Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Fiorenzo A. Peverali"'
Autor:
Paola Crociara, Maria Novella Chieppa, Elena Vallino Costassa, Elena Berrone, Marina Gallo, Monica Lo Faro, Maria Domenica Pintore, Barbara Iulini, Antonio D'Angelo, Giovanni Perona, Alberto Botter, Donato Formicola, Alberto Rainoldi, Marianna Paulis, Paolo Vezzoni, Federica Meli, Fiorenzo Antonio Peverali, Caterina Bendotti, Maria Chiara Trolese, Laura Pasetto, Valentina Bonetto, Giovanna Lazzari, Roberto Duchi, Andrea Perota, Irina Lagutina, Corinne Quadalti, Maria Silvia Gennero, Daniela Dezzutto, Rosanna Desiato, Marina Boido, Matilde Ghibaudi, Maria Consuelo Valentini, Maria Caramelli, Cesare Galli, Cristina Casalone, Cristiano Corona
Publikováno v:
Neurobiology of Disease, Vol 124, Iss , Pp 263-275 (2019)
Amyotrophic Lateral Sclerosis (ALS) is a neural disorder gradually leading to paralysis of the whole body. Alterations in superoxide dismutase SOD1 gene have been linked with several variants of familial ALS. Here, we investigated a transgenic (Tg) c
Externí odkaz:
https://doaj.org/article/a0482bdf80404e0594753d7ba9be41dd
Autor:
Giulia Branca, Miria Stefanini, Bruno Vaz, Fiorenzo A. Peverali, Tiziana Nardo, Manuela Mura, Manuela Lanzafame, Donata Orioli, Mingyue Qiang, Debora Ferri, Sebastian Iben, Luca Bini, Claudia Landi
Publikováno v:
Nucleic Acids Research
CSA and CSB proteins are key players in transcription-coupled nucleotide excision repair (TC-NER) pathway that removes UV-induced DNA lesions from the transcribed strands of expressed genes. Additionally, CS proteins play relevant but still elusive r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa2d7c0513cc6738d5c3d85eb6e5d84f
https://pubmed.ncbi.nlm.nih.gov/34581821
https://pubmed.ncbi.nlm.nih.gov/34581821
Autor:
Anita, Lombardi, Lavinia, Arseni, Roberta, Carriero, Emmanuel, Compe, Elena, Botta, Debora, Ferri, Martina, Uggè, Giuseppe, Biamonti, Fiorenzo A, Peverali, Silvia, Bione, Donata, Orioli
Publikováno v:
Proc Natl Acad Sci U S A
The cancer-free photosensitive trichothiodystrophy (PS-TTD) and the cancer-prone xeroderma pigmentosum (XP) are rare monogenic disorders that can arise from mutations in the same genes, namely ERCC2/XPD or ERCC3/XPB. Both XPD and XPB proteins belong
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::335a5f7eb05783df37a82472b3ef4b77
https://pubmed.ncbi.nlm.nih.gov/34155103
https://pubmed.ncbi.nlm.nih.gov/34155103
Autor:
Emmanuel Compe, Roberta Carriero, Anita Lombardi, Elena Botta, Martina Uggè, Silvia Bione, Lavinia Arseni, Giuseppe Biamonti, Donata Orioli, Fiorenzo A. Peverali, Debora Ferri
Publikováno v:
Proceedings of the National Academy of Sciences. 118
The cancer-free photosensitive trichothiodystrophy (PS-TTD) and the cancer-prone xeroderma pigmentosum (XP) are rare monogenic disorders that can arise from mutations in the same genes, namely ERCC2/XPD or ERCC3/XPB Both XPD and XPB proteins belong t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::861916b43e50e2190ad46cfcd2ec61f2
https://doi.org/10.1073/pnas.2024502118
https://doi.org/10.1073/pnas.2024502118
Autor:
Sara Seneca, Laura Baranello, Kathelijn Keymolen, Donata Orioli, E. Heller, Manuela Lanzafame, Elena Botta, Robert M. Stephens, Alan R. Lehmann, John J. DiGiovanna, Christiane Kuschal, Roberta Ricotti, Tiziana Nardo, David Levens, Yongmei Zhao, Fiorenzo A. Peverali, Sikandar G. Khan, Deborah Tamura, Miria Stefanini, Kenneth H. Kraemer, Giuseppina Caligiuri
Publikováno v:
The American Journal of Human Genetics. 98:627-642
The general transcription factor IIE (TFIIE) is essential for transcription initiation by RNA polymerase II (RNA pol II) via direct interaction with the basal transcription/DNA repair factor IIH (TFIIH). TFIIH harbors mutations in two rare genetic di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1031b65a93a4b682718aced4078f80cc
