Sfoglia per Titolo
NK1 Receptor Antagonists as a New Treatment for Corneal Neovascularization
2014-01-01 Bignami, F; Giacomini, C; Lorusso, A; Aramini, A; Rama, P; Ferrari, G
NKp46-expressing human gut-resident intraepithelial Vδ1 T cell subpopulation exhibits high anti-tumor activity against colorectal cancer
2019-01-01 Mikulak, Joanna; Oriolo, Ferdinando; Bruni, Elena; Roberto, Alessandra; Colombo, Federico S; Villa, Anna; Bosticardo, Marita; Bortolomai, Ileana; Lo Presti, Elena; Meraviglia, Serena; Dieli, Francesco; Vetrano, Stefania; Danese, Silvio; Della Bella, Silvia; Carvello, Michele M; Sacchi, Matteo; Cugini, Giovanni; Colombo, Giovanni; Klinger, Marco; Spaggiari, Paola; Roncalli, Massimo; Prinz, Immo; Ravens, Sarina; di Lorenzo, Biagio; Marcenaro, Emanuela; Silva-Santos, Bruno; Spinelli, Antonino; Mavilio, Domenico
Nkx2-5+/Islet1+ mesenchymal progenitors generate distinct spleen stromal cell subsets and participate in restoring stromal network integrity
2013-01-01 Castagnaro, L; Lenti, E; Spinardi, L; Maruzzelli, S; Migliori, E; Farinello, D; Sitia, G; Harrelson, Z; Evans, S; Guidotti, Luca; Harvey, Rp; Brendolan, A.
NLRP1 influences the systemic sclerosis phenotype: a new clue for the contribution of innate immunity in systemic sclerosis-related fibrosing alveolitis pathogenesis
2011-01-01 Dieudé, P; Guedj, M; Wipff, J; Ruiz, B; Riemekasten, G; Airo, P; Melchers, I; Hachulla, E; MATUCCI CERINIC, Marco; Diot, E; Hunzelmann, N; Caramaschi, P; Sibilia, J; Tiev, K; Mouthon, L; Riccieri, V; Cracowski, Jl; Carpentier, Ph; Distler, J; Amoura, Z; Tarner, I; Avouac, J; Meyer, O; Kahan, A; Boileau, C; Allanore, Y.
NMO spectrum disorder and optic neuritis: are VEPs useful?
2010-01-01 Straffi, L.; Radaelli, M.; Bianco, M.; Gonzalez-Rosa, J. J.; Moiola, L.; Dalla Libera, D.; Rodegher, M.; Martinelli, V.; Comi, G.; Leocani, L.
NMO Spectrum Disorder: The Importance of NMO-IgG in Clinical Practice
2011-01-01 Radaelli, M; Martinelli, V; Esposito, F; Moiola, L; Dalla Libera, D; Privitera, D; Furlan, R; Fazio, R; Comi, G
NMR spectroscopic analysis of the DNA conformation induced by the human testis determining factor SRY
1995-01-01 Werner, M H; Bianchi, M E; Gronenborn, A M; Clore, G M
NMR-Based Metabolomic Approach Tracks Potential Serum Biomarkers of Disease Progression in Patients with Type 2 Diabetes Mellitus
2019-01-01 Del Coco, Laura; Vergara, Daniele; De Matteis, Serena; Mensà, Emanuela; Sabbatinelli, Jacopo; Prattichizzo, Francesco; Bonfigli, Anna Rita; Storci, Gianluca; Bravaccini, Sara; Pirini, Francesca; Ragusa, Andrea; Casadei-Gardini, Andrea; Bonafè, Massimiliano; Maffia, Michele; Fanizzi, Francesco Paolo; Olivieri, Fabiola; Giudetti, Anna Maria
No association between eating disorders, obsessive-compulsive disorder and 1438G/A 5-HT2A promoter polymorphism in an Italian population.
2000-01-01 Di Bella, D; Cavallini, Mc; Riboldi, C; Manzato, M; Bellodi, Laura
No association between obsessive-compulsive disorder and the 5-HT1D beta receptor gene
2002-01-01 Di Bella, D; Cavallini, Mc; Bellodi, Laura
No association between polyomaviruses and primary central nervous system lymphomas of HIV-seronegative and HIV-positive patients.
2004-01-01 Martini, F; Dolcetti, R; Ferreri, Aj; Ponzoni, Maurilio; Fumagalli, L; Reni, M; Terreni, Mr; Mariuzzi, L; Tognon, M.
