Pedro Miguel Teixeira Brites
AuthID: R-000-TER
31
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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ResearcherID
ORCID | ResearcherID32
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
ORCID | ResearcherID33
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 | ResearcherID34
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
ResearcherID35
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
Scopus IN MY: ORCID
ORCID36
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
ORCID | ResearcherID37
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
38
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
IN MY: ORCID | ResearcherID
ORCID | ResearcherID39
TITLE: Mutational analysis of an X-linked adrenoleukodystrophy (ALD) patient with detectable ALD protein
AUTHORS: Jorge, P ; Brites, P; Nogueira, A; Aubourg, P;
PUBLISHED: 1996, SOURCE: International Symposium on Peroxisomes - Biology and Role in Toxicology and Disease in PEROXISOMES: BIOLOGY AND ROLE IN TOXICOLOGY AND DISEASE, VOLUME: 804, ISSUE: 1 Peroxisomes
AUTHORS: Jorge, P ; Brites, P; Nogueira, A; Aubourg, P;
PUBLISHED: 1996, SOURCE: International Symposium on Peroxisomes - Biology and Role in Toxicology and Disease in PEROXISOMES: BIOLOGY AND ROLE IN TOXICOLOGY AND DISEASE, VOLUME: 804, ISSUE: 1 Peroxisomes
40
TITLE: Spray drying as a method for preparing concentrated cultures of Lactobacillus bulgaricus
AUTHORS: Teixeira, P; Castro, H; Kirby, R;
PUBLISHED: 1995, SOURCE: Journal of Applied Bacteriology, VOLUME: 78, ISSUE: 4
AUTHORS: Teixeira, P; Castro, H; Kirby, R;
PUBLISHED: 1995, SOURCE: Journal of Applied Bacteriology, VOLUME: 78, ISSUE: 4
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