Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Tirzah Braz Petta"'
Autor:
Jordi Gonzalez‐Molina, Paula Hahn, Raul Maia Falcão, Okan Gultekin, Georgia Kokaraki, Valentina Zanfagnin, Tirzah Braz Petta, Kaisa Lehti, Joseph W. Carlson
Publikováno v:
Molecular Oncology, Vol 18, Iss 4, Pp 850-865 (2024)
Fibrillar collagen deposition, stiffness and downstream signalling support the development of leiomyomas (LMs), common benign mesenchymal tumours of the uterus, and are associated with aggressiveness in multiple carcinomas. Compared with epithelial c
Externí odkaz:
https://doaj.org/article/ce0b7c7310a54a3d94cc48e84d821fb1
Autor:
Tirzah Braz Petta, Joseph Carlson
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 19, p 10427 (2024)
Approximately 50% of patients diagnosed with ovarian cancer harbor tumors with mutations in BRCA1, BRCA2, or other genes involved in homologous recombination repair (HR). The presence of homologous recombination deficiency (HRD) is an approved biomar
Externí odkaz:
https://doaj.org/article/63f2a7aa7bcf4b6a8e2b8d20b626d15f
Autor:
Ana Rafaela de Souza Timoteo, Isabel Cristina Pinheiro de Almeida, Andrey A Yurchenko, Sheila Ramos de Miranda Henriques, Paulo de Souza Segundo, Fatemeh Rajabi, Sergey Nikolaev, Tirzah Braz Petta
Publikováno v:
BMC Medical Genomics, Vol 16, Iss 1, Pp 1-7 (2023)
Abstract Background Xeroderma pigmentosum group E (XP-E) is one of the least common forms of XP, a rare syndrome where patients are prone to develop skin cancer in exposed sunlight areas. XP-E patients are generally not diagnosed until they are adult
Externí odkaz:
https://doaj.org/article/630851bae18e40af9ec8f0b92234caf2
Autor:
Ligia Pereira Castro, Danilo Batista-Vieira, Tiago Antonio de Souza, Ana Rafaela de Souza Timoteo, Jessica Dayanna Landivar Coutinho, Isabel Cristina Pinheiro de Almeida, Sheila Ramos de Miranda Henriques, Fabio Medeiros de Azevedo, Reginaldo Cruz Alves Rosa, Patricia L Kannouche, Alain Sarasin, Carlos Frederico Martins Menck, Tirzah Braz Petta
Publikováno v:
Frontiers in Genetics, Vol 12 (2022)
Xeroderma pigmentosum (XP) is a rare genetic condition in which exposure to sunlight leads to a high tumor incidence due to defective DNA repair machinery. Herein, we investigated seven patients clinically diagnosed with XP living in a small city, Mo
Externí odkaz:
https://doaj.org/article/f25b319a39694d058ff782d4ec67f61e
Autor:
Vera Maria Dantas, Cassandra Teixeira Valle, Roberta Piccin de Oliveira, Mylena Taíse Azevedo L. Bezerra, Cleia Teixeira do Amaral, Raissa Anielle S. Brandão, Jussara M. Cerqueira Maia, Tirzah Braz Petta
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Familial hemophagocytic lymphohistiocytosis (FHL) is a rare, potentially fatal autosomal-recessive immunodeficiency, and STXBP2 mutations have been associated with FHL type 5 (FHL-5). Here, we report a case of a 2-year-old boy who presented with recu
Externí odkaz:
https://doaj.org/article/bb7ea2be0fa54b0d9d9adb0809545805
Autor:
Tirzah Braz Petta Lajus
Publikováno v:
Revista de Saúde Pública, Vol 49, Iss 0, Pp 1-4 (2015)
The Brazilian National Regulatory Agency for Private Health Insurance and Plans has recently published a technical note defining the criteria for the coverage of genetic testing to diagnose hereditary cancer. In this study we show the case of a patie
Externí odkaz:
https://doaj.org/article/eb68cd96e19b4f9a93d310ba6831ba52
Autor:
Pinheiro, Daniele Maria Lopes, de Oliveira, Ana Helena Sales, Coutinho, Leonam Gomes, Fontes, Fabrícia Lima, de Medeiros Oliveira, Rayssa Karla, Oliveira, Thais Teixeira, Faustino, André Luís Fonseca, Lira da Silva, Vandeclécio, de Melo Campos, Julliane Tamara Araújo, Lajus, Tirzah Braz Petta, de Souza, Sandro José, Agnez-Lima, Lucymara Fassarella
Publikováno v:
In Free Radical Biology and Medicine January 2019 130:8-22
Autor:
Andrey A. Yurchenko, Fatemeh Rajabi, Tirzah Braz-Petta, Hiva Fassihi, Alan Lehmann, Chikako Nishigori, Jinxin Wang, Ismael Padioleau, Konstantin Gunbin, Leonardo Panunzi, Fanny Morice-Picard, Pierre Laplante, Caroline Robert, Patricia L. Kannouche, Carlos F. M. Menck, Alain Sarasin, Sergey I. Nikolaev
Publikováno v:
Nature Communications. 14
Xeroderma pigmentosum (XP) is a genetic disorder caused by mutations in genes of the Nucleotide Excision Repair (NER) pathway (groups A-G) or in Translesion Synthesis DNA polymerase η (V). XP is associated with an increased skin cancer risk, reachin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b98e6828b79e50e04995d654700d3d62
https://doi.org/10.1038/s41467-023-38311-0
https://doi.org/10.1038/s41467-023-38311-0
Autor:
Jordi Gonzalez‐Molina, Paula Hahn, Raul Maia Falcão, Okan Gultekin, Georgia Kokaraki, Valentina Zanfagnin, Tirzah Braz Petta, Kaisa Lehti, Joseph W. Carlson
Publikováno v:
Molecular Oncology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47a8d9f885387db8ef810505a819d9d5
https://doi.org/10.1002/1878-0261.13440
https://doi.org/10.1002/1878-0261.13440
Autor:
Sandra Wessman, Beatriz Bohorquez Fuentes, Josefin Severin-Karlsson, Sofia Westbom-Fremer, Monica Nistér, Georgia Kokaraki, Tirzah Braz Petta, Felix Haglund, Joseph W. Carlson
Publikováno v:
International Journal of Gynecological Pathology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2697d7dfa6132c63dc8865989deb2299
https://doi.org/10.1097/pgp.0000000000000953
https://doi.org/10.1097/pgp.0000000000000953