No beta cell desensitisation after a median of 68 months on glibenclamide therapy in patients with KCNJ11-associated permanent neonatal diabetes
2011-01-01 Iafusco, D; Bizzarri, C; Cadario, F; Pesavento, R; Tonini, G; Tumini, S; Cauvin, V; Colombo, C; Bonfanti, R; Barbetti, F
No changes in plasma insulin and cortisol during ANF infusion in essential hypertension
1989-01-01 Tonolo, G; Manunta, Paolo; Richards, Am; Soro, A; Madeddu, P; Maioli, M; Glorioso, N.
No difference in penetrance between truncating and missense/aberrant splicing pathogenic variants in mlh1 and msh2: A prospective lynch syndrome database study
2021-01-01 Dominguez-Valentin, M.; Plazzer, J. -P.; Sampson, J. R.; Engel, C.; Aretz, S.; Jenkins, M. A.; Sunde, L.; Bernstein, I.; Capella, G.; Balaguer, F.; Macrae, F.; Winship, I. M.; Thomas, H.; Evans, D. G.; Burn, J.; Greenblatt, M.; de Vos tot Nederveen Cappel, W. H.; Sijmons, R. H.; Nielsen, M.; Bertario, L.; Bonanni, B.; Tibiletti, M. G.; Cavestro, G. M.; Lindblom, A.; Della Valle, A.; Lopez-Kostner, F.; Alvarez, K.; Gluck, N.; Katz, L.; Heinimann, K.; Vaccaro, C. A.; Nakken, S.; Hovig, E.; Green, K.; Lalloo, F.; Hill, J.; Vasen, H. F. A.; Perne, C.; Buttner, R.; Gorgens, H.; Holinski-Feder, E.; Morak, M.; Holzapfel, S.; Huneburg, R.; Doeberitz, M. V. K.; Loeffler, M.; Rahner, N.; Weitz, J.; Steinke-Lange, V.; Schmiegel, W.; Vangala, D.; Crosbie, E. J.; Pineda, M.; Navarro, M.; Brunet, J.; Moreira, L.; Sanchez, A.; Serra-Burriel, M.; Mints, M.; Kariv, R.; Rosner, G.; Pinero, T. A.; Pavicic, W. H.; Kalfayan, P.; Ten Broeke, S. W.; Mecklin, J. -P.; Pylvanainen, K.; Renkonen-Sinisalo, L.; Lepisto, A.; Peltomaki, P.; Hopper, J. L.; Win, A. K.; Buchanan, D. D.; Lindor, N. M.; Gallinger, S.; Marchand, L. L.; Newcomb, P. A.; Figueiredo, J. C.; Thibodeau, S. N.; Therkildsen, C.; Hansen, T. V. O.; Lindberg, L.; Rodland, E. A.; Neffa, F.; Esperon, P.; Tjandra, D.; Moslein, G.; Seppala, T. T.; Moller, P.
No evidence for association and linkage disequilibrium between dyslexia and markers of four dopamine-related genes
2003-01-01 Marino, C; Giorda, R; Vanzin, L; Molteni, M; Lorusso, Ml; Nobile, M; Baschirotto, C; Alda, M; Battaglia, MARCO MARIA
No evidence for cell-to-cell transmission of the unfolded protein response in cell culture
2020-01-01 van Ziel, Am; Wolzak, K; Nolle, A; Hoetjes, Pj; Berenjeno-Correa, E; van Anken, E; Struys, Ea; Scheper, W
No evidence for genetically determined alteration in insulin secretion or sensitivity predisposing the type 1 diabetes - A study of identical twins
2005-01-01 Hawa, Mi; Castelli, Md; Bonfanti, R; Beyan, H; Valeri, C; Leslie, Rdg
No evidence of ATP142 involvment in 12 multiplex italian families with benign familial infantile seizures
2005-01-01 MARTINELLI BONESCHI, F; Aridon, P; Zara, F; Guerrini, R; Marini, C; DE FUSCO, M; Comi, Giancarlo; Casari, GIORGIO NEVIO
No evidence of ATP1A2 involvement in 12 multiplex Italian families with benign familial infantile seizures
2005-01-01 Boneschi, Fm; Aridon, P; Zara, F; Guerrini, R; Marini, C; De Fusco, M; Comi, G; Casari, G
No evidence of cortical lesions in migraine patients: a study with double inversin recovery sequence.
