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Results: 1-12 |
Results: 12
EXPRESSION OF MELANOCORTIN-5 RECEPTOR IN SECRETORY EPITHELIA SUPPORTSA FUNCTIONAL-ROLE IN EXOCRINE AND ENDOCRINE GLANDS
Authors: VANDERKRAAN M ADAN RAH ENTWISTLE ML GISPEN WH BURBACH JPH TATRO JB
Citation: M. Vanderkraan et al., EXPRESSION OF MELANOCORTIN-5 RECEPTOR IN SECRETORY EPITHELIA SUPPORTSA FUNCTIONAL-ROLE IN EXOCRINE AND ENDOCRINE GLANDS, Endocrinology, 139(5), 1998, pp. 2348-2355
MOLECULAR PHARMACOLOGY OF NEURAL MELANOCORTIN RECEPTORS
Authors: ADAN RAH OOSTEROM J TOONEN RFG VANDERKRAAN M BURBACH JPH GISPEN WH
Citation: Rah. Adan et al., MOLECULAR PHARMACOLOGY OF NEURAL MELANOCORTIN RECEPTORS, Receptors & channels, 5(3-4), 1997, pp. 215
2 EXTREMES OF THE CLINICAL SPECTRUM OF GLYCOGEN-STORAGE-DISEASE TYPE-II IN ONE FAMILY - A MATTER OF GENOTYPE
Authors: KROOS MA VANDERKRAAN M VANDIGGELEN OP KLEIJER WJ REUSER AJJ
Citation: Ma. Kroos et al., 2 EXTREMES OF THE CLINICAL SPECTRUM OF GLYCOGEN-STORAGE-DISEASE TYPE-II IN ONE FAMILY - A MATTER OF GENOTYPE, Human mutation, 9(1), 1997, pp. 17-22
DEFINITION OF AN EXTENDED MHC CLASS-II PEPTIDE BINDING MOTIF FOR THE AUTOIMMUNE DISEASE-ASSOCIATED LEWIS RAT RT1.B-L MOLECULE
Authors: WAUBEN MHM VANDERKRAAN M GROSFELDSTULEMEYER MC JOOSTEN I
Citation: Mhm. Wauben et al., DEFINITION OF AN EXTENDED MHC CLASS-II PEPTIDE BINDING MOTIF FOR THE AUTOIMMUNE DISEASE-ASSOCIATED LEWIS RAT RT1.B-L MOLECULE, International immunology, 9(2), 1997, pp. 281-290
PREVALENT MUTATIONS IN THE GALC GENE OF PATIENTS WITH KRABBE-DISEASE OF DUTCH AND OTHER EUROPEAN ORIGIN
Authors: KLEIJER WJ KEULEMANS JLM VANDERKRAAN M GEILEN GG VANDERHELM RM RAFI MA LUZI P WENGER DA HALLEY DJJ VANDIGGELEN OP
Citation: Wj. Kleijer et al., PREVALENT MUTATIONS IN THE GALC GENE OF PATIENTS WITH KRABBE-DISEASE OF DUTCH AND OTHER EUROPEAN ORIGIN, Journal of inherited metabolic disease, 20(4), 1997, pp. 587-594
MELANOCORTIN RECEPTORS MEDIATE ALPHA-MSH-INDUCED STIMULATION OF NEURITE OUTGROWTH IN NEURO 2A CELLS
Authors: ADAN RAH VANDERKRAAN M DOORNBOS RP BAR PR BURBACH JPH
Citation: Rah. Adan et al., MELANOCORTIN RECEPTORS MEDIATE ALPHA-MSH-INDUCED STIMULATION OF NEURITE OUTGROWTH IN NEURO 2A CELLS, Molecular brain research, 36(1), 1996, pp. 37-44
HOMOZYGOUS DELETION OF EXON-18 LEADS TO DEGRADATION OF THE LYSOSOMAL ALPHA-GLUCOSIDASE PRECURSOR AND TO THE INFANTILE FORM OF GLYCOGEN-STORAGE-DISEASE TYPE-II
