Sfoglia per Autore
Platelet glycohydrolase activities: characterization and release
1995-03-01 Emiliani, C; Martino, S; Orlacchio, A; Vezza, R; Nenci, G; Gresele, P
On the identification of two beta-D-mannosidase forms in human kidney and urine
1996-01-01 Ricard, B; Emiliani, C; Orlacchio, A; Foglietti, M; Bernard, M
Purification and properties of human urinary beta-D-mannosidase
1996-03-07 Guadalupi, R; Bernard, M; Orlacchio, A; Foglietti, M; Emiliani, C
Hexosaminidase in Trichinella spiralis is a single protein with alpha- and beta-subunits catalytic activities
1997-09-01 Costanzi, E; Beccari, T; Della Fazia, M; Servillo, G; Orlacchio, A; Tassi, C; Bruschi, F
Constitutive expression of beta-N-acetylhexosaminidase in a microglial cell line: transcriptional modulation by lipopolysaccharide and serum factors
1997-10-01 Beccari, T; Orlacchio, A; Costanzi, E; Grazia Appolloni, M; Laurenzi, Ar; Bocchini, V
Activity levels of a beta1,6 N-acetylglucosaminyltransferase in lymphomonocytes from multiple sclerosis patients
1997-10-22 Orlacchio, A; Sarchielli, P; Gallai, V; Datti, A; Saccardi, C; Palmerini, C
Cytokine secretion and nitric oxide production by mononuclear cells of patients with multiple sclerosis
1997-12-01 Sarchielli, P; Orlacchio, A; Vicinanza, F; Pelliccioli, G; Tognoloni, M; Saccardi, C; Gallai, V
1H-MRS in patients with multiple sclerosis undergoing treatment with interferon beta-1a: results of a preliminary study
1998-02-01 Sarchielli, P; Presciutti, O; Tarducci, R; Gobbi, G; Alberti, A; Pelliccioli, G; Orlacchio, A; Gallai, V
Absence of association between Alzheimer disease and the -491 regulatory region polymorphism of APOE
1998-07-10 Song, Y; Rogaeva, E; Premkumar, S; Brindle, N; Kawarai, T; Orlacchio, A; Yu, G; Levesque, G; Nishimura, M; Ikeda, M; Pei, Y; O'Toole, C; Duara, R; Barker, W; Sorbi, S; Freedman, M; Farrer, L; St George Hyslop, P
Beta-N-acetylhexosaminidase in peripheral blood lymphocytes and monocytes in the different forms and stages of multiple sclerosis
1998-09-01 Orlacchio, A; Martino, S; Sarchielli, P; Gallai, V; Emiliani, C
Promoter characterization and structure of the gene encoding mouse lysosomal alpha-d-mannosidase
1998-11-01 Stinchi, S; Orlacchio, A; Costanzi, E; Stirling, J; Menghini, A; Orlacchio, A; Beccari, T
An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease
1999-05-01 Rogaeva, E; Premkumar, S; Grubber, J; Serneels, L; Scott, W; Kawarai, T; Song, Y; Hill, D; Abou Donia, S; Martin, E; Vance, J; Yu, G; Orlacchio, A; Pei, Y; Nishimura, M; Supala, A; Roberge, B; Saunders, A; Roses, A; Schmechel, D; Crane Gatherum, A; Sorbi, S; Bruni, A; Small, G; Conneally, P; Haines, J; Van Leuven, F; St George Hyslop, P; Farrer, L; Pericak Vance, M
Elevated beta-N-acetylhexosaminidase activity in focal dystonia fibroblasts
1999-10-01 Costanzi, E; Beccari, T; Tassi, C; Orlacchio, A; Rossi, A
Platelets release their lysosomal content in vivo in humans upon activation
2000-01-01 Ciferri, S; Emiliani, C; Guglielmini, G; Orlacchio, A; Nenci, G; Gresele, P
Absence of linkage between familial amyotrophic lateral sclerosis and copper chaperone for the superoxide dismutase gene locus in two Italian pedigrees
2000-05-12 Orlacchio, A; Kawarai, T; Massaro, A; St George Hyslop, P; Sorbi, S
