Export 19 results:
Autore Titolo [ Tipo] Anno Filtri: Autore è Girardelli, Martina [Clear All Filters]
Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome results. Mol Med Rep 2015;12(4):6128-32.
. Putative modifier genes in mevalonate kinase deficiency. Mol Med Rep 2016;13(4):3181-9.
. Protective Role of BST2 Polymorphisms in Mother-to-Child Transmission of HIV-1 and Adult AIDS Progression. J Acquir Immune Defic Syndr 2016;72(3):237-41.
. Polymorphisms in inflammasome' genes and susceptibility to HIV-1 infection. J Acquir Immune Defic Syndr 2012;59(2):121-5.
. Polimorphisms in inflammasome genes are involved in the predisposition to systemic lupus erythematosus. Autoimmunity 2012;45(4):271-8.
. Novel missense mutation in the NOD2 gene in a patient with early onset ulcerative colitis: causal or chance association?. Int J Mol Sci 2014;15(3):3834-41.
. NLRP1 polymorphisms in patients with asbestos-associated mesothelioma. Infect Agent Cancer 2012;7(1):25.
. Mevalonate kinase deficiency and IBD: shared genetic background. Gut 2014;63(8):1367-8.
. Lovastatin-induced apoptosis is modulated by geranylgeraniol in a neuroblastoma cell line. Int J Dev Neurosci 2012;30(6):451-6.
. Inflammation profile of four early onset Crohn patients. Gene 2012;493(2):282-5.
. Geranylgeraniol and Neurological Impairment: Involvement of Apoptosis and Mitochondrial Morphology. Int J Mol Sci 2016;17(3):365.
. Genetics of inflammatory bowel disease from multifactorial to monogenic forms. World J Gastroenterol 2015;21(43):12296-310.
.