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Results: 1-25 | 26-50 | 51-75 | 76-98
Results: 1-25/98
MRI AS A TOOL TO STUDY BRAIN STRUCTURE FROM MOUSE MODELS OF MENTAL-RETARDATION
Authors: KOOY F REYNIERS E VERHOYE M SIJBERS J FRANSEN E OOSTRA BA WILLEMS PJ VANDERLINDEN A
Citation: F. Kooy et al., MRI AS A TOOL TO STUDY BRAIN STRUCTURE FROM MOUSE MODELS OF MENTAL-RETARDATION, European journal of human genetics, 6, 1998, pp. 306-306
KNOCKOUT MOUSE MODEL OF GLYCOGEN-STORAGE-DISEASE TYPE-II - ENZYME THERAPY AT THE TEST
Authors: BIJVOET AGA VANDEKAMP EHM KROOS MA VANHIRTUM JP SCHONEVELD JLM DING JH YANG BZ VISSER P VERBEET MP OOSTRA BA REUSER AJJ VANDERPLOEG AT
Citation: Aga. Bijvoet et al., KNOCKOUT MOUSE MODEL OF GLYCOGEN-STORAGE-DISEASE TYPE-II - ENZYME THERAPY AT THE TEST, European journal of human genetics, 6, 1998, pp. 806-806
OLIGOMERIZATION AND INTRACELLULAR-TRANSPORT OF THE FRAGILE-X MENTAL-RETARDATION PROTEIN
Authors: TAMANINI F VANUNEN L BONTEKOE C",BAKKER,"WILLEMSEN R OOSTRA BA HOOGEVEEN AT
Citation: F. Tamanini et al., OLIGOMERIZATION AND INTRACELLULAR-TRANSPORT OF THE FRAGILE-X MENTAL-RETARDATION PROTEIN, European journal of human genetics, 6, 1998, pp. 905-905
GENERALIZED GLYCOGEN-STORAGE AND CARDIOMEGALY IN A KNOCKOUT MOUSE MODEL OF POMPE-DISEASE
Authors: BIJVOET AGA VANDEKAMP EHM KROOS MA DING JH YANG BZ VISSER P BAKKER CE VERBEET MP OOSTRA BA REUSER AJJ VANDERPLOEG AT
Citation: Aga. Bijvoet et al., GENERALIZED GLYCOGEN-STORAGE AND CARDIOMEGALY IN A KNOCKOUT MOUSE MODEL OF POMPE-DISEASE, Human molecular genetics, 7(1), 1998, pp. 53-62
IN-VITRO REACTIVATION OF THE FMR1 GENE INVOLVED IN FRAGILE-X-SYNDROME
Authors: CHIURAZZI P POMPONI MG WILLEMSEN R OOSTRA BA NERI G
Citation: P. Chiurazzi et al., IN-VITRO REACTIVATION OF THE FMR1 GENE INVOLVED IN FRAGILE-X-SYNDROME, Human molecular genetics, 7(1), 1998, pp. 109-113
NO EVIDENCE FOR DISRUPTION OF NORMAL PATTERNS OF MESSENGER-RNA LOCALIZATION IN DENDRITES OR DENDRITIC TRANSPORT OF RECENTLY SYNTHESIZED MESSENGER-RNA IN FMR1 KNOCKOUT MICE, A MODEL FOR HUMAN FRAGILE-X MENTAL-RETARDATION SYNDROME
Authors: STEWARD O BAKKER CE WILLEMS PJ OOSTRA BA
Citation: O. Steward et al., NO EVIDENCE FOR DISRUPTION OF NORMAL PATTERNS OF MESSENGER-RNA LOCALIZATION IN DENDRITES OR DENDRITIC TRANSPORT OF RECENTLY SYNTHESIZED MESSENGER-RNA IN FMR1 KNOCKOUT MICE, A MODEL FOR HUMAN FRAGILE-X MENTAL-RETARDATION SYNDROME, NeuroReport, 9(3), 1998, pp. 477-481
INCOMPLETE ECORI DIGESTION MAY LEAD TO FALSE DIAGNOSIS OF FRAGILE-X-SYNDROME
Authors: STORM K HANDIG I REYNIERS E OOSTRA BA KOOY RF WILLEMS PJ
Citation: K. Storm et al., INCOMPLETE ECORI DIGESTION MAY LEAD TO FALSE DIAGNOSIS OF FRAGILE-X-SYNDROME, Human genetics, 102(1), 1998, pp. 54-56
FRAGILE-X-SYNDROME IS CAUSED BY A FRAGILE GENE
Authors: OOSTRA BA
Citation: Ba. Oostra, FRAGILE-X-SYNDROME IS CAUSED BY A FRAGILE GENE, American journal of medical genetics, 81(6), 1998, pp. 452-453
