21
TITLE: Pleiotropic effects of fenretinide in neuroblastoma cell lines and multicellular tumor spheroids
AUTHORS: Roos Cuperus; Godelieve A M Tytgat; Rene Leen; Pedro Brites; Johannes Bras; Huib N Caron; Andre B P Van Kuilenburg;
PUBLISHED: 2008, SOURCE: INTERNATIONAL JOURNAL OF ONCOLOGY, VOLUME: 32, ISSUE: 5
INDEXED IN: Scopus WOS
22
TITLE: Organization and integration of biomedical knowledge with concept maps for key peroxisomal pathways  Full Text
AUTHORS: Willemsen, AM; Jansen, GA; Komen, JC; van Hooff, S; Waterham, HR; Brites, PMT; Wanders, RJA; van Kampen, AHC;
PUBLISHED: 2008, SOURCE: Joint Meeting of the 7th European Conference on Computational Biology/5th Meeting of the Bioinformatics-Italian-Society in BIOINFORMATICS, VOLUME: 24, ISSUE: 16
INDEXED IN: Scopus WOS CrossRef
23
TITLE: Ataxia with loss of Purkinje cells in a mouse model for Refsum disease
AUTHORS: Sacha Ferdinandusse; Anna W M Zomer; Jasper C Komen; Christina E van den Brink; Melissa Thanos; Frank P T Hamers; Ronald J A Wanders; Paul T van der Saag; Bwee Tien Poll The; Pedro Brites;
PUBLISHED: 2008, SOURCE: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, VOLUME: 105, ISSUE: 46
INDEXED IN: Scopus WOS CrossRef
24
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
INDEXED IN: Scopus WOS CrossRef: 67
25
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
INDEXED IN: Scopus CrossRef
IN MY: ORCID
26
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
INDEXED IN: Scopus WOS CrossRef
27
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
INDEXED IN: Scopus WOS CrossRef
28
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
INDEXED IN: WOS
29
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
INDEXED IN: Scopus WOS CrossRef
30
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
INDEXED IN: Scopus WOS CrossRef
Page 3 of 4. Total results: 32.