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Results: 1-25 | 26-50 | 51-71
Results: 1-25/71
MISSENSE MUTATIONS IN THE CHROMOSOME-14 FAMILIAL ALZHEIMERS-DISEASE PRESENILIN-1 GENE
Authors: POORKAJ P SHARMA V ANDERSON L NEMENS E ALONSO ME ORR H WHITE J HESTON L BIRD TD SCHELLENBERG GD
Citation: P. Poorkaj et al., MISSENSE MUTATIONS IN THE CHROMOSOME-14 FAMILIAL ALZHEIMERS-DISEASE PRESENILIN-1 GENE, Human mutation, 11(3), 1998, pp. 216-221
HOT PAPERS - AGING AND GENETICS - POSITIONAL CLONING OF THE WERNERS-SYNDROME GENE BY YU,C.E., OSHIMA,J., FU,Y.H., WIJSMAN,E.M., HISAMA,F., ALISCH,R., MATTHEWS,S., NAKURA,J., MIKI,T., OUAIS,S., MARTIN,G.M., MULLIGAN,J., SCHELLENBERG,G.D. - COMMENTS
Authors: SCHELLENBERG GD
Citation: Gd. Schellenberg, HOT PAPERS - AGING AND GENETICS - POSITIONAL CLONING OF THE WERNERS-SYNDROME GENE BY YU,C.E., OSHIMA,J., FU,Y.H., WIJSMAN,E.M., HISAMA,F., ALISCH,R., MATTHEWS,S., NAKURA,J., MIKI,T., OUAIS,S., MARTIN,G.M., MULLIGAN,J., SCHELLENBERG,G.D. - COMMENTS, The Scientist, 12(18), 1998, pp. 11-11
COMPARISON OF METHODS FOR IDENTIFYING TRANSCRIPTION UNITS AND TRANSCRIPTION MAP OF THE WERNER-SYNDROME GENE REGION
Authors: HISAMA FM OSHIMA J YU CE FU YH MULLIGAN J WEISSMAN SM SCHELLENBERG GD
Citation: Fm. Hisama et al., COMPARISON OF METHODS FOR IDENTIFYING TRANSCRIPTION UNITS AND TRANSCRIPTION MAP OF THE WERNER-SYNDROME GENE REGION, Genomics (San Diego, Calif.), 52(3), 1998, pp. 352-357
A NOVEL LONG AND UNSTABLE CAG CTG TRINUCLEOTIDE REPEAT ON CHROMOSOME 17Q/
Authors: IKEUCHI T SANPEI K TAKANO H SASAKI H TASHIRO K CANCEL G BRICE A BIRD TD SCHELLENBERG GD PERICAKVANCE MA WELSHBOHMER KA CLARK LN WILHELMSEN K TSUJI S
Citation: T. Ikeuchi et al., A NOVEL LONG AND UNSTABLE CAG CTG TRINUCLEOTIDE REPEAT ON CHROMOSOME 17Q/, Genomics, 49(2), 1998, pp. 321-326
AN EXPRESSION MAP FROM HUMAN-CHROMOSOME 14Q24.3
Authors: SHARMA V POORKAJ P HISAMA F BONNYCASTLE L YU CE MASSA H TRASK B CLANCY KP PATTERSON D WEISSMAN SM SCHELLENBERG GD
Citation: V. Sharma et al., AN EXPRESSION MAP FROM HUMAN-CHROMOSOME 14Q24.3, Genomics, 47(2), 1998, pp. 314-318
TAU IS A CANDIDATE GENE FOR CHROMOSOME-17 FRONTOTEMPORAL DEMENTIA
Authors: POORKAJ P BIRD TD WIJSMAN E NEMENS E GARRUTO RM ANDERSON L ANDREADIS A WIEDERHOLT WC RASKIND M SCHELLENBERG GD
Citation: P. Poorkaj et al., TAU IS A CANDIDATE GENE FOR CHROMOSOME-17 FRONTOTEMPORAL DEMENTIA, Annals of neurology, 43(6), 1998, pp. 815-825
