Microconversion between pseudogene and CYP21A2 reduces the transcriptional activity causing nonclassical form of 21-hydroxylase deficiency
R. S. Araujo A. S Barbosa; B. B Mendonça; C. J Lin; C. J Billerbeck; J. A. M Marcondes; T. A. S. S Bachega; Annual Meeting of the Sociedad Latinoamericana de Endocrinologia Pediátrica (SLEP) (17. 2004 Angra dos Reis)
Journal of pediatric endocrinology and metabolism London v. 17, n. suppl.5, p. 1334, res. Oral 7, 2004
London 2004
Localização:
FM - Fac. Medicina
(BCSEP 355 2004 ) e outros locais(Acessar)
Phylogenetic analysis of hepatitis B virus genotype F complete genome sequences from chilean patients with chronic infection
Mauricio Venegas Mónica V Alvarado-Mora; Rodrigo A Villanueva; João R. Rebello Pinho; Flair José Carrilho; Stephen Locarnini; Lilly Yuen; Javier Brahma
Journal of medical virology New York v. 83, n. 9, p. 1530-1536, 2011
New York 2011
Localização:
FM - Fac. Medicina
(BCSEP 201 2011 )(Acessar)
Novel Molecular Pathways Elicited by Mutant FGFR2 May Account for Brain Abnormalities in Apert Syndrome
Erika Yeh Roberto D Fanganiello; Daniele Y Sunaga; Xueyan Zhou; Gregory Holmes; Katia M Rocha; Nivaldo Alonso; Hamilton Matushita; Yingli Wang; Ethylin W Jabs; Maria Rita Passos-Bueno
Plos One San Francisco v. 8, n. 4, 7 p., art. e60439, 2013
San Francisco 2013
Localização:
FM - Fac. Medicina
(BECEP 034 2013 )(Acessar)