Lattante, Serena
Lattante, Serena
Analysis of STMN2 CA repeats in italian ALS patients shows no association
2023 Doronzio, Paolo Niccolo'; Lattante, Serena; Marangi, Giuseppe; Martello, Francesco; Conte, A.; Bisogni, G.; Bernardo, D.; Patanella, A. K.; Meleo, Emiliana; Zollino, Marcella; Sabatelli, Mario
Characterization of SOD1-DT, a Divergent Long Non-Coding RNA in the Locus of the SOD1 Human Gene
2023 Guerra, Marika; Meola, Lucia; Lattante, Serena; Conte, Amelia; Sabatelli, Mario; Sette, Claudio; Bernardini, Camilla
Evaluating the contribution of the gene TARDBP in Italian patients with amyotrophic lateral sclerosis
2023 Lattante, Serena; Sabatelli, Mario; Bisogni, Giulia.; Marangi, Giuseppe; Doronzio, Paolo Niccolò; Martello, Francesco; Renzi, Anna Gloria; Del Giudice, Elda; Leon, Alberta; Cimbolli, Paola; Marchione, Daniela; Costantino, Umberto; Lucioli, Gabriele; Bernardo, Daniela; Meleo, Emiliana; Patanella, Agata Katia; Romano, Angela; Zollino, Marcella; Conte, Amelia
Allele-specific silencing as therapy for familial amyotrophic lateral sclerosis caused by the p.G376D TARDBP mutation
2022 Romano, R.; De Luca, M.; Del Fiore, V. S.; Pecoraro, M.; Lattante, Serena; Sabatelli, Mario; La Bella, V.; Bucci, C.
Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients
2022 Perciballi, E.; Bovio, F.; Rosati, J.; Arrigoni, F.; D'Anzi, A.; Lattante, Serena; Gelati, M.; De Marchi, F.; Lombardi, I.; Ruotolo, G.; Forcella, M.; Mazzini, L.; D'Alfonso, S.; Corrado, L.; Sabatelli, Mario; Conte, A.; De Gioia, L.; Martino, S.; Vescovi, A. L.; Fusi, P.; Ferrari, D.
FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees
2022 Brenner, D.; Muller, K.; Lattante, Serena; Yilmaz, R.; Knehr, A.; Freischmidt, A.; Ludolph, A. C.; Andersen, P. M.; Weishaupt, J. H.
Generation of an induced pluripotent stem cell line (UCSCi002-A) from a patient with a variant in TARDBP gene associated with familial amyotrophic lateral sclerosis and frontotemporal dementia
2022 Martello, Francesco; Lattante, Serena; Doronzio, Paolo Niccolo'; Conte, A.; Bisogni, G.; Orteschi, D.; Luigetti, Marco; Marrucci, M. A.; Zollino, Marcella; Sabatelli, Mario; Marangi, Giuseppe
Clinical Heterogeneity of ALS-Implications for Models and Therapeutic Development
2021 Lattante, Serena; Sabatelli, Mario
Generation of an induced pluripotent stem cell line (CSS012-A (7672)) carrying the p.G376D heterozygous mutation in the TARDBP protein
2021 D'Anzi, A.; Altieri, F.; Perciballi, E.; Ferrari, D.; Torres, B.; Bernardini, L.; Lattante, Serena; Sabatelli, Mario; Vescovi, A. L.; Rosati, J.
Generation of an induced pluripotent stem cell line (UCSCi001-A) from a patient with early-onset amyotrophic lateral sclerosis carrying a FUS variant
2021 Martello, F.; Lattante, S.; Doronzio, P. N.; Conte, A.; Bisogni, G.; Orteschi, D.; Pirozzi, F.; Sabatelli, M.; Zollino, M.; Marangi, G.