PRESENILIN-1 MUTATION ALTERS NGF-INDUCED NEURITE OUTGROWTH, CALCIUM HOMEOSTASIS, AND TRANSCRIPTION FACTOR (AP-1) ACTIVATION IN PC12 CELLS
Authors: FURUKAWA KS GUO Q SCHELLENBERG GD MATTSON MP
Citation: Ks. Furukawa et al., PRESENILIN-1 MUTATION ALTERS NGF-INDUCED NEURITE OUTGROWTH, CALCIUM HOMEOSTASIS, AND TRANSCRIPTION FACTOR (AP-1) ACTIVATION IN PC12 CELLS, Journal of neuroscience research, 52(5), 1998, pp. 618-624
GENE-TOXIN INTERACTION AS A PUTATIVE RISK FACTOR FOR PARKINSONS-DISEASE WITH DEMENTIA
Authors: HUBBLE JP KURTH JH GLATT SL KURTH MC SCHELLENBERG GD HASSANEIN RES LIEBERMAN A KOLLER WC
Citation: Jp. Hubble et al., GENE-TOXIN INTERACTION AS A PUTATIVE RISK FACTOR FOR PARKINSONS-DISEASE WITH DEMENTIA, Neuroepidemiology, 17(2), 1998, pp. 96-104
MIDLIFE CARDIOVASCULAR RISK-FACTORS, APOE, AND COGNITIVE DECLINE IN ELDERLY MALE TWINS
Authors: CARMELLI D SWAN GE REED T MILLER B WOLF PA JARVIK GP SCHELLENBERG GD
Citation: D. Carmelli et al., MIDLIFE CARDIOVASCULAR RISK-FACTORS, APOE, AND COGNITIVE DECLINE IN ELDERLY MALE TWINS, Neurology, 50(6), 1998, pp. 1580-1585
CEREBROSPINAL-FLUID AND PLASMA-INSULIN LEVELS IN ALZHEIMERS-DISEASE -RELATIONSHIP TO SEVERITY OF DEMENTIA AND APOLIPOPROTEIN-E GENOTYPE
Authors: CRAFT S PESKIND E SCHWARTZ MW SCHELLENBERG GD RASKIND M PORTE D
Citation: S. Craft et al., CEREBROSPINAL-FLUID AND PLASMA-INSULIN LEVELS IN ALZHEIMERS-DISEASE -RELATIONSHIP TO SEVERITY OF DEMENTIA AND APOLIPOPROTEIN-E GENOTYPE, Neurology, 50(1), 1998, pp. 164-168
AGING-ASSOCIATED NEUROPATHOLOGY IN WERNER-SYNDROME
Authors: LEVERENZ JB YU CE SCHELLENBERG GD
Citation: Jb. Leverenz et al., AGING-ASSOCIATED NEUROPATHOLOGY IN WERNER-SYNDROME, Acta Neuropathologica, 96(4), 1998, pp. 421-424
CLINICOPATHOLOGICAL CORRELATIONS OF SOLUBLE AMYLOID BETA-PROTEIN PRECURSOR IN CEREBROSPINAL-FLUID IN PATIENTS WITH ALZHEIMER-DISEASE AND CONTROLS
Authors: PESKIND ER LEVERENZ J FARLOW MR ITO RK PROVOW SA SIEGEL RS CLEVELAND M MORGAN CH PANDIAN MR CORBIN S NOCHLIN D SCHELLENBERG GD RASKIND MA WAGNER SL
Citation: Er. Peskind et al., CLINICOPATHOLOGICAL CORRELATIONS OF SOLUBLE AMYLOID BETA-PROTEIN PRECURSOR IN CEREBROSPINAL-FLUID IN PATIENTS WITH ALZHEIMER-DISEASE AND CONTROLS, Alzheimer disease and associated disorders, 11(4), 1997, pp. 201-206
ALZHEIMERS-DISEASE AND HISTORY OF BLOOD-TRANSFUSION BY APOLIPOPROTEIN-E GENOTYPE
Authors: OMEARA ES KUKULL WA SCHELLENBERG GD BOWEN JD MCCORMICK WC TERI L PFANSCHMIDT M THOMPSON JD LARSON EB
