CTC - Centro de Terapia Celular

• Processo: 13/08135-2
• Modalidade de apoio: Auxílio à Pesquisa - Centros de Pesquisa, Inovação e Difusão - CEPIDs
• Vigência: 01 de junho de 2013 - 31 de maio de 2026
• Área do conhecimento: Ciências da Saúde - Medicina - Clínica Médica
• Pesquisador responsável: Dimas Tadeu Covas
• Beneficiário: Dimas Tadeu Covas
• Instituição Sede: Hemocentro de Ribeirão Preto. Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da USP (HCMRP). Secretaria da Saúde (São Paulo - Estado). Ribeirão Preto , SP, Brasil
• Pesquisadores principais:( Atuais ): Eduardo Magalhães Rego ; Fabíola Traina ; Flávio Vieira Meirelles ; Lewis Joel Greene ; Lygia da Veiga Pereira ; Marco Antonio Zago ; Maria Carolina de Oliveira Rodrigues ; Roberto Passetto Falcão ; Rodrigo do Tocantins Calado de Saloma Rodrigues ; Vanderson Geraldo Rocha ; Vitor Marcel Faça ; Wilson Araújo da Silva Junior
• Pesquisadores principais:( Anteriores ): Dimas Tadeu Covas
• Pesquisadores associados: Andréia Machado Leopoldino ; Ângela Merice de Oliveira Leal ; Antonio Roberto Lucena de Araújo ; Bart Roep ; Belinda Pinto Simoes ; Carlos Eduardo Ambrósio ; Christina Ramires Ferreira ; Clarice Izumi ; Daniele dos Santos Martins ; Davide Ruggero ; Dominique Farge ; Elisa Maria de Sousa Russo ; Fabíola Traina ; Felipe Perecin ; Gene Yeo ; Gerhard Coetzee ; Hau Kwaan ; Houtan Noushmehr ; Jeanne Loring ; Joanna Poulton ; José César Rosa ; Kamilla Swiech Antonietto ; Kelen Cristina Ribeiro Malmegrim de Farias ; Lawrence Charles Smith ; Lucas Eduardo Botelho de Souza ; Lygia da Veiga Pereira ; Maria Angelica Miglino ; Maria Carolina de Oliveira Rodrigues ; Marisa Ramos Barbieri ; Marjorie Barnett ; Renato Luiz Guerino Cunha ; Richard Burt ; Rodrigo Alexandre Panepucci ; Simone Kashima Haddad ; Stefan Bohlander ; Valeria Valente ; Virginia Picanço e Castro ; Vitor Marcel Faça ; Willian Alan King
• Auxílios(s) vinculado(s): 19/27075-7 - Maturação epigenética do oócito e totipotência - o potencial do oócito e sua relação com nicho folicular ovariano, AV.EXT; 20/05367-3 - Uso de plasma de doador convalescente para tratar pacientes com infecção grave pelo SARS-CoV-2 (COVID-19), AP.R; 18/00440-4 - iPSCs: A Decade of Progress and Beyond, AR.EXT; + mais auxílios vinculados 16/22858-5 - Scale-up and Manufacturing of Cell-based Therapies V, AR.EXT; 15/50339-0 - Building metabolomics capacity in livestock research: focus on cattle and application to reproductive biotechnology, AP.R SPRINT; 14/23427-2 - EMU concedido no processo n. 2013/08135-2 equipamento: citômetro de fluxo cell soter com acessórios, AP.EMU; 13/50385-6 - Integrated transcriptome and methylome analysis of undifferentiated and differentiated Brazilian pluripotent cell lines, AP.R - menos auxílios vinculados
• Bolsa(s) vinculada(s): 24/04661-6 - Geração de células CAR-T humanas capazes de eliminar macrófagos associados a tumores., BP.MS; 23/12849-2 - Caracterização da inativação do cromossomo x em blastóides humanos derivados de células-tronco pluripotentes induzidas, BP.PD; 23/12977-0 - Manipulação da via Wnt/b-catenina durante a MIV de oócitos suínos visando a produção de clones por TNCS, BP.DD; + mais bolsas vinculadas 23/10316-7 - Treinamento técnico na área de inovação tecnológica, BP.TT; 23/11375-7 - Modelos animais para estudos de câncer., BP.TT; 23/11306-5 - Modelos animais para estudos de câncer, BP.TT; 23/04099-3 - Treinamento administrativo em acompanhamento, controle de aquisições execução financeira dos recursos elaboração de prestação de contas em projeto de pesquisa, BP.TT; 22/09926-2 - Avaliação da coexpressão de GITRL na eficiência terapêutica e resistência à imunossupressão de células T-CAR anti-GD2 em um modelo pré-clínico de Glioblastoma Multiforme, BP.DD; 22/07503-7 - Indução de hemoglobina fetal como estratégia de tratamento para anemia falciforme utilizando terapia gênica, BP.DR; 22/09643-0 - Análise imunofenotípica e funcional de células CD34 circulantes em pacientes com anemia falciforme sob regime de transfusão crônica