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    1. Hoogenraad, CC; Akhmanova, A; Howell, SA; Dortland, BR; De Zeeuw, CI; Willemsen, R; Visser, P; Grosveld, F; Galjart, N
      Mammalian Golgi-associated Bicaudal-D2 functions in the dynein-dynactin pathway by interacting with these complexes

      EMBO JOURNAL
    2. Rosso, SM; Kamphorst, W; de Graaf, B; Willemsen, R; Ravid, R; Niermeijer, MF; Spillantini, MG; Heutink, P; van Swieten, JC
      Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q2l-22

      BRAIN
    3. Kooy, RF; Willemsen, R; Oostra, BA
      Fragile X syndrome at the turn of the century

      MOLECULAR MEDICINE TODAY
    4. Nauta, J; Goedbloed, MA; Van Herck, H; Hesselink, DA; Visser, P; Willemsen, R; Van Dokkum, RPE; Wright, CJ; Guay-Woodford, LM
      New rat model that phenotypically resembles autosomal recessive polycystickidney disease

      JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
    5. Rizzu, P; Joosse, M; Ravid, R; Hoogeveen, A; Kamphorst, W; van Swieten, JC; Willemsen, R; Heutink, P
      Mutation-dependent aggregation of tau protein and its selective depletion from the soluble fraction in brain of P301L FTDP-17 patients

      HUMAN MOLECULAR GENETICS
    6. Bakker, CE; Kooy, RF; D'Hooge, R; Tamanini, F; Willemsen, R; Nieuwenhuizen, I; De Vries, BBA; Reyniers, E; Hoogeveen, AT; Willems, PJ; De Deyn, PP; Oostra, BA
      Introduction of a FMR1 transgene in the fragile X knockout mouse.

      NEUROSCIENCE RESEARCH COMMUNICATIONS
    7. Arocena, DG; de Diego, Y; Oostra, BA; Willemsen, R; Rodriguez, MM
      A fragile X case with an amplification/deletion mosaic pattern

      HUMAN GENETICS
    8. Willemsen, R; Oostra, BA
      FMRP detection assay for the diagnosis of the fragile X syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    9. Tuncbilek, E; Alikasifoglu, M; Aktas, D; Duman, F; Yanik, H; Anar, B; Oostra, B; Willemsen, R
      Screening for the fragile X syndrome among mentally retarded males by hairroot analysis

      AMERICAN JOURNAL OF MEDICAL GENETICS
    10. Willemsen, R; Olmer, R; Otero, YD; Oostra, BA
      Twin sisters, monozygotic with the fragile X mutation, but with a different phenotype

      JOURNAL OF MEDICAL GENETICS
    11. Bakker, CE; Otero, YD; Bontekoe, C; Raghoe, P; Luteijn, T; Hoogeveen, AT; Oostra, BA; Willemsen, R
      Immunocytochemical and biochemical characterization of FMRP, FXR1P, and FXR2P in the mouse

      EXPERIMENTAL CELL RESEARCH
    12. de Crom, R; van Haperen, R; Janssens, R; Visser, P; Willemsen, R; Grosveld, F; van der Kamp, A
      Gp96/GRP94 is a putative high density lipoprotein binding protein in liver

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
    13. Mancini, GMS; Stojanov, L; Willemsen, R; Kleijer, WJ; Huijmans, JGM; van Diggelen, OP; de Klerk, JBC; Vuzevski, VD; Oranje, AP
      Juvenile hyaline fibromatosis: Clinical heterogeneity in three patients

      DERMATOLOGY
    14. Stone, DL; van Diggelen, OP; de Klerk, JBC; Gaillard, JLJ; Niermeijer, MF; Willemsen, R; Tayebi, N; Sidransky, E
      Is the perinatal lethal form of Gaucher disease more common than classic type 2 Gaucher disease?