Citation: Es. Omeara et al., ALZHEIMERS-DISEASE AND HISTORY OF BLOOD-TRANSFUSION BY APOLIPOPROTEIN-E GENOTYPE, Neuroepidemiology, 16(2), 1997, pp. 86-93
EVIDENCE FOR ASSOCIATION OF HLA-A2 ALLELE WITH ONSET AGE OF ALZHEIMERS-DISEASE
Authors: PAYAMI H SCHELLENBERG GD ZAREPARSI S KAYE J SEXTON GJ HEAD MA MATSUYAMA SS JARVIK LF MILLER B MCMANUS DQ BIRD TD KATZMAN R HESTON L NORMAN D SMALL GW
Citation: H. Payami et al., EVIDENCE FOR ASSOCIATION OF HLA-A2 ALLELE WITH ONSET AGE OF ALZHEIMERS-DISEASE, Neurology, 49(2), 1997, pp. 512-518
CHROMOSOME-17 AND HEREDITARY DEMENTIA - LINKAGE STUDIES IN 3 NON-ALZHEIMER FAMILIES AND KINDREDS WITH LATE-ONSET FAD
Authors: BIRD TD WIJSMAN EM NOCHLIN D LEEHEY M SUMI SM PAYAMI H POORKAJ P NEMENS E RAFKIND M SCHELLENBERG GD
Citation: Td. Bird et al., CHROMOSOME-17 AND HEREDITARY DEMENTIA - LINKAGE STUDIES IN 3 NON-ALZHEIMER FAMILIES AND KINDREDS WITH LATE-ONSET FAD, Neurology, 48(4), 1997, pp. 949-954
EVIDENCE THAT THE APOLIPOPROTEIN-E GENOTYPE EFFECTS ON LIPID-LEVELS CAN CHANGE WITH AGE IN MALES - A LONGITUDINAL ANALYSIS
Authors: JARVIK GP GOODE EL AUSTIN MA AUWERX J DEEB S SCHELLENBERG GD REED T
Citation: Gp. Jarvik et al., EVIDENCE THAT THE APOLIPOPROTEIN-E GENOTYPE EFFECTS ON LIPID-LEVELS CAN CHANGE WITH AGE IN MALES - A LONGITUDINAL ANALYSIS, American journal of human genetics, 61(1), 1997, pp. 171-181
MUTATIONS IN THE CONSENSUS HELICASE DOMAINS OF THE WERNER SYNDROME GENE
Authors: YU CE OSHIMA J WIJSMAN EM NAKURA J MIKI T PIUSSAN C MATTHEWS S FU YH MULLIGAN J MARTIN GM SCHELLENBERG GD BURG G EPSTEIN CJ FISCHER W FUJIWARA Y FUKUCHI KI HOEHN H HURLIMANN AF KISO S MATTHEWS J MELARAGNO MI MURANO S OUAIS S POOT M RIZZO M SAIDA T TANNOCK TCA UYENO B
Citation: Ce. Yu et al., MUTATIONS IN THE CONSENSUS HELICASE DOMAINS OF THE WERNER SYNDROME GENE, American journal of human genetics, 60(2), 1997, pp. 330-341
HEAD-INJURY AND RISK OF ALZHEIMERS-DISEASE BY APOLIPOPROTEIN-E GENOTYPE
Authors: OMEARA ES KUKULL WA SHEPPARD L BOWEN JD MCCORMICK WC TERI L PFANSCHMIDT M THOMPSON JD SCHELLENBERG GD LARSON EB
Citation: Es. Omeara et al., HEAD-INJURY AND RISK OF ALZHEIMERS-DISEASE BY APOLIPOPROTEIN-E GENOTYPE, American journal of epidemiology, 146(5), 1997, pp. 373-384
HOMOZYGOUS AND COMPOUND HETEROZYGOUS MUTATIONS AT THE WERNER SYNDROMELOCUS
Authors: OSHIMA J YU CE PIUSSAN C KLEIN G JABKOWSKI J BALCI S MIKI T NAKURA J OGIHARA T ELLS J SMITH MDC MELARAGNO MI FRACCARO M SCAPPATICCI S MATTHEWS J OUAIS S JARZEBOWICZ A SCHELLENBERG GD MARTIN GM
