Zobrazeno 1 - 8 of 8 pro vyhledávání: '"Betsaida Urtremari"'
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Akademický článek
Toxicological, genotoxic and antioxidant potential of Pyrostegia venusta
Autor: Amanda Martins Viel, Luciana Pereira Silva, Gustavo Rafagnin Martins, Betsaida Urtremari, Alline Sekiya, Anne Lígia Dokkedal, Edislane Barreiros de Sousa, Isabel Cristina Cherici Camargo, Regildo Márcio Gonçalves Silva
Publikováno v: Bioscience Journal, Vol 35, Iss 2 (2018)
Pyrostegia venusta is usually found in the secondary growth of the Atlantic forests, and in the Brazilian Savanna. Flowers and leaves of this plant are used in folk remedies for treating a wide variety of healthy conditions, this way is important eva
Externí odkaz: https://doaj.org/article/5d8621ff5e8244e6a652db36c7ec457f
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2
Toxicological, genotoxic and antioxidant potential of Pyrostegia venusta
Autor: Anne Lígia Dokkedal, Alline Sekiya, Gustavo Rafagnin Martins, Regildo Márcio Gonçalves da Silva, Betsaida Urtremari, Amanda Martins Viel, Edislane Barreiros de Sousa, Isabel Cristina Cherici Camargo, Luciana Pereira Silva
Publikováno v: Bioscience Journal, Vol 35, Iss 2 (2018)
Bioscience Journal ; Vol. 35 No. 2 (2019): Mar./Apr.; 570-585
Bioscience Journal ; v. 35 n. 2 (2019): Mar./Apr.; 570-585
Bioscience journal
Universidade Federal de Uberlândia (UFU)
instacron:UFU
Pyrostegia venusta is usually found in the secondary growth of the Atlantic forests, and in the Brazilian Savanna. Flowers and leaves of this plant are used in folk remedies for treating a wide variety of healthy conditions, this way is important eva
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a912bddcd31e35e9d3903a079759967d
https://doi.org/10.14393/bj-v35n2a20198-41790
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3
Padronização e aplicação de painel baseado em sequenciamento paralelo em larga escala direcionado ao diagnóstico genético de neoplasia endócrina múltipla tipo 1
Autor: Betsaida Urtremari
Publikováno v: Biblioteca Digital de Teses e Dissertações da USP
Universidade de São Paulo (USP)
instacron:USP
A neoplasia endócrina múltipla tipo 1 (MEN1) é uma doença genética, de herança autossômica dominante, caracterizada pelo desenvolvimento de tumores endócrinos que acometem, principalmente, hipófise, paratireoide e pâncreas/duodeno endócrin
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::209ce1ecf0acc7d70206faccfa9b8c6c
https://doi.org/10.11606/d.5.2020.tde-29012020-122521
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4
Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencing
Autor: Elisangela P S Quedas, Antonio M. Lerario, Sergio P. A. Toledo, Viviane C. Longuini, Betsaida Urtremari, Delmar M. Lourenço, Fábio Luiz de Menezes Montenegro, Alexander A. L. Jorge, Tomoko Sekiya, Stephen J. Marx, Lucas Santos de Santana, Rodrigo A. Toledo, Rafael Arrabaça Carvalho
Publikováno v: European Journal of Endocrinology. 179:391-407
Background Loss-of-function germline MEN1 gene mutations account for 75–95% of patients with multiple endocrine neoplasia type 1 (MEN1). It has been postulated that mutations in non-coding regions of MEN1 might occur in some of the remaining patien
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0c32a7ea17a82a9c0174f47653e3b55
https://doi.org/10.1530/eje-18-0430
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5
Comprehensive Analysis of Clinical Features in Index Cases With Multiple Endocrine Neoplasia Type 1 Refine the Risk Rate for Detection of Mutation Distinguishing Negative-Mutation (Phenocopies) and Positive-Mutation Cases
Autor: Louise V Antonio, Betsaida Urtremari, Delmar M. Lourenço, Flavio G Ribeiro, Elisangela P S Quedas, Lucas Santos de Santana, Rafael Aquino de Carvalho, Palloma C Lugeiro
Publikováno v: Journal of the Endocrine Society
Background: Index cases clinically diagnosed with multiple endocrine neoplasia type 1 (MEN1) are declared as MEN1 phenocopies if no germline MEN1 mutation is identified. In comparison with positive-mutation cases, most phenocopies have been diagnosed
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6f9b552363a7f03dec0f91a66468e55
http://europepmc.org/articles/PMC8089159
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6
SUN-046 Identification of Clinical Predictors for Detection of Mutations in Multiple Endocrine Neoplasia Type 1
Autor: Betsaida Urtremari, Delmar M. Lourenço, Rafael Cardoso Carvalho, Elisangela P S Quedas
Publikováno v: Journal of the Endocrine Society
Context: Guidelines has systematically suggested genetic testing for a wide spectrum of phenotypes in order to confirm or exclude surely the diagnosis of multiple endocrine neoplasia type 1 (MEN1). However, the probability of find a germline MEN1 mut
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::899b75fd01bb50089e9cbc907e5bcf56
http://europepmc.org/articles/PMC6552916
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7
Comparative Analysis of Different International Criteria (ACMG-AMP vs. TENGEN) Applied to Classification of Missense Germline Allelic Variants in Patients With Multiple Endocrine Neoplasia Type 1 or Suspected to this Syndrome
Autor: Betsaida Urtremari, Delmar M. Lourenço, Lucas Santos de Santana, Palloma C Lugeiro, Elisangela P S Quedas
Publikováno v: Journal of the Endocrine Society
Context: Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant genetic syndrome caused by germline pathogenic allele variants (PAV) in the MEN1 tumor suppressor gene, which predispose MEN1 carriers to the increased risk of several e
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9e690616edae4b77bb39e249a496dca
https://doi.org/10.1210/jendso/bvab048.2074
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