FAMILIAL AGGREGATION IN FRONTOTEMPORAL DEMENTIA
Authors: STEVENS M VANDUIJN CM KAMPHORST W DEKNIJFF P HEUTINK P VANGOOL WA SCHELTENS P RAVID R OOSTRA BA NIERMEIJER MF VANSWIETEN JC
Citation: M. Stevens et al., FAMILIAL AGGREGATION IN FRONTOTEMPORAL DEMENTIA, Neurology, 50(6), 1998, pp. 1541-1545
ASSOCIATION OF MISSENSE AND 5'-SPLICE-SITE MUTATIONS IN TAU WITH THE INHERITED DEMENTIA FTDP-17
Authors: HUTTON M LENDON CL RIZZU P BAKER M FROELICH S HOULDEN H PICKERINGBROWN S CHAKRAVERTY S ISAACS A GROVER A HACKETT J ADAMSON J LINCOLN S DICKSON D DAVIES P PETERSEN RC STEVENS M DEGRAAFF E WAUTERS E VANBAREN J HILLEBRAND M JOOSSE M KWON JM NOWOTNY P CHE LK NORTON J MORRIS JC REED LA TROJANOWSKI J BASUN H LANNFELT L NEYSTAT M FAHN S DARK F TANNENBERG T DODD PR HAYWARD N KWOK JBJ SCHOFIELD PR ANDREADIS A SNOWDEN J CRAUFURD D NEARY D OWEN F OOSTRA BA HARDY J GOATE A VANSWIETEN J MANN D LYNCH T HEUTINK P
Citation: M. Hutton et al., ASSOCIATION OF MISSENSE AND 5'-SPLICE-SITE MUTATIONS IN TAU WITH THE INHERITED DEMENTIA FTDP-17, Nature, 393(6686), 1998, pp. 702-705
THE FRAGILE-X-SYNDROME
Authors: DEVRIES BBA HALLEY DJJ OOSTRA BA NIERMEIJER MF
Citation: Bba. Devries et al., THE FRAGILE-X-SYNDROME, Journal of Medical Genetics, 35(7), 1998, pp. 579-589
MACROORCHIDISM IN FMR1 KNOCKOUT MICE IS CAUSED BY INCREASED SERTOLI-CELL PROLIFERATION DURING TESTICULAR DEVELOPMENT
Authors: SLEGTENHORSTEEGDEMAN KE DEROOIJ DG VERHOEFPOST M VANDEKANT HJG BAKKER CE OOSTRA BA GROOTEGOED JA THEMMEN APN
Citation: Ke. Slegtenhorsteegdeman et al., MACROORCHIDISM IN FMR1 KNOCKOUT MICE IS CAUSED BY INCREASED SERTOLI-CELL PROLIFERATION DURING TESTICULAR DEVELOPMENT, Endocrinology, 139(1), 1998, pp. 156-162
CHARACTERIZATION OF THE FULL FRAGILE-X-SYNDROME MUTATION IN FETAL GAMETES
Authors: MALTER HE IBER JC WILLEMSEN R DEGRAAFF E TARLETON JC LEISTI J WARREN ST OOSTRA BA
Citation: He. Malter et al., CHARACTERIZATION OF THE FULL FRAGILE-X-SYNDROME MUTATION IN FETAL GAMETES, Nature genetics, 15(2), 1997, pp. 165-169
FMR1 PREMUTATION ALLELE (CGG)(81) IS STABLE IN MICE
Authors: BONTEKOE CJM DEGRAAFF E NIEUWENHUIZEN IM WILLEMSEN R OOSTRA BA
Citation: Cjm. Bontekoe et al., FMR1 PREMUTATION ALLELE (CGG)(81) IS STABLE IN MICE, European journal of human genetics, 5(5), 1997, pp. 293-298
DIFFERENTIAL EXPRESSION OF FMR1, FXR1 AND FXR2 PROTEINS IN HUMAN BRAIN AND TESTIS
Authors: TAMANINI F WILLEMSEN R VANUNEN L BONTEKOE C GALJAARD H OOSTRA BA HOOGEVEEN AT
Citation: F. Tamanini et al., DIFFERENTIAL EXPRESSION OF FMR1, FXR1 AND FXR2 PROTEINS IN HUMAN BRAIN AND TESTIS, Human molecular genetics, 6(8), 1997, pp. 1315-1322
FMR2 EXPRESSION IN FAMILIES WITH FRAXE MENTAL-RETARDATION
Authors: GECZ J OOSTRA BA HOCKEY A CARBONELL P TURNER G HAAN EA SUTHERLAND GR MULLEY JC
Citation: J. Gecz et al., FMR2 EXPRESSION IN FAMILIES WITH FRAXE MENTAL-RETARDATION, Human molecular genetics, 6(3), 1997, pp. 435-441