Lack of SOD1 gene mutations and activity alterations in two Italian families with amyotrophic lateral sclerosis
2000-08-11 Gestri, D; Cecchi, C; Tedde, A; Latorraca, S; Orlacchio, A; Grassi, E; Massaro, A; Liguri, G; St George Hyslop, P; Sorbi, S
Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer disease
2000-10-01 Devi, G; Fotiou, A; Jyrinji, D; Tycko, B; Dearmand, S; Rogaeva, E; Song, Y; Medieros, H; Liang, Y; Orlacchio, A; Williamson, J; St George Hyslop, P; Mayeux, R
beta-hexosaminidase, alpha-D-mannosidase, and beta-mannosidase expression in serum from patients with carbohydrate-deficient glycoprotein syndrome type I
2000-12-01 Beccari, T; Mancuso, F; Costanzi, E; Tassi, C; Barone, R; Fiumara, A; Orlacchio, A; Aisa, M; Orlacchio, A
Alpha2-macroglobulin polymorphisms in Italian sporadic and familial Alzheimer's disease
2001-02-16 Nacmias, B; Tedde, A; Cellini, E; Forleo, P; Orlacchio, A; Guarnieri, B; Petruzzi, C; D'Andrea, F; Serio, A; Sorbi, S
Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease
2001-10-01 Nicolaou, M; Song, Y; Sato, C; Orlacchio, A; Kawarai, T; Medeiros, H; Liang, Y; Sorbi, S; Richard, E; Rogaev, E; Moliaka, Y; Bruni, A; Jorge, R; Percy, M; Duara, R; Farrer, L; St Georg Hyslop, P; Rogaeva, E
Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
---|---|---|---|---|
1-mar-1995 | Platelet glycohydrolase activities: characterization and release | Emiliani, C; Martino, S; Orlacchio, A; Vezza, R; Nenci, G; Gresele, P | Articolo su rivista | |
1-gen-1996 | On the identification of two beta-D-mannosidase forms in human kidney and urine | Ricard, B; Emiliani, C; Orlacchio, A; Foglietti, M; Bernard, M | Articolo su rivista | |
7-mar-1996 | Purification and properties of human urinary beta-D-mannosidase | Guadalupi, R; Bernard, M; Orlacchio, A; Foglietti, M; Emiliani, C | Articolo su rivista | |
1-set-1997 | Hexosaminidase in Trichinella spiralis is a single protein with alpha- and beta-subunits catalytic activities | Costanzi, E; Beccari, T; Della Fazia, M; Servillo, G; Orlacchio, A; Tassi, C; Bruschi, F | Articolo su rivista | |
1-ott-1997 | Constitutive expression of beta-N-acetylhexosaminidase in a microglial cell line: transcriptional modulation by lipopolysaccharide and serum factors | Beccari, T; Orlacchio, A; Costanzi, E; Grazia Appolloni, M; Laurenzi, Ar; Bocchini, V | Articolo su rivista | |
22-ott-1997 | Activity levels of a beta1,6 N-acetylglucosaminyltransferase in lymphomonocytes from multiple sclerosis patients | Orlacchio, A; Sarchielli, P; Gallai, V; Datti, A; Saccardi, C; Palmerini, C | Articolo su rivista | |
1-dic-1997 | Cytokine secretion and nitric oxide production by mononuclear cells of patients with multiple sclerosis | Sarchielli, P; Orlacchio, A; Vicinanza, F; Pelliccioli, G; Tognoloni, M; Saccardi, C; Gallai, V | Articolo su rivista | |
1-feb-1998 | 1H-MRS in patients with multiple sclerosis undergoing treatment with interferon beta-1a: results of a preliminary study | Sarchielli, P; Presciutti, O; Tarducci, R; Gobbi, G; Alberti, A; Pelliccioli, G; Orlacchio, A; Gallai, V | Articolo su rivista | |
