STRINA, DARIO
STRINA, DARIO
Istituto di Ricerca Genetica e Biomedica - IRGB
Exonic knockout and knockin gene editing in hematopoietic stem and progenitor cells rescues RAG1 immunodeficiency
2024 Castiello, M. C.; Brandas, C.; Ferrari, S.; Porcellini, S.; Sacchetti, N.; Canarutto, D.; Draghici, E.; Merelli, I.; Barcella, M.; Pelosi, G.; Vavassori, V.; Varesi, A.; Jacob, A.; Scala, S.; Ricci, L. B.; Paulis, M.; Strina, D.; Di Verniere, M.; Sergi, L. S.; Serafini, M.; Holland, S. M.; Bergerson, J. R. E.; De Ravin, S. S.; Malech, H. L.; Pala, F.; Bosticardo, M.; Brombin, C.; Cugnata, F.; Calzoni, E.; Crooks, G. M.; Notarangelo, L. D.; Genovese, P.; Naldini, L.; Villa, A.
A novel intronic variant in PIGB in Acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects
2021 Palagano E.; Gordon C.T.; Uva P.; Strina D.; Dimartino C.; Villa A.; Amiel J.; GuionAlmeida M.L.; VendraminiPittoli S.; KokitsuNakata N.M.; ZechiCeide R.M.; Sobacchi C.
Chromosome Transplantation: A Possible Approach to Treat Human X-linked Disorders
2020 Paulis, M; Susani, L; Castelli, A; Suzuki, T; Hara, T; Straniero, L; Duga, S; Strina, D; Mantero, S; Caldana, E; Sergi, Ls; Villa, A; Vezzoni, P
Generation of an immunodeficient mouse model of tcirg1-deficient autosomal recessive osteopetrosis
2020 Palagano E.; Muggeo S.; Crisafulli L.; Tourkova I.L.; Strina D.; Mantero S.; Fontana E.; Locatelli S.L.; Monari M.; Morenghi E.; CarloStella C.; Barnett J.B.; Blair H.C.; Vezzoni P.; Villa A.; Sobacchi C.; Ficara F.
Absence of Dipeptidyl Peptidase 3 Increases Oxidative Stress and Causes Bone Loss
2019 Menale, C; Robinson, Lj; Palagano, E; Rigoni, R; Erreni, M; Almarza, Aj; Strina, D; Mantero, S; Lizier, M; Forlino, A; Besio, R; Monari, M; Vezzoni, P; Cassani, B; Blair, Hc; Villa, A; Sobacchi, C
Chromosome Transplantation: Correction of the Chronic Granulomatous Disease Defect in Mouse Induced Pluripotent Stem Cells
2019 Castelli A.; Susani L.; Menale C.; Muggeo S.; Caldana E.; Strina D.; Cassani B.; Recordati C.; Scanziani E.; Ficara F.; Villa A.; Vezzoni P.; Paulis M.
Targeted gene correction in osteopetrotic-induced pluripotent stem cells for the generation of functional osteoclasts
2015 Neri T.; Muggeo S.; Paulis M.; Caldana M.E.; Crisafulli L.; Strina D.; Focarelli M.L.; Faggioli F.; Recordati C.; Scaramuzza S.; Scanziani E.; Mantero S.; Buracchi C.; Sobacchi C.; Lombardo A.; Naldini L.; Vezzoni P.; Villa A.; Ficara F.
RANK-dependent autosomal recessive osteopetrosis: characterisation of 5 new cases with novel mutations.
2012 Pangrazio A; Cassani B; Guerrini MM; Crockett JC; Marrella V; Zammataro L; Strina D; Schulz A; Schlack C; Kornak U; Mellis DJ; Duthie A; Helfrich MH; Durandy A; Moshous D; Vellodi A; Chiesa R; Veys P; Lo Iacono N; Vezzoni P; Fischer A; Villa A; Sobacchi C.
Homeostatic expansion of autoreactive immunoglobulin-secreting cells in the Rag2 mouse model of Omenn syndrome.
2010 Cassani, B; Poliani, Pl; Marrella, V; Schena, F; Sauer, Av; Ravanini, M; Strina, D; Busse, Ce; Regenass, S; Wardemann, H; Martini, A; Facchetti, F; van der Burg, M; Rolink, Ag; Vezzoni, P; Grassi, F; Traggiai, E; Villa, A
The ZNF75 zinc finger gene subfamily: Isolation and mapping of the four members in humans and great apes
1996 Villa A.; Strina D.; Frattini A.; Faranda S.; Macchi P.; Finelli P.; Bozzi F.; Susani L.; Archidiacono N.; Rocchi M.; Vezzoni P.
