Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Thaise Nayane Ribeiro Carneiro"'
Autor:
Paula Diana, Thaise Nayane Ribeiro Carneiro, Janete Maria Cerutti, Reginaldo Massanobu Kuroshu, Gianna Maria Griz Carvalheira
Publikováno v:
Genes and Diseases, Vol 11, Iss 4, Pp 101094- (2024)
Externí odkaz:
https://doaj.org/article/a1bb0ff9b3364489bf179731c9f53566
Autor:
Luis Eduardo Barbalho de Mello, Thaise Nayane Ribeiro Carneiro, Aline Neves Araujo, Camila Xavier Alves, Pedro Alexandre Favoretto Galante, Vanessa Candiotti Buzatto, Maria das Graças de Almeida, Karina Marques Vermeulen-Serpa, Sancha Helena de Lima Vale, Fernando José de Pinto Paiva, José Brandão-Neto, Janete Maria Cerutti
Publikováno v:
Endocrine Connections, Vol 11, Iss 1, Pp 1-16 (2022)
The genetics underlying non-syndromic familial non-medullary thyroid carcinoma (FNMTC) is still poorly understood. To identify susceptibility genes for FNMTC, we performed whole-exome sequencing (WES) in a Brazilian family affected by papilla ry thyr
Externí odkaz:
https://doaj.org/article/f670244863574267afc9a41fd4900eee
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USPUniversidade de São PauloUSP.
Deficiência intelectual (DI), associada ou não a outras alterações congênitas, é a razão mais frequente de procura por aconselhamento genético pelas famílias. Até alguns anos atrás, a realização de cariótipo, triagem para doenças metab
Autor:
Luis Eduardo Barbalho de Mello, Thaise Nayane Ribeiro Carneiro, Aline Neves Araujo, Camila Xavier Alves, Pedro Alexandre Favoretto Galante, Vanessa Candiotti Buzatto, Maria das Graças de Almeida, Karina Marques Vermeulen-Serpa, Sancha Helena de Lima Vale, Fernando José de Pinto Paiva, José Brandão-Neto, Janete Maria Cerutti
Publikováno v:
Endocrine Connections, Vol 11, Iss 1, Pp 1-16 (2022)
The genetics underlying non-syndromic familial non-medullary thyroid carcinoma (FNMTC) is still poorly understood. To identify susceptibility genes for FNMTC, we performed whole-exome sequencing (WES) in a Brazilian family affected by papillary thyro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e98e24eb7ff9b5614f0974b2b60f42a6
https://pubmed.ncbi.nlm.nih.gov/34941562
https://pubmed.ncbi.nlm.nih.gov/34941562
Autor:
Paula Fontes Asprino, Vanessa Buzatto, Larissa V. Bim, Janete M. Cerutti, Thaise Nayane Ribeiro Carneiro, Pedro Alexandre Favoretto Galante, Vanessa Galdeno, Eunjung Lee
Publikováno v:
Cancers, Vol 13, Iss 2306, p 2306 (2021)
Cancers
Volume 13
Issue 10
Cancers
Volume 13
Issue 10
Simple Summary RAS mutations have been reported in a wide range of thyroid cancer histological types, from benign to aggressive phenotypes. The presence of RAS mutations in benign lesions suggests that the mutation alone is unlikely to lead to a mali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6383e790b5537ad2211aa4584a4c0b78
https://www.mdpi.com/2072-6694/13/10/2306
https://www.mdpi.com/2072-6694/13/10/2306
Autor:
Vanessa Buzatto, Eunjung Lee, Gabriel Avelar Colozza-Gama, Pedro Alexandre Favoretto Galante, Janete M. Cerutti, Debora Mota Dias Thomaz, Larissa V. Bim, Fernanda C. Koyama, Ana Carolina de Jesus Paniza, Thaise Nayane Ribeiro Carneiro
Publikováno v:
Cancers, Vol 13, Iss 5184, p 5184 (2021)
Cancers
Volume 13
Issue 20
Cancers
Volume 13
Issue 20
Simple Summary Thyroid cancer is the most common endocrine malignancy. However, the cytological diagnosis of certain malignant thyroid tumors and their benign counterparts is a challenge for preoperative diagnosis, as nearly 20–30% of biopsied thyr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f335f34f79dc0d3da8d9df5c77cf4eb4
https://doi.org/10.3390/cancers13205184
https://doi.org/10.3390/cancers13205184
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USP
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Deficiência intelectual (DI), associada ou não a outras alterações congênitas, é a razão mais frequente de procura por aconselhamento genético pelas famílias. Até alguns anos atrás, a realização de cariótipo, triagem para doenças metab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24dc04f915b50961bb22d260183bc71d
https://doi.org/10.11606/d.41.2017.tde-28032017-153312
https://doi.org/10.11606/d.41.2017.tde-28032017-153312
