Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Juliana Garcia Carneiro"'
Autor:
Bianca Gomes-Fernandes, Luísa Martins Trindade, Marcela de Castro Bastos Rodrigues, João Pedro Duarte Cardoso, Frederico Temponi Lima, Luíza Rogerio, Simone de Vasconcelos Generoso, Juliana Garcia Carneiro, Rodrigo Gomes da Silva, Renan Pedra de Souza, Luiz De Marco, Luciana Bastos-Rodrigues
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)
Abstract Colorectal cancer (CRC) is a leading cause of morbidity and mortality worldwide. Detection before metastasis and efficient treatment of disease significantly improve patient survival and quality of life. However, limitations in diagnosis and
Externí odkaz:
https://doaj.org/article/ff51d7bd66d045c6bb430029f271fac5
Autor:
Júlia Zanon Pereira, Juliana Garcia Carneiro, Mariana Sousa Vieira, Bruna Mattioly Valente, Pâmella Zorzan de Oliveira, Carolina Lins Mello, Caroline Leonel Vasconcelos de Campos, Karina Braga Gomes
Publikováno v:
Molecular biology reports. 49(10)
About 5-10% of breast cancer cases are related to genetic and hereditary factors. The application of Next Generation Sequencing (NGS) in oncology has allowed the identification of genetic variants present in several genes related to the increased ris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2b62bc2066e8b4fd5efabc1ac5fad2e
https://pubmed.ncbi.nlm.nih.gov/35980532
https://pubmed.ncbi.nlm.nih.gov/35980532
Scenery of multilocus inherited neoplasia alleles syndrome (MINAS) in a single Brazilian institution
Publikováno v:
Journal of Clinical Oncology. 40:10598-10598
10598 Background: Genetic testing of hereditary cancer using comprehensive gene panels can identify patients with more than one pathogenic mutation in high and/or moderate-risk-associated cancer genes. This phenomenon is known as multilocus inherited
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1e66c0060fe48839694885a1e037cd0
https://doi.org/10.1200/jco.2022.40.16_suppl.10598
https://doi.org/10.1200/jco.2022.40.16_suppl.10598
Autor:
Felipe Filardi da Rocha, Juliana Garcia Carneiro, Patrícia de Araújo Pereira, Humberto Correa, Antonio Lúcio Teixeira
Publikováno v:
Brazilian Journal of Psychiatry, Vol 30, Iss 2, Pp 173-174 (2008)
Externí odkaz:
https://doaj.org/article/b85f1536c582472e9f241b0e25858321
Autor:
Juliana Garcia Carneiro, Cláudia Bianka de Souza Manhães, Fabiana O. Melo, Mariana Balbino da Silva, Melania Maria Ramos de Amorim, Adriana Suely de Oliveira Melo
Publikováno v:
Obstetrics & Gynecology. 129:S164-S165
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddde7acb4de76fa4063b20f290ce6549
https://doi.org/10.1097/01.aog.0000514077.54388.3c
https://doi.org/10.1097/01.aog.0000514077.54388.3c
Autor:
Gomes-Fernandes, Bianca1 (AUTHOR), Trindade, Luísa Martins2 (AUTHOR), de Castro Bastos Rodrigues, Marcela3 (AUTHOR), Cardoso, João Pedro Duarte1 (AUTHOR), Lima, Frederico Temponi1 (AUTHOR), Rogerio, Luíza4 (AUTHOR), de Vasconcelos Generoso, Simone2 (AUTHOR), Carneiro, Juliana Garcia5 (AUTHOR), da Silva, Rodrigo Gomes4 (AUTHOR), de Souza, Renan Pedra6 (AUTHOR), De Marco, Luiz1,7 (AUTHOR), Bastos-Rodrigues, Luciana1,2 (AUTHOR) lu.bastosr@gmail.com
Publikováno v:
Scientific Reports. 11/2/2024, Vol. 14 Issue 1, p1-8. 8p.
Autor:
Leonardo Agostinho de Castro Silva, Marília de Souza Dantas, Bruno Luiz Fonseca Schamber-Reis, Juliana Garcia Carneiro, Victor Augusto Moraes da Silva
Publikováno v:
BioMed Research International, Vol 2015 (2015)
BioMed Research International
BioMed Research International
Schizophrenia (SZ) is a debilitating mental disorder characterized by psychotic events, abnormal social behavior, false beliefs, and auditory hallucinations. Hypermethylation of the promoter region of reelin (RELN), a gene involved in regulation of n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9f3d3efb73a510559f6edb4e80d203b
https://doaj.org/article/5b319111fb5d46aeb17060de29c905fc
https://doaj.org/article/5b319111fb5d46aeb17060de29c905fc
Autor:
Pereira, Júlia Zanon, Carneiro, Juliana Garcia, Vieira, Mariana Sousa, Valente, Bruna Mattioly, de Oliveira, Pâmella Zorzan, Mello, Carolina Lins, de Campos, Caroline Leonel Vasconcelos, Gomes, Karina Braga
Publikováno v:
Molecular Biology Reports; Oct2022, Vol. 49 Issue 10, p9509-9520, 12p
Autor:
Vanessa Waisberg
Publikováno v:
Repositório Institucional da UFMG
Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
RESUMO Alterações Genéticas e Oftalmológicas na Neurofibromatose Tipo 2 Introdução: Neurofibromatose tipo 2 (NF2) é uma doença autossômica dominante caracterizada por schwannomas vestibulares bilaterais, múltiplos tumores do sistema nervoso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::e188fb1d928605a8b85cb195310cc202
