Neuromuscular disorders: genes, genetic counseling and therapeutic trials

Por Zatz, Mayana, Passos-Bueno, Maria Rita, Vainzof, Mariz
Publicado no Genet Mol Biol (2016)

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

Por Sertie, Andrea L, de Alencastro, Gustavo, De Paula, Vanessa J, Passos-Bueno, Maria Rita
Publicado em 2010

Genetics and Management of the Patient with Orofacial Cleft

Por Brito, Luciano Abreu, Meira, Joanna Goes Castro, Kobayashi, Gerson Shigeru, Passos-Bueno, Maria Rita
Publicado em 2012

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

Por Clouthier, David E., Passos Bueno, Maria Rita, Tavares, Andre L.P., Lyonnet, Stanislas, Amiel, Jeanne, Gordon, Christopher T.
Publicado em 2013

Genetics and genomics in Brazil: a promising future

Por Passos-Bueno, Maria Rita, Bertola, Debora, Horovitz, Dafne Dain Gandelman, de Faria Ferraz, Victor Evangelista, Brito, Luciano Abreu
Publicado em 2014

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

Por Alvizi, Lucas, Ke, Xiayi, Brito, Luciano Abreu, Seselgyte, Rimante, Moore, Gudrun E., Stanier, Philip, Passos-Bueno, Maria Rita
Publicado no Sci Rep (2017)

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

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

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

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

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

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

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

Por Yeh, Erika, Atique, Rodrigo, Ishiy, Felipe A. A., Fanganiello, Roberto Dalto, Alonso, Nivaldo, Matushita, Hamilton, da Rocha, Katia Maria, Passos-Bueno, Maria Rita
Publicado no Stem Cell Rev (2013)

A Novel Autosomal Recessive GJA1 Missense Mutation Linked to Craniometaphyseal Dysplasia

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

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

Por 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
Publicado no Stem Cells Int (2015)

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

Por 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
Publicado no 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

Por 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
Publicado em 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...

Por 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
Publicado em 2014

Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17

Por 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
Publicado em 2001-01-01

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

Por 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
Publicado em 2013

Novel pathogenic mutations and skin biopsy analysis in Knobloch syndrome

Por Suzuki, Oscar, Kague, Erika, Bagatini, Kelly, Tu, Hongmin, Heljasvaara, Ritva, Carvalhaes, Lorenza, Gava, Elisandra, de Oliveira, Gisele, Godoi, Paulo, Oliva, Glaucius, Kitten, Gregory, Pihlajaniemi, Taina, Passos-Bueno, Maria-Rita
Publicado em 2009

Deletion of the Basement Membrane Heparan Sulfate Proteoglycan Type XVIII Collagen Causes Hypertriglyceridemia in Mice and Humans

Por Bishop, Joseph R., Passos-Bueno, Maria Rita, Fong, Loren, Stanford, Kristin I., Gonzales, Jon C., Yeh, Erika, Young, Stephen G., Bensadoun, Andre, Witztum, Joseph L., Esko, Jeffrey D., Moulton, Karen S.
Publicado em 2010

Is bone transplantation the gold standard for repair of alveolar bone defects?

Por Raposo-Amaral, Cassio Eduardo, Bueno, Daniela Franco, Almeida, Ana Beatriz, Jorgetti, Vanda, Costa, Cristiane Cabral, Gouveia, Cecília Helena, Vulcano, Luiz Carlos, Fanganiello, Roberto D, Passos-Bueno, Maria Rita, Alonso, Nivaldo
Publicado em 2014