Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Valentina ZANIN"'
Autor:
Liza Vecchi Brumatti, Annalisa Marcuzzi, Paola Maura Tricarico, Valentina Zanin, Martina Girardelli, Anna Monica Bianco
Publikováno v:
Molecules, Vol 19, Iss 12, Pp 21127-21153 (2014)
Curcumin belongs to the family of natural compounds collectively called curcuminoids and it possesses remarkable beneficial anti-oxidant, anti-inflammatory, anti-cancer, and neuroprotective properties. Moreover it is commonly assumed that curcumin ha
Externí odkaz:
https://doaj.org/article/676c8b8c3b114ce39724c84de7180e82
Autor:
Valentina Zanin, Ludovica Segat, Anna Monica Bianco, Lara Padovan, Nathalia de Alencar Cunha Tavares, Sergio Crovella
Publikováno v:
Clinics, Vol 67, Iss 4, Pp 395-398 (2012)
Externí odkaz:
https://doaj.org/article/6d6f5aebdd144422b3af8ca7cc2023cf
Publikováno v:
Mediators of Inflammation, Vol 2013 (2013)
Growing knowledge about the cytokine network response has led to a better comprehension of mechanisms of pathologies and to the development of new treatments with biological drugs, able to block specific molecules of the immune response. Indeed, when
Externí odkaz:
https://doaj.org/article/4ccd717322274a9fb236e50a36c57cac
Publikováno v:
Obstetrics and Gynecology Research.
Autor:
Valentina ZANIN, Lorenza DRIUL, Silvia ZOLETTO, Stefano RESTAINO, Angelica TULISSO, Michela BULFONI, Maria ORSARIA
Publikováno v:
Minerva obstetrics and gynecology.
SARS-CoV-2 disease mechanisms are not yet fully understood, especially in cases affecting pregnant women. In fact, although they suffer from the same symptoms as non-pregnant women, they are more susceptible to adverse outcomes of COVID-19 as well as
Autor:
Stefano, Restaino, Alessia, Sala, Marta, Angelini, Valentina, Zanin, Alice, Poli, Cristina, Angeli, Francesca, Ferrara, Vanni, Pezzarini, Giuseppe, Vizzielli, Lorenza, Driul
Publikováno v:
Minerva Obstetrics and Gynecology.
Glutaric aciduria type II (GA II) is a genetic disorder that interferes with the body's ability to break down proteins and fats in order to produce energy. Signs and symptoms vary greatly depending on the age of onset and severity of the condition. P
Group B streptococcus (GBS) is the leading cause of neonatal morbidity and mortality in developed countries. This study aims primarily to estimate the prevalence of maternal GBS positivity and secondarily to evaluate the compliance and the effectiven
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::75f6ab102d6232308052efdd0c73451a
http://hdl.handle.net/11567/1081048
http://hdl.handle.net/11567/1081048
Autor:
Francesco De Seta, Valentina Zanin, Carlo Contini, Pierlanfranco D'Agaro, Silva Seraceni, Rossella Del Savio, Giuliano Pesel, Manola Comar, Claudia Colli
Publikováno v:
Infectious Agents and Cancer
Background: Chlamydia trachomatis interaction with HR-HPV types has highlighted a central role in cervical cancer development. The aim of this study was to investigate HPV prevalence and genotypes distribution in women at risk for C. trachomatis infe
Autor:
Francesco Napoletano, Ilaria Nisoli, J. P. Chauvin, Bernard Charroux, Valentina Zanin, Manolis Fanto, Piera Calamita
Publikováno v:
Cell Death and Differentiation
Cell Death and Differentiation, Nature Publishing Group, 2010, 17 (10), pp.1577-87. ⟨10.1038/Cdd.2010.31⟩
Cell Death and Differentiation, 2010, 17 (10), pp.1577-87. ⟨10.1038/Cdd.2010.31⟩
Cell Death and Differentiation, Nature Publishing Group, 2010, 17 (10), pp.1577-87. ⟨10.1038/Cdd.2010.31⟩
Cell Death and Differentiation, 2010, 17 (10), pp.1577-87. ⟨10.1038/Cdd.2010.31⟩
Polyglutamine pathologies are neurodegenerative diseases that manifest both general polyglutamine toxicity and mutant protein-specific effects. Dentatorubral-pallidoluysian Atrophy (DRPLA) is one of these disorders caused by mutations in the Atrophin
Autor:
Lorenzo Monasta, Elisa Piscianz, Giulio Kleiner, Annalisa Marcuzzi, Sergio Crovella, Valentina Zanin, Paola Maura Tricarico
Publikováno v:
BioMed Research International
BioMed Research International, Vol 2013 (2013)
BioMed Research International, Vol 2013 (2013)
Mevalonate Kinase Deficiency (MKD) is a rare autosomal recessive inborn disorder of cholesterol biosynthesis caused by mutations in the mevalonate kinase (MK) gene, leading to MK enzyme decreased activity. The consequent shortage of mevalonate-derive