Reply to Lombardo, 2020: An additional route of investigation: what are the mechanisms controlling ribosomal protein genes dysregulation in autistic neuronal cells?

מאת Griesi-Oliveira, Karina, Passos-Bueno, Maria Rita
הוצא לאור ב Mol Psychiatry (2020)

Neuromuscular disorders: genes, genetic counseling and therapeutic trials

מאת Zatz, Mayana, Passos-Bueno, Maria Rita, Vainzof, Mariz
הוצא לאור ב Genet Mol Biol (2016)

Collybistin and gephyrin are novel components of the eukaryotic translation initiation factor 3 complex

מאת Sertie, Andrea L, de Alencastro, Gustavo, De Paula, Vanessa J, Passos-Bueno, Maria Rita
יצא לאור 2010

Genetics and Management of the Patient with Orofacial Cleft

מאת Brito, Luciano Abreu, Meira, Joanna Goes Castro, Kobayashi, Gerson Shigeru, Passos-Bueno, Maria Rita
יצא לאור 2012

Understanding the Basis of Auriculocondylar Syndrome: Insights From Human and Mouse Genetic Studies

מאת Clouthier, David E., Passos Bueno, Maria Rita, Tavares, Andre L.P., Lyonnet, Stanislas, Amiel, Jeanne, Gordon, Christopher T.
יצא לאור 2013

Genetics and genomics in Brazil: a promising future

מאת Passos-Bueno, Maria Rita, Bertola, Debora, Horovitz, Dafne Dain Gandelman, de Faria Ferraz, Victor Evangelista, Brito, Luciano Abreu
יצא לאור 2014

Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effects

מאת Alvizi, Lucas, Ke, Xiayi, Brito, Luciano Abreu, Seselgyte, Rimante, Moore, Gudrun E., Stanier, Philip, Passos-Bueno, Maria Rita
הוצא לאור ב Sci Rep (2017)

Optimization of Parameters for a More Efficient Use of Adipose-Derived Stem Cells in Regenerative Medicine Therapies

מאת Aguena, Meire, Dalto Fanganiello, Roberto, Tissiani, Luiz Alexandre Lorico, Ishiy, Felipe Augusto André, Atique, Rodrigo, Alonso, Nivaldo, Passos-Bueno, Maria Rita
יצא לאור 2012

Reduced transcription of TCOF1 in adult cells of Treacher Collins syndrome patients

מאת Masotti, Cibele, Ornelas, Camila C, Splendore-Gordonos, Alessandra, Moura, Ricardo, Félix, Têmis M, Alonso, Nivaldo, Camargo, Anamaria A, Passos-Bueno, Maria Rita
יצא לאור 2009

FGFR2 Mutation Confers a Less Drastic Gain of Function in Mesenchymal Stem Cells Than in Fibroblasts

מאת Yeh, Erika, Atique, Rodrigo, Ishiy, Felipe A. A., Fanganiello, Roberto Dalto, Alonso, Nivaldo, Matushita, Hamilton, da Rocha, Katia Maria, Passos-Bueno, Maria Rita
יצא לאור 2011

Erratum to: FGFR2 Mutation Confers a Less Drastic Gain of Function in Mesenchymal Stem Cells than in Fibroblasts

מאת Yeh, Erika, Atique, Rodrigo, Ishiy, Felipe A. A., Fanganiello, Roberto Dalto, Alonso, Nivaldo, Matushita, Hamilton, da Rocha, Katia Maria, Passos-Bueno, Maria Rita
הוצא לאור ב Stem Cell Rev (2013)

A Novel Autosomal Recessive GJA1 Missense Mutation Linked to Craniometaphyseal Dysplasia

מאת Hu, Ying, Chen, I-Ping, de Almeida, Salome, Tiziani, Valdenize, Do Amaral, Cassio M. Raposo, Gowrishankar, Kalpana, Passos-Bueno, Maria Rita, Reichenberger, Ernst J.
יצא לאור 2013

