نتائج البحث - Rodrigo Coutinho de Almeida

تنقيح النتائج
  1. 1
    Shared genetics in coeliac disease and other immune-mediated diseases

    Shared genetics in coeliac disease and other immune-mediated diseases حسب Javier Gutierrez‐Achury, Rodrigo Coutinho de Almeida, Cisca Wijmenga

    منشور في 2011
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  2. 2
    Genetic variation in the non-coding genome: Involvement of micro-RNAs and long non-coding RNAs in disease

    Genetic variation in the non-coding genome: Involvement of micro-RNAs and long non-coding RNAs in disease حسب Barbara Hrdličková, Rodrigo Coutinho de Almeida, Z Borek, Sebo Withoff

    منشور في 2014
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  3. 3
    Integrative Analysis Identifies Genetic Variants Associated With Autoimmune Diseases Affecting Putative MicroRNA Binding Sites

    Integrative Analysis Identifies Genetic Variants Associated With Autoimmune Diseases Affecting Putative MicroRNA Binding Sites حسب Rodrigo Coutinho de Almeida, Vinicius S Chagas, Mauro A. A. Castro, Maria Luiza Petzl‐Erler

    منشور في 2018
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  4. 4
    Serologic screening and genetic testing among brazilian patients with celiac disease and their first degree relatives

    Serologic screening and genetic testing among brazilian patients with celiac disease and their first degree relatives حسب Rita Martins, Lenora Gandolfi, Inês Cristina Modelli, Rodrigo Coutinho de Almeida, Luiz Cláudio Castro, Riccardo Pratesi

    منشور في 2010
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  5. 5
    Prevalence of celiac disease among first degree relatives of Brazilian celiac patients

    Prevalence of celiac disease among first degree relatives of Brazilian celiac patients حسب Patrícia Lopes de Almeida, Lenora Gandolfi, Inês Cristina Modelli, Rita Martins, Rodrigo Coutinho de Almeida, Riccardo Pratesi

    منشور في 2008
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  6. 6
    Besides Pathology: Long Non-Coding RNA in Cell and Tissue Homeostasis

    Besides Pathology: Long Non-Coding RNA in Cell and Tissue Homeostasis حسب Amanda Salviano‐Silva, Sara Cristina Lobo‐Alves, Rodrigo Coutinho de Almeida, Danielle Malheiros, Maria Luiza Petzl‐Erler

    منشور في 2018
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  7. 7
    Screening the full leucocyte receptor complex genomic region revealed associations with pemphigus that might be explained by gene regulation

    Screening the full leucocyte receptor complex genomic region revealed associations with pemphigus that might be explained by gene regulation حسب Ticiana D.J. Farias, Danillo G. Augusto, Rodrigo Coutinho de Almeida, Danielle Malheiros, Maria Luiza Petzl‐Erler

    منشور في 2018
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  8. 8
    Serological screening for celiac disease in symptomatic 12 to 36 month-old children

    Serological screening for celiac disease in symptomatic 12 to 36 month-old children حسب Inês Cristina Modelli, Lenora Gandolfi, Rodrigo Coutinho de Almeida, Gloria Araujo, Marilúcia de Almeida Rocha Picanço, Riccardo Pratesi

    منشور في 2010
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  9. 9
    Screening for celiac disease among patients with Turner syndrome in Brasília, DF, midwest region of Brazil

    Screening for celiac disease among patients with Turner syndrome in Brasília, DF, midwest region of Brazil حسب Maria do Carmo Sorci Dias, Luiz Cláudio Castro, Lenora Gandolfi, Rodrigo Coutinho de Almeida, Mara S. Córdoba, Riccardo Pratesi

    منشور في 2010
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  10. 10
    Autism spectrum disorder and celiac disease: no evidence for a link

    Autism spectrum disorder and celiac disease: no evidence for a link حسب Icaro Camargo Batista, Lenora Gandolfi, Yanna Karla de Medeiros Nóbrega, Rodrigo Coutinho de Almeida, Lucas Malta Almeida, Dioclécio Campos, Riccardo Pratesi

    منشور في 2012
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  11. 11
    Sparking Fire Under the Skin? Answers From the Association of Complement Genes With Pemphigus Foliaceus

    Sparking Fire Under the Skin? Answers From the Association of Complement Genes With Pemphigus Foliaceus حسب Valéria Bumiller‐Bini, Gabriel Adelman Cipolla, Rodrigo Coutinho de Almeida, Maria Luiza Petzl‐Erler, Danillo G. Augusto, Angelica Beate Winter Boldt

    منشور في 2018
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  12. 12
    An epigenome-wide view of osteoarthritis in primary tissues

    An epigenome-wide view of osteoarthritis in primary tissues حسب Peter Kreitmaier, Matthew Suderman, Lorraine Southam, Rodrigo Coutinho de Almeida, Konstantinos Hatzikotoulas, Ingrid Meulenbelt, Julia Steinberg, Caroline L. Relton, J. Mark Wilkinson, Eleftheria Zeggini

    منشور في 2022
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  13. 13
    Long noncoding <scp>RNA</scp> polymorphisms influence susceptibility to endemic pemphigus foliaceus

