Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Renan Barbosa Lemes"'
Autor:
Eliniete de Jesus Fidelis Baniwa, Eliene Rodrigues Putira Sacuena, Rosilene Reis Della Noce, Vanessa Barroso Quaresma, Teodora Honorato Alencar, Renan Barbosa Lemes, Antônia Cherlly Araújo, Izaura Maria Vieira Cayres-Vallinoto, João Farias Guerreiro
Publikováno v:
BMC Public Health, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Background Available data show that the epidemiological profile of most indigenous Brazilian populations is characterized by the coexistence of long-standing health problems (high prevalence of infectious and parasitic diseases, malnutrition
Externí odkaz:
https://doaj.org/article/73f0840f6ec84ea78bc36d97f794ddc7
Autor:
Alice Nagai, Renan Barbosa Lemes, José Geraldo Mill, Alexandre Costa Pereira, Rafael Elias Marques, Tábita Hünemeier
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
The COVID-19 pandemic caused a significant loss of human lives and a worldwide decline in quality of life. Although our understanding of the pandemic has improved significantly since the beginning, the natural history of COVID-19 and its impacts on u
Externí odkaz:
https://doaj.org/article/e06dcb8b7fc74986a8ac6a5a26920b0d
Autor:
Lucas Schenatto Sena, Renan Barbosa Lemes, Gabriel Vasata Furtado, Maria Luiza Saraiva-Pereira, Laura Bannach Jardim
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Spinocerebellar ataxia types 2 (SCA2) and 3 (SCA3/MJD) are diseases due to dominant unstable expansions of CAG repeats (CAGexp). Age of onset of symptoms (AO) correlates with the CAGexp length. Repeat instability leads to increases in the
Externí odkaz:
https://doaj.org/article/00c474dee72541f393c1f57b03ac1b7f
Autor:
Rodrigo Barbosa de Souza, Renan Barbosa Lemes, Orestes Foresto-Neto, Luara Lucena Cassiano, Dieter P Reinhardt, Keith M Meek, Ivan Hong Jun Koh, Philip N Lewis, Lygia V Pereira
Publikováno v:
PLoS ONE, Vol 18, Iss 5, p e0285418 (2023)
Fibrillin-1 is a pivotal structural component of the kidney's glomerulus and peritubular tissue. Mutations in the fibrillin-1 gene result in Marfan syndrome (MFS), an autosomal dominant disease of the connective tissue. Although the kidney is not con
Externí odkaz:
https://doaj.org/article/9b61dbdc740445ba97f4a1ca1dc341ef
Publikováno v:
Genetics and Molecular Biology, Vol 43, Iss 2 (2020)
Abstract This article deals with a Windows (© Microsoft Inc.) executable, user-friendly program that tests the hypothesis of Hardy-Weinberg (HW) proportions from autosomal multiallelic data using different methods that include parametric, nonparamet
Externí odkaz:
https://doaj.org/article/143933cb1c0a47968db31947e15f2aee
Autor:
Allysson Allan de Farias, Kelly Nunes, Renan Barbosa Lemes, Ronald Moura, Gustavo Ribeiro Fernandes, Uirá Souto Melo, Mayana Zatz, Fernando Kok, Silvana Santos
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-8 (2018)
Abstract The mutation age and local ancestry of chromosomal segments harbouring mutations associated with autosomal recessive (AR) disorders in Brazilian admixed populations remain unknown; additionally, inbreeding levels for these affected individua
Externí odkaz:
https://doaj.org/article/d723e7e4b3614cfe81131cb8fa90adec
Autor:
Renan Barbosa Lemes
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USPUniversidade de São PauloUSP.
A porção paulista do Vale do Ribeira concentra a maior quantidade de comunidades remanescentes de quilombos do estado de São Paulo, abrangendo uma área de cerca de 10% de seu território. Por meio das análises de marcadores moleculares, de frequ
Publikováno v:
Genética na Escola. 17:41-52
De onde vieram nossos antepassados? Essa pergunta tem guiado milhares de pessoas em uma busca por suas origens, alimentada pela divulgação de testes genéticos nas redes sociais, comercializados por empresas privadas que oferecem respostas para que
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5e0506270e623791c188831baa8d3d7
https://doi.org/10.55838/1980-3540.ge.2022.421
https://doi.org/10.55838/1980-3540.ge.2022.421
Autor:
Larissa Nascimento Antunes, Lilian Kimura, Renan Barbosa Lemes, Regina Célia Mingroni Netto, Ana Carla Batissoco
Publikováno v:
Genética na Escola. 16:158-167
A perda auditiva ou surdez é um dos mais importantes defeitos sensoriais para os seres humanos, com enorme impacto na comunicação. A perda auditiva é um fenótipo de estudo complexo, dada a sua natureza heterogênea. Pode ser causada por fatores
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e531a922cf6110fadec934d8ab05b39
https://doi.org/10.55838/1980-3540.ge.2021.364
https://doi.org/10.55838/1980-3540.ge.2021.364
Autor:
Steffany Larissa Galdino Galisa, Priscila Lima Jacob, Allysson Allan de Farias, Renan Barbosa Lemes, Leandro Ucela Alves, Júlia Cristina Leite Nóbrega, Mayana Zatz, Silvana Santos, Mathias Weller
Publikováno v:
Genetics and Molecular Biology, Volume: 45, Issue: 1, Article number: e20210172, Published: 02 FEB 2022
Genetics and Molecular Biology v.45 n.1 2022
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Genetics and Molecular Biology v.45 n.1 2022
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Admixed populations have not been examined in detail in cancer genetic studies. Here, we inferred the local ancestry of cancer-associated single nucleotide polymorphisms (SNPs) and haplotypes of a highly admixed Brazilian population. SNP array was us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::353c8c2e1177d6e3347232ec8de767af
https://doi.org/10.1590/1678-4685-gmb-2021-0172
https://doi.org/10.1590/1678-4685-gmb-2021-0172