Understanding the WHIM syndrome: molecular analysis of CXCR4 functions in lymphocyte activation
2011-01-01 Kallikourdis, M; Trovato, Ae; Anselmi, F; Sarukhan, A; Roselli, G; Tassone, L; Badolato, R; Viola, A
In vitro effects of loratadine and its active metabolite an T lymphocytes
1998-01-01 Cagnoni, F.; Mincarini, M.; Passalacqua, G.; Semino, C.; Pietra, G.; Melioli, G.; Canonica, G. W.
State of the art of rare bleeding disorders database (RBDD)
2008-01-01 Spreafico, M.; Menegatti, M.; Palla, R.; Garagiola, I.; Tagliabue, L.; Cairo, A.; Lavoretano, S.; Asselta, R.; Duga, S.; Mannucci, P. M.; Peyvandi, F.
A Published Pharmacogenetic Algorithm Was Poorly Predictive of Tacrolimus Clearance in An Independent Cohort of Renal Transplant Recipients
2012-01-01 Boughton, O; Borgulya, G; Cecconi, M; Macphee, Iam
The lymphatic system controls intestinal inflammation and inflammation-associated colon cancer through the chemokine decoy receptor D6
2009-01-01 Vetrano, S.; Borroni, E.; Bonecchi, R.; Correale, C.; Sarukhan, A.; Vincenzo, A.; Fantini, M.; Roncalli, M.; Malesci, A.; Vecchi, A.; Mantovani, A.; Locati, M.; Danese, S.
Low risk of hepatitis B reactivation in patients with chronic hepatitis C and concurrent inactive hepatitis B infection treated with interferon and ribavirin
2008-01-01 Iavarone, M.; Aghemo, A.; Viganò, M.; Rumi, M. G.; Agnelli, F.; Lampertico, P.; Donato, M. F.; Colombo, M.
In vivo and in vitro effect of ribavirin and interferon on erythropoiesis in patients with hepatitis C
2009-01-01 Ronzoni, L.; Colancecco, A.; Cattaneo, A.; Aghemo, A.; Monico, S.; Rumi, M.; Colombo, M.; Cappellini, M. D.
Five new point mutations in fibrinogen alpha-chain gene causing afibrinogenemia
2000-01-01 Asselta, R; Duga, S; Malcovati, M; Simonic, T; Santagostino, E; Mannucci, Pm; Tenchini, Ml
Congenital afibrinogenemia: two novel fibrinogen gene mutations identified in two patients from Iran
2006-01-01 Monaldini, L; Asselta, R; Duga, S; Peyvandi, F; Malcovati, M; Tenchini, Ml
CHRNA3/CHRNA5/CHRNB4 cluster and autosomal dominant nocturnal frontal lobe epilepsy
2000-01-01 Bonati, Mt; Asselta, R; Duga, S; Malcovati, M; Tenchini, Ml; Oldani, A; Zucconi, M; Ferini-Strambi, L; Dalprà, L
Molecular genetic analysis of coagulation factor XI deficiency in Italian patients
2003-01-01 Zadra, G; Asselta, R; Santagostino, E; Mannucci, Pm; Malcovati, M; Tenchini, Ml; Duga, S
Severe factor V deficiency: identification and molecular characterization of three novel splicing mutations
2006-01-01 Asselta, R; Dall’Osso, C; Duga, S; Locatelli, N; Malcovati, M; Tenchini, Ml
Congenital afibrinogenemia: In Vitro Expression of Two Novel Missense Mutations in the Fibrinogen Bbeta-Chain Gene Demonstrates That One of Them Acts as a Splicing Mutation
2002-01-01 Asselta, R; Spena, S; Duga, S; Malcovati, M; Peyvandi, F; Mannucci, Pm; Tenchini, Ml
Two cases of congenital afibrinogenemia caused by potentially elusive mutations
2003-01-01 Spena, S; Duga, S; Asselta, R; Malcovati, M; Tenchini, Ml
Congenital afibrinogenemia, identification of four novel homozygous mutations in the fibrinogen gene cluster: three point mutations and a 15-kb deletion