Characterization of nine novel mutations in the CD40 ligand gene in patients with X-linked hyper IgM syndrome of various ancestry.
1995 Macchi, Paolo; Villa, Anna; Strina, Dario; Grazia Sacco, Maria; Morali, Federica; Brugnoni, Duilio; Giliani, Silvia; Mantuano, Elide; Fasth, Anders; Andersson, Bengt; M Zegers, Ben J; Cavagni, Giovanni; Reznick, Igor; Levy, Jacov; Zanbar, Israel; Porat, Yael; Airo, Paolo; Plebani, Alessandro; Vezzoni, Paolo; D Notarangelo, Luigi
X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP gene
1995 Villa, Anna; Notarangelo, Luigi; Macchi, Paolo; Mantuano, Elide; Cavagni, Giovanni; Brugnoni, Duilio; Strina, Dario; Cristina Patrosso, M; Ramenghi, Ugo; Grazia Sacco, Maria; Ugazio, Alberto; Vezzoni, Paolo
Organization of the -human CD40L gene: Ixaplications for molecular defects in X-chromosomehlinked hyper-IgM syndrome and prenatal diagnosis
1994 ANNA VILLA; LUIGI D. NOTARANGELO JAMES P. Di SANTO; PAOLO P. MACCHI; DARIO STRINA;ANNALISA FRATTINI; FRANCO LUCCHINI; CRISTINA M. PATROSSO; SILVIA GILIANI; ELIDE MANTUANO;SILVANO AGOSTI; GIANFRANCO NOCERA; RICHARD A. KROCZEKII; ALAIN FISCHER; ALBERTO G. UGAZIO;GENEVItVE DE SAINT BASILE; AND PAOLO VEZZONI
Rapid isolation of cDNA clones by aliquot testing via PCR amplification
1994 Di Bacco, A.; Susani, L.; Villa, A.; Strina, D.; Frattini, A.; Vezzoni, P.; Zucchi, I.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Exonic knockout and knockin gene editing in hematopoietic stem and progenitor cells rescues RAG1 immunodeficiency | 1-gen-2024 | Castiello, M. C.; Brandas, C.; Ferrari, S.; Porcellini, S.; Sacchetti, N.; Canarutto, D.; Draghici, E.; Merelli, I.; Barcella, M.; Pelosi, G.; Vavassori, V.; Varesi, A.; Jacob, A.; Scala, S.; Ricci, L. B.; Paulis, M.; Strina, D.; Di Verniere, M.; Sergi, L. S.; Serafini, M.; Holland, S. M.; Bergerson, J. R. E.; De Ravin, S. S.; Malech, H. L.; Pala, F.; Bosticardo, M.; Brombin, C.; Cugnata, F.; Calzoni, E.; Crooks, G. M.; Notarangelo, L. D.; Genovese, P.; Naldini, L.; Villa, A. | |
| A novel intronic variant in PIGB in Acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects | 1-gen-2021 | Palagano E.; Gordon C.T.; Uva P.; Strina D.; Dimartino C.; Villa A.; Amiel J.; GuionAlmeida M.L.; VendraminiPittoli S.; KokitsuNakata N.M.; ZechiCeide R.M.; Sobacchi C. | |
| Chromosome Transplantation: A Possible Approach to Treat Human X-linked Disorders | 1-gen-2020 | Paulis, M; Susani, L; Castelli, A; Suzuki, T; Hara, T; Straniero, L; Duga, S; Strina, D; Mantero, S; Caldana, E; Sergi, Ls; Villa, A; Vezzoni, P | |
| Generation of an immunodeficient mouse model of tcirg1-deficient autosomal recessive osteopetrosis | 1-gen-2020 | Palagano E.; Muggeo S.; Crisafulli L.; Tourkova I.L.; Strina D.; Mantero S.; Fontana E.; Locatelli S.L.; Monari M.; Morenghi E.; CarloStella C.; Barnett J.B.; Blair H.C.; Vezzoni P.; Villa A.; Sobacchi C.; Ficara F. | |
| Absence of Dipeptidyl Peptidase 3 Increases Oxidative Stress and Causes Bone Loss | 1-gen-2019 | Menale, C; Robinson, Lj; Palagano, E; Rigoni, R; Erreni, M; Almarza, Aj; Strina, D; Mantero, S; Lizier, M; Forlino, A; Besio, R; Monari, M; Vezzoni, P; Cassani, B; Blair, Hc; Villa, A; Sobacchi, C | |
