Search Results - "Pezzi, Eduarda Heidrich"

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

“…The TP53 3'UTR variant rs78378222 A>C has been detected in different tumor types as a somatic alteration that reduces p53 expression through modification of…”
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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

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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

“…PURPOSELi-Fraumeni Syndrome (LFS) is a rare cancer predisposing condition caused by germline pathogenic TP53 variants, in which core tumors comprise sarcomas,…”
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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

“…Li-Fraumeni Syndrome (LFS) is a rare cancer predisposing condition caused by germline pathogenic TP53 variants, in which core tumors comprise sarcomas, breast,…”
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