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Results: 1-25 | 26-34 |
Results: 26-34/34
THE EFFECT OF A SINGLE-BASE PAIR DELETION (DELTA-T525) AND A C1634T MISSENSE MUTATION (PRO545LEU) ON THE EXPRESSION OF LYSOSOMAL ALPHA-GLUCOSIDASE IN PATIENTS WITH GLYCOGEN-STORAGE-DISEASE TYPE-II
Authors: HERMANS MMP DEGRAAFF E KROOS MA MOHKAMSING S EUSSEN BJ JOOSSE M WILLEMSEN R KLEIJER WJ OOSTRA BA REUSER AJJ
Citation: Mmp. Hermans et al., THE EFFECT OF A SINGLE-BASE PAIR DELETION (DELTA-T525) AND A C1634T MISSENSE MUTATION (PRO545LEU) ON THE EXPRESSION OF LYSOSOMAL ALPHA-GLUCOSIDASE IN PATIENTS WITH GLYCOGEN-STORAGE-DISEASE TYPE-II, Human molecular genetics, 3(12), 1994, pp. 2213-2218
AN EVALUATION OF THE POTENTIAL SIDE-EFFECTS OF ALPHA-GLUCOSIDASE INHIBITORS USED FOR THE MANAGEMENT OF DIABETES-MELLITUS
Authors: REUSER AJJ WISSELAAR HA
Citation: Ajj. Reuser et Ha. Wisselaar, AN EVALUATION OF THE POTENTIAL SIDE-EFFECTS OF ALPHA-GLUCOSIDASE INHIBITORS USED FOR THE MANAGEMENT OF DIABETES-MELLITUS, European journal of clinical investigation, 24, 1994, pp. 19-24
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
LYSOSOMAL STORAGE DISEASES - CELLULAR PATHOLOGY, CLINICAL AND GENETIC-HETEROGENEITY, THERAPY
Authors: REUSER AJJ KROOS MA VISSER WJ WILLEMSEN R
Citation: Ajj. Reuser et al., LYSOSOMAL STORAGE DISEASES - CELLULAR PATHOLOGY, CLINICAL AND GENETIC-HETEROGENEITY, THERAPY, Annales de biologie clinique, 52(10), 1994, pp. 721-728
2 MUTATIONS AFFECTING THE TRANSPORT AND MATURATION OF LYSOSOMAL ALPHA-GLUCOSIDASE IN AN ADULT CASE OF GLYCOGEN-STORAGE-DISEASE TYPE-II
Authors: HERMANS MMP KROOS MA DEGRAAFF E OOSTRA BA REUSER AJJ
Citation: Mmp. Hermans et al., 2 MUTATIONS AFFECTING THE TRANSPORT AND MATURATION OF LYSOSOMAL ALPHA-GLUCOSIDASE IN AN ADULT CASE OF GLYCOGEN-STORAGE-DISEASE TYPE-II, Human mutation, 2(4), 1993, pp. 268-273
SYNTHESIS AND IN-SITU LOCALIZATION OF LYSOSOMAL ALPHA-GLUCOSIDASE IN MUSCLE OF AN UNUSUAL VARIANT OF GLYCOGEN-STORAGE-DISEASE TYPE-II
Authors: WILLEMSEN R VANDERPLOEG AT BUSCH HFM ZONDERVAN PE VANNOORDEN CJF REUSER AJJ
Citation: R. Willemsen et al., SYNTHESIS AND IN-SITU LOCALIZATION OF LYSOSOMAL ALPHA-GLUCOSIDASE IN MUSCLE OF AN UNUSUAL VARIANT OF GLYCOGEN-STORAGE-DISEASE TYPE-II, Ultrastructural pathology, 17(5), 1993, pp. 515-527
CHARACTERIZATION AND LOCALIZATION OF THE FMR-1 GENE-PRODUCT ASSOCIATED WITH FRAGILE-X SYNDROME
Authors: VERHEIJ C BAKKER CE DEGRAAFF E KEULEMANS J WILLEMSEN R VERKERK AJMH GALJAARD H REUSER AJJ HOOGEVEEN AT OOSTRA BA
Citation: C. Verheij et al., CHARACTERIZATION AND LOCALIZATION OF THE FMR-1 GENE-PRODUCT ASSOCIATED WITH FRAGILE-X SYNDROME, Nature, 363(6431), 1993, pp. 722-724
MOLECULAR-BIOLOGY, THERAPEUTIC TRIALS AND ANIMAL-MODELS OF LYSOSOMAL STORAGE DISEASES - TYPE-II GLYCOGENOSIS AS AN EXAMPLE
Authors: REUSER AJJ
Citation: Ajj. Reuser, MOLECULAR-BIOLOGY, THERAPEUTIC TRIALS AND ANIMAL-MODELS OF LYSOSOMAL STORAGE DISEASES - TYPE-II GLYCOGENOSIS AS AN EXAMPLE, Annales de biologie clinique, 51(3-5), 1993, pp. 218-219
IDENTIFICATION AND LOCALIZATION OF THE FMR-1 PROTEIN PRODUCT
Authors: VERHEIJ C HOOGEVEEN AT VERKERK AJMH DEGRAAFF E BAKKER C REUSER AJJ OOSTRA BA
Citation: C. Verheij et al., IDENTIFICATION AND LOCALIZATION OF THE FMR-1 PROTEIN PRODUCT, American journal of human genetics, 53(3), 1993, pp. 739-739
Risultati: 1-25 | 26-34 |