10-lug-1998 | Absence of association between Alzheimer disease and the -491 regulatory region polymorphism of APOE | Song, Y; Rogaeva, E; Premkumar, S; Brindle, N; Kawarai, T; Orlacchio, A; Yu, G; Levesque, G; Nishimura, M; Ikeda, M; Pei, Y; O'Toole, C; Duara, R; Barker, W; Sorbi, S; Freedman, M; Farrer, L; St George Hyslop, P | Articolo su rivista | |
1-set-1998 | Beta-N-acetylhexosaminidase in peripheral blood lymphocytes and monocytes in the different forms and stages of multiple sclerosis | Orlacchio, A; Martino, S; Sarchielli, P; Gallai, V; Emiliani, C | Articolo su rivista | |
1-nov-1998 | Promoter characterization and structure of the gene encoding mouse lysosomal alpha-d-mannosidase | Stinchi, S; Orlacchio, A; Costanzi, E; Stirling, J; Menghini, A; Orlacchio, A; Beccari, T | Articolo su rivista | |
1-mag-1999 | An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease | Rogaeva, E; Premkumar, S; Grubber, J; Serneels, L; Scott, W; Kawarai, T; Song, Y; Hill, D; Abou Donia, S; Martin, E; Vance, J; Yu, G; Orlacchio, A; Pei, Y; Nishimura, M; Supala, A; Roberge, B; Saunders, A; Roses, A; Schmechel, D; Crane Gatherum, A; Sorbi, S; Bruni, A; Small, G; Conneally, P; Haines, J; Van Leuven, F; St George Hyslop, P; Farrer, L; Pericak Vance, M | Articolo su rivista | |
1-ott-1999 | Elevated beta-N-acetylhexosaminidase activity in focal dystonia fibroblasts | Costanzi, E; Beccari, T; Tassi, C; Orlacchio, A; Rossi, A | Articolo su rivista | |
1-gen-2000 | Platelets release their lysosomal content in vivo in humans upon activation | Ciferri, S; Emiliani, C; Guglielmini, G; Orlacchio, A; Nenci, G; Gresele, P | Articolo su rivista | |
12-mag-2000 | Absence of linkage between familial amyotrophic lateral sclerosis and copper chaperone for the superoxide dismutase gene locus in two Italian pedigrees | Orlacchio, A; Kawarai, T; Massaro, A; St George Hyslop, P; Sorbi, S | Articolo su rivista | |
11-ago-2000 | Lack of SOD1 gene mutations and activity alterations in two Italian families with amyotrophic lateral sclerosis | Gestri, D; Cecchi, C; Tedde, A; Latorraca, S; Orlacchio, A; Grassi, E; Massaro, A; Liguri, G; St George Hyslop, P; Sorbi, S | Articolo su rivista | |
1-ott-2000 | Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer disease | Devi, G; Fotiou, A; Jyrinji, D; Tycko, B; Dearmand, S; Rogaeva, E; Song, Y; Medieros, H; Liang, Y; Orlacchio, A; Williamson, J; St George Hyslop, P; Mayeux, R | Articolo su rivista | |
1-dic-2000 | beta-hexosaminidase, alpha-D-mannosidase, and beta-mannosidase expression in serum from patients with carbohydrate-deficient glycoprotein syndrome type I | Beccari, T; Mancuso, F; Costanzi, E; Tassi, C; Barone, R; Fiumara, A; Orlacchio, A; Aisa, M; Orlacchio, A | Articolo su rivista | |
16-feb-2001 | Alpha2-macroglobulin polymorphisms in Italian sporadic and familial Alzheimer's disease | Nacmias, B; Tedde, A; Cellini, E; Forleo, P; Orlacchio, A; Guarnieri, B; Petruzzi, C; D'Andrea, F; Serio, A; Sorbi, S | Articolo su rivista | |
1-ott-2001 | Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease | Nicolaou, M; Song, Y; Sato, C; Orlacchio, A; Kawarai, T; Medeiros, H; Liang, Y; Sorbi, S; Richard, E; Rogaev, E; Moliaka, Y; Bruni, A; Jorge, R; Percy, M; Duara, R; Farrer, L; St Georg Hyslop, P; Rogaeva, E | Articolo su rivista |
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