Pulmonary fibrosis is related to TGF-ß and BMP-7 gene expression in murine asthma (2008)
- Authors:
- USP affiliated authors: LANDGRAF, RICHARDT GAMA - ICB ; NEGRO, SONIA JANCAR - ICB ; CÂMARA, NIELS OLSEN SARAIVA - ICB
- Unidade: ICB
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: Ribeirão Preto
- Date published: 2008
- Source:
- Título do periódico: Resumos
- Conference titles: Congress of the Brazilian Society for Immunology - SBI
-
ABNT
STUMM, Camila Leindecker et al. Pulmonary fibrosis is related to TGF-ß and BMP-7 gene expression in murine asthma. 2008, Anais.. Ribeirão Preto: Instituto de Ciências Biomédicas, Universidade de São Paulo, 2008. . Acesso em: 06 fev. 2023. -
APA
Stumm, C. L., Landgraf, R. G., Campanholle, G., Câmara, N. O. S., & Jancar, S. (2008). Pulmonary fibrosis is related to TGF-ß and BMP-7 gene expression in murine asthma. In Resumos. Ribeirão Preto: Instituto de Ciências Biomédicas, Universidade de São Paulo. -
NLM
Stumm CL, Landgraf RG, Campanholle G, Câmara NOS, Jancar S. Pulmonary fibrosis is related to TGF-ß and BMP-7 gene expression in murine asthma. Resumos. 2008 ;[citado 2023 fev. 06 ] -
Vancouver
Stumm CL, Landgraf RG, Campanholle G, Câmara NOS, Jancar S. Pulmonary fibrosis is related to TGF-ß and BMP-7 gene expression in murine asthma. Resumos. 2008 ;[citado 2023 fev. 06 ] - IL-4 and IL-5 reduced expression promotes downregulation of the lung allergic response after renal ischemia and reperfusion injury
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- Renal ischemia and reperfusion injury modulates the lung allergic response through TH1/TH2 balance
- Pulmonary damages associated with renal ischemia and reperfusion injury
- Isquemia e reperfusão renal induz resposta inflamatória sistemica com danos pulmonares
- Fibrose pulmonar e sua relação com a expressão gênica de TGF-Beta e BMP-7 na asma murina
- Prostaglandins, leukotrienes and PAF selectively modulate lymphocyte subset and eosinophil infiltration into the airways in a murine model of asthma
- Small bowel injury associated to allergy is triggered by platelet-activating factor, mast cells, neutrophils and protected by nitric oxide
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