      EUROPEAN JOURNAL OF HUMAN GENETICS
    15. Guy, J; Willemsen, R; Langeveld, A; Grosveld, F; Drabek, D
      Murine MHC class II locus control region drives expression of human beta-glucocerebrosidase in antigen presenting cells of transgenic mice

      GENE THERAPY
    16. Tamanini, F; Bontekoe, C; Bakker, CE; van Unen, L; Anar, B; Willemsen, R; Yoshida, M; Galjaard, H; Oostra, BA; Hoogeveen, AT
      Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations

      HUMAN MOLECULAR GENETICS
    17. Willemsen, R; Breynaert, J; Lauwers, S
      The influence of alcohol disinfection of nail samples in the laboratory

      MYCOSES
    18. Lambiris, N; Peters, H; Bollmann, R; Leschik, G; Leisti, J; Salonen, R; Cobet, G; Oostra, BA; Willemsen, R
      Rapid FMR1-protein analysis of fetal blood: an enhancement of prenatal diagnostics

      HUMAN GENETICS
    19. Tassone, F; Hagerman, RJ; Ikle, DN; Dyer, PN; Lampe, M; Willemsen, R; Oostra, BA; Taylor, AK
      FMRP expression as a potential prognostic indicator in fragile X syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    20. Helderman-van den Enden, ATJM; Maaswinkel-Mooij, PD; Hoogendoorn, E; Willemsen, R; Maat-Kievit, JA; Losekoot, M; Oostra, BA
      Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities

      JOURNAL OF MEDICAL GENETICS
    21. Willemsen, R; Anar, B; Otero, YD; de Vries, BBA; Hilhorst-Hofstee, Y; Smits, A; van Looveren, E; Willems, PJ; Galjaard, H; Oostra, BA
      Noninvasive test for fragile X syndrome, using hair root analysis

      AMERICAN JOURNAL OF HUMAN GENETICS
    22. TAMANINI F; VANUNEN L; BONTEKOE C; BAKKER; WILLEMSEN R; OOSTRA BA; HOOGEVEEN AT
      OLIGOMERIZATION AND INTRACELLULAR-TRANSPORT OF THE FRAGILE-X MENTAL-RETARDATION PROTEIN

      European journal of human genetics
    23. FRANSEN E; DHOOGE R; VANCAMP G; VERHOYE M; SIJBERS J; REYNIERS E; SORIANO P; KAMIGUCHI H; WILLEMSEN R; KOEKKOEK SKE; DEZEEUW CI; DEDEYN PP; VANDERLINDEN A; LEMMON V; KOOY RF; WILLEMS PJ
      L1 KNOCKOUT MICE SHOW DILATED VENTRICLES, VERMIS HYPOPLASIA AND IMPAIRED EXPLORATION PATTERNS

      Human molecular genetics
    24. CHIURAZZI P; POMPONI MG; WILLEMSEN R; OOSTRA BA; NERI G
      IN-VITRO REACTIVATION OF THE FMR1 GENE INVOLVED IN FRAGILE-X-SYNDROME

      Human molecular genetics
    25. SACCHI N; TAMANINI F; WILLEMSEN R; DENISDONINI S; CAMPIGLIO S; HOOGEVEEN AT
      SUBCELLULAR-LOCALIZATION OF THE ONCOPROTEIN MTG8 (CDR ETO) IN NEURAL CELLS/

      Oncogene
    26. de Vries, BBA; Mohkamsing, S; van den Ouweland, AMW; Halley, DJJ; Niermeijer, MF; Oostra, BA; Willemsen, R
      Screening with the FMR1 protein test among mentally retarded males

      HUMAN GENETICS
    27. WILLEMSEN R; SCHOTS R; SHAHABPOUR M; PIERARD D
      PSEUDALLESCHERIA-BOYDII TENOSYNOVITIS

      Journal de mycologie medicale
    28. MALTER HE; IBER JC; WILLEMSEN R; DEGRAAFF E; TARLETON JC; LEISTI J; WARREN ST; OOSTRA BA
      CHARACTERIZATION OF THE FULL FRAGILE-X-SYNDROME MUTATION IN FETAL GAMETES

      Nature genetics
    29. BONTEKOE CJM; DEGRAAFF E; NIEUWENHUIZEN IM; WILLEMSEN R; OOSTRA BA
      FMR1 PREMUTATION ALLELE (CGG)(81) IS STABLE IN MICE

      European journal of human genetics
    30. TAMANINI F; WILLEMSEN R; VANUNEN L; BONTEKOE C; GALJAARD H; OOSTRA BA; HOOGEVEEN AT
      DIFFERENTIAL EXPRESSION OF FMR1, FXR1 AND FXR2 PROTEINS IN HUMAN BRAIN AND TESTIS

