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Filtri: Autore è Crovella, Sergio and First Letter Of Title is M [Clear All Filters]
Mannose binding lectin gene (MBL2) functional polymorphisms are associated with systemic lupus erythematosus in southern Brazilians. Hum Immunol 2011;72(6):516-21.
. Mannose-binding lectin gene (MBL-2) polymorphism in oral lichen planus. Clin Oral Investig 2011;15(5):699-704.
. MBL1 gene in nonhuman primates. Hum Immunol 2011;72(11):1084-90.
. The missense variation Q705K in CIAS1/NALP3/NLRP3 gene and an NLRP1 haplotype are associated with celiac disease. Am J Gastroenterol 2011;106(3):539-44.
. Mevalonate kinase deficiency: disclosing the role of mevalonate pathway modulation in inflammation. Curr Pharm Des 2012;18(35):5746-52.
. Mevalonate kinase deficiency and IBD: shared genetic background. Gut 2014;63(8):1367-8.
. MBL2 polymorphisms in women with atypical squamous cells of undetermined significance. J Med Virol 2015;87(5):851-9.
. Meta-analysis and time series modeling allow a systematic review of primary HIV-1 drug-resistant prevalence in Latin America and Caribbean. Curr HIV Res 2015;13(2):125-42.
. Meta-analysis of Brazilian genetic admixture and comparison with other Latin America countries. Am J Hum Biol 2015;27(5):674-80.
. Mevalonate Pathway Blockade, Mitochondrial Dysfunction and Autophagy: A Possible Link. Int J Mol Sci 2015;16(7):16067-84.
. Microglia activation and interaction with neuronal cells in a biochemical model of mevalonate kinase deficiency. Apoptosis 2015;20(8):1048-55.
. MBL2 genetic polymorphisms and HIV-1 mother-to-child transmission in Zambia. Immunol Res 2016;64(3):775-84.
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