Ana Paula Costa Santos Peralta Leandro


AuthID: R-000-19T

Publications Awaiting Confirmation

81
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
IN MY: ResearcherID
82
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
IN MY: ResearcherID
83
TITLE: Assembly of hybrid heteroallelic mutant forms of human phenylalanine hydroxylase produced in a prokaryotic dual vector expression system  Full Text
AUTHORS: Almeida, R; Leandro, J; Cristo, I; Tavares I de Almeida; Leandro, P;
PUBLISHED: 2008, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 31
INDEXED IN: WOS
IN MY: ResearcherID
84
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
IN MY: ResearcherID
85
TITLE: Interallelic complementation and phenylketonuria: Isolation of hybrid forms of human phenylalanine hydroxylase (HPAH)  Full Text
AUTHORS: Leandro, J; de Almeida I Tavares; Leandro, P; Flatmark, T;
PUBLISHED: 2008, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 31
INDEXED IN: WOS
IN MY: ResearcherID
86
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
IN MY: ResearcherID
87
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
IN MY: ResearcherID
88
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
IN MY: ResearcherID
89
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
IN MY: ResearcherID
90
TITLE: Biochemical characterization of chimerical mutant forms of human phenylalanine hydroxylase: a contribution to the understanding of enzyme stabilization  Full Text
AUTHORS: Nascimento, C; Coelho, C; Leandro, J; de Almeida, IT; Leandro, P;
PUBLISHED: 2005, SOURCE: IUBMB 50th Anniversary Symposium in FEBS JOURNAL, VOLUME: 272
INDEXED IN: WOS
IN MY: ResearcherID
Page 9 of 10. Total results: 97.

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