2003-01-01 Duga, S; Asselta, R; Spena, S; Peyvandi, F; Malcovati, M; Mannucci, Pm; Tenchini, Ml
Characterization of the F11 alternative splicing pattern: identification of a novel coagulation FXI isoform
2007-01-01 Guella, I; Asselta, R; Rimoldi, V; Tenchini, Ml; Duga, S
A novel mechanism for congenital afibrinogenemia based on pseudoexon activation in the fibrinogen gamma-chain gene
2007-01-01 Spena, S; Asselta, R; Platè, M; Castaman, G; Duga, S; Tenchini, Ml
Eight novel mutations in FXI gene
2005-01-01 G., Castaman; R., Ghiotto; G., Rossetti; D., Habart; A., Tagliaferri; Duga, S
Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients
2009-01-01 Solda, G; Paraboschi, Em; Gemmati, D; Zamboni, P; Duga, S; Asselta, R
Characterization of productive and unproductive mRNA splicings in F11: identification of a novel coagulation FXI isoform
2008-01-01 Rimoldi, V; Guella, I; Asselta, R; De Cristofaro, R; Peyvandi, F; Mannucci, Pm; Duga, S
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Understanding the WHIM syndrome: molecular analysis of CXCR4 functions in lymphocyte activation | 1-gen-2011 | Kallikourdis, M; Trovato, Ae; Anselmi, F; Sarukhan, A; Roselli, G; Tassone, L; Badolato, R; Viola, A | |
| In vitro effects of loratadine and its active metabolite an T lymphocytes | 1-gen-1998 | Cagnoni, F.; Mincarini, M.; Passalacqua, G.; Semino, C.; Pietra, G.; Melioli, G.; Canonica, G. W. | |
| State of the art of rare bleeding disorders database (RBDD) | 1-gen-2008 | Spreafico, M.; Menegatti, M.; Palla, R.; Garagiola, I.; Tagliabue, L.; Cairo, A.; Lavoretano, S.; Asselta, R.; Duga, S.; Mannucci, P. M.; Peyvandi, F. | |
| A Published Pharmacogenetic Algorithm Was Poorly Predictive of Tacrolimus Clearance in An Independent Cohort of Renal Transplant Recipients | 1-gen-2012 | Boughton, O; Borgulya, G; Cecconi, M; Macphee, Iam | |
| The lymphatic system controls intestinal inflammation and inflammation-associated colon cancer through the chemokine decoy receptor D6 | 1-gen-2009 | Vetrano, S.; Borroni, E.; Bonecchi, R.; Correale, C.; Sarukhan, A.; Vincenzo, A.; Fantini, M.; Roncalli, M.; Malesci, A.; Vecchi, A.; Mantovani, A.; Locati, M.; Danese, S. | |
| Low risk of hepatitis B reactivation in patients with chronic hepatitis C and concurrent inactive hepatitis B infection treated with interferon and ribavirin | 1-gen-2008 | Iavarone, M.; Aghemo, A.; Viganò, M.; Rumi, M. G.; Agnelli, F.; Lampertico, P.; Donato, M. F.; Colombo, M. | |
| In vivo and in vitro effect of ribavirin and interferon on erythropoiesis in patients with hepatitis C | 1-gen-2009 | Ronzoni, L.; Colancecco, A.; Cattaneo, A.; Aghemo, A.; Monico, S.; Rumi, M.; Colombo, M.; Cappellini, M. D. | |
| Five new point mutations in fibrinogen alpha-chain gene causing afibrinogenemia | 1-gen-2000 | Asselta, R; Duga, S; Malcovati, M; Simonic, T; Santagostino, E; Mannucci, Pm; Tenchini, Ml | |
| Congenital afibrinogenemia: two novel fibrinogen gene mutations identified in two patients from Iran | 1-gen-2006 | Monaldini, L; Asselta, R; Duga, S; Peyvandi, F; Malcovati, M; Tenchini, Ml | |
