Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Daniela T. Soltys"'
Autor:
Mateus P. Mori, Rute A. P. Costa, Daniela T. Soltys, Thiago de S. Freire, Franco A. Rossato, Ignácio Amigo, Alicia J. Kowaltowski, Aníbal E. Vercesi, Nadja C. de Souza-Pinto
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-15 (2017)
Abstract Genomic instability drives tumorigenesis and DNA repair defects are associated with elevated cancer. Metabolic alterations are also observed during tumorigenesis, although a causal relationship between these has not been clearly established.
Externí odkaz:
https://doaj.org/article/8c3abd91e76c4e26a1355a84576051ac
Autor:
Valquiria Tiago dos Santos, Carlos Frederico Martins Menck, Clarissa Ribeiro Reily Rocha, Veridiana Munford, Leticia K. Lerner, Daniela T. Soltys, Camila Carrião Machado Garcia, Alain Sarasin, Natália Cestari Moreno
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Nucleotide excision repair (NER) is a conserved, flexible mechanism responsible for the removal of bulky, helix-distorting DNA lesions, like ultraviolet damage or cisplatin adducts, but its role in the repair of lesions generated by oxidative stress
Autor:
Felipe C Beckedorff, Ana C Ayupe, Renan Crocci-Souza, Murilo S Amaral, Helder I Nakaya, Daniela T Soltys, Carlos F M Menck, Eduardo M Reis, Sergio Verjovski-Almeida
Publikováno v:
PLoS Genetics, Vol 9, Iss 8, p e1003705 (2013)
The down-regulation of the tumor-suppressor gene RASSF1A has been shown to increase cell proliferation in several tumors. RASSF1A expression is regulated through epigenetic events involving the polycomb repressive complex 2 (PRC2); however, the molec
Externí odkaz:
https://doaj.org/article/ec6e8151289d4678a4989b51ca3aa8c0
Autor:
Aysegul Ekmekcioglu, Daniela T. Soltys, Ugur Sezerman, Asli Semerci, Nadja C. de Souza-Pinto, Meltem Muftuoglu, Mehmet Oguz Gok, Tugce Ertuzun, Mehmet Emin Cakir
Publikováno v:
PLoS ONE, Vol 14, Iss 8, p e0221362 (2019)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
PLoS ONE
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
PLoS ONE
Base excision repair (BER) defects and concomitant oxidative DNA damage accumulation play a role in the etiology and progression of late-onset Alzheimer's disease (LOAD). However, it is not known whether genetic variant(s) of specific BER genes contr
Autor:
Ligia Pereira Castro, Vanesa Gottifredi, Alain Sarasin, Alexandre T. Vessoni, Guilherme Francisco, Silvina Odete Bustos, Annabel Quinet, Daniela T. Soltys, Roger Chammas, Taynah I.P. David, Leticia K. Lerner, Bryan E. Strauss, Carlos Frederico Martins Menck, Anne Stary, Clarissa Ribeiro Reily Rocha
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Nucleic Acids Research
Nucleic Acids Research, Oxford University Press, 2017, 45 (3), pp.1270-1280. ⟨10.1093/nar/gkw1196⟩
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Universidade de São Paulo (USP)
instacron:USP
Nucleic Acids Research
Nucleic Acids Research, Oxford University Press, 2017, 45 (3), pp.1270-1280. ⟨10.1093/nar/gkw1196⟩
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Genome lesions trigger biological responses that help cells manage damaged DNA, improving cell survival. Pol eta is a translesion synthesis (TLS) polymerase that bypasses lesions that block replicative polymerases, avoiding continued stalling of repl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c632e78bf42211a64ddaf21fcf039d4
Publikováno v:
The Base Excision Repair Pathway: Molecular Mechanisms and Role in Disease Development and Therapeutic Design
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::553fb03d99f58b6eee72e9a3d88ae672
https://doi.org/10.1142/9789814719735_0019
https://doi.org/10.1142/9789814719735_0019
Autor:
Daniela T. Soltys
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USP
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
O NER é uma via de reparo de DNA capaz de lidar com uma ampla variedade de lesões. Participam do NER diversas proteínas, entre elas a endonuclease XPG. Pacientes que possuem mutações no gene XPG apresentam a síndrome XP, e em alguns casos XP/CS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c0aa6f75c3ab6d7d656cfc5d846eec9
https://doi.org/10.11606/t.42.2010.tde-05082010-114429
https://doi.org/10.11606/t.42.2010.tde-05082010-114429
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Most human tissues used in research are of post mortem origin. This is the case for all brain samples, and due to the difficulty in obtaining a good number of samples, especially in the case of neurodegenerative diseases, male and female samples are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8bde238510ae5a91e6ee615071dac4c
Autor:
Murilo S. Amaral, Daniela T. Soltys, Felipe Beckedorff, Renan Crocci-Souza, Eduardo M. Reis, Carlos Frederico Martins Menck, Helder I. Nakaya, Ana C. Ayupe, Sergio Verjovski-Almeida
Publikováno v:
PLoS Genetics
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
PLoS Genetics, Vol 9, Iss 8, p e1003705 (2013)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
PLoS Genetics, Vol 9, Iss 8, p e1003705 (2013)
The down-regulation of the tumor-suppressor gene RASSF1A has been shown to increase cell proliferation in several tumors. RASSF1A expression is regulated through epigenetic events involving the polycomb repressive complex 2 (PRC2); however, the molec
Autor:
Alain Sarasin, Tiziana Nardo, Veridiana Munford, Fernanda C. Cabral, Carlos Frederico Martins Menck, Clarissa Ribeiro Reily Rocha, Januário B. Cabral-Neto, Daniela T. Soltys, Miria Stefanini, Leticia K. Lerner, Tiago Antonio de Souza
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Nucleotide excision repair (NER) is the most flexible of all known DNA-repair mechanisms, and XPG is a 3′-endonuclease that participates in NER. Mutations in this gene (ERCC5) may result in the human syndrome xeroderma pigmentosum (XP) and, in some