Pedro Miguel Teixeira Brites
AuthID: R-000-TER
31
TITLE: Endoplasmic reticulum stress associated with extracellular aggregates - Evidence from transthyretin deposition in familial amyloid polyneuropathy
AUTHORS: Pedro Filipe Teixeira; Filipe Cerca; Sofia D Santos; Maria Joao Saraiva ;
PUBLISHED: 2006, SOURCE: JOURNAL OF BIOLOGICAL CHEMISTRY, VOLUME: 281, ISSUE: 31
AUTHORS: Pedro Filipe Teixeira; Filipe Cerca; Sofia D Santos; Maria Joao Saraiva ;
PUBLISHED: 2006, SOURCE: JOURNAL OF BIOLOGICAL CHEMISTRY, VOLUME: 281, ISSUE: 31
32
TITLE: The mouse as a model to understand peroxisomal biogenesis and its disorders Full Text
AUTHORS: Brites, P; Wanders, RJA; Waterham, HR;
PUBLISHED: 2004, SOURCE: Drug Discovery Today: Disease Models, VOLUME: 1, ISSUE: 3
AUTHORS: Brites, P; Wanders, RJA; Waterham, HR;
PUBLISHED: 2004, SOURCE: Drug Discovery Today: Disease Models, VOLUME: 1, ISSUE: 3
33
TITLE: Functions and biosynthesis of plasmalogens in health and disease Full Text
AUTHORS: Brites, P; Waterham, HR; Wanders, RJA;
PUBLISHED: 2004, SOURCE: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, VOLUME: 1636, ISSUE: 2-3
AUTHORS: Brites, P; Waterham, HR; Wanders, RJA;
PUBLISHED: 2004, SOURCE: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, VOLUME: 1636, ISSUE: 2-3
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TITLE: Identification of PEX7 as the second gene involved in Refsum disease
AUTHORS: van den Brink, DM; Brites, P; Haasjes, J; Wierzbicki, AS; Mitchell, J; Lambert Hamill, M; de Belleroche, J; Jansen, GA; Waterham, HR; Wanders, RJA;
PUBLISHED: 2003, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 72, ISSUE: 2
AUTHORS: van den Brink, DM; Brites, P; Haasjes, J; Wierzbicki, AS; Mitchell, J; Lambert Hamill, M; de Belleroche, J; Jansen, GA; Waterham, HR; Wanders, RJA;
PUBLISHED: 2003, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 72, ISSUE: 2
IN MY: ORCID | ResearcherID
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TITLE: Impaired neuronal migration and endochondral ossification in Pex7 knockout mice: a model for rhizomelic chondrodysplasia punctata
AUTHORS: Brites, P; Motley, AM; Gressens, P; Mooyer, PAW; Ploegaert, I; Everts, V; Evrard, P; Carmeliet, P; Dewerchin, M; Schoonjans, L; Duran, M; Waterham, HR; Wanders, RJA; Baes, M;
PUBLISHED: 2003, SOURCE: HUMAN MOLECULAR GENETICS, VOLUME: 12, ISSUE: 18
AUTHORS: Brites, P; Motley, AM; Gressens, P; Mooyer, PAW; Ploegaert, I; Everts, V; Evrard, P; Carmeliet, P; Dewerchin, M; Schoonjans, L; Duran, M; Waterham, HR; Wanders, RJA; Baes, M;
PUBLISHED: 2003, SOURCE: HUMAN MOLECULAR GENETICS, VOLUME: 12, ISSUE: 18
IN MY: ORCID | ResearcherID
ORCID | ResearcherID36
TITLE: Identification of PEX7 as the second gene involved in Refsum disease
AUTHORS: Van den Brink, DM; Brites, P; Haasjes, J; Wierzbicki, AS; Mitchell, J; Lambert Hamill, M; De Belleroche, J; Jansen, GA; Waterham, HR; Wanders, RJA;
