Domenico Bordo
Genoa, 16132, Italy
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 16 publications
LncRNA EPR-induced METTL7A1 modulates target gene translation.
Journal: Nucleic acids research
Published: February 03, 2022
In uveal melanoma Gα-protein GNA11 mutations convey a shorter disease-specific survival and are more strongly associated with loss of BAP1 and chromosomal alterations than Gα-protein GNAQ mutations.
Journal: European journal of cancer (Oxford, England : 1990)
Published: January 13, 2022
Novel ACTG2 variants disclose allelic heterogeneity and bi-allelic inheritance in pediatric chronic intestinal pseudo-obstruction.
Journal: Clinical genetics
Published: June 01, 2020
miRNA-Mediated KHSRP Silencing Rewires Distinct Post-transcriptional Programs during TGF-β-Induced Epithelial-to-Mesenchymal Transition.
Journal: Cell reports
Published: February 22, 2016
Diverse roles of the nucleic acid-binding protein KHSRP in cell differentiation and disease.
Journal: Wiley interdisciplinary reviews. RNA
Published: September 30, 2015
ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism.
Journal: Brain : a journal of neurology
Published: August 23, 2015
ABCB4 mutations in adult patients with cholestatic liver disease: impact and phenotypic expression.
Journal: Journal of gastroenterology
Published: June 09, 2015
H19 long noncoding RNA controls the mRNA decay promoting function of KSRP.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: November 12, 2014
A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype.
Journal: Human molecular genetics
Published: February 22, 2014
Last Updated: 09/26/2026