Novel variants and cellular studies on patients' primary fibroblasts support a role for NEK1 missense variants in ALS pathogenesis
2021 Lattante, Serena; Doronzio, Paolo Niccolo'; Conte, Amelia; Marangi, Giuseppe; Martello, Francesco; Bisogni, Giulia; Meleo, Emiliana; Colavito, Davide; Del Giudice, Elda; Patanella, Agata Katia; Bernardo, Daniela; Romano, Angela; Zollino, Marcella; Sabatelli, Mario
SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration
2021 Barbier, M.; Camuzat, A.; Hachimi, K. E.; Guegan, J.; Rinaldi, D.; Lattante, Serena; Houot, M.; Sanchez-Valle, R.; Sabatelli, Mario; Antonell, A.; Molina-Porcel, L.; Clot, F.; Couratier, P.; Van Der Ende, E.; Van Der Zee, J.; Manzoni, C.; Camu, W.; Cazeneuve, C.; Sellal, F.; Didic, M.; Golfier, V.; Pasquier, F.; Duyckaerts, C.; Rossi, G.; Bruni, A. C.; Alvarez, V.; Gomez-Tortosa, E.; De Mendonca, A.; Graff, C.; Masellis, M.; Nacmias, B.; Oumoussa, B. M.; Jornea, L.; Forlani, S.; Van Deerlin, V.; Rohrer, J. D.; Gelpi, E.; Rademakers, R.; Van Swieten, J.; Le Guern, E.; Van Broeckhoven, C.; Ferrari, R.; Genin, E.; Brice, A.; Le Ber, I.
Targeting S100A4 with niclosamide attenuates inflammatory and profibrotic pathways in models of amyotrophic lateral sclerosis
2021 Milani, M.; Mammarella, E.; Rossi, S.; Miele, C.; Lattante, Serena; Sabatelli, Mario; Cozzolino, M.; D'Ambrosi, N.; Apolloni, S.
Adult phenotype in Koolen-de Vries/KANSL1 haploinsufficiency syndrome
2020 Amenta, S.; Frangella, S.; Marangi, G.; Lattante, S.; Ricciardi, S.; Doronzio, P. N.; Orteschi, D.; Veredice, C.; Contaldo, I.; Zampino, G.; Gentile, M.; Scarano, E.; Graziano, C.; Zollino, M.
ALS skin fibroblasts reveal oxidative stress and ERK1/2-mediated cytoplasmic localization of TDP-43
2020 Romano, Nicla; Catalani, Alessia; Lattante, Serena; Belardo, Antonio; Proietti, Silvia; Bertini, Laura; Silvestri, Federica; Catalani, Elisabetta; Cervia, Davide; Zolla, Lello; Sabatelli, Mario; Welshhans, Kristy; Ceci, Marcello
High-throughput genetic testing in ALS: The challenging path of variant classification considering the acmg guidelines
2020 Lattante, Serena; Marangi, Giuseppe; Doronzio, Paolo Niccolo'; Conte, A.; Bisogni, G.; Zollino, Marcella; Sabatelli, Mario
SOD1 p.D12Y variant is associated with ALS/distal myopathy spectrum
2020 Tasca, Giorgio; Lattante, Serena; Marangi, Giuseppe; Conte, Amelia; Bernardo, Daniela; Bisogni, Giulia; Mandich, Paola; Zollino, Marcella; Ragozzino, Elvira; Udd, Bjarne; Sabatelli, Mario
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS
2019 Lattante, Serena; Doronzio, Paolo Niccolo'; Marangi, Giuseppe; Conte, Amelia; Bisogni, Giulia; Bernardo, Daniela; Russo, Tommaso; Lamberti, Dante; Patrizi, Sara; Paolo Apollo, Francesco; Lunetta, Christian; Scarlino, Stefania; Pozzi, Laura; Zollino, Marcella; Riva, Nilo; Sabatelli, Mario
Germline pathogenic variant in PIK3CA leading to symmetrical overgrowth with marked macrocephaly and mild global developmental delay