Citation: J. Oshima et al., HOMOZYGOUS AND COMPOUND HETEROZYGOUS MUTATIONS AT THE WERNER SYNDROMELOCUS, Human molecular genetics, 5(12), 1996, pp. 1909-1913
APOLIPOPROTEIN-E IN ALZHEIMERS-DISEASE RISK AND CASE DETECTION - A CASE-CONTROL STUDY
Authors: KUKULL WA SCHELLENBERG GD BOWEN JD MCCORMICK WC YU CE TERI L THOMSON JD OMEARA ES LARSON EB
Citation: Wa. Kukull et al., APOLIPOPROTEIN-E IN ALZHEIMERS-DISEASE RISK AND CASE DETECTION - A CASE-CONTROL STUDY, Journal of clinical epidemiology, 49(10), 1996, pp. 1143-1148
NARROWING THE POSITION OF THE WERNER SYNDROME LOCUS BY HOMOZYGOSITY ANALYSIS - EXTENSION OF HOMOZYGOSITY ANALYSIS
Authors: NAKURA J MIKI T YE L MITSUDA N ZHAO Y KIHARA K YU CE OSHIMA J FUKUCHI K WIJSMAN EM SCHELLENBERG GD MARTIN GM MURANO S HASHIMOTO K FUJIWARA Y OGIHARA T
Citation: J. Nakura et al., NARROWING THE POSITION OF THE WERNER SYNDROME LOCUS BY HOMOZYGOSITY ANALYSIS - EXTENSION OF HOMOZYGOSITY ANALYSIS, Genomics, 36(1), 1996, pp. 130-141
A YAC, P1, AND COSMID CONTIG AND 17 NEW POLYMORPHIC MARKERS FOR THE WERNER SYNDROME REGION AT 8P12-P21
Authors: YU CE OSHIMA J HISAMA FM MATTHEWS S TRASK BJ SCHELLENBERG GD
Citation: Ce. Yu et al., A YAC, P1, AND COSMID CONTIG AND 17 NEW POLYMORPHIC MARKERS FOR THE WERNER SYNDROME REGION AT 8P12-P21, Genomics, 35(3), 1996, pp. 431-440
THE CLINICAL PHENOTYPE OF 2 MISSENSE MUTATIONS IN THE PRESENILIN-I GENE IN JAPANESE PATIENTS
Authors: IKEDA M SHARMA V SUMI M ROGAEVA EA POORKAJ P SHERRINGTON R NEE L TSUDA T ODA N WATANABE M AOKI M SHOJI M ABE K ITOYAMA Y HIRAI S SCHELLENBERG GD BIRD TD STGEORGEHYSLOP PH
Citation: M. Ikeda et al., THE CLINICAL PHENOTYPE OF 2 MISSENSE MUTATIONS IN THE PRESENILIN-I GENE IN JAPANESE PATIENTS, Annals of neurology, 40(6), 1996, pp. 912-917
WIDE-RANGE IN AGE-OF-ONSET FOR CHROMOSOME 1-RELATED FAMILIAL ALZHEIMERS-DISEASE
Authors: BIRD TD LEVYLAHAD E POORKAJ P SHARMA V NEMENS E LAHAD A LAMPE TH SCHELLENBERG GD
Citation: Td. Bird et al., WIDE-RANGE IN AGE-OF-ONSET FOR CHROMOSOME 1-RELATED FAMILIAL ALZHEIMERS-DISEASE, Annals of neurology, 40(6), 1996, pp. 932-936
POSITIONAL CLONING OF THE WARNERS SYNDROME GENE
Authors: YU CE OSHIMA J FU YH WIJSMAN EM HISAMA F ALISCH R MATTHEWS S NAKURA J MIKI T OUAIS S MARTIN GM MULLIGAN J SCHELLENBERG GD
Citation: Ce. Yu et al., POSITIONAL CLONING OF THE WARNERS SYNDROME GENE, Science, 272(5259), 1996, pp. 258-262
Risultati: 1-25 | 26-50 | 51-71