15 results for author:"Messina S." in Literature citations
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| Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy. Bello L., Piva L., Barp A., Taglia A., Picillo E., Vasco G., Pane M., Previtali S.C., Torrente Y., Gazzerro E. et al. Neurology 79:159-162(2012) · Mapped (8) |
| Dual-specificity phosphatase DUSP6 has tumor-promoting properties in human glioblastomas. Messina S., Frati L., Leonetti C., Zuchegna C., Di Zazzo E., Calogero A., Porcellini A. Oncogene 30:3813-3820(2011) · Mapped (4) |
| Telomere shortening is associated to TRF1 and PARP1 overexpression in Duchenne muscular dystrophy. Aguennouz M., Vita G.L., Messina S., Cama A., Lanzano N., Ciranni A., Rodolico C., Di Giorgio R.M., Vita G. Neurobiol. Aging 32:2190-2197(2011) · Mapped (11) |
| SMN transcript levels in leukocytes of SMA patients determined by absolute real-time PCR. Tiziano F.D., Pinto A.M., Fiori S., Lomastro R., Messina S., Bruno C., Pini A., Pane M., D'Amico A., Ghezzo A. et al. Eur. J. Hum. Genet. 18:52-58(2010) · Mapped (7) |
| Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study. Mercuri E., Messina S., Bruno C., Mora M., Pegoraro E., Comi G.P., D'Amico A., Aiello C., Biancheri R., Berardinelli A. et al. |
| POMT1 and POMT2 mutations in CMD patients: a multicentric Italian study. Messina S., Mora M., Pegoraro E., Pini A., Mongini T., D'Amico A., Pane M., Aiello C., Bruno C., Biancheri R. et al. Neuromuscul. Disord. 18:565-571(2008) · Mapped (12) |
| VEGF overexpression via adeno-associated virus gene transfer promotes skeletal muscle regeneration and enhances muscle function in mdx mice. Messina S., Mazzeo A., Bitto A., Aguennouz M., Migliorato A., De Pasquale M.G., Minutoli L., Altavilla D., Zentilin L., Giacca M. et al. FASEB J. 21:3737-3746(2007) · Mapped (5) |
| POMT2 mutation in a patient with 'MEB-like' phenotype. Mercuri E., D'Amico A., Tessa A., Berardinelli A., Pane M., Messina S., van Reeuwijk J., Bertini E., Muntoni F., Santorelli F.M. Neuromuscul. Disord. 16:446-448(2006) · UniProtKB (1) |
| Lipid peroxidation inhibition blunts nuclear factor-kappaB activation, reduces skeletal muscle degeneration, and enhances muscle function in mdx mice. Messina S., Altavilla D., Aguennouz M., Seminara P., Minutoli L., Monici M.C., Bitto A., Mazzeo A., Marini H., Squadrito F. et al. Am. J. Pathol. 168:918-926(2006) · Mapped (8) |
| Nuclear factor kappa-B blockade reduces skeletal muscle degeneration and enhances muscle function in Mdx mice. Messina S., Bitto A., Aguennouz M., Minutoli L., Monici M.C., Altavilla D., Squadrito F., Vita G. Exp. Neurol. 198:234-241(2006) · Mapped (8) |
| Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene. Jungbluth H., Zhou H., Hartley L., Halliger-Keller B., Messina S., Longman C., Brockington M., Robb S.A., Straub V., Voit T. et al. |
| Specific matrix metalloproteinase expression in focal myositis: an immunopathological study. Rodolico C., Mazzeo A., Toscano A., Messina S., Aguennouz M., Gaeta M., Messina C., Vita G. Acta Neurol. Scand. 112:173-177(2005) · Mapped (13) |
| Magnetic resonance imaging of muscle in congenital myopathies associated with RYR1 mutations. Jungbluth H., Davis M.R., Muller C., Counsell S., Allsop J., Chattopadhyay A., Messina S., Mercuri E., Laing N.G., Sewry C.A. et al. Neuromuscul. Disord. 14:785-790(2004) · Mapped (6) |
| The expression of the thyroid-stimulating hormone (TSH) receptor and the cAMP-dependent protein kinase RII beta regulatory subunit confers TSH-cAMP-dependent growth to mouse fibroblasts. Porcellini A., Messina S., De Gregorio G., Feliciello A., Carlucci A., Barone M., Picascia A., De Blasi A., Avvedimento E.V. J. Biol. Chem. 278:40621-40630(2003) · Mapped (4) |
| Specific interactions of neuronal focal adhesion kinase isoforms with Src kinases and amphiphysin. Messina S., Onofri F., Bongiorno-Borbone L., Giovedi S., Valtorta F., Girault J.A., Benfenati F. J. Neurochem. 84:253-265(2003) · Mapped (2) |