Sfoglia per Rivista NATURE NEUROSCIENCE
Acetylcholine receptor M3 domain: stereochemical and volume contribution to channel gating
1999 Wang, Hl; Milone, M; Ohno, K; Shen, Xm; Tsujino, A; Batocchi, Anna Paola; Tonali, Pietro Attilio; Brengman, J; Engel, Ag; Sine, S. m.
The changing tree in Parkinson's disease
2015 Calabresi, Paolo; Di Filippo, M.
Hyperkinetic disorders and loss of synaptic downscaling
2016 Calabresi, Paolo; Pisani, A.; Rothwell, J.; Ghiglieri, V.; Obeso, J. A.; Picconi, B.
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
2014 Johnson, Jo; Pioro, Ep; Boehringer, A; Chia, R; Feit, H; Renton, Ae; Pliner, Ha; Abramzon, Y; Marangi, Giuseppe; Winborn, Bj; Gibbs, Jr; Nalls, Ma; Morgan, S; Shoai, M; Hardy, J; Pittman, A; Orrell, Rw; Malaspina, A; Sidle, Kc; Fratta, P; Harms, Mb; Baloh, Rh; Pestronk, A; Weihl, Cc; Rogaeva, E; Zinman, L; Drory, Ve; Borghero, G; Mora, G; Calvo, A; Rothstein, Jd; Drepper, C; Sendtner, M; Singleton, Ab; Taylor, Jp; Cookson, Mr; Restagno, G; Sabatelli, Mario; Bowser, R; Chiò, A; Traynor, Bj; Conte, Amelia; Luigetti, Marco; Zollino, Marcella; Lattante, Serena
A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability
2007 Zalfa, Francesca; Eleuteri, Boris; S Dickson, Kirsten; Mercaldo, Valentina; De Rubeis, Silvia; di Penta, Alessandra; Tabolacci, Elisabetta; Chiurazzi, Pietro; Neri, Giovanni; N Grant, Seth G; Bagni, Claudia
| Data di pubblicazione | Titolo | Autore(i) | File |
|---|---|---|---|
| 1-gen-1999 | Acetylcholine receptor M3 domain: stereochemical and volume contribution to channel gating | Wang, Hl; Milone, M; Ohno, K; Shen, Xm; Tsujino, A; Batocchi, Anna Paola; Tonali, Pietro Attilio; Brengman, J; Engel, Ag; Sine, S. m. | |
| 1-gen-2015 | The changing tree in Parkinson's disease | Calabresi, Paolo; Di Filippo, M. | |
| 1-gen-2016 | Hyperkinetic disorders and loss of synaptic downscaling | Calabresi, Paolo; Pisani, A.; Rothwell, J.; Ghiglieri, V.; Obeso, J. A.; Picconi, B. | |
| 1-gen-2014 | Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis | Johnson, Jo; Pioro, Ep; Boehringer, A; Chia, R; Feit, H; Renton, Ae; Pliner, Ha; Abramzon, Y; Marangi, Giuseppe; Winborn, Bj; Gibbs, Jr; Nalls, Ma; Morgan, S; Shoai, M; Hardy, J; Pittman, A; Orrell, Rw; Malaspina, A; Sidle, Kc; Fratta, P; Harms, Mb; Baloh, Rh; Pestronk, A; Weihl, Cc; Rogaeva, E; Zinman, L; Drory, Ve; Borghero, G; Mora, G; Calvo, A; Rothstein, Jd; Drepper, C; Sendtner, M; Singleton, Ab; Taylor, Jp; Cookson, Mr; Restagno, G; Sabatelli, Mario; Bowser, R; Chiò, A; Traynor, Bj; Conte, Amelia; Luigetti, Marco; Zollino, Marcella; Lattante, Serena | |
| 1-gen-2007 | A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability | Zalfa, Francesca; Eleuteri, Boris; S Dickson, Kirsten; Mercaldo, Valentina; De Rubeis, Silvia; di Penta, Alessandra; Tabolacci, Elisabetta; Chiurazzi, Pietro; Neri, Giovanni; N Grant, Seth G; Bagni, Claudia |
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