BIUNNO, IDA
BIUNNO, IDA
Istituto di Ricerca Genetica e Biomedica - IRGB
A collection of 33 novel human mt DNA homoplasmic variants
2002 Crimi, M; Sciacco, M; Galbiati, S; Bordoni, A; Malferrari, G; Debo, R; Biunno, I; Bresolin, N; Comi, G
A itochondrial tRNA (His) gene mutation causing pigmentary retinopathy and neurosensorial deafness
2003 Crimi, M; Galbiati, S; Perini, Mp; Bordoni, A; Malferrari, G; Sciacco, M; Biunno, I; Strazzer, S; Moggio, M; Bresolin, N; Comi, G
A miRNA signature in human cord blood stem and progenitor cells as potential biomarker of specific acute myeloid leukemia subtypes
2014 Cattaneo M; Pelosi E; Castelli G; Cerio AM; D'Angià A; Porretti L; Rebulla P; Pavesi L; Russo G; Giordano A; Turri J; Cicconi L; LoCoco F; Testa U; Biunno I.
A missense mutation in the mitochondrial ND5 gene associated with a Leigh MELAS overlap syndrome
2003 Crimi, M; Galbiati, S; Moroni, I; Bordoni, A; Perini, Mp; Lamantea, E; Sciacco, M; Zeviani, M; Biunno, I; Moggio, M; Scarlato, G; Comi, G
A new mutation in ABCC8 gene discoverd in an infant with congenital hyperinsulinism
2007 Dicandia, S; Bosio, L; Proverbio, Mc; Zamproni, I; Mora, S; Valin, Ps; Bove, M; Grechi, E; Biagiotti, L; Biunno, I; Patricelli, Mg; Chiumello, G
A novel polymorphism in SEL1L confers susceptibility to Alzheimer's disease
2006 Saltini, G; Dominici, R; Lovati, C; Cattaneo, M; Michelini, S; Malferrari, G; Caprera, A; Milanesi, L; Finazzi, D; Bertora, P; Scarpini, E; Galimberti, D; Venturelli, E; Musicco, M; Adorni, F; Mariani, C; Biunno, I
A simple extraction method useful to purify DNA from difficult biological sources
2006 Oliveri, C; Frequin, M; Malferrari, G; Saltini, G; Gramegna, M; Tagliabue, R; Deblasio, P; Biunno, I; Biagiotti, L
Additional congeners of the macrolide neaumycin: structure revision and biological activity.
2015 Simone, M; Maffioli, Si; Tocchetti, A; Tretter, S; Cattaneo, M; Biunno, I; Gaspari, E; Donadio, S
Allelic polymorphisms in the transcriptional regulatory regionof human SEL1L
2001 Cattaneo M.; Zollo M.; Malferrari G.; orlandi R.; D'Angelo A.; Menard S.; Biunno I
An analysis in human lymphomas of a J alpha region involved in ac-myc/J alpha translocation:relationship with TCR alpha, beta and gamma rearrangements
1988 Villa A.; Sacco MG.; Cairo G.; Biunno I.; MathieuMahul D.; Larsen J.; Vezzoni P
An association study of single alzheimer candidate genes by mean allelic discrimination technology
2005 Caristina L.; Spinelli R.; Finazzi D.; Caprera A.; Callegaro A.; Bicciato S.; Beltrame L.; Biunno I.; Milanesi L.; Saltini G.; Malferrari G.; Galimberti D.; Lovati C.; Mariani C.; Battaglia C.