      Human molecular genetics
    31. ZHOU XY; VANDERSPOEL A; ROTTIER R; HALE G; WILLEMSEN R; BERRY GT; STRISCIUGLIO P; MORRONE A; ZAMMARCHI E; ANDRIA G; DAZZO A
      MOLECULAR AND BIOCHEMICAL-ANALYSIS OF PROTECTIVE PROTEIN CATHEPSIN A MUTATIONS - CORRELATION WITH CLINICAL SEVERITY IN GALACTOSIALIDOSIS (VOL 5, PG 1977, 1996)/

      Human molecular genetics
    32. WILLEMSEN R; SMITS A; MOHKAMSING S; VANBEERENDONK H; DEHAAN A; DEVRIES B; VANDENOUWELAND A; SISTERMANS E; GALJAARD H; OOSTRA BA
      RAPID ANTIBODY-TEST FOR DIAGNOSING FRAGILE-X-SYNDROME - A VALIDATION OF THE TECHNIQUE

      Human genetics
    33. BREEDVELD B; SCHOONDERWOERD K; VERHOEVEN AJM; WILLEMSEN R; JANSEN H
      HEPATIC LIPASE IS LOCALIZED AT THE PARENCHYMAL-CELL MICROVILLI IN RAT-LIVER

      Biochemical journal
    34. WILLEMSEN R; LOS F; MOHKAMSING S; VANDENOUWELAND A; DEELEN W; GALJAARD H; OOSTRA B
      RAPID ANTIBODY-TEST FOR PRENATAL-DIAGNOSIS OF FRAGILE-X-SYNDROME ON AMNIOTIC-FLUID CELLS - A NEW APPRAISAL

      Journal of Medical Genetics
    35. LOSEKOOT M; HOOGENDOORN E; OLMER R; JANSEN CCAM; OOSTERWIJK JC; VANDENOUWELAND AMW; HALLEY DJJ; WARREN ST; WILLEMSEN R; OOSTRA BA; BAKKER E
      PRENATAL-DIAGNOSIS OF THE FRAGILE-X-SYNDROME - LOSS OF MUTATION OWINGTO A DOUBLE RECOMBINANT OR GENE CONVERSION EVENT AT THE FMR1 LOCUS

      Journal of Medical Genetics
    36. HOOGEVEEN AT; TAMANINI F; WILLEMSEN R; VANUNEN L; BONTEKOE CJM; GALJAARD H; OOSTRA BA
      FMR1, FXR1 AND FXR2 PROTEINS IN HUMAN BRAIN AND TESTIS

      American journal of human genetics
    37. SACCHI N; TAMANINI F; WILLEMSEN R; HOOGEVEEN AT
      THE MTG8 (CDR ETO) PROTEIN DISRUPTED BY THE (8-21)TRANSLOCATION IN ACUTE MYELOID-LEUKEMIA IS EXPRESSED IN NEURONS BOTH IN THE NUCLEUS AND THE NEURITES/

      American journal of human genetics
    38. CHIURAZZI P; POMPONI MG; WILLEMSEN R; OOSTRA BA; NERI G
      IN-VITRO REACTIVATION OF THE FRAGILE-X-SYNDROME GENE

      American journal of human genetics
    39. TASSONE F; HAGERMAN RJ; IKLE D; DYER PN; LAMPE M; WILLEMSEN R; OOSTRA BA; TAYLOR AK
      FMRP EXPRESSION AS A POTENTIAL PROGNOSTIC INDICATOR IN FRAGILE-X-SYNDROME

      American journal of human genetics
    40. ZHOU XY; VANDERSPOEL A; ROTTIER R; HALE G; WILLEMSEN R; BERRY GT; STRISCIUGLIO P; ANDRIA G; DAZZO A
      MOLECULAR AND BIOCHEMICAL-ANALYSIS OF PROTECTIVE PROTEIN CATHEPSIN-A MUTATIONS - CORRELATION WITH CLINICAL SEVERITY IN GALACTOSIALIDOSIS/

      Human molecular genetics
    41. DEGRAAFF E; DEVRIES BBA; WILLEMSEN R; VANHEMEL JO; MOHKAMSING S; OOSTRA BA; VANDENOUWELAND AMW
      THE FRAGILE-X PHENOTYPE IN A MOSAIC MALE WITH A DELETION SHOWING EXPRESSION OF THE FMR1 PROTEIN IN 28-PERCENT OF THE CELLS

