Torgeir Flatmark
AuthID: R-001-HXG
1
TITLE: PKU mutation p.G46S prevents the stereospecific binding of L-phenylalanine to the dimer of human phenylalanine hydroxylase regulatory domain
AUTHORS: Joao Leandro; Jaakko Saraste; Paula Leandro; Torgeir Flatmark;
PUBLISHED: 2017, SOURCE: FEBS OPEN BIO, VOLUME: 7, ISSUE: 2
AUTHORS: Joao Leandro; Jaakko Saraste; Paula Leandro; Torgeir Flatmark;
PUBLISHED: 2017, SOURCE: FEBS OPEN BIO, VOLUME: 7, ISSUE: 2
2
TITLE: High molecular weight forms of human phenylalanine hydroxylase: the role of the ACT domain in the balance between a fully functional protein and the large inactive aggregates Full Text
AUTHORS: Leandro, J; Amaro, MP; Lino, PR; Flatmark, T; Leandro, P;
PUBLISHED: 2013, SOURCE: 38th Congress of the Federation-of-European-Biochemical-Societies (FEBS) in FEBS JOURNAL, VOLUME: 280
AUTHORS: Leandro, J; Amaro, MP; Lino, PR; Flatmark, T; Leandro, P;
PUBLISHED: 2013, SOURCE: 38th Congress of the Federation-of-European-Biochemical-Societies (FEBS) in FEBS JOURNAL, VOLUME: 280
INDEXED IN: 
WOS
WOS3
TITLE: Heterotetrameric forms of human phenylalanine hydroxylase: Co-expression of wild-type and mutant forms in a bicistronic system Full Text
AUTHORS: Joao Leandro ; Paula Leandro ; Torgeir Flatmark;
PUBLISHED: 2011, SOURCE: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, VOLUME: 1812, ISSUE: 5
AUTHORS: Joao Leandro ; Paula Leandro ; Torgeir Flatmark;
PUBLISHED: 2011, SOURCE: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, VOLUME: 1812, ISSUE: 5
4
TITLE: The G46S-hPAH mutant protein: A model to study the rescue of aggregation-prone PKU mutations by chaperones Full Text
AUTHORS: Joao Leandro ; Jaakko Saraste; Paula Leandro ; Torgeir Flatmark;
PUBLISHED: 2011, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 104, ISSUE: SUPPL.
AUTHORS: Joao Leandro ; Jaakko Saraste; Paula Leandro ; Torgeir Flatmark;
PUBLISHED: 2011, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 104, ISSUE: SUPPL.
5
TITLE: THE EFFECT OF LOW-MOLECULAR-WEIGHT COMPOUNDS ON THE IN VITRO POLYMERIZATION/FIBRIL FORMATION PROCESS OF MUTANT G46S-HPAH Full Text
AUTHORS: Leandro, J; Simonsen, N; Tavares T de Almeida; Leandro, P; Flatmark, T;
PUBLISHED: 2009, SOURCE: 11th International Conference of Inborn Errors of Metabolism in MOLECULAR GENETICS AND METABOLISM, VOLUME: 98, ISSUE: 1-2
AUTHORS: Leandro, J; Simonsen, N; Tavares T de Almeida; Leandro, P; Flatmark, T;
PUBLISHED: 2009, SOURCE: 11th International Conference of Inborn Errors of Metabolism in MOLECULAR GENETICS AND METABOLISM, VOLUME: 98, ISSUE: 1-2
INDEXED IN: WOS
WOS6
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
WOS7
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
WOS