Paola Riva
Mental retardation and cardiovascular malformations in NF1 microdeleted patients point to candidate genes in 17q11.2.
Journal of medical genetics 2004;41(1):35-41.
2002: Cristina Gervasini; Angela Bentivegna; Marco Venturin; Lucia Corrado; Lidia Larizza; Paola Riva
Tandem duplication of the NF1 gene detected by high-resolution FISH in the 17q11.2 region.
Human genetics 2002;110(4):314-21.
2001: Angela Bentivegna; Marco Venturin; Cristina Gervasini; Lucia Corrado; Lidia Larizza; Paola Riva
Identification of duplicated genes in 17q11.2 using FISH on stretched chromosomes and DNA fibers.
Human genetics 2001;109(1):48-54.
2001: Angela Bentivegna; Marco Venturin; Cristina Gervasini; Lucia Corrado; Lidia Larizza; Paola Riva
FISH with locus-specific probes on stretched chromosomes: a useful tool for genome organization studies.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2001;9(2):167-70.