      American journal of medical genetics
    42. OOSTRA B; DEGRAAF E; ZHONG N; WILLEMSEN R
      INSTABILITY OF THE CGG REPEAT AND EXPRESSION OF FMR1 PROTEIN IN A MALE-PATIENT WITH A LUNG-TUMOR

      American journal of medical genetics
    43. OOSTRA BA; WILLEMSEN R; MANDEL JL; DEVRIES B; DEVYS D
      RAPID SCREENING-TEST FOR FRAGILE-X SYNDROME

      American journal of medical genetics
    44. WILLEMSEN R; OOSTERWIJK JC; LOS FJ; GALJAARD H; OOSTRA BA
      PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME

      Lancet
    45. MCCABE ERB; FINE BA; GOLBUS MS; GREENHOUSE JB; MCGRATH GL; NEW M; OBRIEN WE; ROWLEY PT; SLY WS; SPENCE MA; STOCKMAN JA; WHYTE M; WILSON W; WOLF B; AERTS JMFG; BARRANGER JA; BARTON NW; BEUTLER E; BRADY RO; COX TM; EKSTEIN J; ENG CM; ERIKSON A; FINDLING DM; GARBER AM; GINNS EI; GRABOWSKI GA; HILL SC; HOLLACK CEM; KABACK MM; LEE RE; MANKIN HJ; MISTRY PK; MOSCICKI RA; MURRAY GJ; NATOWICZ M; PASTORES GM; MIRANDA MCS; SIDRANSKY E; WARE JE; WILLEMSEN R; ZAIZOV R; ZIMRAN A; BEITINS IZ; BERMAN RE; ELLIOTT JM; FERGUSON JH; HALL WH; MCKEON C; NITKIN RM; SCHLESINGER SL; SHERIDAN PH; WEEKS M; COWDRY RW; ALEXANDER DF; GORDEN P; HALL ZW; VAITUKAITIS JL; COLLINS FS; GROFT S
      GAUCHER DISEASE - CURRENT ISSUES IN DIAGNOSIS AND TREATMENT

      JAMA, the journal of the American Medical Association
    46. KEULEMANS JLM; REUSER AJJ; KROOS MA; WILLEMSEN R; HERMANS MMP; VANDENOUWELAND AMW; DEJONG JGN; WEVERS RA; RENIER WO; SCHINDLER D; COLL MJ; CHABAS A; SAKURABA H; SUZUKI Y; VANDIGGELEN OP
      HUMAN ALPHA-N-ACETYLGALACTOSAMINIDASE (ALPHA-NAGA) DEFICIENCY - NEW MUTATIONS AND THE PARADOX BETWEEN GENOTYPE AND PHENOTYPE

      Journal of Medical Genetics
    47. DEVRIES BBA; JANSEN CCAM; DUITS AA; VERHEIJ C; WILLEMSEN R; VANHEMEL JO; VANDENOUWELAND AMW; NIERMEIJER MF; OOSTRA BA; HALLEY DJJ
      VARIABLE FMR1 GENE METHYLATION OF LARGE EXPANSIONS LEADS TO VARIABLE PHENOTYPE IN 3 MALES FROM ONE FRAGILE-X FAMILY

      Journal of Medical Genetics
    48. KOKEN MHM; HOOGERBRUGGE JW; JASPERSDEKKER I; DEWIT J; WILLEMSEN R; ROEST HP; GROOTEGOED JA; HOEIJMAKERS JHJ
      EXPRESSION OF THE UBIQUITIN-CONJUGATING DNA-REPAIR ENZYMES HHR6A AND HHR6B SUGGESTS A ROLE IN SPERMATOGENESIS AND CHROMATIN MODIFICATION

      Developmental biology
    49. WILLEMSEN R; BONTEKOE C; TAMANINI F; GALJAARD H; HOOGEVEEN A; OOSTRA B
      ASSOCIATION OF FMRP WITH RIBOSOMAL PRECURSOR PARTICLES IN THE NUCLEOLUS