https://doi.org/10.1016/j.ajhg.2016.02.008
https://doi.org/10.1016/j.ajhg.2016.02.008
Autor:
Luca Diamanti, Francesca Polveraccio, Matteo Bordoni, Orietta Pansarasa, Gabriellla Tedeschi, Michela Dell'Orco, Fiorenzo A. Peverali, Elisa Maffioli, Mauro Ceroni, Valentina Sardone, Laura Arrigoni, Pamela Milani, Cristina Cereda
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1859:315-323
Background It is still unclear whether oxidative stress (OS) is a disease consequence or is directly involved in the etiology of neurodegenerative disorders (NDs) onset and/or progression; however, many of these conditions are associated with increas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8e26b53d259b9ff0338d8341f1d1449
https://doi.org/10.1016/j.bbagrm.2015.11.009
https://doi.org/10.1016/j.bbagrm.2015.11.009
Autor:
Federica Meli, Paolo Vezzoni, Maria Chiara Trolese, Valentina Bonetto, Caterina Bendotti, Cristina Casalone, Maria Consuelo Valentini, Maria Novella Chieppa, Donato Formicola, Matilde Ghibaudi, Elena Vallino Costassa, Giovanna Lazzari, Marina Boido, Barbara Iulini, Maria Domenica Pintore, Elena Berrone, Monica Lo Faro, Paola Crociara, Laura Pasetto, Fiorenzo Antonio Peverali, Corinne Quadalti, Andrea Perota, Irina Lagutina, Alberto Botter, Cesare Galli, Marianna Paulis, Roberto Duchi, Marina Gallo, Maria Silvia Gennero, Antonio D'Angelo, Giovanni Perona, Maria Caramelli, Daniela Dezzutto, Alberto Rainoldi, Cristiano Corona, Rosanna Desiato
Publikováno v:
Neurobiology of Disease, Vol 124, Iss, Pp 263-275 (2019)
Amyotrophic Lateral Sclerosis (ALS) is a neural disorder gradually leading to paralysis of the whole body. Alterations in superoxide dismutase SOD1 gene have been linked with several variants of familial ALS. Here, we investigated a transgenic (Tg) c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85219416c8c893b24c11d7fd05e7d272
https://pubmed.ncbi.nlm.nih.gov/30471417
https://pubmed.ncbi.nlm.nih.gov/30471417
Autor:
Elena Botta, Emmanuel Compe, Tiziana Nardo, Fiorenzo A. Peverali, Christophe Giraudon, Donata Orioli, Miria Stefanini, Laura Arrigoni, Manuela Mura, Jean-Marc Egly
Publikováno v:
Human Molecular Genetics. 22:1061-1073
Mutations in the XPD subunit of the transcription/DNA repair factor (TFIIH) give rise to trichothiodystrophy (TTD), a rare hereditary multisystem disorder with skin abnormalities. Here, we show that TTD primary dermal fibroblasts contain low amounts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::226f3e0723a68dd508ee6192b9726107
https://doi.org/10.1093/hmg/dds508
https://doi.org/10.1093/hmg/dds508
Autor:
Paola Fortugno, Fiorenzo A. Peverali, Emmanuel Compe, António Afonso-Barroso, Miria Stefanini, Donata Orioli, Giovanna Zambruno, Jean-Marc Egly, Lavinia Arseni, Manuela Lanzafame, Alan R. Lehmann
Mutations in the XPD subunit of the DNA repair/transcription factor TFIIH result in distinct clinical entities, including the cancer-prone xeroderma pigmentosum (XP) and the multisystem disorder trichothiodystrophy (TTD), which share only cutaneous p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a60f77263a62692ef15ad550cf34f912
https://europepmc.org/articles/PMC4321311/
https://europepmc.org/articles/PMC4321311/
To date, a complete understanding of the molecular events leading to DNA replication origin activation in mammalian cells still remains elusive. In this work, we report the results of a high resolution chromatin immunoprecipitation study to detect pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f33ff9b58d228e474e6805d37f948405
https://europepmc.org/articles/PMC4352957/
https://europepmc.org/articles/PMC4352957/