Sfoglia per Autore RAMPOLDI, LUCA
Identification of genetic factors for alachlor tolerance in maize by molecular markers analysis
1996-01-01 Sarigorla, M; Rampoldi, L; Binelli, G; Frova, C; Pe, Me
The preliminary transcript map of a human skeletal muscle RID E-2182-2011 RID G-8211-2011
1997-01-01 Pallavicini, A; Zimbello, R; Tiso, N; Muraro, T; Rampoldi, L; Bortoluzzi, S; Valle, G; Lanfranchi, G; Danieli, Ga
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
1997-01-01 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
1997-01-01 Rampoldi, L; Zimbello, R; Bortoluzzi, S; Tiso, N; 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
1998-01-01 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
2000-01-01 Mostacciuolo, Ml; Rampoldi, L; Righetti, E; Vazza, G; Schiavon, F; Angelini, C
McLeod neuroacanthocytosis: Genotype and phenotype
2001-01-01 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
Identification and characterisation of the gene for chorea-acanthocytosis
2001-01-01 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
2001-01-01 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
Chorea-Acanthocytosis
2002-01-01 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
2002-01-01 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
2002-01-01 Rampoldi, L; Danek, A; Monaco, Ap
Mutations of UMOD in the tubulo-interstitial diseases MCKD and FJHN associate with intracellular aggregates and excretion reduction of uromodulin
2003-01-01 Rampoldi, L; Caridi, G; Boaretto, F; Bernascone, I; Santon, D; Lamorte, G; Tardanico, R; Colussi, G; Scolari, F; Amoroso, A; Ghiggeri, G; Casan, G
Chorea-acanthocytosis: Clinical and genetic findings in three families from the Arabian peninsula
2003-01-01 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
2003-01-01 Scolari, F; Viola, Bf; Ghiggeri, Gm; Caridi, G; Amoroso, A; Rampoldi, L; Casari, GIORGIO NEVIO
A reduced activity of the Na-K ATPase is responsible for familial hemiplegic migraine
2003-01-01 Casari, G; De Fusco, M; Aridon, P; Silvestri, L; Atorino, L; Rampoldi, L; Ballabio, A; Marconi, R
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics
2003-01-01 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
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha 2 subunit associated with familial hemiplegic migraine type 2
2003-01-01 De Fusco, M; Marconi, R; Silvestri, L; Atorino, L; Rampoldi, L; Morgante, L; Ballabio, A; Aridon, P; Casari, GIORGIO NEVIO
Functional consequences of a novel uromodulin mutation in a family with familial juvenile hyperuricaemic nephropathy
2004-01-01 Tinschert, S; Ruf, N; Bernascone, I; Sacherer, K; Lamorte, G; Neumayer, Hh; Nurnberg, P; Luft, Fc; Rampoldi, L
Uromodulin storage diseases: Clinical aspects and mechanisms
2004-01-01 Scolari, F; Caridi, G; Rampoldi, L; Tardanico, R; Izzi, C; Pirulli, D; Amoroso, A; Casari, GIORGIO NEVIO; Ghiggeri, Gm
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
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 | |
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 | |
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 | |
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 | |
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 | |
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 | |
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 | |
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 | |
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 | |
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 | |
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 | |
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 | |
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 | |
Uromodulin storage diseases: Clinical aspects and mechanisms | 1-gen-2004 | Scolari, F; Caridi, G; Rampoldi, L; Tardanico, R; Izzi, C; Pirulli, D; Amoroso, A; Casari, GIORGIO NEVIO; Ghiggeri, Gm |
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