GOMEZ, Maria Macarena
GOMEZ, Maria Macarena
DIPARTIMENTO DI NEUROSCIENZE, BIOMEDICINA E MOVIMENTO
3,5-dicaffeoylquinic acid lowers 3T3-L1 mitotic clonal expansion and adipocyte differentiation by enhancing heme oxygenase-1 expression
2021-01-01 Raineri, Alice; Campagnari, Rachele; Dal Toso, Roberto; Copetti, Stefano; Gomez-Lira, Macarena; Menegazzi, Marta
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease
1995-01-01 Gomez-Lira, M.; Perusi, C.; Brutti, N.; Farnetani, M. A.; Margollicci, M. A.; Rizzuto, N.; Pignatti, P. F.; Salviati, A.
A base substitution at IVS-19 3' splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta
1994-01-01 Mottes, Monica; Sangalli, Antonella; Valli, M.; Forlino, A.; Gomez, Maria Macarena; Antoniazzi, Franco; CONSTANTINOU DELTAS, C. D.; Cetta, G.; Pignatti, Pierfranco
A base substitution at IVS-19 3'-end splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta
1994-01-01 Mottes, M.; Sangalli, A.; Valli, M.; Forlino, A.; Gomez-Lira, M.; Antoniazzi, F.; Constantinou-Deltas, C. D.; Cetta, G.; Pignatti, P. F.
A Case-control study of myelin oligodendrocyte glycoprotein and CD45 polymorphisms in multiple sclerosis in Verona, Italy
2004-01-01 Gomez, Maria Macarena; S., Ottaviani; S., Mazzola; A., Salviati; Gajofatto, Alberto; E., Turri; A., Fiumani; L., Deotto; G., Moretto; N., Rizzuto; Benedetti, Mariadonata
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients.
1995-01-01 Gomez, Maria Macarena; Sangalli, Antonella; Mottes, Monica; Perusi, C; Pignatti, Pierfranco; Rizzuto, Nicolo'; Salviati, Alessandro
A de novo G to T transversion in a pro-alpha 1(I) collagen gene for a moderate case of osteogenesis imperfecta. Substitution of cysteine for glycine 178 in the triple helical domain
1991-01-01 Valli, M.; Mottes, Monica; Tenni, R.; Sangalli, Antonella; Gomez, Maria Macarena; Rossi, A.; Antoniazzi, Franco; Cetta, G.; Pignatti, Pierfranco
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease
2001-01-01 Gomez-Lira, M.; Mottes, M.; Perusi, C.; Pignatti, P. F.; Rizzuto, N.; Gatti, R.; Salviati, A.
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene
1997-01-01 C., Perusi; Gomez, Maria Macarena; Mottes, Monica; Pignatti, Pierfranco; Rizzuto, Nicolo'; Salviati, Alessandro
Adult-onset MLD: A gene mutation with isolated polyneuropathy
2000-01-01 Felice, K. J.; Gomez Lira, M.; Natowicz, M.; Grunnet, M. L.; Tsongalis, G. J.; Sima, A. A. F.; Kaplan, R. F.
Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation
2011-01-01 Gomez, Maria Macarena; Tessari, Gianpaolo; Mazzola, Silvia; Malerba, Giovanni; Rugiu, Carlo; Naldi, L; Nacchia, Francesco; Valerio, F; Anna, B; Forni, Alberto; Boschiero, Luigino; Sandrini, S; Faggian, Giuseppe; Girolomoni, Giampiero; Turco, Alberto
Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis.
2001-01-01 Castellani, C; Gomez, Maria Macarena; Frulloni, Luca; Delmarco, A; Marzari, M; Bonizzato, A; Cavallini, Giorgio; Pignatti, Pierfranco; Mastella, G.
Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation.
2007-01-01 Gomez, Maria Macarena; Mazzola, Silvia; Tessari, Gianpaolo; Malerba, Giovanni; Ortombina, M.; Naldi, L.; Remuzzi, G.; Boschiero, Luigino; Forni, Alberto; Rugiu, Carlo; Piaserico, S.; Girolomoni, Giampiero; Turco, Alberto
Association of microRNA 146a polymorphism rs2910164 and the risk of melanoma in an Italian population
2015-01-01 Gomez, Maria Macarena; Ferronato, Silvia; Orlandi, Elisa; Dal Molin, Anna; Malerba, Giovanni; Frigerio, Simona; Rodolfo, Monica; Romanelli, Maria
Association of promoter polymorphism -765G>C in the PTGS2 gene with malignant melanoma in Italian patients and its correlation to gene expression in dermal fibroblasts.
2014-01-01 Gomez, Maria Macarena; Ferronato, Silvia; Malerba, Giovanni; Santinami, M; Maurichi, A; Sangalli, Antonella; Turco, Alberto; Perego, P; Rodolfo, M.
