User profiles for "author:Marco Venturin"

Marco Venturin

University of Milan
Verified email at unimi.it
Cited by 1245

The long non-coding RNAs in neurodegenerative diseases: novel mechanisms of pathogenesis

P Riva, A Ratti, M Venturin - Current Alzheimer Research, 2016 - ingentaconnect.com
Background: Long-non-coding RNAs (lncRNAs), RNA molecules longer than 200
nucleotides, have been involved in several biological processes and in a growing number of …

[HTML][HTML] Psychiatric disorders and lncRNAs: a synaptic match

F Rusconi, E Battaglioli, M Venturin - International Journal of Molecular …, 2020 - mdpi.com
Psychiatric disorders represent a heterogeneous class of multifactorial mental diseases
whose origin entails a pathogenic integration of genetic and environmental influences …

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

A Salvi, C Sabelli, S Moncini, M Venturin… - The FEBS …, 2009 - Wiley Online Library
Urokinase‐type plasminogen activator (uPA) and c‐met play a major role in cancer invasion
and metastasis. Evidence has suggested that uPA and c‐met overexpression may be …

[HTML][HTML] The Role of miR-103 and miR-107 in Regulation of CDK5R1 Expression and in Cellular Migration

S Moncini, A Salvi, P Zuccotti, G Viero, A Quattrone… - PloS one, 2011 - journals.plos.org
CDK5R1 encodes p35, a specific activator of the serine/threonine kinase CDK5, which plays
crucial roles in CNS development and maintenance. CDK5 activity strongly depends on p35 …

[HTML][HTML] Emerging role of genetic alterations affecting exosome biology in neurodegenerative diseases

P Riva, C Battaglia, M Venturin - International journal of molecular …, 2019 - mdpi.com
The abnormal deposition of proteins in brain tissue is a common feature of
neurodegenerative diseases (NDs) often accompanied by the spread of mutated proteins …

The miR-15/107 family of microRNA genes regulates CDK5R1/p35 with implications for Alzheimer's disease pathogenesis

S Moncini, M Lunghi, A Valmadre, M Grasso… - Molecular …, 2017 - Springer
Cyclin-dependent kinase 5 regulatory subunit 1 (CDK5R1) encodes p35, the main activatory
subunit of cyclin-dependent kinase 5 (CDK5). The p35/CDK5 active complex plays a …

[HTML][HTML] Multiple Layers of CDK5R1 Regulation in Alzheimer's Disease Implicate Long Non-Coding RNAs

M Spreafico, B Grillo, F Rusconi, E Battaglioli… - International journal of …, 2018 - mdpi.com
Cyclin-dependent kinase 5 regulatory subunit 1 (CDK5R1) gene encodes for p35, the main
activator of Cyclin-dependent kinase 5 (CDK5). The active p35/CDK5 complex is involved in …

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

M Venturin, C Gervasini, F Orzan, A Bentivegna… - Human genetics, 2004 - Springer
NF1 microdeletion syndrome is caused by haploinsufficiency of the NF1 gene and of gene
(s) located in adjacent flanking regions. Most of the NF1 deletions originate by non-allelic …

ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome

M Venturin, S Carra, G Gaudenzi, S Brunelli… - Journal of Medical …, 2014 - jmg.bmj.com
Background Cardiovascular malformations have a higher incidence in patients with NF1
microdeletion syndrome compared to NF1 patients with intragenic mutation, presumably …

[HTML][HTML] Candidate genes and MiRNAs linked to the inverse relationship between cancer and alzheimer's disease: insights from data mining and enrichment analysis

C Battaglia, M Venturin, A Sojic, N Jesuthasan… - Frontiers in …, 2019 - frontiersin.org
The incidence of cancer and Alzheimer's disease (AD) increases exponentially with age. A
growing body of epidemiological evidence and molecular investigations inspired the …