Microsomal triglyceride transfer protein (MTP) 493 G/T polymorphism is associated with insulin resistance in chronic hepatitis (CHC) genotype infection (2008)
- Authors:
- USP affiliated authors: CARRILHO, FLAIR JOSÉ - FM ; OLIVEIRA, CLAUDIA PINTO MARQUES SOUZA DE - FM
- Unidade: FM
- Subjects: FÍGADO GORDUROSO; HEPATITE CRÔNICA; POLIMORFISMO
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of Hepatology
- ISSN: 0168-8278
- Volume/Número/Paginação/Ano: v. 48, n. 4, p. 791A, res. 1084, 2008
- Conference titles: Annual Meeting of the European Association for the Study of the Liver
-
ABNT
SIQUEIRA, E. R. F. et al. Microsomal triglyceride transfer protein (MTP) 493 G/T polymorphism is associated with insulin resistance in chronic hepatitis (CHC) genotype infection. Journal of Hepatology. Amsterdam: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 28 abr. 2024. , 2008 -
APA
Siqueira, E. R. F., Gianella, M. L. C., Oliveira, C. P. M. S., Stefano, J. T., Cavaleiro, A. M., Fortes, M. A. Z., et al. (2008). Microsomal triglyceride transfer protein (MTP) 493 G/T polymorphism is associated with insulin resistance in chronic hepatitis (CHC) genotype infection. Journal of Hepatology. Amsterdam: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Siqueira ERF, Gianella MLC, Oliveira CPMS, Stefano JT, Cavaleiro AM, Fortes MAZ, Muniz MTC, Carrilho FJ, Silva KA, Silva FS, Pereira LB. Microsomal triglyceride transfer protein (MTP) 493 G/T polymorphism is associated with insulin resistance in chronic hepatitis (CHC) genotype infection. Journal of Hepatology. 2008 ; 48( 4): 791A.[citado 2024 abr. 28 ] -
Vancouver
Siqueira ERF, Gianella MLC, Oliveira CPMS, Stefano JT, Cavaleiro AM, Fortes MAZ, Muniz MTC, Carrilho FJ, Silva KA, Silva FS, Pereira LB. Microsomal triglyceride transfer protein (MTP) 493 G/T polymorphism is associated with insulin resistance in chronic hepatitis (CHC) genotype infection. Journal of Hepatology. 2008 ; 48( 4): 791A.[citado 2024 abr. 28 ] - S-Nitroso-N-acetylcysteine induces de-differentiation of activated hepatic stellate cells and promotes antifibrotic effects in vitro
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