72
TITLE: Molecular analysis of medium-chain acyl-CoA dehydrogenase deficiency in Portugal  Full Text
AUTHORS: Luz, A; Violante, S; Gaspar, A; Antunes M Lobo; Rivera, IA; Silva, MFB; Ramos, A; Rocha, H; Sousa, C; Marcao, A; Fonseca, H; Ventura, FV; Leandro, P ; Vilarinho, L; de Almeida Tavares;
PUBLISHED: 2008, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 31
INDEXED IN: WOS
73
TITLE: PAH deficiency in Portugal: Identification of potential BH4-responsive patients  Full Text
AUTHORS: Rivera, I; Leandro, P ; Queiros, A; Gaspar, A; Antunes M Lobo; Vilarinho, L; de Almeida Tavares;
PUBLISHED: 2008, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 31
INDEXED IN: WOS
74
TITLE: Phenylketonuria as a protein misfolding disease: Mutant PG46S human phenylalanine hydroxylase has a propensity to self-associate and form amyloid fibrils  Full Text
AUTHORS: Leandro, J; Simonsen, N; Tavares I de Almeida; Leandro, P ; Flatmark, T;
PUBLISHED: 2008, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 31
INDEXED IN: WOS
75
TITLE: Protein misfolding in conformational disorders: Rescue of folding defects and chemical chaperoning
AUTHORS: Paula Leandro ; Claudio M Gomes ;
PUBLISHED: 2008, SOURCE: MINI-REVIEWS IN MEDICINAL CHEMISTRY, VOLUME: 8, ISSUE: 9
INDEXED IN: Scopus WOS CrossRef
76
TITLE: Studies on the interaction of mutant forms of human phenylalanine hydroxylase with molecular chaperones  Full Text
AUTHORS: Cristo, I; Almeida, R; Leandro, J; de Almeida Tavares; Leandro, P ;
PUBLISHED: 2008, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 31
INDEXED IN: WOS
77
TITLE: The lytic cassette of mycobacteriophage Ms6 encodes an enzyme with lipolytic activity
AUTHORS: Filipa Gil; Maria Joao Catalao ; Jose Moniz Pereira ; Paula Leandro ; Michael McNeil; Madalena Pimentel ;
PUBLISHED: 2008, SOURCE: MICROBIOLOGY-SGM, VOLUME: 154, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef
78
TITLE: Folding rescue of mild PKU mutations by chemical chaperones  Full Text
AUTHORS: Nascimento, C; Botelho, HM ; Tavares De Almeida, I; Gomes, CM; Leandro, P ;
PUBLISHED: 2007, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 30
INDEXED IN: WOS
79
TITLE: Modification of phenylalanine hydroxylase by site-directed mutagenesis: Production of chimerical proteins with higher stability  Full Text
AUTHORS: Nascimento, C; Coelho, C; Acosta, C; Oliveira, C; Tavares de Almeida, I; Leandro, P ;
PUBLISHED: 2007, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 30
INDEXED IN: WOS
80
TITLE: The human carnitine acylcarnitine translocase (hCACT): Strategies for its heterologous expression, purification and crystallization  Full Text
AUTHORS: Ventura FV; Violante, S; Gomes, C; Carvalho, AL; Romao, MJ; Gaspar, MM ; Cruz, MEM; Soveral, G; Wanders, RJ; Leandro, P ; Tavares T de Almeida;
PUBLISHED: 2007, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 30
INDEXED IN: WOS
Page 8 of 10. Total results: 96.