Biopsychosocial model of resilience in young adults with multiple sclerosis (BPS-ARMS): an observational study protocol exploring psychological reactions early after diagnosis
2019-01-01 Gajofatto, Alberto; Donisi, Valeria; Busch, Isolde Martina; Gobbin, Francesca; Butturini, Elena; Calabrese, Massimiliano; Carcereri de Prati, Alessandra; Cesari, Paola; Del Piccolo, Lidia; Donadelli, Massimo; Fabene, Paolo; Fochi, Stefania; Gomez-Lira, Macarena; Magliozzi, Roberta; Malerba, Giovanni; Mariotti, Raffaella; Mariotto, Sofia; Milanese, Chiara; Romanelli, Maria Grazia; Sbarbati, Andrea; Schena, Federico; Mazzi, Maria Angela; Rimondini, Michela
Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia
2003-01-01 Patuzzo, Cristina; Castellani, C.; Sagramoso, C.; Gomez, Maria Macarena; Bonamini, D.; Belpinati, F.; Dechecchi, M. C.; Assael, B. M.; Pignatti, Pierfranco
CD14(++) CD16(-) monocytes are the main source of 11β-HSD type 1 after IL-4 stimulation
2017-01-01 Kunnathully, VIDYA SATHEESN; Gomez, Maria Macarena; Bassi, Giulio; Poli, Fabio; Zoratti, Elisa; LA VERDE, Valentina; Idolazzi, Luca; Gatti, Davide; Viapiana, Ombretta; Adami, Silvano; Rossini, Maurizio
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers
2003-01-01 Gomez, Maria Macarena; Liguori, M.; Magnani, C.; Bonamini, D.; Salviati, Alessandro; Leone, M.; Andreoli, V.; Trojano, M.; Valentino, P.; Savatteri, G.; Quattrone, A.; Pignatti, Pierfranco; Momigliano Richiardi, P.; Giordano, M.
CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia
2001-01-01 Gomez, Maria Macarena; Patuzzo, Cristina; C., Castellani; Bovo, Paolo; Cavallini, Giorgio; G., Mastella; Pignatti, Pierfranco
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 3,5-dicaffeoylquinic acid lowers 3T3-L1 mitotic clonal expansion and adipocyte differentiation by enhancing heme oxygenase-1 expression | 1-gen-2021 | Raineri, Alice; Campagnari, Rachele; Dal Toso, Roberto; Copetti, Stefano; Gomez-Lira, Macarena; Menegazzi, Marta | |
| A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease | 1-gen-1995 | Gomez-Lira, M.; Perusi, C.; Brutti, N.; Farnetani, M. A.; Margollicci, M. A.; Rizzuto, N.; Pignatti, P. F.; Salviati, A. | |
| A base substitution at IVS-19 3' splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta | 1-gen-1994 | Mottes, Monica; Sangalli, Antonella; Valli, M.; Forlino, A.; Gomez, Maria Macarena; Antoniazzi, Franco; CONSTANTINOU DELTAS, C. D.; Cetta, G.; Pignatti, Pierfranco | |
| A base substitution at IVS-19 3'-end splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta | 1-gen-1994 | Mottes, M.; Sangalli, A.; Valli, M.; Forlino, A.; Gomez-Lira, M.; Antoniazzi, F.; Constantinou-Deltas, C. D.; Cetta, G.; Pignatti, P. F. | |
| A Case-control study of myelin oligodendrocyte glycoprotein and CD45 polymorphisms in multiple sclerosis in Verona, Italy | 1-gen-2004 | Gomez, Maria Macarena; S., Ottaviani; S., Mazzola; A., Salviati; Gajofatto, Alberto; E., Turri; A., Fiumani; L., Deotto; G., Moretto; N., Rizzuto; Benedetti, Mariadonata | |
| A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. | 1-gen-1995 | Gomez, Maria Macarena; Sangalli, Antonella; Mottes, Monica; Perusi, C; Pignatti, Pierfranco; Rizzuto, Nicolo'; Salviati, Alessandro | |
| A de novo G to T transversion in a pro-alpha 1(I) collagen gene for a moderate case of osteogenesis imperfecta. Substitution of cysteine for glycine 178 in the triple helical domain | 1-gen-1991 | Valli, M.; Mottes, Monica; Tenni, R.; Sangalli, Antonella; Gomez, Maria Macarena; Rossi, A.; Antoniazzi, Franco; Cetta, G.; Pignatti, Pierfranco | |
| A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease | 1-gen-2001 | Gomez-Lira, M.; Mottes, M.; Perusi, C.; Pignatti, P. F.; Rizzuto, N.; Gatti, R.; Salviati, A. | |
