Search Results - Brussa Reis, Larissa

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  1. 1
    Systems Biology Approaches Reveal Potential Phenotype-Modifier Genes in Neurofibromatosis Type 1

    Systems Biology Approaches Reveal Potential Phenotype-Modifier Genes in Neurofibromatosis Type 1 by Woycinck Kowalski, Thayne, Brussa Reis, Larissa, Finger Andreis, Tiago, Ashton-Prolla, Patricia, Rosset, Clévia

    Published in Cancers
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  2. 2
    The paradox of autophagy in Tuberous Sclerosis Complex

    The paradox of autophagy in Tuberous Sclerosis Complex by Reis, Larissa Brussa, Filippi-Chiela, Eduardo C, Ashton-Prolla, Patricia, Visioli, Fernanda, Rosset, Clévia

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  3. 3
    The Role of Co-Deleted Genes in Neurofibromatosis Type 1 Microdeletions: An Evolutive Approach

    The Role of Co-Deleted Genes in Neurofibromatosis Type 1 Microdeletions: An Evolutive Approach by Brussa Reis, Larissa, Turchetto-Zolet, Andreia Carina, Fonini, Maievi, Ashton-Prolla, Patricia, Rosset, Clévia

    Published in Genes
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  4. 4
    Primary cells derived from Tuberous Sclerosis Complex patients show autophagy alteration in the haploinsufficiency state

    Primary cells derived from Tuberous Sclerosis Complex patients show autophagy alteration in the haploinsufficiency state by Rosset, Clévia, Jaeger, Mariane da Cunha, Filippi-Chiela, Eduardo, Reis, Larissa Brussa, Sartor, Ivaine Taís Sauthier, Oliveira Netto, Cristina Brinckmann, Farias, Caroline Brunetto de, Roesler, Rafael, Ashton-Prolla, Patricia

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  5. 5
    MIR605 rs2043556 is associated with the occurrence of multiple primary tumors in TP53 p.(Arg337His) mutation carriers

    MIR605 rs2043556 is associated with the occurrence of multiple primary tumors in TP53 p.(Arg337His) mutation carriers by Bandeira, Isabel Cristina, Vieira, Igor Araujo, Andreis, Tiago Finger, Brussa Reis, Larissa, Macedo, Gabriel S., Vianna, Fernanda Sales Luiz, Santos-Silva, Patricia, Palmero, Edenir Inez, Galvão, Henrique de Campos Reis, Ramos, Cintia Regina Niederauer, Santiago, Karina Miranda, Achatz, Maria Isabel, da Costa, Alexandre André Balieiro Anastácio, Ashton-Prolla, Patricia

    Published in Cancer genetics
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  6. 6
    Functional pri-miR-34b/c rs4938723 and KRAS 3′UTR rs61764370 SNPs: Novel phenotype modifiers in Li-Fraumeni Syndrome?

    Functional pri-miR-34b/c rs4938723 and KRAS 3′UTR rs61764370 SNPs: Novel phenotype modifiers in Li-Fraumeni Syndrome? by Vieira, Igor Araujo, Pezzi, Eduarda Heidrich, Bandeira, Isabel Cristina, Reis, Larissa Brussa, de Araújo Rocha, Yasminne Marinho, Fernandes, Bruna Vieira, Siebert, Marina, Miyamoto, Kendi Nishino, Siqueira, Monique Banik, Achatz, Maria I., Galvão, Henrique de Campos Reis, Garcia, Felipe Antonio de Oliveira, Campacci, Natalia, Carraro, Dirce Maria, Formiga, Maria Nirvana, Vianna, Fernanda Sales Luiz, Palmero, Edenir Inez, Macedo, Gabriel S., Ashton-Prolla, Patricia

    Published in Gene
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  7. 7
    Tuberous Sclerosis Complex with rare associated findings in the gastrointestinal system: a case report and review of the literature

    Tuberous Sclerosis Complex with rare associated findings in the gastrointestinal system: a case report and review of the literature by Reis, Larissa Brussa, Konzen, Daniele, Netto, Cristina Brinckmann Oliveira, Braghini, Pedro Moacir Braghirolli, Prolla, Gabriel, Ashton-Prolla, Patricia

    Published in BMC gastroenterology
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  8. 8
    Functional pri-miR-34b/c rs4938723 and KRAS 3'UTR rs61764370 SNPs: Novel phenotype modifiers in Li-Fraumeni Syndrome?

    Functional pri-miR-34b/c rs4938723 and KRAS 3'UTR rs61764370 SNPs: Novel phenotype modifiers in Li-Fraumeni Syndrome? by Vieira, Igor Araujo, Pezzi, Eduarda Heidrich, Bandeira, Isabel Cristina, Reis, Larissa Brussa, de Araújo Rocha, Yasminne Marinho, Fernandes, Bruna Vieira, Siebert, Marina, Miyamoto, Kendi Nishino, Siqueira, Monique Banik, Achatz, Maria I, Galvão, Henrique de Campos Reis, Garcia, Felipe Antonio de Oliveira, Campacci, Natalia, Carraro, Dirce Maria, miga, Maria Nirvana, Vianna, Fernanda Sales Luiz, Palmero, Edenir Inez, Macedo, Gabriel S, Ashton-Prolla, Patricia

    Published in Gene
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  9. 9
    Functional pri-miR-34b/c rs4938723 and KRAS 3'UTR rs61764370 SNPs: novel phenotype modifiers in Li-Fraumeni syndrome?

    Functional pri-miR-34b/c rs4938723 and KRAS 3'UTR rs61764370 SNPs: novel phenotype modifiers in Li-Fraumeni syndrome? by Araujo Vieira, Igor, Heidrich Pezzi, Eduarda, Cristina Bandeira, Isabel, Brussa Reis, Larissa, Marinho de Araújo Rocha, Yasminne, Vieira Fernandes, Bruna, Siebert, Marina, Nishino Miyamoto, Kendi, Banik Siqueira, Monique, Isabel Achatz, Maria, de Campos Reis Galvão, Henrique, Antonio O Garcia, Felipe, Campacci, Natalia, Maria Carraro, Dirce, Nirvana Formiga, Maria, Sales Luiz Vianna, Fernanda, Inez Palmero, Edenir, Macedo, Gabriel S, Ashton-Prolla, Patricia

    Published in Gene
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