ReP USP - Resultado da busca

Filtros : "Musso, Camila M" Removido: "Gardham, Alice" Limpar

Filtros

USP affiliated authors
- bertola, débora romeo (1)
- bueno, maria rita dos santos e passos (1)
- caires júnior, luiz carlos de (1)
- ceide, roseli maria zechi (1)
- costa, antonio richieri da (1)

Date published
- 2018 (~1)
- 2017 (~1)
Subjects
- anormalidades craniofaciais (1)
- células-tronco (1)
- disostose mandibulofacial (1)
- doenças genéticas (1)
- malformações (1)

Collaboration
Normalized affiliation
Non normalized affiliation
- department of informatics (deinfo), universidade estadual de ponta grossa (uepg), ponta grossa, paraná 84030-900, brazil (1)
- department of medicine, laboratory of endocrinology and translational medicine, universidade federal de são paulo (unifesp/epm), são paulo, são paulo, brazil (1)
- department of molecular genetics and microbiology, duke university medical center, durham, nc, usa (1)
- department of molecular genetics and microbiology, duke university medical center, durham, nc, usa; department of neurobiology; department of cell biology and duke institute for brain sciences, duke university medical center, durham, nc, usa (1)
- department of neurosurgery and neurology, laboratory of neuroscience, universidade federal de são paulo (unifesp/epm), são paulo, são paulo, brazil (1)

Artigo de periodico
Down Syndrome iPSC-Derived Astrocytes Impair Neuronal Synaptogenesis and the mTOR Pathway In Vitro (2018)
Araújo, Bruno H. S ; Kaid, Carolini ; Souza, Janaina S. De; Silva, Sérgio Gomes da ; Goulart, Ernesto ; Caires, Luiz C. J. ; Musso, Camila M ; Torres, Laila B; Ferrasa, Adriano ; Herai, Roberto ; Zatz, Mayana ; Okamoto, Oswaldo Keith ; Cavalheiro, Esper A
Source: Molecular Neurobiology. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, SÍNDROME DE DOWN, CÉLULAS-TRONCO, NEURÔNIOS, PESSOAS COM DEFICIÊNCIA INTELECTUAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ARAÚJO, Bruno H. S et al. Down Syndrome iPSC-Derived Astrocytes Impair Neuronal Synaptogenesis and the mTOR Pathway In Vitro. Molecular Neurobiology, v. 55, n. 7, p. 5962-5975, 2018Tradução . . Disponível em: https://doi.org/10.1007/s12035-017-0818-6. Acesso em: 25 out. 2025.
APA
Araújo, B. H. S., Kaid, C., Souza, J. S. D., Silva, S. G. da, Goulart, E., Caires, L. C. J., et al. (2018). Down Syndrome iPSC-Derived Astrocytes Impair Neuronal Synaptogenesis and the mTOR Pathway In Vitro. Molecular Neurobiology, 55( 7), 5962-5975. doi:10.1007/s12035-017-0818-6
NLM
Araújo BHS, Kaid C, Souza JSD, Silva SG da, Goulart E, Caires LCJ, Musso CM, Torres LB, Ferrasa A, Herai R, Zatz M, Okamoto OK, Cavalheiro EA. Down Syndrome iPSC-Derived Astrocytes Impair Neuronal Synaptogenesis and the mTOR Pathway In Vitro [Internet]. Molecular Neurobiology. 2018 ; 55( 7): 5962-5975.[citado 2025 out. 25 ] Available from: https://doi.org/10.1007/s12035-017-0818-6
Vancouver
Araújo BHS, Kaid C, Souza JSD, Silva SG da, Goulart E, Caires LCJ, Musso CM, Torres LB, Ferrasa A, Herai R, Zatz M, Okamoto OK, Cavalheiro EA. Down Syndrome iPSC-Derived Astrocytes Impair Neuronal Synaptogenesis and the mTOR Pathway In Vitro [Internet]. Molecular Neurobiology. 2018 ; 55( 7): 5962-5975.[citado 2025 out. 25 ] Available from: https://doi.org/10.1007/s12035-017-0818-6
Artigo de periodico
EIF4A3 deficient human iPSCs and mouse models demonstrate neural crest defects that underlie Richieri-Costa-Pereira syndrome (2017)
Miller, Emily E; Kobayashi, Gerson S; Musso, Camila M; Allen, Miranda; Ishiy, Felipe A. A; Caires Jr, Luiz Carlos de; Goulart, Ernesto ; Griesi-Oliveira, Karina; Zechi-Ceide, Roseli Maria; Richieri-Costa, Antonio; Bertola, Débora Romeo; Passos-Bueno, Maria Rita ; Silver, Debra L
Source: Human Molecular Genetics. Unidades: HRAC, IB
Subjects: ANORMALIDADES CRANIOFACIAIS, MUTAÇÃO GENÉTICA, MODELOS ANIMAIS, MALFORMAÇÕES, DISOSTOSE MANDIBULOFACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MILLER, Emily E et al. EIF4A3 deficient human iPSCs and mouse models demonstrate neural crest defects that underlie Richieri-Costa-Pereira syndrome. Human Molecular Genetics, v. 26, n. 12, p. 2177-2191, 2017Tradução . . Disponível em: https://doi.org/10.1093/hmg/ddx078. Acesso em: 25 out. 2025.
APA
Miller, E. E., Kobayashi, G. S., Musso, C. M., Allen, M., Ishiy, F. A. A., Caires Jr, L. C. de, et al. (2017). EIF4A3 deficient human iPSCs and mouse models demonstrate neural crest defects that underlie Richieri-Costa-Pereira syndrome. Human Molecular Genetics, 26( 12), 2177-2191. doi:10.1093/hmg/ddx078
NLM
Miller EE, Kobayashi GS, Musso CM, Allen M, Ishiy FAA, Caires Jr LC de, Goulart E, Griesi-Oliveira K, Zechi-Ceide RM, Richieri-Costa A, Bertola DR, Passos-Bueno MR, Silver DL. EIF4A3 deficient human iPSCs and mouse models demonstrate neural crest defects that underlie Richieri-Costa-Pereira syndrome [Internet]. Human Molecular Genetics. 2017 ; 26( 12): 2177-2191.[citado 2025 out. 25 ] Available from: https://doi.org/10.1093/hmg/ddx078
Vancouver
Miller EE, Kobayashi GS, Musso CM, Allen M, Ishiy FAA, Caires Jr LC de, Goulart E, Griesi-Oliveira K, Zechi-Ceide RM, Richieri-Costa A, Bertola DR, Passos-Bueno MR, Silver DL. EIF4A3 deficient human iPSCs and mouse models demonstrate neural crest defects that underlie Richieri-Costa-Pereira syndrome [Internet]. Human Molecular Genetics. 2017 ; 26( 12): 2177-2191.[citado 2025 out. 25 ] Available from: https://doi.org/10.1093/hmg/ddx078

Digital Library of Intellectual Production of Universidade de São Paulo 2012 - 2025