PUBLISHED: 2003, SOURCE: International Symposium on Peroxisomal Disorders and Requlation of Genes in PEROXISOMAL DISORDERS AND REGULATION OF GENES, VOLUME: 544
AUTHORS: Van den Brink, DM; Brites, P; Haasjes, J; Wierzbicki, AS; Mitchell, J; Lambert Hamill, M; De Belleroche, J; Jansen, GA; Waterham, HR; Wanders, RJA;
PUBLISHED: 2003, SOURCE: International Symposium on Peroxisomal Disorders and Requlation of Genes in PEROXISOMAL DISORDERS AND REGULATION OF GENES, VOLUME: 544
INDEXED IN: WOS
WOS IN MY: ResearcherID
ResearcherID37
TITLE: Identification of PEX7 as the second gene involved in Refsum disease
AUTHORS: Daan M Van Den Brink; Pedro Brites; Janet Haasjes; Anthony S Wierzbicki; John Mitchell; Michelle Lambert Hamill; Jacqueline De Belleroche; Gerbert A Jansen; Hans R Waterham; Ronald J A Wanders;
PUBLISHED: 2003, SOURCE: Advances in Experimental Medicine and Biology, VOLUME: 544
AUTHORS: Daan M Van Den Brink; Pedro Brites; Janet Haasjes; Anthony S Wierzbicki; John Mitchell; Michelle Lambert Hamill; Jacqueline De Belleroche; Gerbert A Jansen; Hans R Waterham; Ronald J A Wanders;
PUBLISHED: 2003, SOURCE: Advances in Experimental Medicine and Biology, VOLUME: 544
INDEXED IN: 
Scopus
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ORCID38
TITLE: Mutational spectrum in the PEX7 gene and functional analysis of mutant alleles in 78 patients with rhizomelic chondrodysplasia punctata type 1
AUTHORS: Motley, AM; Brites, P; Gerez, L; Hogenhout, E; Haasjes, J; Benne, R; Tabak, HF; Wanders, RJA; Waterham, HR;
PUBLISHED: 2002, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 70, ISSUE: 3
AUTHORS: Motley, AM; Brites, P; Gerez, L; Hogenhout, E; Haasjes, J; Benne, R; Tabak, HF; Wanders, RJA; Waterham, HR;
PUBLISHED: 2002, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 70, ISSUE: 3
IN MY: ORCID | ResearcherID
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TITLE: Molecular basis of rhizomelic chondrodysplasia punctata type I: High frequency of the Leu-292 Stop mutation in 38 patients
AUTHORS: Brites P.; Motley A.; Hogenhout E.; Hettema E.; Wijburg F.; Heijmans H.; Tabak H.; Distel B.; Wanders R.;
PUBLISHED: 1998, SOURCE: Journal of Inherited Metabolic Disease, VOLUME: 21, ISSUE: 3
AUTHORS: Brites P.; Motley A.; Hogenhout E.; Hettema E.; Wijburg F.; Heijmans H.; Tabak H.; Distel B.; Wanders R.;
PUBLISHED: 1998, SOURCE: Journal of Inherited Metabolic Disease, VOLUME: 21, ISSUE: 3
40
TITLE: Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor
AUTHORS: Motley, AM; Hettema, EH; Hogenhout, EM; Brites, P; tenAsbroek, ALMA; Wijburg, FA; Baas, F; Heijmans, HS; Tabak, HF; Wanders, RJA; Distel, B;
PUBLISHED: 1997, SOURCE: NATURE GENETICS, VOLUME: 15, ISSUE: 4
AUTHORS: Motley, AM; Hettema, EH; Hogenhout, EM; Brites, P; tenAsbroek, ALMA; Wijburg, FA; Baas, F; Heijmans, HS; Tabak, HF; Wanders, RJA; Distel, B;
PUBLISHED: 1997, SOURCE: NATURE GENETICS, VOLUME: 15, ISSUE: 4
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