Sfoglia per SSD
A 12-bp deletion (7818del12) in the c-kit protooncogene in a large Italian kindred with piebaldism
1995 P. Riva, N. Milani, P. Gandolfi, L. Larizza
A comparative analysis of collagen III, IV, laminin and fibronectin in Duchenne muscular dystrophy biopsies and cell cultures
1986 E. Rampoldi, G. Meola, A. M. Conti, M. Velicogna, L. Larizza
A dual acting compound releasing nitric oxide (NO) and ibuprofen, NCX 320, shows significant therapeutic effects in a mouse model of muscular dystrophy
2011 C. Sciorati, D. Miglietta, R. Buono, V. Pisa, D. Cattaneo, E. Azzoni, S. Brunelli, E. Clementi
A functional variant in ERAP1 predisposes to multiple sclerosis
2012 F.R. Guerini, R. Cagliani, D. Forni, C. Agliardi, D. Caputo, A. Cassinotti, D. Galimberti, C. Fenoglio, M. Biasin, R. Asselta, E. Scarpini, G.P. Comi, N. Bresolin, M.S. Clerici, M. Sironi
A genomic and proteomic study of obesity-related non-alcoholic fatty liver disease (NAFLD)
2004 K. Schlauch, L. O'Reilly, T. Born, K. Ziegler, J. Ong, H. Elariny, F. Gorreta, L. Del Giacco, A. Younoszai, G. Grant, V. Chandhoke, Z. Goodman, Z. Younossi
A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy
2012 D.S. Cabianca, V. Casa, B. Bodega, A. Xynos, E. Ginelli, Y. Tanaka, D. Gabellini
A mitochondrial mechanism is involved in apoptosis of Robertsonian mouse male germ cells
2008 V. Merico, G.D. de Barboza, C. Vasco, R. Ponce, V. Rodriguez, S. Garagna, N.T. de Talamoni
A new aspect of neuritin-1 (cpg15) : induction of cell migration
2011 A. Zito, G. Cappelletti, D. Cartelli, A.M. Cariboni, A. Poletti, M. Galbiati
A new BRCA1 germline mutation (E879X) in a Malaysian breast cancer patient of Chinese descent
2000 A.S. Khoo, P. Balraj, L. Volpi, S. Nair
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing
2011 M. Robusto, R. Asselta, P. Primignani, P. Castorina, E. Benzoni, A. Cesarani, U. Ambrosetti, S. Duga, G. Soldà
A novel mutation in MIR96 in an Italian family with nonsyndromic inherited hearing loss
2011 G.M. Soldà, M. Robusto, R. Asselta, P. Primignani, D. Coviello, P. Castorina, U. Ambrosetti, S. Duga
A novel mutation within the MIR96 gene causes nonsyndromic inherited hearing loss in an Italian family by altering pre-miRNA processing
2011 M. Robusto, G. Soldà, P. Primignani, P. Castorina, E. Benzoni, A. Cesarani, U. Ambrosetti, R. Asselta, S. Duga
A novel role for neuritin (cpg15) : the regulation of neuronal migration
2010 M. Galbiati, G. Cappelletti, D. Cartelli, A.M. Cariboni, A. Zito, A. Poletti
A novel, highly regulated, rapidly inducible system for the expression of chicken progesterone receptor, cPRA, in Saccharomyces cerevisiae
1992 A. Poletti, N.L. Weigel, D.P. McDonnell, W.T. Schrader, B.W. O'Malley, O.M. Conneely
A presynaptically toxic secreted phospholipase A2 is internalized into motoneuron-like cells where it is rapidly translocated into the cytosol
2008 Z.J. Praznikar, L. Kovacic, E.G. Rowan, R. Romih, P. Rusmini, A. Poletti, I. Krizaj, J. Pungercar
A rapid method for monitoring DNA labelling reactions with haptens
1990 A. Corti, P. Tripputi, G. Cassani
A rare chromosome 5 heterochromatic variant derived from insertion of 9qh satellite 3 sequences
1998 L. Doneda, P. Gandolfi, G. Nocera, L. Larizza
A role of small heat shock protein B8 (HspB8) in the autophagic removal of misfolded proteins responsible for neurodegenerative diseases
2010 V. Crippa, S. Carra, P. Rusmini, D. Sau, E. Bolzoni, C. Bendotti, S. De Biasi, A. Poletti
A satellite DNA isolated from human tissues
1967 G. Corneo, E. Ginelli, E. Polli
A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome
2010 E. Martinoli, G.V. Zuccotti, L. Pogliani, M. Volontè, M. Venturin, P. Fortina, A. Ertel, S. Redaelli, P.V. Riva, L. Dalprà
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