ou Hidroxiuréia., BP.IC; 22/09764-2 - Uso de CRISPR para marcar o lncRNA RMEL3 endógeno para estudo de suas interações moleculares e localização subcelular, BP.IC; 22/08235-6 - Treinamento administrativo em acompanhamento, controle de aquisições e estoque de materiais de pesquisa, BP.TT; 21/06359-7 - Terapia com células NK-CAR anti-MAGE-A4 para o tratamento de Melanoma, BP.DR; 21/05465-8 - Modificação genética de células NK com CAR anti-CD19 expressando GITRL para aumentar a função efetora das células NK para o tratamento de leucemias e linfomas, BP.DR; 22/03271-4 - Modelos animais para estudos de câncer, BP.TT; 21/11568-4 - Investigação do efeito da expressão de KMT2E em Leucemia Mieloide Aguda na resposta ao tratamento com ácido all-trans-retinóico (ATRA) e SLIT2, BP.DD; 21/08755-7 - Efeito de UM171 na expansão in vitro de células-tronco hematopoéticas de pacientes com telomeropatias, BP.DR; 20/13463-2 - Análise proteômica e fosfoproteômica dos eventos moleculares e sinalização celular no modelo de células CAR-T Anti-CD-19 usado no tratamento de Leucemia e Linfoma, BP.DD; 20/03108-0 - Estabelecimento de modelo cardiovascular in vitro derivado de células-tronco pluripotentes humanas (hiPSC) para análise funcional da Hipertensão, BP.DR; 19/26007-8 - Fenótipo endotelial como determinante da relação genótipo/fenótipo na Síndrome de Marfan, BP.PD; 21/06467-4 - Treinamento administrativo em acompanhamento, controle de aquisições e estoque de materiais de pesquisa, BP.TT; 20/11413-8 - Desenvolvimento de uma nova imunoterapia para tumores sólidos utilizando linfócitos T modificados geneticamente para expressar um TCR projetado anti-NY-ESO-1, BP.DR; 21/01462-4 - Caracterização imunofenotípica do compartimento de células-tronco e progenitoras hematopoéticas em pacientes com telomeropatias, BP.IC; 21/04120-7 - Modelos animais para estudos de câncer, BP.TT; 21/03976-5 - Treinamento administrativo em acompanhamento, controle de aquisições e estoque de materiais de pesquisa, BP.TT; 21/03063-0 - Treinamento técnico e de aperfeiçoamento na área jurídica, a fim de colaborar para incremento das atividades em geral de assessoria jurídica consultiva, garantindo a segurança legal no planejamento e efetivação dos negócios, BP.TT; 21/02211-5 - Treinamento administrativo em acompanhamento, controle de aquisições execução financeira dos recursos elaboração de prestação de contas em projeto de pesquisa, BP.TT; 20/09206-4 - Prospecção de rotas tecnológicas em imunoterapia na área de terapia gênica, BP.DR; 20/08279-8 - Estabelecimento de uma plataforma para geração de células NK-CAR com maior eficácia terapêutica in vitro e in vivo, BP.PD; 20/10804-3 - Desenvolvimento e validação de células T-CAR anti-BCMA com perfil de diferenciação de memória para tratamento de Mieloma Múltiplo, BP.PD; 20/13460-3 - Treinamento administrativo em acompanhamento, controle de aquisições e elaboração de prestação de contas em projeto de pesquisa, BP.TT; 20/02043-2 - Estabelecimento de uma metodologia de edição gênica por CRISPR/Cas9 para a geração de linfócitos T-CAR alogênicos prontos para o uso, BP.MS; 19/22155-2 - Caracterização celular dos nichos hematopoéticos de modelo murino da anemia falciforme, BP.MS; 19/05722-0 - Investigação dos efeitos celulares e moleculares do tratamento com metformina em neoplasias mielóides raras, BP.DR; 19/18702-8 - Geração e avaliação da eficiência antitumoral de linfócitos T CAR com fenótipo T helper 17, BP.MS; 19/18672-1 - Avaliação da persistência in vivo de linfócitos T expressando receptores de antígeno quiméricos anti-CD19, BP.IC; 19/14084-8 - Investigação do papel da proteína SLIT2 em células tronco estromais e a sua influência no microambiente medular na leucemia mielóide aguda, BP.MS; 19/04738-0 - LncRNAs no desenvolvimento inicial e reconstrução de embriões bovinos, BP.PD; 19/01285-5 - A regulação pós-traducional de RAS pelo complexo EMC: um potencial alvo para terapia anti-oncogênica, BP.DR; 18/16254-5 - Análise do efeito de mutações em FBN1 em células endoteliais