| Chromosome Transplantation: Correction of the Chronic Granulomatous Disease Defect in Mouse Induced Pluripotent Stem Cells | 1-gen-2019 | Castelli A.; Susani L.; Menale C.; Muggeo S.; Caldana E.; Strina D.; Cassani B.; Recordati C.; Scanziani E.; Ficara F.; Villa A.; Vezzoni P.; Paulis M. | |
| Targeted gene correction in osteopetrotic-induced pluripotent stem cells for the generation of functional osteoclasts | 1-gen-2015 | Neri T.; Muggeo S.; Paulis M.; Caldana M.E.; Crisafulli L.; Strina D.; Focarelli M.L.; Faggioli F.; Recordati C.; Scaramuzza S.; Scanziani E.; Mantero S.; Buracchi C.; Sobacchi C.; Lombardo A.; Naldini L.; Vezzoni P.; Villa A.; Ficara F. | |
| RANK-dependent autosomal recessive osteopetrosis: characterisation of 5 new cases with novel mutations. | 1-gen-2012 | Pangrazio A; Cassani B; Guerrini MM; Crockett JC; Marrella V; Zammataro L; Strina D; Schulz A; Schlack C; Kornak U; Mellis DJ; Duthie A; Helfrich MH; Durandy A; Moshous D; Vellodi A; Chiesa R; Veys P; Lo Iacono N; Vezzoni P; Fischer A; Villa A; Sobacchi C. | |
| Homeostatic expansion of autoreactive immunoglobulin-secreting cells in the Rag2 mouse model of Omenn syndrome. | 1-gen-2010 | Cassani, B; Poliani, Pl; Marrella, V; Schena, F; Sauer, Av; Ravanini, M; Strina, D; Busse, Ce; Regenass, S; Wardemann, H; Martini, A; Facchetti, F; van der Burg, M; Rolink, Ag; Vezzoni, P; Grassi, F; Traggiai, E; Villa, A | |
| The ZNF75 zinc finger gene subfamily: Isolation and mapping of the four members in humans and great apes | 1-gen-1996 | Villa A.; Strina D.; Frattini A.; Faranda S.; Macchi P.; Finelli P.; Bozzi F.; Susani L.; Archidiacono N.; Rocchi M.; Vezzoni P. | |
| Characterization of nine novel mutations in the CD40 ligand gene in patients with X-linked hyper IgM syndrome of various ancestry. | 1-gen-1995 | Macchi, Paolo; Villa, Anna; Strina, Dario; Grazia Sacco, Maria; Morali, Federica; Brugnoni, Duilio; Giliani, Silvia; Mantuano, Elide; Fasth, Anders; Andersson, Bengt; M Zegers, Ben J; Cavagni, Giovanni; Reznick, Igor; Levy, Jacov; Zanbar, Israel; Porat, Yael; Airo, Paolo; Plebani, Alessandro; Vezzoni, Paolo; D Notarangelo, Luigi | |
| X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP gene | 1-gen-1995 | Villa, Anna; Notarangelo, Luigi; Macchi, Paolo; Mantuano, Elide; Cavagni, Giovanni; Brugnoni, Duilio; Strina, Dario; Cristina Patrosso, M; Ramenghi, Ugo; Grazia Sacco, Maria; Ugazio, Alberto; Vezzoni, Paolo | |
| Organization of the -human CD40L gene: Ixaplications for molecular defects in X-chromosomehlinked hyper-IgM syndrome and prenatal diagnosis | 1-gen-1994 | ANNA VILLA; LUIGI D. NOTARANGELO JAMES P. Di SANTO; PAOLO P. MACCHI; DARIO STRINA;ANNALISA FRATTINI; FRANCO LUCCHINI; CRISTINA M. PATROSSO; SILVIA GILIANI; ELIDE MANTUANO;SILVANO AGOSTI; GIANFRANCO NOCERA; RICHARD A. KROCZEKII; ALAIN FISCHER; ALBERTO G. UGAZIO;GENEVItVE DE SAINT BASILE; AND PAOLO VEZZONI | |
| Rapid isolation of cDNA clones by aliquot testing via PCR amplification | 1-gen-1994 | Di Bacco, A.; Susani, L.; Villa, A.; Strina, D.; Frattini, A.; Vezzoni, P.; Zucchi, I. |