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A functional variant in ERAP1 predisposes to multiple sclerosis
2012-01-01 Guerini, Fr; Cagliani, R; Forni, D; Agliardi, C; Caputo, D; Cassinotti, A; Galimberti, D; Fenoglio, C; Biasin, M; Asselta, R; Scarpini, E; Comi, Gp; Bresolin, N; Clerici, M; Sironi, M
A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death
2024-01-01 Minnai, Francesca; Biscarini, Filippo; Esposito, Martina; Dragani, Tommaso A; Bujanda, Luis; Rahmouni, Souad; Alarcón-Riquelme, Marta E; Bernardo, David; Carnero-Montoro, Elena; Buti, Maria; Zeberg, Hugo; Asselta, Rosanna; Romero-Gómez, Manuel; Fernandez-Cadenas, Israel; Fallerini, Chiara; Zguro, Kristina; Croci, Susanna; Baldassarri, Margherita; Bruttini, Mirella; Furini, Simone; Renieri, Alessandra; Colombo, Francesca
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest.
2018-01-01 Samarani, M; Loberto, N; Solda, G; Straniero, L; Asselta, R; Duga, S; Lunghi, G; Zucca, Fa; Mauri, L; Ciampa, Mg; Schiumarini, D; Bassi, R; Giussani, P; Chiricozzi, E; Prinetti, A; Aureli, M; Sonnino, S.
A new biallelic polymorphism in intron 1 of the CHRNA4 gene may cause erroneous genotyping of a closely linked CA repeat marker
2000-01-01 Bonati, Mt; Duga, S; Asselta, R; Ferinistrambi, L; Oldani, A; Zucconi, M; Malcovati, M; Dalpra, L; Tenchini, Ml
A new exon in the 5’ untranslated region of bovine Connexin32 gene
1999-01-01 Duga, S.; Asselta, R.; Giacco, L. D.; Malcovati, M.; Ronchi, S.; Tenchini, M. L.; Simonic, T.
A new genetic mechanism for congenital afibrinogenemia: maternal uniparental isodisomy for chromosome 4 containing a 15-kb deletion in fibrinogen Aalpha-chain gene
2004-01-01 Duga, S; Spena, S; Asselta, R; Peyandi, F; Mahasandana, C; Malcovati, M; Mannucci, Pm; Tenchini, Ml
A novel 15-kb deletion involving fibrinogen Aalpha-chain gene causes congenital afibrinogenemia as a consequence of uniparental isodisomy of chromosome 4
2004-01-01 Spena, S; Asselta, R; Duga, S; Monaldini, L; Malcovati, M; Mannucci, Pm; Tenchini, Ml
A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing
2011-01-01 Robusto, M; Asselta, Rosanna; Primignani, P; Castorina, P; Benzoni, E; Cesarani, A; Ambrosetti, U; Duga, Stefano; Solda', Giulia
A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency
2007-01-01 Bozzao, C; Rimoldi, V; Asselta, R; Landau, M; Ghiotto, R; Tenchini, Ml; DE CRISTOFARO, R; Castaman, G; Duga, S
A novel in-frame deletion in the factor V C1 domain associated with severe coagulation factor V deficiency in a Korean family
2009-01-01 Song, J; Guella, I; Kwon, K. Y.; Cho, H; Park, R; Asselta, R; Choi, J. R.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A functional variant in ERAP1 predisposes to multiple sclerosis | 1-gen-2012 | Guerini, Fr; Cagliani, R; Forni, D; Agliardi, C; Caputo, D; Cassinotti, A; Galimberti, D; Fenoglio, C; Biasin, M; Asselta, R; Scarpini, E; Comi, Gp; Bresolin, N; Clerici, M; Sironi, M | |
| A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death | 1-gen-2024 | Minnai, Francesca; Biscarini, Filippo; Esposito, Martina; Dragani, Tommaso A; Bujanda, Luis; Rahmouni, Souad; Alarcón-Riquelme, Marta E; Bernardo, David; Carnero-Montoro, Elena; Buti, Maria; Zeberg, Hugo; Asselta, Rosanna; Romero-Gómez, Manuel; Fernandez-Cadenas, Israel; Fallerini, Chiara; Zguro, Kristina; Croci, Susanna; Baldassarri, Margherita; Bruttini, Mirella; Furini, Simone; Renieri, Alessandra; Colombo, Francesca | |