derivadas de hiPSCs, BP.IC; 18/14897-6 - Geração de células endoteliais humanas derivadas de linhagens de hiPSC com mutações em FBN1, BP.IC; 18/04232-7 - Análise funcional das vesículas extracelulares derivadas de células estromais mesenquimais humanas usadas em terapia celular, BP.MS; 17/24027-6 - Análise de vias gênicas reguladas pelo gene HOXB2 em glioblastoma, BP.MS; 17/12140-2 - Remodelamento do cromossomo X durante a reprogramação de células sanguíneas humanas à células pluripotentes induzidas (iPSCs) e sua indução em células germinativas primordiais in vitro (iCGPs)., BP.PD; 17/21737-2 - Adaptação para cultivo em suspensão e meio de cultura livre de soro fetal bovino da linhagem celular HEK-293T para produção em larga escala de vetores lentivirais, BP.IC; 17/08057-2 - O switching de globinas na diferenciação hematopoética in vitro, BP.MS; 17/15208-7 - Investigação das funções da HJURP na aquisição de capacidade de auto-renovação e proliferação das linhagens de glioblastoma, BP.DR; 17/19825-0 - Mecanismos do acúmulo lipídico oocitário na obesidade, BP.PD; 17/12663-5 - Caracterização in vivo de células-tronco mesenquimais murinas da medula óssea e do osso compacto quanto à capacidade de geração de nicho hematopoético heterotópico, BP.MS; 17/20686-5 - Modelos animais transgênicos gerados e usados para estudos básicos e pré-clínicos, BP.TT; 16/24443-7 - Avaliação imunofenotípica, funcional e gênica de subpopulações de células B em pacientes com esclerose sistêmica submetidos ao transplante autólogo de células-tronco hematopoiéticas, BP.DR; 17/09428-4 - Hematopoese clonal em pacientes com disfunção telomérica, BP.PD; 17/15823-3 - Modelos animais transgênicos gerados e usados para estudos básicos e pré-clínicos, BP.TT; 17/03102-0 - Análise do impacto do silenciamento da HJURP no controle do estresse replicativo em células de GBM, BP.IC; 17/09491-8 - Modelos murinos de Leucemia/Linfoma Linfoides para avaliar os efeitos antitumorais de células T modificadas com CAR-CD19, BP.PD; 17/07545-3 - Colaboração no planejamento, execução, avaliação e divulgação de atividades da Casa da Ciência, BP.TT; 17/07506-8 - Modelos animais transgênicos gerados e usados para estudos básicos e pré-clínicos, BP.TT; 16/22790-1 - Vesículas extracelulares na comunicação inter-embrionária e materno-embrionária durante o desenvolvimento in vitro de embriões bovinos, BP.PD; 16/20650-8 - Avaliação de hepatócitos derivados de hiPSC como modelo para estudo da responsividade a losartan in vitro, BP.MS; 16/13416-9 - Uso do corpo cetônico ácido beta-hidroxibutírico como ferramenta para estudar a conexão entre metabolismo, epigenética e reprodução em bovinos, BP.PD; 16/17643-0 - Modelos animais transgênicos gerados e usados para estudos básicos e pre-clinicos, BP.TT; 15/23469-0 - Identificação de genes modificadores de anemia falciforme por análise exômica, BP.PD; 16/10862-8 - Estudo do papel da miosina-Va nos processos da dinâmica mitocondrial e mitofagia, BP.DD; 16/14199-1 - Modelos animais transgênicos gerados e usados para estudos básicos e pré-clínicos, BP.TT; 16/08374-5 - Modificação de linfócitos T com receptor de antígenos quimérico anti-CD19, BP.MS; 16/08373-9 - Obtenção de eritrócitos a partir de células-tronco de pluripotência induzida em cultivo feeder-free com meio xeno-free, BP.MS; 16/02459-9 - Pós-graduandos no programa Pequeno Cientista: caracterização e organização de dados, BP.TT; 15/16329-7 - Análise in vitro do papel dos genes HOXA10, HOXC9, HOXC10 e HOXC13 na tumorigênese do câncer de cabeça e pescoço, BP.IC; 15/23454-2 - Modelos animais transgênicos de leucemia promielocítica aguda gerados e usados para estudos básicos e pré-clínicos, BP.TT; 15/08070-3 - Análise em larga-escala da função dos microRNAs no ciclo celular, pluripotência, auto-renovação e diferenciação de células-tronco utilizando High Content Screening, BE.PQ; 15/20655-7 - Modelos animais transgênicos de leucemia promielocítica aguda gerados e usados para estudos básicos e pré-clínicos, BP.TT; 15/15225-3 - Avaliação dos perfis