IRIS

PERSICHETTI, Francesca

PERSICHETTI, Francesca  

Dipartimento di Scienze della Salute  

Mostra records
Risultati 1 - 20 di 59 (tempo di esecuzione: 0.03 secondi).
Titolo Data di pubblicazione Autore(i) File
A human minisatellite hosts an alternative transcription start site for NPRL3 driving its expression in a repeat number-dependent manner 1-gen-2020 Bertuzzi, M.; Tang, D.; Calligaris, R.; Vlachouli, C.; Finaurini, S.; Sanges, R.; Goldwurm, S.; Catalan, M.; Antonutti, L.; Manganotti, P.; Pizzolato, G.; Pezzoli, G.; Persichetti, F.; Carninci, P.; Gustincich, S.
Amyloid formation by mutant huntingtin: threshold, progressivity and recruitment of normal polyglutamine proteins 1-gen-1998 Huang, Cc; Faber, Pw; Persichetti, Francesca; Mittal, V; Vonsattel, Jp; Macdonald, Me; Gusella, Jf
An additional HindIII polymorphism at the coagulation factor XIII A locus 1-gen-1990 Iodice, C; Novelletto, A; Malaspina, P; Persichetti, Francesca
An Air-well sparging minifermenter system for high-throughput protein production. 1-gen-2014 Deantonio, Cecilia; Sedini, V; Cesaro, Patrizia; Quasso, Fabio; Cotella, Diego; Persichetti, Francesca; Santoro, Claudio Ventura; Sblattero, Daniele
Analysis of LINE1 Retrotransposons in Huntington's Disease 1-gen-2022 Floreani, Lavinia; Ansaloni, Federico; Mangoni, Damiano; Agostoni, Elena; Sanges, Remo; Persichetti, Francesca; Gustincich, Stefano
Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington’s disease 1-gen-1994 Novelletto, A; Persichetti, Francesca; Sabbadini, G; Mandich, P; Bellone, E; Ajmar, F; Pergola, M; DEL SENNO, L; Macdonald, Me; Gusella, Jf; Frontali, M.
Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases 1-gen-2019 Zucchelli, Silvia; Fedele, Stefania; Vatta, Paolo; Calligaris, Raffaella; Heutink, Peter; Rizzu, Patrizia; Itoh, Masayoshi; Persichetti, Francesca; Santoro, Claudio; Kawaji, Hideya; Lassmann, Timo; Hayashizaki, Yoshihide; Carninci, Piero; Forrest, Alistair R R; Gustincich, Stefano
Autosomal dominant pure cerebellar ataxia 1-gen-1992 Frontali, M; Spadaro, M; Giunti, P; Bianco, F; Iodice, C; Persichetti, Francesca; Colazza, Gb; Lulli, P; Terrenato, L; Morocutti, C.
CEPH consortium map of chromosome 14 1-gen-1995 Cox, Dw; Billingsley, Gd; Bale, Ae; COOPERATIVE HUMAN LINKAGE, Center; DONIS KELLER, H; Edwards, Jh; Litt, M; Mcbride, W; Persichetti, Francesca; Spurr, Nk; Weber, Jl; Weissenbach, J; White, Rl
Differential expression of normal and mutant Huntington’s disease gene alleles 1-gen-1996 Persichetti, Francesca; Carlee, L; Faber, Pw; Mcneil, Sm; Ambrose, Cm; Srinidhi, J; Anderson, Ma; Barnes, Gt; Gusella, Jf; Macdonald, Me
Disequilibrium of multiple DNA markers on the human Y chromosome 1-gen-1992 Persichetti, Francesca; Blasi, P; Hammer, M; Malaspina, P; Iodice, C; Terrenato, L; Novelletto, A.
Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cells 1-gen-2000 Trettel, F; Rigamonti, D; HILDITCH MAGUIRE, P; Wheeler, Vc; Sharp, Ah; Persichetti, Francesca; Cattaneo, E; Macdonald, Me
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia 1 1-gen-1994 Iodice, C; Malaspina, P; Persichetti, Francesca; Novelletto, A; Spadaro, M; Giunti, P; Morocutti, C; Terrenato, L; Harding, Ae; Frontali, M.
Effects of Pin1 loss in HdhQ111 knock-in mice 1-gen-2016 Agostoni, Elena; Michelazzi, Silvia; Maurutto, Marta; Carnemolla, Alisia; Ciani, Yari; Vatta, Paolo; Roncaglia, Paola; Zucchelli, Silvia; Leanza, Giampiero; Mantovani, Fiamma; Gustincich, Stefano; Santoro, Claudio Ventura; Piazza, Silvano; Del Sal, Giannino; Persichetti, Francesca
Engineering Translation in Mammalian Cell Factories to Increase Protein Yield: The Unexpected Use of Long Non-Coding SINEUP RNAs 1-gen-2016 Zucchelli, Silvia; Patrucco, Laura; Persichetti, Francesca; Gustincich, Stefano; Cotella, Diego
Entrapment into liposomes of fusicoccin binding sites 1-gen-1986 Patrizia, Aducci; Alessandro, Ballio; Maria Rosaria, Fullone; Persichetti, Francesca
Expression analysis of the long non-coding RNA antisense to Uchl1 (AS Uchl1) during dopaminergic cells' differentiation in vitro and in neurochemical models of Parkinson's disease 1-gen-2015 Claudia, Carrieri; Alistair R. R., Forrest; Santoro, Claudio Ventura; Persichetti, Francesca; Piero, Carninci; Zucchelli, Silvia; Stefano, Gustincich
Factors Associated with HD CAG repeat instability in Huntington's disease 1-gen-2007 Wheeler, V; Persichetti, Francesca; Mcneil, S; Mysore, J; Mysore, S; Macdonald, M; Myers, R; Gusella, J; Wexler, N; Wexler, Tu
Genome-wide analysis of mammalian promoter architecture and evolution 1-gen-2006 Carninci, P; Sandelin, A; Lenhard, B; Katayama, S; Shimokawa, K; Ponjavic, J; Semple, Ca; Taylor, Ms; Engstrom, Pg; Frith, Mc; Forrest, Ar; Alkema, Wb; Tan, Sl; Plessy, C; Kodzius, R; Ravasi, T; Kasukawa, T; Fukuda, S; KANAMORI KATAYAMA, M; Kitazume, Y; Kawaji, H; Kai, C; Nakamura, M; Konno, H; Nakano, K; MOTTAGUI TABAR, S; Arner, P; Chesi, A; Gustincich, S; Persichetti, Francesca; Suzuki, H; Grimmond, Sm; Wells, Ca; Orlando, V; Wahlestedt, C; Liu, Et; Harbers, M; Kawai, J; Bajic, Vb; Hume, Da; Hayashizaki, Y.
Heterogeneous topographic and cellular distribution of huntingtin expression in the normal human neostriatum 1-gen-1997 Ferrante, Rj; Gutekunst, Ca; Persichetti, Francesca; Mcneil, Sm; Kowall, Nw; Gusella, Jf; Macdonald, Me; Beal, Fm; Hersch, Sm