| A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest. | 1-gen-2018 | Samarani, M; Loberto, N; Solda, G; Straniero, L; Asselta, R; Duga, S; Lunghi, G; Zucca, Fa; Mauri, L; Ciampa, Mg; Schiumarini, D; Bassi, R; Giussani, P; Chiricozzi, E; Prinetti, A; Aureli, M; Sonnino, S. | |
| A new biallelic polymorphism in intron 1 of the CHRNA4 gene may cause erroneous genotyping of a closely linked CA repeat marker | 1-gen-2000 | Bonati, Mt; Duga, S; Asselta, R; Ferinistrambi, L; Oldani, A; Zucconi, M; Malcovati, M; Dalpra, L; Tenchini, Ml | |
| A new exon in the 5’ untranslated region of bovine Connexin32 gene | 1-gen-1999 | Duga, S.; Asselta, R.; Giacco, L. D.; Malcovati, M.; Ronchi, S.; Tenchini, M. L.; Simonic, T. | |
| A new genetic mechanism for congenital afibrinogenemia: maternal uniparental isodisomy for chromosome 4 containing a 15-kb deletion in fibrinogen Aalpha-chain gene | 1-gen-2004 | Duga, S; Spena, S; Asselta, R; Peyandi, F; Mahasandana, C; Malcovati, M; Mannucci, Pm; Tenchini, Ml | |
| A novel 15-kb deletion involving fibrinogen Aalpha-chain gene causes congenital afibrinogenemia as a consequence of uniparental isodisomy of chromosome 4 | 1-gen-2004 | Spena, S; Asselta, R; Duga, S; Monaldini, L; Malcovati, M; Mannucci, Pm; Tenchini, Ml | |
| A novel deafness-associated mutation within the microRNA MIR96 gene alters pre-miRNA folding and processing | 1-gen-2011 | Robusto, M; Asselta, Rosanna; Primignani, P; Castorina, P; Benzoni, E; Cesarani, A; Ambrosetti, U; Duga, Stefano; Solda', Giulia | |
| A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency | 1-gen-2007 | Bozzao, C; Rimoldi, V; Asselta, R; Landau, M; Ghiotto, R; Tenchini, Ml; DE CRISTOFARO, R; Castaman, G; Duga, S | |
| A novel in-frame deletion in the factor V C1 domain associated with severe coagulation factor V deficiency in a Korean family | 1-gen-2009 | Song, J; Guella, I; Kwon, K. Y.; Cho, H; Park, R; Asselta, R; Choi, J. R. |
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Opzioni
Scopri
Tipologia
- 1 Contributo su Rivista 267
- 1 Contributo su Rivista::1.1 Arti... 189
- 1 Contributo su Rivista::1.5 Abst... 68
- 4 Contributo in Atti di Convegno ... 64
- 4 Contributo in Atti di Convegno ... 56
- 1 Contributo su Rivista::1.2 Rece... 9
- 4 Contributo in Atti di Convegno ... 4
- 4 Contributo in Atti di Convegno ... 4
- 1 Contributo su Rivista::1.7 Lettera 1
- 2 Contributo in Volume 1
- 2 Contributo in Volume::2.1 Contr... 1
Data di pubblicazione
- 2020 - 2024 60
- 2010 - 2019 100
- 2000 - 2009 153
- 1995 - 1999 19
Editore
- Nature Publishing Group 4
- Wiley Blackwell 2
- Blackwell 1
- piccin 1
Rivista
- JOURNAL OF THROMBOSIS AND HAEMOST... 26
- HAEMATOLOGICA 23
- BLOOD 19
- EUROPEAN JOURNAL OF HUMAN GENETICS 14
- HAEMOPHILIA 11
- THROMBOSIS AND HAEMOSTASIS 11
- PARKINSONISM & RELATED DISORDERS 6
- PLOS ONE 6
- HUMAN MOLECULAR GENETICS 5
- INTERNATIONAL JOURNAL OF MOLECULA... 5
Keyword
- Humans 12
- COVID-19 9
- SARS-CoV-2 8
- Female 6
- Male 6
- Mutation 5
- Aged 4
- autoimmunity 4
- Genetic 4
- Genetic Predisposition to Disease 4
Lingua
- eng 263
- ita 26
Accesso al fulltext
- no fulltext 316
- open 9
- reserved 7