Authors: AUSEMS MGEM KROOS MA VANDERKRAAN M SMEITINK JAM KLEIJER WJ VANAMSTEL HKP REUSER AJJ
Citation: Mgem. Ausems et al., HOMOZYGOUS DELETION OF EXON-18 LEADS TO DEGRADATION OF THE LYSOSOMAL ALPHA-GLUCOSIDASE PRECURSOR AND TO THE INFANTILE FORM OF GLYCOGEN-STORAGE-DISEASE TYPE-II, Clinical genetics, 49(6), 1996, pp. 325-328
PRENATAL-DIAGNOSIS OF ISOVALERIC ACIDEMIA BY ENZYME AND METABOLITE ASSAY IN THE FIRST AND 2ND TRIMESTERS
Authors: KLEIJER WJ VANDERKRAAN M HUIJMANS JGM VANDENHEUVEL CMM JAKOBS C
Citation: Wj. Kleijer et al., PRENATAL-DIAGNOSIS OF ISOVALERIC ACIDEMIA BY ENZYME AND METABOLITE ASSAY IN THE FIRST AND 2ND TRIMESTERS, Prenatal diagnosis, 15(6), 1995, pp. 527-533
PRENATAL-DIAGNOSIS OF GLYCOGEN-STORAGE-DISEASE TYPE-II - ENZYME ASSAYOR MUTATION ANALYSIS
Authors: KLEIJER WJ VANDERKRAAN M KROOS MA GROENER JEM VANDIGGELEN OP REUSER AJJ VANDERPLOEG AT
Citation: Wj. Kleijer et al., PRENATAL-DIAGNOSIS OF GLYCOGEN-STORAGE-DISEASE TYPE-II - ENZYME ASSAYOR MUTATION ANALYSIS, Pediatric research, 38(1), 1995, pp. 103-106
GLYCOGEN-STORAGE-DISEASE TYPE-II - FREQUENCY OF 3 COMMON MUTANT ALLELES AND THEIR ASSOCIATED CLINICAL PHENOTYPES STUDIED IN 121 PATIENTS
Authors: KROOS MA VANDERKRAAN M VANDIGGELEN OP KLEIJER WJ REUSER AJJ VANDENBOOGAARD MJ AUSEMS MGEM VANAMSTEL HKP
Citation: Ma. Kroos et al., GLYCOGEN-STORAGE-DISEASE TYPE-II - FREQUENCY OF 3 COMMON MUTANT ALLELES AND THEIR ASSOCIATED CLINICAL PHENOTYPES STUDIED IN 121 PATIENTS, Journal of Medical Genetics, 32(10), 1995, pp. 836-837
PRENATAL-DIAGNOSIS OF ATAXIA-TELANGIECTASIA AND NIJMEGEN-BREAKAGE-SYNDROME BY THE ASSAY OF RADIORESISTANT DNA-SYNTHESIS
Authors: KLEIJER WJ VANDERKRAAN M LOS FJ JASPERS NGJ
Citation: Wj. Kleijer et al., PRENATAL-DIAGNOSIS OF ATAXIA-TELANGIECTASIA AND NIJMEGEN-BREAKAGE-SYNDROME BY THE ASSAY OF RADIORESISTANT DNA-SYNTHESIS, International journal of radiation biology, 66(6), 1994, pp. 167-174
DELETION OF EXON-18 IS A FREQUENT MUTATION IN GLYCOGEN-STORAGE-DISEASE TYPE-II
Authors: VANDERKRAAN M KROOS MA JOOSSE M BIJVOET AGA VERBEET MP KLEIJER WJ REUSER AJJ
Citation: M. Vanderkraan et al., DELETION OF EXON-18 IS A FREQUENT MUTATION IN GLYCOGEN-STORAGE-DISEASE TYPE-II, Biochemical and biophysical research communications, 203(3), 1994, pp. 1535-1541
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