Search Results - "Raiol, Milene"

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    Investigation of INDEL variants in apoptosis: the relevance to gastric cancer by Cavalcante, Giovanna Chaves, de Moraes, Milene Raiol, Valente, Cristina Maria Duarte, Silva, Caio Santos, Modesto, Antônio André Conde, de Assumpção, Paula Baraúna, de Assumpção, Paulo Pimentel, Santos, Sidney, Ribeiro-Dos-Santos, Ândrea

    Published in BMC medical genetics (19-10-2020)
    “…Apoptosis is a type of cell death involved in different pathways inherent to the cell and the evasion from this mechanism has been related to cancer, although…”
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    Journal Article
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    Siaα2-3Galβ1- Receptor Genetic Variants Are Associated with Influenza A(H1N1)pdm09 Severity by Maestri, Alvino, Sortica, Vinicius Albuquerque, Tovo-Rodrigues, Luciana, Santos, Mirleide Cordeiro, Barbagelata, Luana, Moraes, Milene Raiol, Alencar de Mello, Wyller, Gusmão, Leonor, Sousa, Rita Catarina Medeiros, Emanuel Batista Dos Santos, Sidney

    Published in PloS one (05-10-2015)
    “…Different host genetic variants may be related to the virulence and transmissibility of pandemic Influenza A(H1N1)pdm09, influencing events such as binding of…”
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    Journal Article
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    Real-time PCR diagnosis of Plasmodium vivax among blood donors by Batista-dos-Santos, Sergio, Raiol, Milene, Santos, Sidney, Cunha, Maristela G, Ribeiro-dos-Santos, Ândrea

    Published in Malaria journal (12-10-2012)
    “…When selecting blood donors in transfusion centres, one important problem is to identify, during screening, individuals with infectious diseases that can be…”
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    Human aging and somatic point mutations in mtDNA: A comparative study of generational differences (grandparents and grandchildren) by do Rosário Marinho, Anderson Nonato, de Moraes, Milene Raiol, Santos, Sidney, Ribeiro-Dos-Santos, Andrea

    Published in Genetics and molecular biology (01-01-2011)
    “…The accumulation of somatic mutations in mtDNA is correlated with aging. In this work, we sought to identify somatic mutations in the HVS-1 region (D-loop) of…”
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    Mixed Plasmodium malariae Infections Were Underdetected in a Malaria Endemic Area in the Amazon Region, Brazil by Cunha, Maristela G, Santos, Camille S, Raiol, Milene, Costa, Sheyla Patrícia T, Ventura, Ana Maria R, Póvoa, Marinete M, Ribeiro-Dos-Santos, Ândrea

    “…Plasmodium malariae infections are often asymptomatic and long-lasting. Mixed infections are often underdetected in areas where P. malariae, P. vivax, and P…”
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    A novel nonsense mutation of the KAL1 gene (p.Trp204) in Kallmann syndrome by El Husny, Antonette Souto, Raiol-Moraes, Milene, Fernandes-Caldato, Milena Coelho, Ribeiro-Dos-Santos, Andrea

    Published in Application of clinical genetics (01-01-2014)
    “…To describe a novel KAL1 mutation in patients affected by Kallmann syndrome. Endocrinology Clinic of the João de Barros Barreto University Hospital - Federal…”
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    A novel nonsense mutation of the KALI gene (p.Trp204 ) in Kallmann syndrome by Husny, Antonette Souto El, Raiol-Moraes, Milene, Fernandes-Caldato, Milena Coelho, Ribeiro-dos-Santos, Andrea

    Published in Application of clinical genetics (01-01-2014)
    “…Objective: To describe a novel KAL1 mutation in patients affected by Kallmann syndrome. Setting: Endocrinology Clinic of the Joao de Barros Barreto University…”
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    Journal Article
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    Molecular Characterization of TP53 Gene in Human Populations Exposed to Low-Dose Ionizing Radiation by Ribeiro-dos-Santos, Ândrea K. C., Burbano, Rommel Rodríguez, Jati, Schneyder R., Brito, Alexandre W. M., Pessoa, Igor A., Raiol-Moraes, Milene, Alencar, Dayse O., Brasil-Costa, Igor, Santos, Sidney E. B.

    Published in BioMed research international (01-01-2013)
    “…Ionizing radiation, such as that emitted by uranium, may cause mutations and consequently lead to neoplasia in human cells. The TP53 gene acts to maintain…”
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    A novel nonsense mutation of the KAL1 gene (p.Trp204) in Kallmann syndrome by El Husny, Antonette Souto, Raiol-Moraes, Milene, Fernandes-Caldato, Milena Coelho, Ribeiro-Dos-Santos, Andrea

    Published in The application of clinical genetics (01-01-2014)
    “…OBJECTIVETo describe a novel KAL1 mutation in patients affected by Kallmann syndrome. SETTINGEndocrinology Clinic of the João de Barros Barreto University…”
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