Analysis of 21-deoxycortisol, a marker of congenital adrenal hyperplasia, in blood by atmospheric pressure chemical ionization and electrospray ionization using multiple reaction monitoring
2004 S. Cristoni; D. Cuccato; M. Sciannambio; L. RossiBernardi; I. Biunno; P. Gerthoux; G. Russo; G. Weber; S. Mora
Analysis of peptides using partial (no discharge) atmospheric pressure chemical ionization conditions with ion trap mass spectrometry
2002 Cristoni, S; Bernardi, Lr; Biunno, I; Guidugli, F
Analysis of protein ions in the range 3000-12000 Th under partial (no discharge) atmospheric pressure chemical ionization conditions using ion trap mass spectrometry
2002 Cristoni S.; Bernardi LR.; Biunno I.; Guidugli F.
Application of Tissue Microarray Technology to Stem Cell
2014 Alberto La Spada; Barnaba Rainoldi; Andrea De Blasio; Ida Biunno
Association of early onset Alzeimer's disease with an interleukin 1 alpha gene polymorphism
2000 Grimaldi LM.; Casadei VM.; Ferri C.; Veglia F.; Licastro F.; Annoni G.; Biunno I.; DeBellis G.; Sorbi S.; Mariani C.; Canal N.; Griffin WS.; Francesch M.
Association of early-onset Alzheimer's disease with an interleukin-1alpha gene polymorphism
2000 Grimaldi, Lm; Casadei, Vm; Ferri, C; Veglia, F; Licastro, F; Annoni, G; Biunno, I; De Bellis, G; Sorbi, S; Mariani, C; Canal, N; Griffin, Ws; Franceschi, M
Basal-like phenotype in a breast carcinoma case series from Sudan: prevalence and clinical/pathological correlations.
2010 Awadelkarim KD; Arizzi C; Elamin EO; Hamad HM; De Blasio P; Mekki SO; Osman I; Biunno I; Elwali NE; Barberis MC; MarianiCostantini R.
BGLII polymorphism of the epidermal growth factor receptor (EGF-R) gene
1988 Biunno, I; Pozzi, Mr; Radice, P; Mondini, P; Pierotti, Ma; Haley, J; Waterfield, Md; Della porta, G
Biobanking shifts to precision medicine.
2014 Ntai A; Baronchelli S; Pellegrino T; Biunno
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
A collection of 33 novel human mt DNA homoplasmic variants | 1-gen-2002 | Crimi, M; Sciacco, M; Galbiati, S; Bordoni, A; Malferrari, G; Debo, R; Biunno, I; Bresolin, N; Comi, G | |
A itochondrial tRNA (His) gene mutation causing pigmentary retinopathy and neurosensorial deafness | 1-gen-2003 | Crimi, M; Galbiati, S; Perini, Mp; Bordoni, A; Malferrari, G; Sciacco, M; Biunno, I; Strazzer, S; Moggio, M; Bresolin, N; Comi, G | |
A miRNA signature in human cord blood stem and progenitor cells as potential biomarker of specific acute myeloid leukemia subtypes | 1-gen-2014 | Cattaneo M; Pelosi E; Castelli G; Cerio AM; D'Angià A; Porretti L; Rebulla P; Pavesi L; Russo G; Giordano A; Turri J; Cicconi L; LoCoco F; Testa U; Biunno I. | |
A missense mutation in the mitochondrial ND5 gene associated with a Leigh MELAS overlap syndrome | 1-gen-2003 | Crimi, M; Galbiati, S; Moroni, I; Bordoni, A; Perini, Mp; Lamantea, E; Sciacco, M; Zeviani, M; Biunno, I; Moggio, M; Scarlato, G; Comi, G | |
A new mutation in ABCC8 gene discoverd in an infant with congenital hyperinsulinism | 1-gen-2007 | Dicandia, S; Bosio, L; Proverbio, Mc; Zamproni, I; Mora, S; Valin, Ps; Bove, M; Grechi, E; Biagiotti, L; Biunno, I; Patricelli, Mg; Chiumello, G | |
