PALLOTTI, FRANCESCO
PALLOTTI, FRANCESCO
DIPARTIMENTO DI MEDICINA E CHIRURGIA
A new acute myeloid leukemia case with STAT5B-RARA gene fusion due to 17q21.2 interstitial deletion
2017-01-01 Pessina, Chiara; Basilico, Claudia; Genoni, Angelo; Meroni, Emanuela; Elli, Lorenzo; Granata, Paola; Righi, Rossana; Pallotti, Francesco; Mora, Barbara; Ferrario, Andrea; Passamonti, Francesco; Casalone, Rosario
A particular case of AML patient with the polymorphism G105G (rs11554137) and the missense mutation R132C in IDH1 gene
2019-01-01 Accetta, R.; Campiotti, L.; Elli, L.; Casalone, R.; Pallotti, F.
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV
1999-01-01 Bruno, C; Martinuzzi, A; Tang, Yy; Andreu, Al; Pallotti, Francesco; Bonilla, E; Shanske, S; Fu, J; Sue, Cm; Angelini, C; Dimauro, S; Manfredi, G.
A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck
2014-01-01 Pallotti, Francesco; Binelli, GIORGIO PIETRO MARIO; R., Fabbri; M. L., Valentino; R., Vicenti; M., Macciocca; S., Cevoli; A., Baruzzi; S., Dimauro; V., Carelli
Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB gene
2019-01-01 Marchet, S.; Invernizzi, F.; Blasevich, F.; Bruno, V.; Dusi, S.; Venco, P.; Fiorillo, C.; Baranello, G.; Pallotti, F.; Lamantea, E.; Mora, M.; Tiranti, V.; Lamperti, C.
AN UPDATING OF THE BIOCHEMICAL FUNCTION OF COENZYME-Q IN MITOCHONDRIA
1994-01-01 Lenaz, G; Fato, R; Castelluccio, C; Cavazzoni, M; Estornell, E; Huertas, Jf; Pallotti, Francesco; Castelli, Gp; Rauchova, H.
Analysis of fluorophore labeled glycosaminoglycan disaccharides using polyacrylamide gel electroforesis and HPLC
2005-01-01 Viola, Manuela; Karousou, Evgenia; Vigetti, Davide; A., Genasetti; Rizzi, M.; Pallotti, Francesco; DE LUCA, Giancarlo; Passi, Alberto
Analysis of mtDNA deletions in muscle by in situ hybridization
2000-01-01 Vu, Th; Tanji, K; Pallotti, Francesco; Golzi, V; Hirano, M; Dimauro, S; Bonilla, E.
Analysis of three screening methods for the detection of calreticulin gene mutations
2020-01-01 Accetta, R.; Elli, L.; Libera, L.; Siracusa, C.; Cassavia, F.; Orsini, F.; Orlandi, L.; Passamonti, F.; Casalone, R.; Pallotti, F.
Aortic smooth muscle cells migration and the role of metalloproteinases and hyaluronan.
2008-01-01 Vigetti, Davide; Moretto, P; Viola, Manuela; Genasetti, A; Rizzi, M; Karousou, Evgenia; Clerici, M; Bartolini, B; Pallotti, Francesco; DE LUCA, Giancarlo; Passi, Alberto
Archaeogenomics in Caravate and Cittiglio (Lombardy): from the excavation of ancient human bones to the study of DNA
2022-01-01 Olivieri, Anna; Pallotti, Francesco; Rosario Capodiferro, Marco; Colombo, Giulia; Licata, Marta; Tesi, Chiara; Semino, Ornella; Achilli, Alessandro; Torroni, Antonio
ASSAY CONDITIONS FOR THE MITOCHONDRIAL NADH - COENZYME-Q OXIDOREDUCTASE
1993-01-01 Estornell, E; Fato, R; Pallotti, Francesco; Lenaz, G.