metabólico e de expressão gênica de hepatócitos gerados a partir de células-tronco pluripotentes induzidas (iPSC) de pacientes humanos com telomeropatias, BP.PD; 15/20429-7 - Modelos animais transgênicos de leucemia promielocítica aguda gerados e usados para estudos básicos e pré-clínicos, BP.TT; 15/19640-5 - Edição de Vídeos - Produção de material educacional para a Casa da Ciência, BP.TT; 15/20665-2 - Gestão de materiais, BP.TT; 15/08807-6 - Metilação da H3K9 como regulador da memória epigenética na reprogramação nuclear de bovinos., BP.PD; 15/09575-1 - Edição gênica por CRISPR-Cas9 na correção da distrofia muscular de Duchenne no modelo canino (GRMD) a partir de células de pluripotência induzida, BP.PD; 14/24587-3 - Análise comparativa de neurônios derivados de células-tronco pluripotentes induzidas (iPSC) para avaliar a associação da Doença de Gaucher e Doença de Parkinson, BP.DR; 15/01046-0 - Células tronco embrionárias humanas como um sistema para screening de toxicidade in vitro, BP.IC; 14/27294-7 - Identificação de moduladores genéticos da resposta à imunossupressão na anemia aplástica adquirida por sequenciamento de nova geração, BP.DR; 15/03185-7 - Geração de células-tronco pluripotentes induzidas (iPSCs) a partir de fibroblastos de pacientes com anemia aplástica adquirida, BP.TT; 14/26379-9 - Análise mutacional do gene GATA2 e de alterações imunológicas em pacientes com síndromes de falência medular, BP.MS; 15/00604-9 - Gestão de projetos, BP.TT; 14/20756-5 - Análise funcional em larga-escala para a identificação de microRNAs com potencial antitumoral e antimetastático no câncer de cabeça e pescoço, BP.DR; 15/01060-2 - Estudo da heterogeneidade genética em câncer renal de células claras, BP.TT; 14/20379-7 - Análise do perfil de expressão dos genes da família HOX em um painel de 70 linhagens tumorais, BP.IC; 14/00088-8 - Mecanismos imunológicos e hematológicos envolvidos na resposta terapêutica de pacientes com anemia falciforme submetidos ao transplante alogênico de células-tronco hematopoéticas, BP.DR; 13/25119-0 - Estudo do metabolismo energético na progressão do melanoma com base na instabilidade do genoma mitocondrial, BP.DR; 14/14216-8 - Estabelecimento de banco de células primárias para geração de hiPSCs, BP.TT; 14/07726-0 - Caracterização genômica e funcional de genes de expressão restrita a melanoma (RMELs), BP.DD; 14/03866-1 - Avaliação da função tímica em pacientes com anemia falciforme, BP.DR; 14/09294-0 - Análise qualitativa e quantitativa de lncRNA de tumores metastáticos em sistema nervoso central, BP.TT; 14/02574-7 - Estudo dos mecanismos de geração de células t regulatórias a partir de células T naive: papel da sinalização da adenosina, BP.DR; 13/27061-0 - O papel dos microRNAs na proliferação e diferenciação celular da linhagem pluripotente de carcinoma embrionário humano NTera-2, BP.DR; 13/24199-0 - Avaliação dos níveis de expressão de TERRA e sua correlação com o desequilíbrio telomérico em indivíduos com hemopatias e telomeropatias., BP.DR; 13/11817-8 - Pesquisa de mutações adicionais ao rearranjo PML/RARa por meio da análise do transcriptoma, exoma completo e metiloma em amostras de Leucemia Promielocítica Aguda no diagnóstico, remissão molecular e recaída, BP.PD; 13/18678-3 - Estudo dos mecanismos imunológicos envolvidos na resposta terapêutica de pacientes com esclerose sistêmica ao transplante autólogo de células-tronco hematopoéticas, BP.DR; 13/07675-3 - Estudo da via de sinalização pi3k/akt em leucemia mielóide aguda utilizando o monitoramento seletivo de ions (srm)., BP.PD - menos bolsas vinculadas
• Assunto(s): Terapia baseada em transplante de células e tecidos Células-tronco Hematologia Expressão gênica Neoplasias Financiamento em saúde
• Palavra(s)-Chave do Pesquisador: Células-tronco | células-tronco de pluripotência induzida | células-tronco do câncer | expressão gênica | Hematologia | terapia celular | Clinica Médica
• Publicação FAPESP: https://media.fapesp.br/bv/uploads/pdfs/Multidisciplinary_science_PG76toF_26_27.pdf

