Search Results - "Luiz Simões, Aguinaldo"

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    Mitochondrial DNA variability among eight Tikúna villages: Evidence for an intratribal genetic heterogeneity pattern by MENDES-JUNIOR, Celso Teixeira, LUIZ SIMOES, Aguinaldo

    Published in American journal of physical anthropology (01-11-2009)
    “…To study the genetic structure of the Tikúna tribe, four major Native American mitochondrial DNA (mtDNA) founder haplogroups were analyzed in 187 Amerindians…”
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    Journal Article
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    Genomic ancestry of a sample population from the state of São Paulo, Brazil by Ferreira, Luzitano Brandão, Mendes -Junior, Celso Teixeira, Wiezel, Cláudia Emília Vieira, Luizon, Marcelo Rizzatti, Simões, Aguinaldo Luiz

    Published in American journal of human biology (01-09-2006)
    “…Allelic frequencies of eight autosomal short‐tandem repeat (STR) loci (TH01, TPOx, CSF1PO, vWA, FES/FPS, F13A1, F13B, and CD4) were determined in 400…”
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    Distribution of the CCR5delta32 allele (gene variant CCR5) in Rondônia, Western Amazonian region, Brazil by de Farias, Josileide Duarte, Santos, Marlene Guimarães, de França, Andonai Krauze, Delani, Daniel, Tada, Mauro Shugiro, Casseb, Almeida Andrade, Simões, Aguinaldo Luiz, Engracia, Vera

    Published in Genetics and molecular biology (01-01-2012)
    “…Since around 1723, on the occasion of its initial colonization by Europeans, Rondonia has received successive waves of immigrants. This has been further…”
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    Copy number variation in the susceptibility to systemic lupus erythematosus by Barbosa, Fernanda Bueno, Simioni, Milena, Wiezel, Cláudia Emília Vieira, Torres, Fábio Rossi, Molck, Miriam Coelho, Bonilla, Melvin M, de Araujo, Tânia Kawasaki, Donadi, Eduardo Antônio, Gil-da-Silva-Lopes, Vera Lúcia, Lemos, Bernardo, Simões, Aguinaldo Luiz

    Published in PloS one (28-11-2018)
    “…Systemic lupus erythematosus (SLE) is an autoimmune disease with a strong genetic component and etiology characterized by chronic inflammation and autoantibody…”
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    Y-STR diversity and ethnic admixture in White and Mulatto Brazilian population samples by Ferreira, Luzitano Brandão, Mendes-Junior, Celso Teixeira, Wiezel, Cláudia Emília Vieira, Luizon, Marcelo Rizzatti, Simões, Aguinaldo Luiz

    Published in Genetics and molecular biology (2006)
    “…We investigated 50 Mulatto and 120 White Brazilians for the Y-chromosome short tandem repeat (Y-STR) markers (DYS19, DYS390, DYS391, DYS392 and DYS393) and…”
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    Large-scale selection of highly informative microhaplotypes for ancestry inference and population specific informativeness by de Barros Rodrigues, Maria Luisa, Rodrigues, Marcelo Porto, Norton, Heather L., Mendes-Junior, Celso Teixeira, Simões, Aguinaldo Luiz, Lawson, Daniel John

    Published in Forensic science international : genetics (01-01-2025)
    “…Microhaplotypes (MHs) describe physically close genetic markers that are inherited together and are gaining prominence due to their efficiency in forensic,…”
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    Ancestry informative markers in Amerindians from Brazilian Amazon by Luizon, Marcelo Rizzatti, Mendes-Junior, Celso Teixeira, De Oliveira, Silviene Fabiana, Simões, Aguinaldo Luiz

    Published in American journal of human biology (01-01-2008)
    “…Ancestry informative markers (AIMs) are genetic loci with large frequency differences between the major ethnic groups and are very useful in admixture…”
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    The SCA1 (Spinocerebellar ataxia type 1) and MJD (Machado-Joseph disease) CAG repeats in normal individuals: segregation analysis and allele frequencies by Wiezel, Cláudia Emília Vieira, Canas, Maria do Carmo Tomitão, Simões, Aguinaldo Luiz

    Published in Genetics and molecular biology (2003)
    “…Spinocerebellar ataxia type 1 (SCA1) and Machado-Joseph disease (MJD/SCA3) are autosomal dominant neurodegenerative diseases caused by expansions of a CAG…”
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    Distrofia miotônica tipo 1 em pacientes com catarata: diagnóstico molecular para triagem e aconselhamento genético by Muñoz Rojas, María Verónica, Chimelli, Leila Maria Cardão, Simões, Aguinaldo Luiz

    Published in Arquivos brasileiros de oftalmologia (01-02-2005)
    “…OBJETIVOS: Detectar novos pacientes portadores da mutação e pré-mutação da DM1, entre pacientes com catarata e realizar aconselhamento genético. MÉTODOS: Foi…”
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    Genomic ancestry in urban Afro-Brazilians by Muniz, Yara Costa Netto, Ferreira, Luzitano Brandão, Mendes-Junior, Celso Teixeira, Wiezel, Cláudia Emília Vieira, Simões, Aguinaldo Luiz

    Published in Annals of human biology (2008)
    “…Brazil is the result of interethnic crosses of European, African and Amerindian populations. Allelic frequencies for seven STR loci (TH01, TPOx, CSF1PO, vWA,…”
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