A novel polymorphism in SEL1L confers susceptibility to Alzheimer's disease | 1-gen-2006 | Saltini, G; Dominici, R; Lovati, C; Cattaneo, M; Michelini, S; Malferrari, G; Caprera, A; Milanesi, L; Finazzi, D; Bertora, P; Scarpini, E; Galimberti, D; Venturelli, E; Musicco, M; Adorni, F; Mariani, C; Biunno, I | |
A simple extraction method useful to purify DNA from difficult biological sources | 1-gen-2006 | Oliveri, C; Frequin, M; Malferrari, G; Saltini, G; Gramegna, M; Tagliabue, R; Deblasio, P; Biunno, I; Biagiotti, L | |
Additional congeners of the macrolide neaumycin: structure revision and biological activity. | 1-gen-2015 | Simone, M; Maffioli, Si; Tocchetti, A; Tretter, S; Cattaneo, M; Biunno, I; Gaspari, E; Donadio, S | |
Allelic polymorphisms in the transcriptional regulatory regionof human SEL1L | 1-gen-2001 | Cattaneo M.; Zollo M.; Malferrari G.; orlandi R.; D'Angelo A.; Menard S.; Biunno I | |
An analysis in human lymphomas of a J alpha region involved in ac-myc/J alpha translocation:relationship with TCR alpha, beta and gamma rearrangements | 1-gen-1988 | Villa A.; Sacco MG.; Cairo G.; Biunno I.; MathieuMahul D.; Larsen J.; Vezzoni P | |
An association study of single alzheimer candidate genes by mean allelic discrimination technology | 1-gen-2005 | Caristina L.; Spinelli R.; Finazzi D.; Caprera A.; Callegaro A.; Bicciato S.; Beltrame L.; Biunno I.; Milanesi L.; Saltini G.; Malferrari G.; Galimberti D.; Lovati C.; Mariani C.; Battaglia C. | |
Analysis of 21-deoxycortisol, a marker of congenital adrenal hyperplasia, in blood by atmospheric pressure chemical ionization and electrospray ionization using multiple reaction monitoring | 1-gen-2004 | S. Cristoni; D. Cuccato; M. Sciannambio; L. RossiBernardi; I. Biunno; P. Gerthoux; G. Russo; G. Weber; S. Mora | |
Analysis of peptides using partial (no discharge) atmospheric pressure chemical ionization conditions with ion trap mass spectrometry | 1-gen-2002 | Cristoni, S; Bernardi, Lr; Biunno, I; Guidugli, F | |
Analysis of protein ions in the range 3000-12000 Th under partial (no discharge) atmospheric pressure chemical ionization conditions using ion trap mass spectrometry | 1-gen-2002 | Cristoni S.; Bernardi LR.; Biunno I.; Guidugli F. | |
Application of Tissue Microarray Technology to Stem Cell | 1-gen-2014 | Alberto La Spada; Barnaba Rainoldi; Andrea De Blasio; Ida Biunno | |
Association of early onset Alzeimer's disease with an interleukin 1 alpha gene polymorphism | 1-gen-2000 | Grimaldi LM.; Casadei VM.; Ferri C.; Veglia F.; Licastro F.; Annoni G.; Biunno I.; DeBellis G.; Sorbi S.; Mariani C.; Canal N.; Griffin WS.; Francesch M. | |
Association of early-onset Alzheimer's disease with an interleukin-1alpha gene polymorphism | 1-gen-2000 | Grimaldi, Lm; Casadei, Vm; Ferri, C; Veglia, F; Licastro, F; Annoni, G; Biunno, I; De Bellis, G; Sorbi, S; Mariani, C; Canal, N; Griffin, Ws; Franceschi, M | |
Basal-like phenotype in a breast carcinoma case series from Sudan: prevalence and clinical/pathological correlations. | 1-gen-2010 | Awadelkarim KD; Arizzi C; Elamin EO; Hamad HM; De Blasio P; Mekki SO; Osman I; Biunno I; Elwali NE; Barberis MC; MarianiCostantini R. | |
BGLII polymorphism of the epidermal growth factor receptor (EGF-R) gene | 1-gen-1988 | Biunno, I; Pozzi, Mr; Radice, P; Mondini, P; Pierotti, Ma; Haley, J; Waterfield, Md; Della porta, G | |
Biobanking shifts to precision medicine. | 1-gen-2014 | Ntai A; Baronchelli S; Pellegrino T; Biunno |