2011-01-01 Absinta, M; Rocca, Ma; Colombo, B; Defeo, D; Falini, A; Comi, G; Filippi, Massimo
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| NK1 Receptor Antagonists as a New Treatment for Corneal Neovascularization | 1-gen-2014 | Bignami, F; Giacomini, C; Lorusso, A; Aramini, A; Rama, P; Ferrari, G | |
| NKp46-expressing human gut-resident intraepithelial Vδ1 T cell subpopulation exhibits high anti-tumor activity against colorectal cancer | 1-gen-2019 | Mikulak, Joanna; Oriolo, Ferdinando; Bruni, Elena; Roberto, Alessandra; Colombo, Federico S; Villa, Anna; Bosticardo, Marita; Bortolomai, Ileana; Lo Presti, Elena; Meraviglia, Serena; Dieli, Francesco; Vetrano, Stefania; Danese, Silvio; Della Bella, Silvia; Carvello, Michele M; Sacchi, Matteo; Cugini, Giovanni; Colombo, Giovanni; Klinger, Marco; Spaggiari, Paola; Roncalli, Massimo; Prinz, Immo; Ravens, Sarina; di Lorenzo, Biagio; Marcenaro, Emanuela; Silva-Santos, Bruno; Spinelli, Antonino; Mavilio, Domenico | |
| Nkx2-5+/Islet1+ mesenchymal progenitors generate distinct spleen stromal cell subsets and participate in restoring stromal network integrity | 1-gen-2013 | Castagnaro, L; Lenti, E; Spinardi, L; Maruzzelli, S; Migliori, E; Farinello, D; Sitia, G; Harrelson, Z; Evans, S; Guidotti, Luca; Harvey, Rp; Brendolan, A. | |
| NLRP1 influences the systemic sclerosis phenotype: a new clue for the contribution of innate immunity in systemic sclerosis-related fibrosing alveolitis pathogenesis | 1-gen-2011 | Dieudé, P; Guedj, M; Wipff, J; Ruiz, B; Riemekasten, G; Airo, P; Melchers, I; Hachulla, E; MATUCCI CERINIC, Marco; Diot, E; Hunzelmann, N; Caramaschi, P; Sibilia, J; Tiev, K; Mouthon, L; Riccieri, V; Cracowski, Jl; Carpentier, Ph; Distler, J; Amoura, Z; Tarner, I; Avouac, J; Meyer, O; Kahan, A; Boileau, C; Allanore, Y. | |
| NMO spectrum disorder and optic neuritis: are VEPs useful? | 1-gen-2010 | Straffi, L.; Radaelli, M.; Bianco, M.; Gonzalez-Rosa, J. J.; Moiola, L.; Dalla Libera, D.; Rodegher, M.; Martinelli, V.; Comi, G.; Leocani, L. | |
| NMO Spectrum Disorder: The Importance of NMO-IgG in Clinical Practice | 1-gen-2011 | Radaelli, M; Martinelli, V; Esposito, F; Moiola, L; Dalla Libera, D; Privitera, D; Furlan, R; Fazio, R; Comi, G | |
| NMR spectroscopic analysis of the DNA conformation induced by the human testis determining factor SRY | 1-gen-1995 | Werner, M H; Bianchi, M E; Gronenborn, A M; Clore, G M | |
| NMR-Based Metabolomic Approach Tracks Potential Serum Biomarkers of Disease Progression in Patients with Type 2 Diabetes Mellitus | 1-gen-2019 | Del Coco, Laura; Vergara, Daniele; De Matteis, Serena; Mensà, Emanuela; Sabbatinelli, Jacopo; Prattichizzo, Francesco; Bonfigli, Anna Rita; Storci, Gianluca; Bravaccini, Sara; Pirini, Francesca; Ragusa, Andrea; Casadei-Gardini, Andrea; Bonafè, Massimiliano; Maffia, Michele; Fanizzi, Francesco Paolo; Olivieri, Fabiola; Giudetti, Anna Maria | |
| No association between eating disorders, obsessive-compulsive disorder and 1438G/A 5-HT2A promoter polymorphism in an Italian population. | 1-gen-2000 | Di Bella, D; Cavallini, Mc; Riboldi, C; Manzato, M; Bellodi, Laura | |
| No association between obsessive-compulsive disorder and the 5-HT1D beta receptor gene | 1-gen-2002 | Di Bella, D; Cavallini, Mc; Bellodi, Laura | |
| No association between polyomaviruses and primary central nervous system lymphomas of HIV-seronegative and HIV-positive patients. | 1-gen-2004 | Martini, F; Dolcetti, R; Ferreri, Aj; Ponzoni, Maurilio; Fumagalli, L; Reni, M; Terreni, Mr; Mariuzzi, L; Tognon, M. | |