Assessing Heteroplasmic Load in Leber's Hereditary Optic Neuropathy Mutation 3460G->A/MT-ND1 with A Real-Time PCR Quantitative Approach
2007-01-01 Genasetti, A; Valentino, M. L.; Carelli, V; Vigetti, Davide; Viola, Manuela; Karousou, Evgenia; Melzi, ; D'Eril, G. V.; DE LUCA, Giancarlo; Passi, Alberto; Pallotti, Francesco
Authors’ Reply to Crampe and Langabeer: Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia
2015-01-01 Mattarucchi, Elia; Pallotti, Francesco; Casalone, Rosario
Biochemical analysis of mitochondrial function in cybrid cell lines harboring mtDNA mutations
2003-01-01 Pallotti, Francesco; Baracca, A; HERNANDEZ ROSA, E; Walker, Wf; Solaini, G; Lenaz, G; D'Eril, Gm; Dimauro, S; Schon, Ea; Davidson, Mm
Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations
2004-01-01 Pallotti, Francesco; Baracca, A; HERNANDEZ ROSA, E; Walker, Wf; Solaini, G; Lenaz, G; MELZI D'ERIL, Gv; Dimauro, S; Schon, Ea; Davidson, M. M.
Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation
2002-01-01 Carelli, V; Baracca, A; Barogi, S; Pallotti, Francesco; Valentino, Ml; Montagna, P; Zeviani, M; Pini, A; Lenaz, G; Baruzzi, A; Solaini, G.
Biological variation of procalcitonin in healthy individuals
2004-01-01 A., Barassi; Pallotti, Francesco; G., Massari; A., Nauti; G. V., MELZI DERIL
Biological variation of procalcitonin in healthy individuals
2004-01-01 Barassi, A; Pallotti, Francesco; Massari, G; Nauti, A; D'Eril, Gvm
Biological variation of procalcitonin in healthy individuals
2004-01-01 Barassi, A; Pallotti, Francesco; D'Eril, Gm
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A new acute myeloid leukemia case with STAT5B-RARA gene fusion due to 17q21.2 interstitial deletion | 1-gen-2017 | Pessina, Chiara; Basilico, Claudia; Genoni, Angelo; Meroni, Emanuela; Elli, Lorenzo; Granata, Paola; Righi, Rossana; Pallotti, Francesco; Mora, Barbara; Ferrario, Andrea; Passamonti, Francesco; Casalone, Rosario | |
| A particular case of AML patient with the polymorphism G105G (rs11554137) and the missense mutation R132C in IDH1 gene | 1-gen-2019 | Accetta, R.; Campiotti, L.; Elli, L.; Casalone, R.; Pallotti, F. | |
| A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV | 1-gen-1999 | Bruno, C; Martinuzzi, A; Tang, Yy; Andreu, Al; Pallotti, Francesco; Bonilla, E; Shanske, S; Fu, J; Sue, Cm; Angelini, C; Dimauro, S; Manfredi, G. | |
| A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck | 1-gen-2014 | Pallotti, Francesco; Binelli, GIORGIO PIETRO MARIO; R., Fabbri; M. L., Valentino; R., Vicenti; M., Macciocca; S., Cevoli; A., Baruzzi; S., Dimauro; V., Carelli | |
| Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB gene | 1-gen-2019 | Marchet, S.; Invernizzi, F.; Blasevich, F.; Bruno, V.; Dusi, S.; Venco, P.; Fiorillo, C.; Baranello, G.; Pallotti, F.; Lamantea, E.; Mora, M.; Tiranti, V.; Lamperti, C. | |
| AN UPDATING OF THE BIOCHEMICAL FUNCTION OF COENZYME-Q IN MITOCHONDRIA | 1-gen-1994 | Lenaz, G; Fato, R; Castelluccio, C; Cavazzoni, M; Estornell, E; Huertas, Jf; Pallotti, Francesco; Castelli, Gp; Rauchova, H. | |
