Rare RELN variants affect Reelin–DAB1 signal transduction in autism spectrum disorder
Sánchez‐Sánchez, Sandra M., Magdalon, Juliana, Griesi‐Oliveira, Karina, Yamamoto, Guilherme L., Santacruz‐Perez, Carolina, Fogo, Mariana, Passos‐Bueno, Maria Rita, Sertié, Andrea L.
Published in Human mutation (01.10.2018)
Published in Human mutation (01.10.2018)
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MS‐Driven Metabolic Alterations Are Recapitulated in iPSC‐Derived Astrocytes
Ghirotto, Bruno, Oliveira, Danyllo F., Cipelli, Marcella, Basso, Paulo J., Lima, Jean, Breda, Cristiane N. S., Ribeiro, Henrique C., Silva, Camille C. C., Sertié, Andrea L., Oliveira, Antonio Edson R., Hiyane, Meire I., Caldini, Elia G., Sussulini, Alessandra, Nakaya, Helder I., Kowaltowski, Alicia J., Oliveira, Enedina M. L., Zatz, Mayana, Câmara, Niels O. S.
Published in Annals of neurology (01.05.2022)
Published in Annals of neurology (01.05.2022)
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Different gene expression profiles in iPSC-derived motor neurons from ALS8 patients with variable clinical courses suggest mitigating pathways for neurodegeneration
Oliveira, Danyllo, Morales-Vicente, David A, Amaral, Murilo S, Luz, Livia, Sertié, Andrea L, Leite, Felipe S, Navarro, Claudia, Kaid, Carolini, Esposito, Joyce, Goulart, Ernesto, Caires, Luiz, Alves, Luciana M, Melo, Uirá S, Figueiredo, Thalita, Mitne-Neto, Miguel, Okamoto, Oswaldo K, Verjovski-Almeida, Sergio, Zatz, Mayana
Published in Human molecular genetics (03.06.2020)
Published in Human molecular genetics (03.06.2020)
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Dysfunctional mTORC1 Signaling: A Convergent Mechanism between Syndromic and Nonsyndromic Forms of Autism Spectrum Disorder?
Magdalon, Juliana, Sánchez-Sánchez, Sandra M, Griesi-Oliveira, Karina, Sertié, Andréa L
Published in International journal of molecular sciences (18.03.2017)
Published in International journal of molecular sciences (18.03.2017)
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10q23.31 microduplication encompassing PTEN decreases mTOR signalling activity and is associated with autosomal dominant primary microcephaly
Oliveira, Danyllo, Leal, Gabriela Ferraz, Sertié, Andréa L, Caires Jr, Luiz Carlos, Goulart, Ernesto, Musso, Camila Manso, Oliveira, João Ricardo Mendes de, Krepischi, Ana Cristina Victorino, Vianna-Morgante, Angela Maria, Zatz, Mayana
Published in Journal of medical genetics (01.08.2019)
Published in Journal of medical genetics (01.08.2019)
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Effects of antipsychotics with different weight gain liabilities on human in vitro models of adipose tissue differentiation and metabolism
Sertié, Andréa L., Suzuki, Angela May, Sertié, Rogério A.L., Andreotti, Sandra, Lima, Fábio B., Passos-Bueno, Maria Rita, Gattaz, Wagner F.
Published in Progress in neuro-psychopharmacology & biological psychiatry (01.12.2011)
Published in Progress in neuro-psychopharmacology & biological psychiatry (01.12.2011)
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Apert p.Ser252Trp mutation in FGFR2 alters osteogenic potential and gene expression of cranial periosteal cells
Fanganiello, Roberto D, Sertié, Andréa L, Reis, Eduardo M, Yeh, Erika, Oliveira, Nélio A J, Bueno, Daniela F, Kerkis, Irina, Alonso, Nivaldo, Cavalheiro, Sérgio, Matsushita, Hamilton, Freitas, Renato, Verjovski-Almeida, Sergio, Passos-Bueno, Maria Rita
Published in Molecular medicine (Cambridge, Mass.) (01.07.2007)
Published in Molecular medicine (Cambridge, Mass.) (01.07.2007)
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COL18A1 is highly expressed during human adipocyte differentiation and the SNP c.1136C > T in its "frizzled" motif is associated with obesity in diabetes type 2 patients
Errera, Flavia I V, Canani, Luís H, Yeh, Erika, Kague, Erika, Armelin-Corrêa, Lucia M, Suzuki, Oscar T, Tschiedel, Balduíno, Silva, Maria Elizabeth R, Sertié, Andréa L, Passos-Bueno, Maria Rita
Published in Anais da Academia Brasileira de Ciências (01.03.2008)
Published in Anais da Academia Brasileira de Ciências (01.03.2008)
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Mutations in collagen 18A1 and their relevance to the human phenotype
Passos-Bueno, Maria Rita, Suzuki, Oscar T, Armelin-Correa, Lucia M, Sertié, Andréa L, Errera, Flavia I V, Bagatini, Kelly, Kok, Fernando, Leite, Katia R M
Published in Anais da Academia Brasileira de Ciências (01.03.2006)
Published in Anais da Academia Brasileira de Ciências (01.03.2006)
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A polymorphism in endostatin, an angiogenesis inhibitor, predisposes for the development of prostatic adenocarcinoma
IUGHETTI, Paula, SUZUKI, Oscar, MOREIRA-FILHO, Carlos Alberto, SIMOSON, Andrew, OLIVA, Glaucius, PASSOS-BUENO, Maria Rita, GODOI, Paulo H. C, FERREIRA ALVES, Venancio Avancini, SERTIE, Andrea L, ZORICK, Todd, SOARES, Fernando, CAMARGO, Anamaria, MOREIRA, Eloisa S, DI LORETO, Celso
Published in Cancer research (Chicago, Ill.) (15.10.2001)
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Published in Cancer research (Chicago, Ill.) (15.10.2001)
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Crouzon syndrome: Association with absent pulmonary valve syndrome and severe tracheobronchomalacia
Beck, Raphael, Sertie, Andrea L., Brik, Riva, Shinawi, Marwan
Published in Pediatric pulmonology (01.12.2002)
Published in Pediatric pulmonology (01.12.2002)
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How pathogenic is the p.D104N/endostatin polymorphic allele of COL18A1 in Knobloch syndrome?
Suzuki, Oscar T., Bagatini, Kelly, Sertié, Andréa L., Passos-Bueno, Maria Rita
Published in Human mutation (01.03.2005)
Published in Human mutation (01.03.2005)
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