Improvement of In Vitro Osteogenic Potential through Differentiation of Induced Pluripotent Stem Cells from Human Exfoliated Dental Tissue towards Mesenchymal-Like Stem Cells

מאת Ishiy, Felipe Augusto Andre, Fanganiello, Roberto Dalto, Griesi-Oliveira, Karina, Suzuki, Angela May, Kobayashi, Gerson Shigeru, Morales, Andressa Gois, Capelo, Luciane Portas, Passos-Bueno, Maria Rita
הוצא לאור ב Stem Cells Int (2015)

Importance of Zinc Transporter 8 Autoantibody in the Diagnosis of Type 1 Diabetes in Latin Americans

מאת Gomes, Karla Fabiana Brasil, Semzezem, Cintia, Batista, Rodolfo, Fukui, Rosa Tsuneshiro, Santos, Aritania Sousa, Correia, Márcia Regina, Passos-Bueno, Maria Rita, Silva, Maria Elizabeth Rossi da
הוצא לאור ב Sci Rep (2017)

Human Stem Cell Cultures from Cleft Lip/Palate Patients Show Enrichment of Transcripts Involved in Extracellular Matrix Modeling By Comparison to Controls

מאת Bueno, Daniela Franco, Sunaga, Daniele Yumi, Kobayashi, Gerson Shigeru, Aguena, Meire, Raposo-Amaral, Cassio Eduardo, Masotti, Cibele, Cruz, Lucas Alvizi, Pearson, Peter Lees, Passos-Bueno, Maria Rita
יצא לאור 2010

Array comparative genomic hybridization in confirmation of the deleted genes in a patient with subterminal deletion of the long arm of chromosome 10 associated with sagittal cranio...

מאת Faria, Ágatha Cristhina, Toledo Atique, Ferraz de Rodrigo, Oliveira Rebouças, Maria Regina Galvêas, Cavagnaro, Pablo Federico, Rabbi-Bortolini, Eliete, Passos-Bueno, Maria Rita, Valle Errera, Flávia Imbroisi
יצא לאור 2014

Recapitulation of Neural Crest Specification and EMT via Induction from Neural Plate Border-like Cells

מאת Kobayashi, Gerson Shigeru, Musso, Camila Manso, Moreira, Danielle de Paula, Pontillo-Guimarães, Giovanna, Hsia, Gabriella Shih Ping, Caires-Júnior, Luiz Carlos, Goulart, Ernesto, Passos-Bueno, Maria Rita
הוצא לאור ב Stem Cell Reports (2020)

Complement C4 Is Reduced in iPSC-Derived Astrocytes of Autism Spectrum Disorder Subjects

מאת Mansur, Fernanda, Teles e Silva, André Luiz, Gomes, Ana Karolyne Santos, Magdalon, Juliana, de Souza, Janaina Sena, Griesi-Oliveira, Karina, Passos-Bueno, Maria Rita, Sertié, Andréa Laurato
הוצא לאור ב Int J Mol Sci (2021)

Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17

מאת Nitrini Ricardo, Silva Luís Sidônio Teixeira da, Rosemberg Sérgio, Caramelli Paulo, Carrilho Paulo Eduardo Mestrinelli, Iughetti Paula, Passos-Bueno Maria Rita, Zatz Mayana, Albrecht Stephen, LeBlanc Andrea
יצא לאור 2001-01-01

Novel Molecular Pathways Elicited by Mutant FGFR2 May Account for Brain Abnormalities in Apert Syndrome

מאת Yeh, Erika, Fanganiello, Roberto D., Sunaga, Daniele Y., Zhou, Xueyan, Holmes, Gregory, Rocha, Katia M., Alonso, Nivaldo, Matushita, Hamilton, Wang, Yingli, Jabs, Ethylin W., Passos-Bueno, Maria Rita
יצא לאור 2013