2019 Zollino, Marcella; Ranieri, C.; Grossi, V.; Leoni, Chiara; Lattante, Serena; Mazza', Daniela; Simone, C.; Resta, N.
Relations between C9orf72 expansion size in blood, age at onset, age at collection and transmission across generations in patients and presymptomatic carriers
2019 Fournier, C.; Barbier, M.; Camuzat, A.; Anquetil, V.; Lattante, Serena; Clot, F.; Cazeneuve, C.; Rinaldi, D.; Couratier, P.; Deramecourt, V.; Sabatelli, Mario; Belliard, S.; Vercelletto, M.; Forlani, S.; Jornea, L.; Brice, A.; Auriacombe, S.; Blanc, F.; Bouteleau-Bretonniere, C.; Ceccaldi, M.; Didic, M.; Dubois, B.; Duyckaerts, C.; Etcharry-Bouix, F.; Golfier, V.; Hannequin, D.; Lacomblez, L.; Le Ber, I.; Levy, R.; Michel, B. -F.; Pasquier, F.; Thomas-Anterion, C.; Pariente, J.; Sellal, F.; Benchetrit, E.; Bertin, H.; Bertrand, A.; Bissery, A.; Bombois, S.; Boncoeur, M. -P.; Cassagnaud, P.; Chastan, M.; Chen, Y.; Chupin, M.; Colliot, O.; Delbeucq, X.; Delmaire, C.; Gerardin, E.; Hossein-Foucher, C.; Habert, M. -O.; Lautrette, G.; Lebouvier, T.; Lehericy, S.; Le Toullec, B.; Martineau, K.; Mackowiak, M. -A.; Monteil, J.; Petyt, G.; Pradat, P. -F.; Oya, A. -H.; Rollin-Sillaire, A.; Salachas, F.; Sayah, S.; Wallon, D.; Leguern, E.
| Data di pubblicazione | Titolo | Autore(i) | File |
|---|---|---|---|
| 1-gen-2023 | Analysis of STMN2 CA repeats in italian ALS patients shows no association | Doronzio, Paolo Niccolo'; Lattante, Serena; Marangi, Giuseppe; Martello, Francesco; Conte, A.; Bisogni, G.; Bernardo, D.; Patanella, A. K.; Meleo, Emiliana; Zollino, Marcella; Sabatelli, Mario | |
| 1-gen-2023 | Characterization of SOD1-DT, a Divergent Long Non-Coding RNA in the Locus of the SOD1 Human Gene | Guerra, Marika; Meola, Lucia; Lattante, Serena; Conte, Amelia; Sabatelli, Mario; Sette, Claudio; Bernardini, Camilla | |
| 1-gen-2023 | Evaluating the contribution of the gene TARDBP in Italian patients with amyotrophic lateral sclerosis | Lattante, Serena; Sabatelli, Mario; Bisogni, Giulia.; Marangi, Giuseppe; Doronzio, Paolo Niccolò; Martello, Francesco; Renzi, Anna Gloria; Del Giudice, Elda; Leon, Alberta; Cimbolli, Paola; Marchione, Daniela; Costantino, Umberto; Lucioli, Gabriele; Bernardo, Daniela; Meleo, Emiliana; Patanella, Agata Katia; Romano, Angela; Zollino, Marcella; Conte, Amelia | |
| 1-gen-2022 | Allele-specific silencing as therapy for familial amyotrophic lateral sclerosis caused by the p.G376D TARDBP mutation | Romano, R.; De Luca, M.; Del Fiore, V. S.; Pecoraro, M.; Lattante, Serena; Sabatelli, Mario; La Bella, V.; Bucci, C. | |
| 1-gen-2022 | Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients | Perciballi, E.; Bovio, F.; Rosati, J.; Arrigoni, F.; D'Anzi, A.; Lattante, Serena; Gelati, M.; De Marchi, F.; Lombardi, I.; Ruotolo, G.; Forcella, M.; Mazzini, L.; D'Alfonso, S.; Corrado, L.; Sabatelli, Mario; Conte, A.; De Gioia, L.; Martino, S.; Vescovi, A. L.; Fusi, P.; Ferrari, D. | |