    Long noncoding <scp>RNA</scp> polymorphisms influence susceptibility to endemic pemphigus foliaceus حسب Sara Cristina Lobo‐Alves, Danillo G. Augusto, Wagner C. S. Magalhães, Eduardo Tarazona‐Santos, Maria Fernanda Lima‐Costa, Maurício L. Barreto, Bernardo Lessa Horta, Rodrigo Coutinho de Almeida, Maria Luiza Petzl‐Erler

    منشور في 2019
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  14. 14
    <i>RTNduals</i>: an R/Bioconductor package for analysis of co-regulation and inference of <i>dual regulons</i>

    <i>RTNduals</i>: an R/Bioconductor package for analysis of co-regulation and inference of <i>dual regulons</i> حسب Vinicius S Chagas, Clarice S. Groeneveld, Kelin Gonçalves de Oliveira, Sheyla Trefflich, Rodrigo Coutinho de Almeida, Bruce A.J. Ponder, Kerstin B. Meyer, Steven J.M. Jones, A. Gordon Robertson, Mauro A. A. Castro

    منشور في 2019
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  15. 15
    Does celiac disease occur in Afro‐derived Brazilian populations?

    Does celiac disease occur in Afro‐derived Brazilian populations? حسب Rodrigo Coutinho de Almeida, Lenora Gandolfi, Maria de Nazaré Klautau‐Guimarães, Íris Ferrari, Sandra Mara Bispo Sousa, Kiyoko Abe‐Sandes, Ana Angélica Leal Barbosa, Aguinaldo Luíz Simões, Riccardo Pratesi, Silviene Fabiana de Oliveira

    منشور في 2012
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  16. 16
    A 3′UTR polymorphism marks differential KLRG1 mRNA levels through disruption of a miR-584-5p binding site and associates with pemphigus foliaceus susceptibility

    A 3′UTR polymorphism marks differential KLRG1 mRNA levels through disruption of a miR-584-5p binding site and associates with pemphigus foliaceus susceptibility حسب Gabriel Adelman Cipolla, Jong Kook Park, Liana Alves de Oliveira, Sara Cristina Lobo‐Alves, Rodrigo Coutinho de Almeida, Ticiana D.J. Farias, Débora De Souza Lemos, Danielle Malheiros, Robert M. Lavker, Maria Luiza Petzl‐Erler

    منشور في 2016
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  17. 17
    RNA Sequencing Reveals Interacting Key Determinants of Osteoarthritis Acting in Subchondral Bone and Articular Cartilage: Identification of <i>IL11</i> and <i>CHADL</i> as Attractive Treatment Targets

    RNA Sequencing Reveals Interacting Key Determinants of Osteoarthritis Acting in Subchondral Bone and Articular Cartilage: Identification of <i>IL11</i> and <i>CHADL</i> as Attracti... حسب Margo Tuerlings, Marcella van Hoolwerff, E. Houtman, H. Eka D. Suchiman, Nico Lakenberg, Hailiang Mei, Enrike H. M. J. van der Linden, Rob G. H. H. Nelissen, Y.F. Ramos, Rodrigo Coutinho de Almeida, Ingrid Meulenbelt

    منشور في 2020
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  18. 18
    A genetic variant in microRNA-146a is associated with sporadic breast cancer in a Southern Brazilian Population

    A genetic variant in microRNA-146a is associated with sporadic breast cancer in a Southern Brazilian Population حسب Heloisa Magagnin Brincas, Danillo G. Augusto, Carolina Mathias, Iglenir João Cavalli, Rubens Silveira de Lima, Flávia Kuroda, Cı́cero de Andrade Urban, Daniela Fiori Gradia, Jaqueline Carvalho de Oliveira, Rodrigo Coutinho de Almeida, Enilze Maria de Souza Fonseca Ribeiro

    منشور في 2019
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  19. 19
    RNA sequencing data integration reveals an miRNA interactome of osteoarthritis cartilage

    RNA sequencing data integration reveals an miRNA interactome of osteoarthritis cartilage حسب Rodrigo Coutinho de Almeida, Y.F. Ramos, Ahmed Mahfouz, Wouter den Hollander, Nico Lakenberg, E. Houtman, Marcella van Hoolwerff, H. Eka D. Suchiman, Alejandro Rodríguez Ruiz, P. Eline Slagboom, Hailiang Mei, Szymon M. Kiełbasa, Rob G. H. H. Nelissen, Marcel J. T. Reinders, Ingrid Meulenbelt

    منشور في 2018
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  20. 20
    Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify<i>WNT9A</i>as novel osteoarthritis gene

    Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify<i>WNT9A</i>as novel osteoarthritis gene حسب Cindy G. Boer, Michelle S. Yau, Sarah J. Rice, Rodrigo Coutinho de Almeida, Kathleen Cheung, Unnur Styrkársdóttir, Lorraine Southam, Linda Broer, J. Mark Wilkinson, André G. Uitterlinden, Eleftheria Zeggini, David T. Felson, John Loughlin, Mariel Young, Terence D. Capellini, Ingrid Meulenbelt, Joyce B. J. van Meurs

    منشور في 2020
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