Editorial: Bioinformatics applied to neuroscience by Clevia Rosset, Clevia Rosset, Clevia Rosset, Jaqueline Bohrer Schuch, Mariana Recamonde-Mendoza, Mariana Recamonde-Mendoza, Thayne Woycinck Kowalski, Thayne Woycinck Kowalski, Thayne Woycinck Kowalski, Thayne Woycinck Kowalski

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TSC1 and TSC2 gene mutations and their implications for treatment in Tuberous Sclerosis Complex: a review by Clévia Rosset, Cristina Brinckmann Oliveira Netto, Patricia Ashton-Prolla

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

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

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Fire association with respiratory disease and COVID-19 complications in the State of Pará, Brazil. by Lucas Schroeder, Eniuce Menezes de Souza, Clévia Rosset, Ademir Marques Junior, Juliano André Boquett, Vinicius Francisco Rofatto, Diego Brum, Luiz Gonzaga, Jr., Marcelo Zagonel de Oliveira, Mauricio Roberto Veronez

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An overview of actionable and potentially actionable TSC1 and TSC2 germline variants in an online Database by Arthur Bandeira de Mello Garcia, Guilherme Danielski Viola, Bruno da Silveira Corrêa, Taís da Silveira Fischer, Maria Clara de Freitas Pinho, Grazielle Motta Rodrigues, Patricia Ashton-Prolla, Clévia Rosset

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

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FREQUÊNCIAS ALÉLICAS E GENOTÍPICAS DO POLIMORFISMO RS2228059 T>G NO GENE IL15RΑ EM UMA POPULAÇÃO COM E SEM HISTÓRICO DE INFECÇÃO POR SARS-COV-2 by Grazielle Motta Rodrigues, Maria Clara De Freitas Pinho, Taís da Silveira Fischer, Fabrício Campos, Fernanda de Paris, Fernanda Sales Luiz Vianna, Pâmela Portela da Silva, Patricia Ashton Prolla, Clévia Rosset

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Clinical and molecular characterization of patients fulfilling Chompret criteria for Li-Fraumeni syndrome in Southern Brazil. by Camila Matzenbacher Bittar, Yasminne Marinho de Araújo Rocha, Igor Araujo Vieira, Clévia Rosset, Tiago Finger Andreis, Ivaine Tais Sauthier Sartor, Osvaldo Artigalás, Cristina B O Netto, Barbara Alemar, Gabriel S Macedo, Patricia Ashton-Prolla

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HLA haplotypes and differential regional mortality caused by COVID-19 in Brazil: an ecological study based on a large bone marrow donor bank dataset by JULIANO ANDRÉ BOQUETT, FERNANDA S.L. VIANNA, NELSON J.R. FAGUNDES, LUCAS SCHROEDER, MARCIA BARBIAN, MARCELO ZAGONEL-OLIVEIRA, TIAGO F. ANDREIS, LUIS CRISTÓVÃO M.S. PÔRTO, JOSÉ ARTUR B. CHIES, LAVINIA SCHULER-FACCINI, PATRICIA ASHTON-PROLLA, CLÉVIA ROSSET

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Cancer Risk Factors in Southern Brazil: Report of a Comprehensive, Matched Case-Control Study by Juliana Giacomazzi, Patricia Klarmann Ziegelmann, Samanta da Costa, Camila Matzenbacher Bittar, Fernando Mariano Obst, Clévia Rosset, Gabriel S. Macedo, Hugo Bock, Thais Canal, Mari Ines Paese, Jean Lucas Benvenuti, Maria Carolina Buj, Patricia Ashton-Prolla, José Roberto Goldim, Roberta Pozza

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Germline MLH1, MSH2 and MSH6 variants in Brazilian patients with colorectal cancer and clinical features suggestive of Lynch Syndrome by Nayê Balzan Schneider, Tatiane Pastor, André Escremim de Paula, Maria Isabel Achatz, Ândrea Ribeiro dos Santos, Fernanda Sales Luiz Vianna, Clévia Rosset, Manuela Pinheiro, Patricia Ashton‐Prolla, Miguel Ângelo Martins Moreira, Edenir Inêz Palmero, Brazilian Lynch Syndrome Study Group

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Molecular analysis of TSC1 and TSC2 genes and phenotypic correlations in Brazilian families with tuberous sclerosis. by Clévia Rosset, Filippo Vairo, Isabel Cristina Bandeira, Rudinei Luis Correia, Fernanda Veiga de Goes, Raquel Tavares Boy da Silva, Larissa Souza Mario Bueno, Mireille Caroline Silva de Miranda Gomes, Henrique de Campos Reis Galvão, João I C F Neri, Maria Isabel Achatz, Cristina Brinckmann Oliveira Netto, Patricia Ashton-Prolla

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Exploring the frequency of a TP53 polyadenylation signal variant in tumor DNA from patients diagnosed with lung adenocarcinomas, sarcomas and uterine leiomyomas by Igor Araujo Vieira, Guilherme Danielski Viola, Eduarda Heidrich Pezzi, Thayne Woycinck Kowalski, Bruna Vieira Fernandes, Tiago Finger Andreis, Natascha Bom, Giulianna Sonnenstrahl, Yasminne Marinho de Araújo Rocha, Bruno da Silveira Corrêa, Luiza Mezzomo Donatti, Gabriela dos Santos Sant’Anna, Helena von Eye Corleta, Ilma Simoni Brum, Clévia Rosset, Fernanda Sales Luiz Vianna, Gabriel S. Macedo, Edenir Inez Palmero, Patricia Ashton-Prolla

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