| 1-gen-2022 | FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees | Brenner, D.; Muller, K.; Lattante, Serena; Yilmaz, R.; Knehr, A.; Freischmidt, A.; Ludolph, A. C.; Andersen, P. M.; Weishaupt, J. H. | |
| 1-gen-2022 | Generation of an induced pluripotent stem cell line (UCSCi002-A) from a patient with a variant in TARDBP gene associated with familial amyotrophic lateral sclerosis and frontotemporal dementia | Martello, Francesco; Lattante, Serena; Doronzio, Paolo Niccolo'; Conte, A.; Bisogni, G.; Orteschi, D.; Luigetti, Marco; Marrucci, M. A.; Zollino, Marcella; Sabatelli, Mario; Marangi, Giuseppe | |
| 1-gen-2021 | Clinical Heterogeneity of ALS-Implications for Models and Therapeutic Development | Lattante, Serena; Sabatelli, Mario | |
| 1-gen-2021 | Generation of an induced pluripotent stem cell line (CSS012-A (7672)) carrying the p.G376D heterozygous mutation in the TARDBP protein | D'Anzi, A.; Altieri, F.; Perciballi, E.; Ferrari, D.; Torres, B.; Bernardini, L.; Lattante, Serena; Sabatelli, Mario; Vescovi, A. L.; Rosati, J. | |
| 1-gen-2021 | Generation of an induced pluripotent stem cell line (UCSCi001-A) from a patient with early-onset amyotrophic lateral sclerosis carrying a FUS variant | Martello, F.; Lattante, S.; Doronzio, P. N.; Conte, A.; Bisogni, G.; Orteschi, D.; Pirozzi, F.; Sabatelli, M.; Zollino, M.; Marangi, G. | |
| 1-gen-2021 | Novel variants and cellular studies on patients' primary fibroblasts support a role for NEK1 missense variants in ALS pathogenesis | Lattante, Serena; Doronzio, Paolo Niccolo'; Conte, Amelia; Marangi, Giuseppe; Martello, Francesco; Bisogni, Giulia; Meleo, Emiliana; Colavito, Davide; Del Giudice, Elda; Patanella, Agata Katia; Bernardo, Daniela; Romano, Angela; Zollino, Marcella; Sabatelli, Mario | |
| 1-gen-2021 | SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration | Barbier, M.; Camuzat, A.; Hachimi, K. E.; Guegan, J.; Rinaldi, D.; Lattante, Serena; Houot, M.; Sanchez-Valle, R.; Sabatelli, Mario; Antonell, A.; Molina-Porcel, L.; Clot, F.; Couratier, P.; Van Der Ende, E.; Van Der Zee, J.; Manzoni, C.; Camu, W.; Cazeneuve, C.; Sellal, F.; Didic, M.; Golfier, V.; Pasquier, F.; Duyckaerts, C.; Rossi, G.; Bruni, A. C.; Alvarez, V.; Gomez-Tortosa, E.; De Mendonca, A.; Graff, C.; Masellis, M.; Nacmias, B.; Oumoussa, B. M.; Jornea, L.; Forlani, S.; Van Deerlin, V.; Rohrer, J. D.; Gelpi, E.; Rademakers, R.; Van Swieten, J.; Le Guern, E.; Van Broeckhoven, C.; Ferrari, R.; Genin, E.; Brice, A.; Le Ber, I. | |
| 1-gen-2021 | Targeting S100A4 with niclosamide attenuates inflammatory and profibrotic pathways in models of amyotrophic lateral sclerosis | Milani, M.; Mammarella, E.; Rossi, S.; Miele, C.; Lattante, Serena; Sabatelli, Mario; Cozzolino, M.; D'Ambrosi, N.; Apolloni, S. | |
