au.\*:("WILLEMSEN, R")
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Glazen van Cornelis Van Barlaer Vitraux par Cornelis van BarlaerWILLEMSEN R.Antiek. 1976, Vol 11, Num 5, pp 436-444, issn 0003-5653Article
Die sentimentale Gesellschaft. Zur Begründung einer aktivistischen Literaturtheorie im Werk Robert Musils und Robert Müllers. (La société sentimentale. Les fondements d'une théorie activiste de la littérature dans les oeuvres de R. M. et R. M.)WILLEMSEN, R.Deutsche Vierteljahresschrift für Literaturwissenschaft und Geistesgeschichte Stuttgart. 1984, Vol 58, Num 2, pp 289-316Article
Effects of spraying the herbicides 2,4-D and 2,4,5-T on a population of the tortoise Testudo hermanni in southern GreeceWILLEMSEN, R. E; HAILEY, A.Environmental pollution (1987). 2001, Vol 113, Num 1, pp 71-78, issn 0269-7491Article
INTERACTION OF OXYGEN AND ETHYLENE IN THE RELEASE OF RAGWEED SEEDS FROM DORMANCY.BRENNAN T; WILLEMSEN R; RUDD T et al.1978; BOT. GAZ.; U.S.A.; DA. 1978; VOL. 139; NO 1; PP. 46-49; BIBL. 15 REF.Article
Exceptional good cognitive and phenotypic profile in a male carrying a mosaic mutation in the FMR1 geneGOVAERTS, L. C. P; SMIT, A. E; SARIS, J. J et al.Clinical genetics. 2007, Vol 72, Num 2, pp 138-144, issn 0009-9163, 7 p.Article
Monozygotic twin brothers with the fragile X syndrome : different CGG repeats and different mental capacitiesHELDERMAN-VAN DEN ENDEN, A. T. J. M; MAASWINKEL-MOOIJ, P. D; HOOGENDOORN, E et al.Journal of medical genetics. 1999, Vol 36, Num 3, pp 253-257, issn 0022-2593Article
The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28 % of the cellsDE GRAAFF, E; DE VRIES, B. B. A; WILLEMSEN, R et al.American journal of medical genetics. 1996, Vol 64, Num 2, pp 302-308, issn 0148-7299Article
A monoclonal antibody (ER-HR3) against murine macrophages. I: Ontogeny, distribution and enzyme histochemical characterization of ER-HR3-positive cellsDE JONG, J. P; VOERMAN, J. S. A; VAN DER SLUIJS-GELLING, A. J et al.Cell and tissue research. 1994, Vol 275, Num 3, pp 567-576, issn 0302-766XArticle
The conservative substitution Asp-645 → Glu in lysosomal α-glucosidase affects transport and phosphorylation of the enzyme in an adult patient with glycogen-storage disease type IIHERMANS, M. M. P; DE GRAAFF, E; KROOS, M. A et al.Biochemical journal (London. 1984). 1993, Vol 289, pp 687-693, issn 0264-6021, 3Article
High density lipoprotein-binding proteins in porcine liver : isolation and histological localizationDE CROM, R. P. G; VAN HAPEREN, R; WILLEMSEN, R et al.Arteriosclerosis and thrombosis. 1992, Vol 12, Num 3, pp 325-331Article
Human malignant mesothelioma cell lines express PDGF β-receptors whereas cultured normal mesothelial cells express predominantly PDGF α-receptorsVERSNEL, M. A; CLAESSON-WELSH, L; HELDIN, C.-H et al.Oncogene (Basingstoke). 1991, Vol 6, Num 11, pp 2005-2011, issn 0950-9232Article
Immunological localization of cystic fibrosis candidate gene productsHOOGEVEEN, A. T; KEULEMANS, J; WILLEMSEN, R et al.Experimental cell research. 1991, Vol 193, Num 2, pp 435-437, issn 0014-4827Article
CGG repeat in the FMR1 gene: size mattersWILLEMSEN, R; LEVENGA, J; OOSTRA, B. A et al.Clinical genetics. 2011, Vol 80, Num 3, pp 214-225, issn 0009-9163, 12 p.Article
The FMR1 Gene and Fragile X-Associated Tremor/Ataxia SyndromeBROUWER, J. R; WILLEMSEN, R; OOSTRA, B. A et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2009, Vol 150, Num 6, pp 782-798, issn 1552-4841, 17 p.Article
Altered hypothalamus-pituitary-adrenal gland axis regulation in the expanded CGG-repeat mouse model for fragile X-associated tremor/ataxia syndromeBROUWER, J. R; SEVERIJNEN, E; DE JONG, F. H et al.Psychoneuroendocrinology. 2008, Vol 33, Num 6, pp 863-873, issn 0306-4530, 11 p.Article
The influence of alcohol disinfection of nail samples in the laboratoryWILLEMSEN, R; BREYNAERT, J; LAUWERS, S et al.Mycoses. 1999, Vol 42, Num 11-12, pp 645-647, issn 0933-7407Article
FMRP expression as a potential prognostic indicator in fragile X syndromeTASSONE, F; HAGERMAN, R. J; IKLE, D. N et al.American journal of medical genetics. 1999, Vol 84, Num 3, pp 250-261, issn 0148-7299Article
Screening with the FMR1 protein test among mentally retarded malesDE VRIES, B. B. A; MOHKAMSING, S; VAN DEN OUWELAND, A. M. W et al.Human genetics. 1998, Vol 103, Num 4, pp 520-522, issn 0340-6717Article
Lysosomal storage diseases: cellular pathology, clinical and genetic heterogeneity, therapy = Les maladies lysosomiales: pathologie cellulaire, hétérogénéité clinique et génétique, thérapeutiqueREUSER, A. J. J; KROOS, M. A; VISSER, W. J et al.Annales de biologie clinique (Paris). 1994, Vol 52, Num 10, pp 721-728, issn 0003-3898Article
Characterization and localization of the huntington disease gene productHOOGEVEEN, A. T; WILLEMSEN, R; MEYER, N et al.Human molecular genetics (Print). 1993, Vol 2, Num 12, pp 2069-2073, issn 0964-6906Article
Plasmalemmal vesicles are involved in transendothelial transport of albumin, lysosomal enzymes and mannose 6-phosphate receptor fragments in capillary endotheliumWILLEMSEN, R; WISSELAAR, H. A; VAN DER PLOEG, A. T et al.European journal of cell biology. 1990, Vol 51, Num 2, pp 235-241, issn 0171-9335, 7 p.Article
The X chromosome and fragile X mental retardationOOSTRA, B. A; WILLEMSEN, R.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 257-264, issn 1424-8581, 8 p.Article
Different targets for the fragile X-related proteins revealed by their distinct nuclear localizationsTAMANINI, F; BONTEKOE, C; BAKKER, C. E et al.Human molecular genetics (Print). 1999, Vol 8, Num 5, pp 863-869, issn 0964-6906Article
In vitro reactivation of the FMR1 gene involved in fragile X syndromeCHIURAZZI, P; POMPONI, M. G; WILLEMSEN, R et al.Human molecular genetics (Print). 1998, Vol 7, Num 1, pp 109-113, issn 0964-6906Article
Pseudallescheria boydii tenosynovitisWILLEMSEN, R; SCHOTS, R; SHAHABPOUR, M et al.Journal de mycologie médicale (Paris). 1997, Vol 7, Num 2, pp 100-105, issn 1156-5233Article