ANIMAL-MODEL FOR FRAGILE-X-SYNDROME
Authors: OOSTRA BA HOOGEVEEN AT
Citation: Ba. Oostra et At. Hoogeveen, ANIMAL-MODEL FOR FRAGILE-X-SYNDROME, Annals of medicine, 29(6), 1997, pp. 563-567
HEREDITARY FRONTOTEMPORAL DEMENTIA IS LINKED TO CHROMOSOME-17Q21-Q22 - A GENETIC AND CLINICOPATHOLOGICAL STUDY OF 3 DUTCH FAMILIES
Authors: HEUTINK P STEVENS M RIZZU P BAKKER E KROS JM TIBBEN A NIERMEIJER MF VANDUIJN CM OOSTRA BA VANSWIETEN JC
Citation: P. Heutink et al., HEREDITARY FRONTOTEMPORAL DEMENTIA IS LINKED TO CHROMOSOME-17Q21-Q22 - A GENETIC AND CLINICOPATHOLOGICAL STUDY OF 3 DUTCH FAMILIES, Annals of neurology, 41(2), 1997, pp. 150-159
RAPID ANTIBODY-TEST FOR DIAGNOSING FRAGILE-X-SYNDROME - A VALIDATION OF THE TECHNIQUE
Authors: WILLEMSEN R SMITS A MOHKAMSING S VANBEERENDONK H DEHAAN A DEVRIES B VANDENOUWELAND A SISTERMANS E GALJAARD H OOSTRA BA
Citation: R. Willemsen et al., RAPID ANTIBODY-TEST FOR DIAGNOSING FRAGILE-X-SYNDROME - A VALIDATION OF THE TECHNIQUE, Human genetics, 99(3), 1997, pp. 308-311
MILDLY IMPAIRED WATER MAZE PERFORMANCE IN MALE FMR1 KNOCKOUT MICE
Authors: DHOOGE R NAGELS G FRANCK F BAKKER CE REYNIERS E STORM K KOOY RF OOSTRA BA WILLEMS PJ DEDEYN PP
Citation: R. Dhooge et al., MILDLY IMPAIRED WATER MAZE PERFORMANCE IN MALE FMR1 KNOCKOUT MICE, Neuroscience, 76(2), 1997, pp. 367-376
THE FRAGILE-X-SYNDROME
Authors: HOOGEVEEN AT OOSTRA BA
Citation: At. Hoogeveen et Ba. Oostra, THE FRAGILE-X-SYNDROME, Journal of inherited metabolic disease, 20(2), 1997, pp. 139-151
APOLIPOPROTEIN-E GENE AND SPORADIC FRONTAL-LOBE DEMENTIA
Authors: STEVENS M VANDUIJN CM DEKNIJFF P VANBROECKHOVEN C HEUTINK P OOSTRA BA NIERMEIJER MF VANSWIETEN JC
Citation: M. Stevens et al., APOLIPOPROTEIN-E GENE AND SPORADIC FRONTAL-LOBE DEMENTIA, Neurology, 48(6), 1997, pp. 1526-1529
FAMILIAL AGGREGATION IN FRONTOTEMPORAL DEMENTIA
Authors: STEVENS M VANDUIJN CM OOSTRA BA HEUTINK P VANSWIETEN JC
Citation: M. Stevens et al., FAMILIAL AGGREGATION IN FRONTOTEMPORAL DEMENTIA, Neurology, 48(3), 1997, pp. 5032-5032
ABNORMAL DENDRITIC SPINES IN FRAGILE-X KNOCKOUT MICE - MATURATION ANDPRUNING DEFICITS
Authors: COMERY TA HARRIS JB WILLEMS PJ OOSTRA BA IRWIN SA WEILER IJ GREENOUGH WT
Citation: Ta. Comery et al., ABNORMAL DENDRITIC SPINES IN FRAGILE-X KNOCKOUT MICE - MATURATION ANDPRUNING DEFICITS, Proceedings of the National Academy of Sciences of the United Statesof America, 94(10), 1997, pp. 5401-5404
PRENATAL-DIAGNOSIS OF THE FRAGILE-X-SYNDROME - LOSS OF MUTATION OWINGTO A DOUBLE RECOMBINANT OR GENE CONVERSION EVENT AT THE FMR1 LOCUS
Authors: LOSEKOOT M HOOGENDOORN E OLMER R JANSEN CCAM OOSTERWIJK JC VANDENOUWELAND AMW HALLEY DJJ WARREN ST WILLEMSEN R OOSTRA BA BAKKER E
Citation: M. Losekoot et al., 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, 34(11), 1997, pp. 924-926
Risultati: 1-25 | 26-50 | 51-75 | 76-98