Resumo

O projeto do Centro de Terapia Celular (CTC) tem como foco a realização de pesquisas avançadas, básicas e aplicadas com células-tronco (CT). O CTC congrega 9 pesquisadores principais (Pls) com reconhecida liderança nesta área no Brasil, a equipe se complementa com a participação de 20 pesquisadores associados e 10 colaboradores estrangeiros. A atual proposta continua e expande a experiência adquirida pelo grupo no projeto CEPID em vigor, tanto no aspecto científico: como nos aspectos de disseminação do conhecimento e de transferência tecnológica para a sociedade, como pode ser verificado no sítio: http://ctc.fmrp.usp.br. O projeto científico compreende um ambicioso programa de pesquisa multidisciplinar que objetiva estudar aspectos moleculares, celulares e biológicos das CT normais e patológicas e avaliar, criticamente e o seu papel terapêutico. Os estudos serão conduzidos com CT pluripotentes (CT Embrionária e CT de pluripotência induzida) e CT somáticas (CT Hematopoética, CT Mesenquimal e CP Endotelial). No território das CTE pretendemos a geração de linhagens: brasileiras que possam ser expandidas e usadas em protocolos pré-clínicos e clínicos, bem como contribuir para o, entendimento dos mecanismos da pluripotência. Serão geradas iPSCs derivadas de doentes com Disceratose Congênita: Anemia de Fanconi, Hemofilia A e Doença de Parkinson com o objetivo de entender mecanismos envolvidos na patologia. Na manutenção da pluripotência e no processo de diferenciação celular. No CT Hematopoéticas serão derivadas de CTEs e de iPSCs e estabelecidas linhagens celulares tanto de CT normais como leucêmicas para os estudos dos mecanismos envolvidos no controle da hematopoese normal e neoplásica. Modelos animais transgênicos de leucemia promielocítica aguda serão gerados e usados para estudos básicos e pré-clínicos. No CT do Câncer serão estudadas tendo como foco os mecanismos de trans1o Epitélio-Mesenquimal e Endotélio-Mesenquimal (EMT e EndMT) . Estes mecanismos também serão estudados no contex to d2 reprogramação celular e na geração de CT. Na arena clínica serão realizados ensaios clínicos usando CT mesenquimais no tratamento do diabetes insulino-dependente dos tipos 1 e 2, da Anemia Aplástica grave adquirida refratária, na prevenção da Doença do Enxerto contra o Hospedeiro (DECH) aguda e crônica e da falha de enxertia no transplante alogênico haploidêntico. Por fim, serão desenvolvidos processos de produção de CT em grande escala em condições GMP para permitir o seu uso. (AU)