| 1-gen-2020 | Adult phenotype in Koolen-de Vries/KANSL1 haploinsufficiency syndrome | Amenta, S.; Frangella, S.; Marangi, G.; Lattante, S.; Ricciardi, S.; Doronzio, P. N.; Orteschi, D.; Veredice, C.; Contaldo, I.; Zampino, G.; Gentile, M.; Scarano, E.; Graziano, C.; Zollino, M. | |
| 1-gen-2020 | ALS skin fibroblasts reveal oxidative stress and ERK1/2-mediated cytoplasmic localization of TDP-43 | Romano, Nicla; Catalani, Alessia; Lattante, Serena; Belardo, Antonio; Proietti, Silvia; Bertini, Laura; Silvestri, Federica; Catalani, Elisabetta; Cervia, Davide; Zolla, Lello; Sabatelli, Mario; Welshhans, Kristy; Ceci, Marcello | |
| 1-gen-2020 | High-throughput genetic testing in ALS: The challenging path of variant classification considering the acmg guidelines | Lattante, Serena; Marangi, Giuseppe; Doronzio, Paolo Niccolo'; Conte, A.; Bisogni, G.; Zollino, Marcella; Sabatelli, Mario | |
| 1-gen-2020 | SOD1 p.D12Y variant is associated with ALS/distal myopathy spectrum | Tasca, Giorgio; Lattante, Serena; Marangi, Giuseppe; Conte, Amelia; Bernardo, Daniela; Bisogni, Giulia; Mandich, Paola; Zollino, Marcella; Ragozzino, Elvira; Udd, Bjarne; Sabatelli, Mario | |
| 1-gen-2019 | Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS | Lattante, Serena; Doronzio, Paolo Niccolo'; Marangi, Giuseppe; Conte, Amelia; Bisogni, Giulia; Bernardo, Daniela; Russo, Tommaso; Lamberti, Dante; Patrizi, Sara; Paolo Apollo, Francesco; Lunetta, Christian; Scarlino, Stefania; Pozzi, Laura; Zollino, Marcella; Riva, Nilo; Sabatelli, Mario | |
| 1-gen-2019 | Germline pathogenic variant in PIK3CA leading to symmetrical overgrowth with marked macrocephaly and mild global developmental delay | Zollino, Marcella; Ranieri, C.; Grossi, V.; Leoni, Chiara; Lattante, Serena; Mazza', Daniela; Simone, C.; Resta, N. | |
| 1-gen-2019 | Relations between C9orf72 expansion size in blood, age at onset, age at collection and transmission across generations in patients and presymptomatic carriers | Fournier, C.; Barbier, M.; Camuzat, A.; Anquetil, V.; Lattante, Serena; Clot, F.; Cazeneuve, C.; Rinaldi, D.; Couratier, P.; Deramecourt, V.; Sabatelli, Mario; Belliard, S.; Vercelletto, M.; Forlani, S.; Jornea, L.; Brice, A.; Auriacombe, S.; Blanc, F.; Bouteleau-Bretonniere, C.; Ceccaldi, M.; Didic, M.; Dubois, B.; Duyckaerts, C.; Etcharry-Bouix, F.; Golfier, V.; Hannequin, D.; Lacomblez, L.; Le Ber, I.; Levy, R.; Michel, B. -F.; Pasquier, F.; Thomas-Anterion, C.; Pariente, J.; Sellal, F.; Benchetrit, E.; Bertin, H.; Bertrand, A.; Bissery, A.; Bombois, S.; Boncoeur, M. -P.; Cassagnaud, P.; Chastan, M.; Chen, Y.; Chupin, M.; Colliot, O.; Delbeucq, X.; Delmaire, C.; Gerardin, E.; Hossein-Foucher, C.; Habert, M. -O.; Lautrette, G.; Lebouvier, T.; Lehericy, S.; Le Toullec, B.; Martineau, K.; Mackowiak, M. -A.; Monteil, J.; Petyt, G.; Pradat, P. -F.; Oya, A. -H.; Rollin-Sillaire, A.; Salachas, F.; Sayah, S.; Wallon, D.; Leguern, E. |