Úrsula da Silveira Matte
Researcher Next ID · RN-038025
Researcher · Health Professions
Universidade Federal do Rio Grande do Sul
Porto Alegre, Brazil
- Works count
- 548
- Citation count
- 4,076
- H-index
- 34
- i10-index
- 127
Research interests
Publications
Mucopolysaccharidosis Type I
Diagnostics · 2020 · 10.3390/diagnostics10030161
In vivo genome editing of mucopolysaccharidosis I mice using the CRISPR/Cas9 system
Journal of Controlled Release · 2018 · 10.1016/j.jconrel.2018.08.031
Cationic nanoemulsions as nucleic acids delivery systems
International Journal of Pharmaceutics · 2017 · 10.1016/j.ijpharm.2017.10.030
Delivery Mode and the Transition of Pioneering Gut-Microbiota Structure, Composition and Predicted Metabolic Function
Genes · 2017 · 10.3390/genes8120364
Emerging drugs for the treatment of mucopolysaccharidoses
Expert Opinion on Emerging Drugs · 2016 · 10.1517/14728214.2016.1123690
Photobiomodulation regulates cytokine release and new blood vessel formation during oral wound healing in rats
Lasers in Medical Science · 2016 · 10.1007/s10103-016-1904-0
Birth mode-dependent association between pre-pregnancy maternal weight status and the neonatal intestinal microbiome
Scientific Reports · 2016 · 10.1038/srep23133
miRNA-21 and miRNA-34a Are Potential Minimally Invasive Biomarkers for the Diagnosis of Pancreatic Ductal Adenocarcinoma
Pancreas · 2015 · 10.1097/mpa.0000000000000383
An Analysis of the Global Expression of MicroRNAs in an Experimental Model of Physiological Left Ventricular Hypertrophy
PLoS ONE · 2014 · 10.1371/journal.pone.0093271
Transcoronary gradient of plasma microRNA 423-5p in heart failure: evidence of altered myocardial expression
Biomarkers · 2014 · 10.3109/1354750x.2013.870605
Effects of FTO RS9939906 and MC4R RS17782313 on obesity, type 2 diabetes mellitus and blood pressure in patients with hypertension
Cardiovascular Diabetology · 2013 · 10.1186/1475-2840-12-103
Enzyme replacement therapy started at birth improves outcome in difficult-to-treat organs in mucopolysaccharidosis I mice
Molecular Genetics and Metabolism · 2013 · 10.1016/j.ymgme.2013.03.005
Guidelines for the Management of Mucopolysaccharidosis Type I
The Journal of Pediatrics · 2009 · 10.1016/j.jpeds.2009.07.005
CNS involvement in Fabry disease: Clinical and imaging studies before and after 12 months of enzyme replacement therapy
Journal of Inherited Metabolic Disease · 2004 · 10.1023/b:boli.0000028794.04349.91
Identification and characterization of 13 new mutations in mucopolysaccharidosis type I patients
Molecular Genetics and Metabolism · 2003 · 10.1016/s1096-7192(02)00200-7
Current projects
No projects listed.