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Marcuzzi A, Crovella S, Monasta L, Brumatti LVecchi, Gattorno M, Frenkel J. Mevalonate kinase deficiency: disclosing the role of mevalonate pathway modulation in inflammation. Curr Pharm Des 2012;18(35):5746-52.
Tricarico PMaura, Crovella S, Celsi F. Mevalonate Pathway Blockade, Mitochondrial Dysfunction and Autophagy: A Possible Link. Int J Mol Sci 2015;16(7):16067-84.
Tricarico PMaura, Piscianz E, Monasta L, Kleiner G, Crovella S, Marcuzzi A. Microglia activation and interaction with neuronal cells in a biochemical model of mevalonate kinase deficiency. Apoptosis 2015;20(8):1048-55.
Boding L, Hansen AK, Meroni G, Levring TB, Woetmann A, Ødum N, Bonefeld CM, Geisler C. MID2 can substitute for MID1 and control exocytosis of lytic granules in cytotoxic T cells. APMIS 2015;123(8):682-7.
Stampalija T, Arabin B, Wolf H, Bilardo CM, Lees C. Is middle cerebral artery Doppler related to neonatal and 2-year infant outcome in early fetal growth restriction?. Am J Obstet Gynecol 2017;216(5):521.e1-521.e13.
Boding L, Hansen AK, Meroni G, Johansen BB, Braunstein TH, Bonefeld CM, Kongsbak M, Jensen BAH, Woetmann A, Thomsen AR, Odum N, von Essen MR, Geisler C. Midline 1 directs lytic granule exocytosis and cytotoxicity of mouse killer T cells. Eur J Immunol 2014;44(10):3109-18.
Poillucci G, Degrassi F, Guida E, Pederiva F. "Milky" bowel and malrotation. Surgery 2017;162(2):468-469.
Pastore S, Contorno S, Caddeo G, Calligaris L, Taddio A. A minor trauma revealing linear morphoea in a 4-year-old female. Arch Dis Child 2016;
Zauli G, Voltan R, di Iasio MGrazia, Bosco R, Melloni E, Sana MElena, Secchiero P. miR-34a induces the downregulation of both E2F1 and B-Myb oncogenes in leukemic cells. Clin Cancer Res 2011;17(9):2712-24.
Laganà A, Paone A, Veneziano D, Cascione L, Gasparini P, Carasi S, Russo F, Nigita G, Macca V, Giugno R, Pulvirenti A, Shasha D, Ferro A, Croce CM. miR-EdiTar: a database of predicted A-to-I edited miRNA target sites. Bioinformatics 2012;28(23):3166-8.
Pontillo A, Vendramin A, Catamo E, Fabris A, Crovella S. 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.
Grandone A, Cirillo G, Sasso M, Capristo C, Tornese G, Marzuillo P, Luongo C, Umano GRosaria, Festa A, Coppola R, Del Giudice EMiraglia, Perrone L. MKRN3 levels in girls with central precocious puberty and correlation with sexual hormone levels: a pilot study. Endocrine 2018;59(1):203-208.

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