CTC - Centro de Terapia Celular

• Processo: 13/08135-2
• Modalidade de apoio: Auxílio à Pesquisa - Centros de Pesquisa, Inovação e Difusão - CEPIDs
• Data de Início da vigência: 01 de junho de 2013
• Data de Término da vigência: 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). Ribeirão Preto , SP, Brasil
• Município da Instituição Sede: Ribeirão Preto
• 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
• Auxílio(s) vinculado(s): 25/05909-4 - Isct 2025, AR.EXT; 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; + mais auxílios vinculados 18/00440-4 - iPSCs: A Decade of Progress and Beyond, AR.EXT; 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): 24/20028-1 - Modelagem e alterações epigenéticas na anemia aplástica imune, BP.DR; 25/03164-1 - Inativação Genética de CD33 em Células-Tronco Hematopoiéticas: Uma Estratégia para viabilizar imunoterapia com células CAR-T na Leucemia Mieloide Aguda (LMA), BP.PD; 25/06097-3 - Expansão de células-tronco hematopoéticas de pacientes com anemia aplástica imune e análise do impacto do UM171 no perfil genético e telomérico, BP.TT; + mais bolsas vinculadas 25/01498-0 - Desenvolvimento de Células CAR-T anti-BCMA no Combate ao Mieloma Múltiplo, BP.PD; 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; 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; 22/09764-2 - Uso de CRISPR para marcar o lncRNA RMEL3 endógeno para estudo de suas interações moleculares e localização subcelular, BP.IC; 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; 21/06359-7 - Terapia com células NK-CAR anti-MAGE-A4 para o tratamento de Melanoma, BP.DR; 22/08235-6 - Treinamento administrativo em acompanhamento, controle de aquisições e estoque de materiais de pesquisa, BP.TT; 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; 21/03063-0 - 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; 21/01462-4 - 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; 21/02211-5 - 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; 19/05722-0 - Investigação dos efeitos celulares e moleculares do tratamento com metformina em neoplasias mielóides raras, BP.DR; 19/22155-2 - Caracterização celular dos nichos hematopoéticos de modelo murino da anemia falciforme, BP.MS; 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; 17/24027-6 - Análise de vias gênicas reguladas pelo gene HOXB2 em glioblastoma, BP.MS; 18/04232-7 - Análise funcional das vesículas extracelulares derivadas de células estromais mesenquimais humanas usadas em terapia celular, 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; 17/09491-8 - Modelos murinos de Leucemia/Linfoma Linfoides para avaliar os efeitos antitumorais de células T modificadas com CAR-CD19, BP.PD; 17/03102-0 - Análise do impacto do silenciamento da HJURP no controle do estresse replicativo em células de GBM, BP.IC; 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; 15/20429-7 - Modelos animais transgênicos de leucemia promielocítica aguda gerados e usados para estudos básicos e pré-clínicos, BP.TT; 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; 15/08807-6 - Metilação da H3K9 como regulador da memória epigenética na reprogramação nuclear de bovinos., BP.PD; 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; 15/09575-1 - 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; 15/01060-2 - Estudo da heterogeneidade genética em câncer renal de células claras, BP.TT; 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; 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

(276)

(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)

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)

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)

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)

GOMES DE LIMA, SARAH CAROLINE; CARVALHO FANTACINI, DAIANNE MACIELY; BATISTA, LAIS DE CASTRO; SILVEIRA, ROBERTA MARANINCHI; FURTADO, IZADORA PETER; ROSSETTI, RAFAELA; BRAND, HELOISA; COVAS, DIMAS TADEU; BOTELHO DE SOUZA, LUCAS EDUARDO. Strategies to Enhance the Therapeutic Efficacy, Applicability, and Safety of Genetically Engineered Immune Cells. CRITICAL REVIEWS IN IMMUNOLOGY, v. 41, n. 1, SI, p. 41-67, 2021. (20/02043-2, 19/18702-8, 13/08135-2, 19/18672-1)

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TOFOLI, FABIANO A.; CHIEN, HSIN FEN; BARBOSA, EGBERTO REIS; PEREIRA, V, LYGIA. Generation of three human induced pluripotent stem cell (hiPSC) lines derived from one Gaucher disease patient with Parkinson's disease and two unrelated Parkinson's disease patients with GBA mutations. STEM CELL RESEARCH, v. 39, AUG 2019. (13/08135-2)

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SOBRAL, LAYS M.; COLETTA, RICARDO D.; ALBERICI, LUCIANE C.; CURTI, CARLOS; LEOPOLDINO, ANDREIA M.. SET/I2PP2A overexpression induces phenotypic, molecular, and metabolic alterations in an oral keratinocyte cell line. FEBS Journal, v. 284, n. 17, p. 2774-2785, SEP 2017. (13/08135-2, 10/18544-9, 13/10898-4)

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MARSH, JUDITH C. W.; GUTIERREZ-RODRIGUES, FERNANDA; COOPER, JAMES; JIANG, JIE; GANDHI, SHREYANS; KAJIGAYA, SACHIKO; FENG, XINGMIN; IBANEZ, MARIA DEL PILAR F.; DONAIRES, FLAVIA S.; LOPES DA SILVA, JOAO P.; et al. Heterozygous RTEL1 variants in bone marrow failure and myeloid neoplasms. BLOOD ADVANCES, v. 2, n. 1, p. 36-48, JAN 9 2018. (13/08135-2, 15/19074-0)

MOREIRA DE MELLO, JOANA C.; FERNANDES, GUSTAVO R.; VIBRANOVSKI, MARIA D.; PEREIRA, LYGIA V.. Early X chromosome inactivation during human preimplantation development revealed by single-cell RNA-sequencing. SCIENTIFIC REPORTS, v. 7, SEP 7 2017. (15/20844-4, 09/17481-6, 13/08135-2, 15/03610-0)

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ARAUJO, L. F.; TERRA, JR., A. T.; SARES, C. T. G.; SOBREIRA, C. F. R.; FARIA, E. F.; MACHADO, R. D.; RODRIGUES, JR., A. A.; MUGLIA, V. F.; SILVA, JR., W. A.; REIS, R. B.. Mitochondrial genome analysis in penile carcinoma. MOLECULAR BIOLOGY REPORTS, v. 45, n. 4, p. 591-600, AUG 2018. (13/08135-2, 09/53853-5, 13/25119-0)

FERREIRA, ALINE F.; CALIN, GEORGE A.; PICANCO-CASTRO, VIRGINIA; KASHIMA, SIMONE; COVAS, DIMAS T.; DE CASTRO, FABIOLA A.. Hematopoietic stem cells from induced pluripotent stem cells - considering the role of microRNA as a cell differentiation regulator. Journal of Cell Science, v. 131, n. 4, FEB 2018. (15/21237-4, 13/08135-2)

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LIMA-JUNIOR, JOAO R.; ARRUDA, LUCAS C. M.; GONCALVES, MAYNARA S.; DIAS, JULIANA B. E.; MORAES, DANIELA A.; COVAS, DIMAS T.; SIMOES, BELINDA P.; OLIVEIRA, MARIA CAROLINA; MALMEGRIM, KELEN C. R.. utologous haematopoietic stem cell transplantation restores the suppressive capacity of regulatory B cells in systemic sclerosis patient. RHEUMATOLOGY, v. 60, n. 12, p. 5538-5548, DEC 2021. (18/20343-3, 16/24443-7, 13/08135-2)

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