Publicações científicas

(238)

(Referências obtidas automaticamente do Web of Science e do SciELO, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores)

COMINAL, JUCARA GASTALDI; CACEMIRO, MAIRA DA COSTA; PINTO-SIMOES, BELINDA; KOLB, HANS-JOCHEM; RIBEIRO MALMEGRIM, KELEN CRISTINA; DE CASTRO, FABIOLA ATTIE. Emerging Role of Mesenchymal Stromal Cell-Derived Extracellular Vesicles in Pathogenesis of Haematological Malignancies. STEM CELLS INTERNATIONAL, 2019. (13/08135-2, 14/50947-7, 18/19714-7, 18/01756-5)

MIZUKAMI, AMANDA; SWIECH, KAMILLA. Mesenchymal Stromal Cells: From Discovery to Manufacturing and Commercialization. STEM CELLS INTERNATIONAL, 2018. (13/08135-2, 12/23228-4)

SANGUINET, EDUARDO DE O.; SIQUEIRA, NATALY M.; MENEZES, FELIPE DE C.; RASIA, GISELE M.; LOTHHAMMER, NIVIA; SOARES, ROSANE M. D.; MEIRELLES, FLAVIO V.; BRESSAN, FABIANA F.; BOS-MIKICH, ADRIANA. Interaction of fibroblasts and induced pluripotent stem cells with poly(vinyl alcohol)-based hydrogel substrates. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS, JUN 2019. (15/26818-5, 13/08135-2)

DE FIGUEIREDO PESSOA, LAIS VICARI; LISBOA PIRES, PEDRO RATTO; DEL COLLADO, MAITE; GODOY PIERI, NAIRA CAROLINE; RECCHIA, KAIANA; SOUZA, ALINE FERNANDA; PERECIN, FELIPE; DA SILVEIRA, JULIANO COELHO; CESAR DE ANDRADE, ANDRE FURUGEN; AMBROSIO, CARLOS EDUARDO; et al. Generation and miRNA Characterization of Equine Induced Pluripotent Stem Cells Derived from Fetal and Adult Multipotent Tissues. STEM CELLS INTERNATIONAL, 2019. (08/57877-3, 13/17955-3, 15/26818-5, 13/08135-2, 12/50533-2, 14/22887-0)

BOS-MIKICH, ADRIANA; BRESSAN, FABIANA F.; RUGGERI, RAFAEL R.; WATANABE, YEDA; MEIRELLES, FLAVIO V.. Parthenogenesis and Human Assisted Reproduction. STEM CELLS INTERNATIONAL, 2016. (13/08135-2)

MIZUKAMI, AMANDA; DE ABREU NETO, MARIO SOARES; MOREIRA, FRANCISCO; FERNANDES-PLATZGUMMER, ANA; HUANG, YI-FENG; MILLIGAN, WILLIAM; CABRAL, JOAQUIM M. S.; DA SILVA, CLAUDIA L.; COVAS, DIMAS T.; SWIECH, KAMILLA. A Fully-Closed and Automated Hollow Fiber Bioreactor for Clinical-Grade Manufacturing of Human Mesenchymal Stem/Stromal Cells. STEM CELL REVIEWS AND REPORTS, v. 14, n. 1, p. 141-143, FEB 2018. (13/08135-2, 12/23228-4)

