Ana Paula Costa Santos Peralta Leandro
AuthID: R-000-19T
81
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
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: ORCID | ResearcherID
82
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
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: ORCID | ResearcherID
83
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
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
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84
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
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: ORCID | ResearcherID
85
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
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: ORCID | ResearcherID
86
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
AUTHORS: Nascimento, C; Coelho, C; Leandro, J; de Almeida, IT; Leandro, P;
PUBLISHED: 2005, SOURCE: IUBMB 50th Anniversary Symposium in FEBS JOURNAL, VOLUME: 272
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87
TITLE: The architecture of interphase chromosomes and nucleolar transcription sites in plants Full Text
AUTHORS: Shaw, PJ; Abranches, R ; Santos, AP; Beven, AF; Stoger, E; Wegel, E; Gonzalez Melendi, P;
PUBLISHED: 2002, SOURCE: EMBO Workshop on Functional Organization of the Cell Nucleus in JOURNAL OF STRUCTURAL BIOLOGY, VOLUME: 140, ISSUE: 1-3
AUTHORS: Shaw, PJ; Abranches, R ; Santos, AP; Beven, AF; Stoger, E; Wegel, E; Gonzalez Melendi, P;
PUBLISHED: 2002, SOURCE: EMBO Workshop on Functional Organization of the Cell Nucleus in JOURNAL OF STRUCTURAL BIOLOGY, VOLUME: 140, ISSUE: 1-3
88
TITLE: Prokaryotic expression analysis of I269L and R270K mutations of the phenylalanine hydroxylase gene Full Text
AUTHORS: Paula Leandro; Isabel Rivera; Maria Celeste Lechner; David Konecki; Isabel Tavares de Almeida;
PUBLISHED: 2001, SOURCE: Gene Function & Disease - Gene Funct. Dis., VOLUME: 2, ISSUE: 1
AUTHORS: Paula Leandro; Isabel Rivera; Maria Celeste Lechner; David Konecki; Isabel Tavares de Almeida;
PUBLISHED: 2001, SOURCE: Gene Function & Disease - Gene Funct. Dis., VOLUME: 2, ISSUE: 1
89
TITLE: Identification of a new WT1 mutation in a sporadic Wilms' tumour Full Text
AUTHORS: Santos, AC; Boavida, MG; Costa, A; Osorio Almeida, L;
PUBLISHED: 1998, SOURCE: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, VOLUME: 1407, ISSUE: 2
AUTHORS: Santos, AC; Boavida, MG; Costa, A; Osorio Almeida, L;
PUBLISHED: 1998, SOURCE: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, VOLUME: 1407, ISSUE: 2
90
TITLE: Prokaryotic expression of PAH mutant forms Full Text
AUTHORS: Leandro, P; Rivera, I; de Almedia, IT; Lechner, MC; Konecki, DS;
PUBLISHED: 1998, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 6
AUTHORS: Leandro, P; Rivera, I; de Almedia, IT; Lechner, MC; Konecki, DS;
PUBLISHED: 1998, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 6
INDEXED IN: WOS
IN MY: ORCID | ResearcherID