      Biochemical and biophysical research communications
    50. WILLEMSEN R; TYBULEWICZ V; SIDRANSKY E; ELIASON WK; MARTIN BM; LAMARCA ME; REUSER AJJ; TREMBLAY M; WESTPHAL H; MULLIGAN RC; GINNS EI
      A BIOCHEMICAL AND ULTRASTRUCTURAL EVALUATION OF THE TYPE-2 GAUCHER MOUSE

      Molecular and chemical neuropathology
    51. VERHEIJ C; DEGRAAFF E; BAKKER CE; WILLEMSEN R; WILLEMS PJ; MEIJER N; GALJAARD H; REUSER AJJ; OOSTRA BA; HOOGEVEEN AT
      CHARACTERIZATION OF FMR1 PROTEINS ISOLATED FROM DIFFERENT TISSUES

      Human molecular genetics
    52. SMEETS HJM; SMITS APT; VERHEIJ CE; THEELEN JPG; WILLEMSEN R; VANDEBURGT I; HOOGEVEEN AT; OOSTERWIJK JC; OOSTRA BA
      NORMAL PHENOTYPE IN 2 BROTHERS WITH A FULL FMR1 MUTATION

      Human molecular genetics
    53. WILLEMSEN R; MOHKAMSING S; DEVRIES B; DEVYS D; VANDENOUWELAND A; MANDEL JL; GALJAARD H; OOSTRA B
      RAPID ANTIBODY-TEST FOR FRAGILE-X SYNDROME

      Lancet
    54. BONTEN EJ; GALJART NJ; WILLEMSEN R; USMANY M; VLAK JM; DAZZO A
      LYSOSOMAL PROTECTIVE PROTEIN CATHEPSIN-A - ROLE OF THE LINKER DOMAIN IN CATALYTIC ACTIVATION

      The Journal of biological chemistry
    55. WILLEMSEN R; TIBBE JJM; KROOS MA; MARTIN BM; REUSER AJJ; GINNS EI
      A BIOCHEMICAL AND IMMUNOCYTOCHEMICAL STUDY ON THE TARGETING OF ALGLUCERASE IN MURINE LIVER

      Histochemical Journal
    56. WILLEMSEN R; BAKKER C; MANDEL JL; DEVRIES B; DEVYS D; OOSTRA BA
      RAPID SCREENING-TEST FOR FRAGILE-X SYNDROME

      American journal of human genetics
    57. BAKKER C; DEGRAAFF E; ZHONG N; WILLEMSEN R; OOSTRA B
      INSTABILITY OF THE CGG REPEAT AND EXPRESSION OF FMR1 PROTEIN IN A MALE-PATIENT WITH A LUNG-TUMOR

      American journal of human genetics
    58. DEGRAAFF E; WILLEMSEN R; ZHONG N; DEDIESMULDERS CEM; BROWN WT; FRELING G; OOSTRA B
      INSTABILITY OF THE CGG REPEAT AND EXPRESSION OF THE FMR1 PROTEIN IN AMALE FRAGILE-X PATIENT WITH A LUNG-TUMOR

      American journal of human genetics
    59. DECROM RPG; VANHAPEREN R; VISSER P; WILLEMSEN R; VANDERKAMP AWM
      STRUCTURAL RELATION BETWEEN HDL-BINDING PROTEINS IN PORCINE LIVER

      Arteriosclerosis and thrombosis
    60. HERMANS MMP; DEGRAAFF E; KROOS MA; MOHKAMSING S; EUSSEN BJ; JOOSSE M; WILLEMSEN R; KLEIJER WJ; OOSTRA BA; REUSER AJJ
      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
    61. GINNS EI; YOSHIKAWA H; MCKINNEY CE; STUBBLEFIELD BK; WINFIELD S; CARMON L; MARTIN BM; WILLEMSEN R; SIDRANSKY E; LAMARCA ME
      PROGRESS TOWARD GENERATING TYPE-1 GAUCHER MICE BY INTRODUCTION OF THEN370S POINT MUTATION BY HOMOLOGOUS RECOMBINATION INTO ES CELLS

      Journal of cellular biochemistry
    62. DEJONG JP; VOERMAN JSA; VANDERSLUIJSGELLING AJ; WILLEMSEN R; PLOEMACHER RE
      A MONOCLONAL-ANTIBODY (ER-HR3) AGAINST MURINE MACROPHAGES .1. ONTOGENY, DISTRIBUTION AND ENZYME-HISTOCHEMICAL CHARACTERIZATION OF ER-HR3-POSITIVE CELLS