| Analysis of fluorophore labeled glycosaminoglycan disaccharides using polyacrylamide gel electroforesis and HPLC | 1-gen-2005 | Viola, Manuela; Karousou, Evgenia; Vigetti, Davide; A., Genasetti; Rizzi, M.; Pallotti, Francesco; DE LUCA, Giancarlo; Passi, Alberto | |
| Analysis of mtDNA deletions in muscle by in situ hybridization | 1-gen-2000 | Vu, Th; Tanji, K; Pallotti, Francesco; Golzi, V; Hirano, M; Dimauro, S; Bonilla, E. | |
| Analysis of three screening methods for the detection of calreticulin gene mutations | 1-gen-2020 | Accetta, R.; Elli, L.; Libera, L.; Siracusa, C.; Cassavia, F.; Orsini, F.; Orlandi, L.; Passamonti, F.; Casalone, R.; Pallotti, F. | |
| Aortic smooth muscle cells migration and the role of metalloproteinases and hyaluronan. | 1-gen-2008 | Vigetti, Davide; Moretto, P; Viola, Manuela; Genasetti, A; Rizzi, M; Karousou, Evgenia; Clerici, M; Bartolini, B; Pallotti, Francesco; DE LUCA, Giancarlo; Passi, Alberto | |
| Archaeogenomics in Caravate and Cittiglio (Lombardy): from the excavation of ancient human bones to the study of DNA | 1-gen-2022 | Olivieri, Anna; Pallotti, Francesco; Rosario Capodiferro, Marco; Colombo, Giulia; Licata, Marta; Tesi, Chiara; Semino, Ornella; Achilli, Alessandro; Torroni, Antonio | |
| ASSAY CONDITIONS FOR THE MITOCHONDRIAL NADH - COENZYME-Q OXIDOREDUCTASE | 1-gen-1993 | Estornell, E; Fato, R; Pallotti, Francesco; Lenaz, G. | |
| Assessing Heteroplasmic Load in Leber's Hereditary Optic Neuropathy Mutation 3460G->A/MT-ND1 with A Real-Time PCR Quantitative Approach | 1-gen-2007 | Genasetti, A; Valentino, M. L.; Carelli, V; Vigetti, Davide; Viola, Manuela; Karousou, Evgenia; Melzi, ; D'Eril, G. V.; DE LUCA, Giancarlo; Passi, Alberto; Pallotti, Francesco | |
| Authors’ Reply to Crampe and Langabeer: Technical Issues Behind Molecular Monitoring in Chronic Myeloid Leukemia | 1-gen-2015 | Mattarucchi, Elia; Pallotti, Francesco; Casalone, Rosario | |
| Biochemical analysis of mitochondrial function in cybrid cell lines harboring mtDNA mutations | 1-gen-2003 | Pallotti, Francesco; Baracca, A; HERNANDEZ ROSA, E; Walker, Wf; Solaini, G; Lenaz, G; D'Eril, Gm; Dimauro, S; Schon, Ea; Davidson, Mm | |
| Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations | 1-gen-2004 | Pallotti, Francesco; Baracca, A; HERNANDEZ ROSA, E; Walker, Wf; Solaini, G; Lenaz, G; MELZI D'ERIL, Gv; Dimauro, S; Schon, Ea; Davidson, M. M. | |
| Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation | 1-gen-2002 | Carelli, V; Baracca, A; Barogi, S; Pallotti, Francesco; Valentino, Ml; Montagna, P; Zeviani, M; Pini, A; Lenaz, G; Baruzzi, A; Solaini, G. | |
| Biological variation of procalcitonin in healthy individuals | 1-gen-2004 | A., Barassi; Pallotti, Francesco; G., Massari; A., Nauti; G. V., MELZI DERIL | |
| Biological variation of procalcitonin in healthy individuals | 1-gen-2004 | Barassi, A; Pallotti, Francesco; Massari, G; Nauti, A; D'Eril, Gvm | |
| Biological variation of procalcitonin in healthy individuals | 1-gen-2004 | Barassi, A; Pallotti, Francesco; D'Eril, Gm |