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A model for the involvement of Okazaki fragments in the expansion of triplet repeats associated with hereditary neurological diseases 1-gen-2000 Bellizzi, Dina; Losso, Maria Adele; Sgaramella, V.
A model for the involvement of Okazaki fragments maturation in the expansion of triplet repeats 1-gen-2000 Bellizzi, Dina; Sgaramella, V.; Losso, Maria Adele
Triplet repeats, over-expanded in neuromuscular diseases, are under-represented in mammalian DNA: a survey of models 1-gen-2001 Astolfi, P.; Bellizzi, Dina; Losso, Maria Adele; Sgaramella, V.
Triplet repeats, over-expanded in neuromuscular diseases, are under-represented in mammalian DNA. A model involving discontinuous replication 1-gen-2001 Astolfi, P.; Bellizzi, Dina; Losso, Maria Adele; Sgaramella, V.
A model for the involvment of Okazaki Fragments in the expansion of short tandem repeats responsible of some neuromuscolar diseases 1-gen-2001 Losso, M; Losso, Maria Adele; Sgaramella, V.
Alternative structure sequence-dependent affects a human DNA fragment stability 1-gen-2005 Losso, Maria Adele
Identificazione e caratterizzazione dei geni hly a iap nei sierotipi di Listeria monocytogenes e comparazione con Listeria spp 1-gen-2005 Losso, Maria Adele; Caracciolo, S.; Chiarelli, N.; Lepore, S. M.; Vuono, R.
Identification and characterization of hly and iap genes in L.monocytogenes serotypes and comparison with Listeria spp 1-gen-2005 Losso, Maria Adele; Caracciolo, S.; Chiarelli, N.; Lepore, S. M.; Vuono, R.
A new mutation at position +4 in the intron following exon 10 of the tau gene in a patient with Frontotemporal Dementia 1-gen-2006 Vuono, R; Bruni, A. C.; Bernardi, L; Tomaino, C; Maletta, R; Losso, Maria Adele
Molecular effects of a novel intronic mutation in the tau gene identified in a patient with Frontotemporal dementia 1-gen-2006 Losso, Maria Adele; Vuono, R; Bernardi, L; Maletta, R; Tomaino, C. AND BRUNI A.
A novel intronic 10+4 splice mutation alters tau pre-mRNA splicing 1-gen-2006 Losso, Maria Adele; Bruni, A. C.; Bernardi, L; Tomaino, C; Viola, M. E.; Vuono, R.
A novel intronic 10+4 splice site tau mutation associated to a single patient with Pick disease 1-gen-2007 R., Vuono; L., Bernardi; C., Tomaino; R., Maletta; A. C., Bruni; Losso, Maria Adele
A Clinical, Pathological And Molecular Study Of A Frontotemporal Dementia Sporadic Case 1-gen-2008 Losso, Maria Adele; Vuono, R; Anfossi, M; Bernardi, L; Colao, R; Duyckaerts, C; Foncin, Jf; Frangipane, F; Gallo, M; Geracitano, Silvana; Lamenza, F; Maletta, R; Panno, Ml; Puccio, G; Spillantini, Mg; Tomaino, C; Bruni, Ac
Two novel tau mutations associated to a Frontotemporal Dementia Sporadic case: a clinical and neuropathological study 1-gen-2008 R., Colao; M., Anfossi; C., Tomaino; L., Bernardi; F., Lamenza; G., Zannino; R., Maletta; G., Puccio; F., Frangipane; M., Gallo; S., Geracitano; R., Vuono; Losso, Maria Adele; M. G., Spillantini; J. F., Foncin; C., Duyckaerts; A. C., Bruni
Two novel tau mutations associated to a Frontotemporal Dementia Sporadic case: a molecular study 1-gen-2008 Losso, Maria Adele; Anfossi, M.; Bernardi, L.; Bruni, A. C.; Maletta, R.; Panno, M. L.; Tomaino, C.; Vuono, R.
Frontotemporal Dementia Sporadic Case associating two novel Tau mutations. Part two: molecular effect on Exon 10 alternative splicing 1-gen-2009 Losso, Maria Adele; Anfossi, M; Bernardi, L; Bruni, Ac; Maletta, R; Panno, Ml; Tomaino, C. A. N. D. VUONO R.
Frontotemporal Dementia Sporadic Case associating two novel Tau mutations. Part one: clinico-pathological study 1-gen-2009 Colao, R; Anfossi, M; Clodomino A., TOMAINO C; Bernardi, L; Curcio, Sam; Mirabelli, M; Lamenza, F; Zannino, G.; Maletta, R; Puccio, G; Frangipane, F; Gallo, M; Geracitano, S; Vuono, R; Losso, Maria Adele; Foncin, Jf; Spillantini, Mg; Duyckaerts, C; Bruni, Ac; Bruni, Ac
Two novel MAPT mutations associated to a Frontotemporal Dementia Sporadic case: a clinical, neuropathological and molecular study 1-gen-2009 Vuono, R; Anfossi, M; Bernardi, L; Bruni, Ac; Colao, R; Duyckaerts, C; Foncin, Jf; Frangipane, F; Gallo, M; Geracitano, S; Maletta, R; Panno, Ml; Puccio, G; Spillantini, Mg; Losso, Maria Adele
Frontotemporal Dementia Sporadic case associating two novel tau mutations: a clinico-pathological study 1-gen-2009 Bruni, Ac; Colao, R; Anfossi, M; Clodomiro, A; Tomaino, C; Bernardi, L; Curcio, S; Mirabelli, M; Lamenza, F; Zannino, G; Maletta, R; Puccio, G; Frangipane, F; Gallo, M; Geracitano, S; Vuono, R; Losso, Maria Adele; Foncin, Jf; Spillantini, Mg; Duyckaerts, C.
Compound heterozygosity of 2 novel MAPT mutations in frontotemporal dementia 1-gen-2011 Anfossi, M; Vuono, R; Maletta, R; Virdee, K; Mirabelli, M; Colao, R; Puccio, G; Frangipane, F; Gallo, M; Geracitano, S; Tomaino, C; Curcio, Sam; Zannino, G; Lamenza, F; Duyckaerts, C; Spillantini, Mg; Losso, Maria Adele; Bruni, Ac
Mostrati risultati da 1 a 20 di 26
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