| A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene | 1-gen-1997 | C., Perusi; Gomez, Maria Macarena; Mottes, Monica; Pignatti, Pierfranco; Rizzuto, Nicolo'; Salviati, Alessandro | |
| Adult-onset MLD: A gene mutation with isolated polyneuropathy | 1-gen-2000 | Felice, K. J.; Gomez Lira, M.; Natowicz, M.; Grunnet, M. L.; Tsongalis, G. J.; Sima, A. A. F.; Kaplan, R. F. | |
| Analysis of the 3'UTR of the prostaglandin synthetase-2 (PTGS-2/COX-2) gene in non-melanoma skin cancer after organ transplantation | 1-gen-2011 | Gomez, Maria Macarena; Tessari, Gianpaolo; Mazzola, Silvia; Malerba, Giovanni; Rugiu, Carlo; Naldi, L; Nacchia, Francesco; Valerio, F; Anna, B; Forni, Alberto; Boschiero, Luigino; Sandrini, S; Faggian, Giuseppe; Girolomoni, Giampiero; Turco, Alberto | |
| Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis. | 1-gen-2001 | Castellani, C; Gomez, Maria Macarena; Frulloni, Luca; Delmarco, A; Marzari, M; Bonizzato, A; Cavallini, Giorgio; Pignatti, Pierfranco; Mastella, G. | |
| Association of functional gene variants in the regulatory regions of COX-2 gene (PTGS2) with nonmelanoma skin cancer after organ transplantation. | 1-gen-2007 | Gomez, Maria Macarena; Mazzola, Silvia; Tessari, Gianpaolo; Malerba, Giovanni; Ortombina, M.; Naldi, L.; Remuzzi, G.; Boschiero, Luigino; Forni, Alberto; Rugiu, Carlo; Piaserico, S.; Girolomoni, Giampiero; Turco, Alberto | |
| Association of microRNA 146a polymorphism rs2910164 and the risk of melanoma in an Italian population | 1-gen-2015 | Gomez, Maria Macarena; Ferronato, Silvia; Orlandi, Elisa; Dal Molin, Anna; Malerba, Giovanni; Frigerio, Simona; Rodolfo, Monica; Romanelli, Maria | |
| Association of promoter polymorphism -765G>C in the PTGS2 gene with malignant melanoma in Italian patients and its correlation to gene expression in dermal fibroblasts. | 1-gen-2014 | Gomez, Maria Macarena; Ferronato, Silvia; Malerba, Giovanni; Santinami, M; Maurichi, A; Sangalli, Antonella; Turco, Alberto; Perego, P; Rodolfo, M. | |
| Biopsychosocial model of resilience in young adults with multiple sclerosis (BPS-ARMS): an observational study protocol exploring psychological reactions early after diagnosis | 1-gen-2019 | Gajofatto, Alberto; Donisi, Valeria; Busch, Isolde Martina; Gobbin, Francesca; Butturini, Elena; Calabrese, Massimiliano; Carcereri de Prati, Alessandra; Cesari, Paola; Del Piccolo, Lidia; Donadelli, Massimo; Fabene, Paolo; Fochi, Stefania; Gomez-Lira, Macarena; Magliozzi, Roberta; Malerba, Giovanni; Mariotti, Raffaella; Mariotto, Sofia; Milanese, Chiara; Romanelli, Maria Grazia; Sbarbati, Andrea; Schena, Federico; Mazzi, Maria Angela; Rimondini, Michela | |
| Cationic trypsinogen and pancreatic secretory trypsin inhibitor gene mutations in neonatal hypertrypsinaemia | 1-gen-2003 | Patuzzo, Cristina; Castellani, C.; Sagramoso, C.; Gomez, Maria Macarena; Bonamini, D.; Belpinati, F.; Dechecchi, M. C.; Assael, B. M.; Pignatti, Pierfranco | |
| CD14(++) CD16(-) monocytes are the main source of 11β-HSD type 1 after IL-4 stimulation | 1-gen-2017 | Kunnathully, VIDYA SATHEESN; Gomez, Maria Macarena; Bassi, Giulio; Poli, Fabio; Zoratti, Elisa; LA VERDE, Valentina; Idolazzi, Luca; Gatti, Davide; Viapiana, Ombretta; Adami, Silvano; Rossini, Maurizio | |
| CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers | 1-gen-2003 | Gomez, Maria Macarena; Liguori, M.; Magnani, C.; Bonamini, D.; Salviati, Alessandro; Leone, M.; Andreoli, V.; Trojano, M.; Valentino, P.; Savatteri, G.; Quattrone, A.; Pignatti, Pierfranco; Momigliano Richiardi, P.; Giordano, M. | |
| CFTR and cationic trypsinogen gene mutations in idiopathic pancreatitis and neonatal hypertrypsinemia | 1-gen-2001 | Gomez, Maria Macarena; Patuzzo, Cristina; C., Castellani; Bovo, Paolo; Cavallini, Giorgio; G., Mastella; Pignatti, Pierfranco |