      Cell and tissue research
    63. DEFRESNE MP; NABARRA B; VANVLIET E; WILLEMSEN R; VANDONGEN H; VANEWIJK W
      THE ER-TR4 MONOCLONAL-ANTIBODY RECOGNIZES MURINE THYMIC EPITHELIAL-CELLS (TYPE-1) AND INHIBITS THEIR CAPACITY TO INTERACT WITH IMMATURE THYMOCYTES - IMMUNOELECTRON MICROSCOPIC AND FUNCTIONAL-STUDIES

      Histochemistry
    64. BAKKER CE; VERHEIJ C; WILLEMSEN R; VANDERHELM R; OERLEMANS F; VERMEY M; BYGRAVE A; HOOGEVEEN AT; OOSTRA BA; REYNIERS E; DEBOULLE K; DHOOGE R; CRAS P; VANVELZEN D; NAGELS G; MARTIN JJ; DEDEYN PP; DARBY JK; WILLEMS PJ
      FMR1 KNOCKOUT MICE - A MODEL TO STUDY FRAGILE-X MENTAL-RETARDATION

      Cell
    65. POORTHUIS BJHM; ROMME AE; WILLEMSEN R; WAGEMAKER G
      BONE-MARROW TRANSPLANTATION HAS A SIGNIFICANT EFFECT ON ENZYME LEVELSAND STORAGE OF GLYCOSAMINOGLYCANS IN TISSUES AND IN ISOLATED HEPATOCYTES OF MUCOPOLYSACCHARIDOSIS TYPE-VII MICE

      Pediatric research
    66. DEJONG J; VANDENBERG C; WIJBURG H; WILLEMSEN R; VANDIGGELEN O; SCHINDLER D; HOEVENAARS F; WEVERS R
      ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY WITH MILD CLINICAL MANIFESTATIONS AND DIFFICULT BIOCHEMICAL-DIAGNOSIS

      The Journal of pediatrics
    67. REUSER AJJ; KROOS MA; VISSER WJ; WILLEMSEN R
      LYSOSOMAL STORAGE DISEASES - CELLULAR PATHOLOGY, CLINICAL AND GENETIC-HETEROGENEITY, THERAPY

      Annales de biologie clinique
    68. HOOGEVEEN AT; WILLEMSEN R; MEYER N; DEROOIJ KE; ROOS RAC; VANOMMEN GJB; GALJAARD H
      CHARACTERIZATION AND LOCALIZATION OF THE HUNTINGTON DISEASE GENE-PRODUCT

      Human molecular genetics
    69. WILLEMSEN R; VANDERPLOEG AT; BUSCH HFM; ZONDERVAN PE; VANNOORDEN CJF; REUSER AJJ
      SYNTHESIS AND IN-SITU LOCALIZATION OF LYSOSOMAL ALPHA-GLUCOSIDASE IN MUSCLE OF AN UNUSUAL VARIANT OF GLYCOGEN-STORAGE-DISEASE TYPE-II

      Ultrastructural pathology
    70. VERHEIJ C; BAKKER CE; DEGRAAFF E; KEULEMANS J; WILLEMSEN R; VERKERK AJMH; GALJAARD H; REUSER AJJ; HOOGEVEEN AT; OOSTRA BA
      CHARACTERIZATION AND LOCALIZATION OF THE FMR-1 GENE-PRODUCT ASSOCIATED WITH FRAGILE-X SYNDROME

      Nature
    71. DAZZO A; ZHOU XY; WILLEMSEN R; FRASER P; GROSVELD FG; GROSVELD GC
      LCR-DIRECTED EXPRESSION OF HUMAN PROTECTIVE PROTEIN CATHEPSIN-A IN TRANSGENIC MICE

      American journal of human genetics
    72. ZHOU XY; WILLEMSEN R; GILLEMANS N; MORRONE A; STRISCIUGLIO P; ANDRIA G; APPLEGARTH DA; DAZZO A
      COMMON POINT MUTATIONS IN 4 PATIENTS WITH THE LATE INFANTILE FORM OF GALACTOSIALIDOSIS

      American journal of human genetics


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Documento generato il 29/05/20 alle ore 08:16:21