| CHRNA3/CHRNA5/CHRNB4 cluster and autosomal dominant nocturnal frontal lobe epilepsy | 1-gen-2000 | Bonati, Mt; Asselta, R; Duga, S; Malcovati, M; Tenchini, Ml; Oldani, A; Zucconi, M; Ferini-Strambi, L; Dalprà, L | |
| Molecular genetic analysis of coagulation factor XI deficiency in Italian patients | 1-gen-2003 | Zadra, G; Asselta, R; Santagostino, E; Mannucci, Pm; Malcovati, M; Tenchini, Ml; Duga, S | |
| Severe factor V deficiency: identification and molecular characterization of three novel splicing mutations | 1-gen-2006 | Asselta, R; Dall’Osso, C; Duga, S; Locatelli, N; Malcovati, M; Tenchini, Ml | |
| Congenital afibrinogenemia: In Vitro Expression of Two Novel Missense Mutations in the Fibrinogen Bbeta-Chain Gene Demonstrates That One of Them Acts as a Splicing Mutation | 1-gen-2002 | Asselta, R; Spena, S; Duga, S; Malcovati, M; Peyvandi, F; Mannucci, Pm; Tenchini, Ml | |
| Two cases of congenital afibrinogenemia caused by potentially elusive mutations | 1-gen-2003 | Spena, S; Duga, S; Asselta, R; Malcovati, M; Tenchini, Ml | |
| Congenital afibrinogenemia, identification of four novel homozygous mutations in the fibrinogen gene cluster: three point mutations and a 15-kb deletion | 1-gen-2003 | Duga, S; Asselta, R; Spena, S; Peyvandi, F; Malcovati, M; Mannucci, Pm; Tenchini, Ml | |
| Characterization of the F11 alternative splicing pattern: identification of a novel coagulation FXI isoform | 1-gen-2007 | Guella, I; Asselta, R; Rimoldi, V; Tenchini, Ml; Duga, S | |
| A novel mechanism for congenital afibrinogenemia based on pseudoexon activation in the fibrinogen gamma-chain gene | 1-gen-2007 | Spena, S; Asselta, R; Platè, M; Castaman, G; Duga, S; Tenchini, Ml | |
| Eight novel mutations in FXI gene | 1-gen-2005 | G., Castaman; R., Ghiotto; G., Rossetti; D., Habart; A., Tagliaferri; Duga, S | |
| Differential expression of microRNAs in peripheral blood mononuclear cells of Multiple Sclerosis patients | 1-gen-2009 | Solda, G; Paraboschi, Em; Gemmati, D; Zamboni, P; Duga, S; Asselta, R | |
| Characterization of productive and unproductive mRNA splicings in F11: identification of a novel coagulation FXI isoform | 1-gen-2008 | Rimoldi, V; Guella, I; Asselta, R; De Cristofaro, R; Peyvandi, F; Mannucci, Pm; Duga, S |
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Tipologia
- 1 Contributo su Rivista2152
Data di pubblicazione
- 2020 - 2026113
- 2010 - 20191341
- 2000 - 2009587
- 1990 - 1999110
- 1988 - 19891
Editore
- Nature Publishing Group4
- s.n4
- ICRS3
- Blackwell1
Rivista
- EUROPEAN UROLOGY. SUPPLEMENTS124
- GASTROENTEROLOGY123
- EUROPEAN JOURNAL OF NUCLEAR MEDIC...120
- THE JOURNAL OF UROLOGY111
- DIGESTIVE AND LIVER DISEASE100
- THE JOURNAL OF NUCLEAR MEDICINE80
- ANNALS OF THE RHEUMATIC DISEASES69
- RADIOTHERAPY AND ONCOLOGY59
- ANNALS OF ONCOLOGY57
- JOURNAL OF CLINICAL ONCOLOGY45
Keyword
- Myelodysplastic syndrome8
- Survival4
- biomimetic3
- Mitochondrial ferritin3
- osteochondral3
- Prognosis3
- scaffold3
- Sideroblastic anemia3
- viscosupplementation3
- COLONOSCOPIC SURVEILLANCE2
Lingua
- eng795
- ita24
- und6
Accesso al fulltext
- no fulltext2099
- reserved51
- open2