DE OLIVEIRA GEORGES, JULIANA ANDREA; VERGANI, NAJA; SIQUEIRA FONSECA, SIMONE APARECIDA; FRAGA, ANA MARIA; MOREIRA DE MELLO, JOANA CARVALHO; MACIEL ALBUQUERQUE, MARIA CECILIA R.; FUJIHARA, LITSUKO SHIMABUKURO; PEREIRA, LYGIA VEIGA. Aberrant Patterns of X Chromosome Inactivation in a New Line of Human Embryonic Stem Cells Established in Physiological Oxygen Concentrations. STEM CELL REVIEWS AND REPORTS, v. 10, n. 4, p. 472-479, AUG 2014. (13/08135-2)

GRASSI, MARIANA LOPES; PALMA, CAMILA DE SOUZA; THOME, CAROLINA HASSIBE; LANFREDI, GUILHERME PAUPERIO; POERSCH, ALINE; FACA, VITOR MARCEL. Proteomic analysis of ovarian cancer cells during epithelial-mesenchymal transition (EMT) induced by epidermal growth factor (EGF) reveals mechanisms of cell cycle control. JOURNAL OF PROTEOMICS, v. 151, n. SI, p. 2-11, JAN 16 2017. (12/09682-4, 13/08755-0, 13/07675-3, 13/08135-2, 04/09448-5)

PICANCO-CASTRO, VIRGINIA; MOCO, PABLO DIEGO; MIZUKAMI, AMANDA; VAZ, LETICIA DELFINI; FERNANDES PEREIRA, MARCELO DE SOUZA; SILVESTRE, RENATA NACASAKI; COTTAS DE AZEVEDO, JULIA TEIXEIRA; BOMFIM, ALINE DE SOUSA; DE ABREU NETO, MARIO SOARES; RIBEIRO MALMEGRIM, KELEN CRISTINA; et al. Establishment of a simple and efficient platform for car-t cell generation and expansion: from lentiviral production to in vivo studies. Hematology, Transfusion and Cell Therapy, v. 42, n. 2, p. 150-158, APR-JUN 2020. (17/09491-8, 16/08374-5, 13/08135-2, 12/23228-4)

GODOY PIERI, NAIRA CAROLINE; DE SOUZA, ALINE FERNANDA; BOTIGELLI, RAMON CESAR; DE FIGUEIREDO PESSOA, LAIS VICARI; RECCHIA, KAIANA; MACHADO, LUCAS SIMOES; GLORIA, MAYRA HIRAKAWA; GUIMARAES DE CASTRO, RAQUEL VASCONCELOS; LEAL, DIEGO FEITOSA; NETO, PAULO FANTINATO; et al. Porcine Primordial Germ Cell-Like Cells Generated from Induced Pluripotent Stem Cells Under Different Culture Conditions. STEM CELL REVIEWS AND REPORTS, JUN 2021. (13/08135-2, 15/26818-5, 15/25564-0, 17/14884-9)

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DE CASTRO, RAQUEL V. G.; PIERI, NAIRA C. G.; FANTINATO NETO, PAULO; GRIZENDI, BIANCA M.; DORIA, RENATA G. S.; MEIRELLES, FLAVIO V.; SMITH, LAWRENCE C.; GARCIA, JOAQUIM M.; BRESSAN, FABIANA F.. In Vitro Induction of Pluripotency from Equine Fibroblasts in 20% or 5% Oxygen. STEM CELLS INTERNATIONAL, v. 2020, NOV 26 2020. (13/08135-2, 18/04009-6, 15/26818-5)

SOUSA, LUCAS OLIVEIRA; SOBRAL, LAYS MARTIN; DE ALMEIDA, LUCIANA OLIVEIRA; GARCIA, CRISTIANA BERNADELLI; GREENE, LEWIS JOEL; LEOPOLDINO, ANDREIA MACHADO. SET protein modulates H4 histone methylation status and regulates miR-137 level in oral squamous cell carcinoma. Epigenomics, v. 12, n. 6, p. 475-485, MAR 2020. (10/20384-0, 16/19103-2, 13/10898-4, 13/08135-2)

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