| No beta cell desensitisation after a median of 68 months on glibenclamide therapy in patients with KCNJ11-associated permanent neonatal diabetes | 1-gen-2011 | Iafusco, D; Bizzarri, C; Cadario, F; Pesavento, R; Tonini, G; Tumini, S; Cauvin, V; Colombo, C; Bonfanti, R; Barbetti, F | |
| No changes in plasma insulin and cortisol during ANF infusion in essential hypertension | 1-gen-1989 | Tonolo, G; Manunta, Paolo; Richards, Am; Soro, A; Madeddu, P; Maioli, M; Glorioso, N. | |
| No difference in penetrance between truncating and missense/aberrant splicing pathogenic variants in mlh1 and msh2: A prospective lynch syndrome database study | 1-gen-2021 | Dominguez-Valentin, M.; Plazzer, J. -P.; Sampson, J. R.; Engel, C.; Aretz, S.; Jenkins, M. A.; Sunde, L.; Bernstein, I.; Capella, G.; Balaguer, F.; Macrae, F.; Winship, I. M.; Thomas, H.; Evans, D. G.; Burn, J.; Greenblatt, M.; de Vos tot Nederveen Cappel, W. H.; Sijmons, R. H.; Nielsen, M.; Bertario, L.; Bonanni, B.; Tibiletti, M. G.; Cavestro, G. M.; Lindblom, A.; Della Valle, A.; Lopez-Kostner, F.; Alvarez, K.; Gluck, N.; Katz, L.; Heinimann, K.; Vaccaro, C. A.; Nakken, S.; Hovig, E.; Green, K.; Lalloo, F.; Hill, J.; Vasen, H. F. A.; Perne, C.; Buttner, R.; Gorgens, H.; Holinski-Feder, E.; Morak, M.; Holzapfel, S.; Huneburg, R.; Doeberitz, M. V. K.; Loeffler, M.; Rahner, N.; Weitz, J.; Steinke-Lange, V.; Schmiegel, W.; Vangala, D.; Crosbie, E. J.; Pineda, M.; Navarro, M.; Brunet, J.; Moreira, L.; Sanchez, A.; Serra-Burriel, M.; Mints, M.; Kariv, R.; Rosner, G.; Pinero, T. A.; Pavicic, W. H.; Kalfayan, P.; Ten Broeke, S. W.; Mecklin, J. -P.; Pylvanainen, K.; Renkonen-Sinisalo, L.; Lepisto, A.; Peltomaki, P.; Hopper, J. L.; Win, A. K.; Buchanan, D. D.; Lindor, N. M.; Gallinger, S.; Marchand, L. L.; Newcomb, P. A.; Figueiredo, J. C.; Thibodeau, S. N.; Therkildsen, C.; Hansen, T. V. O.; Lindberg, L.; Rodland, E. A.; Neffa, F.; Esperon, P.; Tjandra, D.; Moslein, G.; Seppala, T. T.; Moller, P. | |
| No evidence for association and linkage disequilibrium between dyslexia and markers of four dopamine-related genes | 1-gen-2003 | Marino, C; Giorda, R; Vanzin, L; Molteni, M; Lorusso, Ml; Nobile, M; Baschirotto, C; Alda, M; Battaglia, MARCO MARIA | |
| No evidence for cell-to-cell transmission of the unfolded protein response in cell culture | 1-gen-2020 | van Ziel, Am; Wolzak, K; Nolle, A; Hoetjes, Pj; Berenjeno-Correa, E; van Anken, E; Struys, Ea; Scheper, W | |
| No evidence for genetically determined alteration in insulin secretion or sensitivity predisposing the type 1 diabetes - A study of identical twins | 1-gen-2005 | Hawa, Mi; Castelli, Md; Bonfanti, R; Beyan, H; Valeri, C; Leslie, Rdg | |
| No evidence of ATP142 involvment in 12 multiplex italian families with benign familial infantile seizures | 1-gen-2005 | MARTINELLI BONESCHI, F; Aridon, P; Zara, F; Guerrini, R; Marini, C; DE FUSCO, M; Comi, Giancarlo; Casari, GIORGIO NEVIO | |
| No evidence of ATP1A2 involvement in 12 multiplex Italian families with benign familial infantile seizures | 1-gen-2005 | Boneschi, Fm; Aridon, P; Zara, F; Guerrini, R; Marini, C; De Fusco, M; Comi, G; Casari, G | |
| No evidence of cortical lesions in migraine patients: a study with double inversin recovery sequence. | 1-gen-2011 | Absinta, M; Rocca, Ma; Colombo, B; Defeo, D; Falini, A; Comi, G; Filippi, Massimo |
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile