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Identification of genetic factors for alachlor tolerance in maize by molecular markers analysis 1-gen-1996 Sarigorla, M; Rampoldi, L; Binelli, G; Frova, C; Pe, Me
Fine mapping of five human skeletal muscle genes: Alpha-tropomyosin, beta-tropomyosin, troponin-I slow-twitch, troponin-I fast-twitch, and troponin-c fast RID E-2182-2011 1-gen-1997 Tiso, N; Rampoldi, L; Pallavicini, A; Zimbello, R; Pandolfo, D; Valle, G; Lanfranchi, G; Danieli, Ga
Chromosomal localization of four MAPK signaling cascade genes: MEK1, MEK3, MEK4 and MEKK5 RID G-8211-2011 RID E-2182-2011 1-gen-1997 Rampoldi, L; Zimbello, R; Bortoluzzi, S; Tiso, N; Valle, G; Lanfranchi, G; Danieli, Ga
The preliminary transcript map of a human skeletal muscle RID E-2182-2011 RID G-8211-2011 1-gen-1997 Pallavicini, A; Zimbello, R; Tiso, N; Muraro, T; Rampoldi, L; Bortoluzzi, S; Valle, G; Lanfranchi, G; Danieli, Ga
A comprehensive, high-resolution genomic transcript map of human skeletal muscle RID G-8211-2011 RID E-7037-2010 RID E-2182-2011 1-gen-1998 Bortoluzzi, S; Rampoldi, L; Simionati, B; Zimbello, R; Barbon, A; D'Alessi, F; Tiso, N; Pallavicini, A; Toppo, S; Cannata, N; Valle, G; Lanfranchi, C; Danieli, Ga
Hereditary spastic paraplegia associated with peripheral neuropathy: a distinct clinical and genetic entity 1-gen-2000 Mostacciuolo, Ml; Rampoldi, L; Righetti, E; Vazza, G; Schiavon, F; Angelini, C
Identification and characterisation of the gene for chorea-acanthocytosis 1-gen-2001 Rampoldi, L; Dobson-Stone, C; Rubio, Jp; Danek, A; Nemeth, Ah; Monaco, Ap
A conserved sorting-associated protein is mutant in chorea-acanthocytosis RID C-2505-2009 RID A-4495-2010 1-gen-2001 Rampoldi, L; Dobson-Stone, C; Rubio, Jp; Danek, A; Chalmers, Rm; Wood, Nw; Verellen, C; Ferrer, X; Malandrini, A; Fabrizi, Gm; Brown, R; Vance, J; Pericak-Vance, M; Rudolf, G; Carre, S; Alonso, E; Manfredi, M; Nemeth, Ah; Monaco, Ap
McLeod neuroacanthocytosis: Genotype and phenotype 1-gen-2001 Danek, A; Rubio, Jp; Rampoldi, L; Ho, Mf; Dobson-Stone, C; Tison, F; Symmans, Wa; Oechsner, M; Kalckreuth, W; Watt, Jm; Corbett, Aj; Hamdalla, Hhm; Marshall, Ag; Sutton, I; Dotti, Mt; Malandrini, A; Walker, Rh; Daniels, G; Monaco, Ap
Chorea-Acanthocytosis 1-gen-2002 Dobson-Stone, C; Rampoldi, L; Bader, B; Velayos Baeza, A; Walker, Rh; Danek, A; Monaco, Ap
Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis 1-gen-2002 Dobson-Stone, C.; Danek, A.; Rampoldi, L.; Hardie, R. J.; Chalmers, R. M.; Wood, N. W.; Bohlega, S.; Dotti, M. T.; Federico, A.; Shizuka, M.; Tanaka, M.; Watanabe, M.; Ikeda, Y.; Brin, M.; Goldfarb, L. G.; Karp, B. I.; Mohiddin, S.; Fananapazir, L.; Storch, A.; Fryer, A. E.; Maddison, P.; Sibon, I.; Trevisol-Bittencourt, P. C.; Singer, C.; Caballero, I. R.; Aasly, J. O.; Schmierer, K.; Dengler, R.; Hiersemenzel, L. -P.; Zeviani, M.; Meiner, V.; Lossos, A.; Johnson, S.; Mercado, F. C.; Sorretino, G.; Dupre, N.; Rouleau, G. A.; Volkmann, J.; Arpa, J.; Lees, A.; Geraud, G.; Chouinard, S.; Nemeth, A.; Monaco, A. P.
Clinical features and molecular bases of neuroacanthocytosis 1-gen-2002 Rampoldi, L; Danek, A; Monaco, Ap
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha 2 subunit associated with familial hemiplegic migraine type 2 1-gen-2003 De Fusco, M; Marconi, R; Silvestri, L; Atorino, L; Rampoldi, L; Morgante, L; Ballabio, A; Aridon, P; Casari, GIORGIO NEVIO
A reduced activity of the Na-K ATPase is responsible for familial hemiplegic migraine 1-gen-2003 Casari, G; De Fusco, M; Aridon, P; Silvestri, L; Atorino, L; Rampoldi, L; Ballabio, A; Marconi, R
Mutations of UMOD in the tubulo-interstitial diseases MCKD and FJHN associate with intracellular aggregates and excretion reduction of uromodulin 1-gen-2003 Rampoldi, L; Caridi, G; Boaretto, F; Bernascone, I; Santon, D; Lamorte, G; Tardanico, R; Colussi, G; Scolari, F; Amoroso, A; Ghiggeri, G; Casan, G
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics 1-gen-2003 Rampoldi, L; Caridi, G; Santon, D; Boaretto, F; Bernascone, I; Lamorte, G; Tardanico, R; Dagnino, M; Colussi, G; Scolari, F; Ghiggeri, Gm; Amoroso, A; Casari, GIORGIO NEVIO
Chorea-acanthocytosis: Clinical and genetic findings in three families from the Arabian peninsula 1-gen-2003 Bohlega, S; Al-Jishi, A; Dobson-Stone, C; Rampoldi, L; Saha, P; Murad, H; Kareem, A; Roberts, G; Monaco, Ap
Towards the identification of (a) gene(s) for autosomal dominant medullary cystic kidney disease 1-gen-2003 Scolari, F; Viola, Bf; Ghiggeri, Gm; Caridi, G; Amoroso, A; Rampoldi, L; Casari, GIORGIO NEVIO
Genetics of hypercalciuria and calcium nephrolithiasis: from the rare monogenic to the common polygenic forms 1-gen-2004 Gambaro, G; Vezzoli, G; Casari, G; Rampoldi, L; D’Angelo, A; Borghi, L
Functional consequences of a novel uromodulin mutation in a family with familial juvenile hyperuricaemic nephropathy 1-gen-2004 Tinschert, S; Ruf, N; Bernascone, I; Sacherer, K; Lamorte, G; Neumayer, Hh; Nurnberg, P; Luft, Fc; Rampoldi, L
Mostrati risultati da 1 a 20 di 84
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