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Results: 51-75/127
LINKAGE MAPPING OF MICRODISSECTED CLONES FROM DISTAL MOUSE CHROMOSOME-16
Authors: WEI JJ DLOUHY SR WANG Y ZHU JG FITZPATRICK L GHETTI B HODES ME
Citation: Jj. Wei et al., LINKAGE MAPPING OF MICRODISSECTED CLONES FROM DISTAL MOUSE CHROMOSOME-16, Somatic cell and molecular genetics, 22(3), 1996, pp. 227-232
CONGENITAL HYPOMYELINATING NEUROPATHY IN 2 CHILDREN WITH LONG-TERM FOLLOW-UP
Authors: PHILLIPS JP GHETTI B GARG BP
Citation: Jp. Phillips et al., CONGENITAL HYPOMYELINATING NEUROPATHY IN 2 CHILDREN WITH LONG-TERM FOLLOW-UP, Annals of neurology, 40(2), 1996, pp. 160-160
MOLECULAR-BASIS OF PHENOTYPIC VARIABILITY IN SPORADIC CREUTZFELDT-JAKOB-DISEASE
Authors: PARCHI P CASTELLANI R CAPELLARI S GHETTI B YOUNG K CHEN SG FARLOW M DICKSON DW SIMA AAF TROJANOWSKI JQ PETERSEN RB GAMBETTI P
Citation: P. Parchi et al., MOLECULAR-BASIS OF PHENOTYPIC VARIABILITY IN SPORADIC CREUTZFELDT-JAKOB-DISEASE, Annals of neurology, 39(6), 1996, pp. 767-778
PHENOTYPIC EFFECTS OF THE WEAVER GENE ARE EVIDENT IN THE EMBRYONIC CEREBELLUM BUT NOT IN THE VENTRAL MIDBRAIN
Authors: BAYER SA WILLS KV WEI JJ FENG Y DLOUHY SR HODES ME VERINA T GHETTI B
Citation: Sa. Bayer et al., PHENOTYPIC EFFECTS OF THE WEAVER GENE ARE EVIDENT IN THE EMBRYONIC CEREBELLUM BUT NOT IN THE VENTRAL MIDBRAIN, Developmental brain research, 96(1-2), 1996, pp. 130-137
PET STUDY OF GLUCOSE-METABOLISM IN AT-RISK AND AFFECTED PATIENTS WITHGERTSMANN-STRAEUSSLER-SCHEINKER DISEASE, INDIANA KINDRED
Authors: HUTCHINS GD FARLOW MR DLOUHY SR PICCARDO P GHETTI B
Citation: Gd. Hutchins et al., PET STUDY OF GLUCOSE-METABOLISM IN AT-RISK AND AFFECTED PATIENTS WITHGERTSMANN-STRAEUSSLER-SCHEINKER DISEASE, INDIANA KINDRED, The Journal of nuclear medicine, 37(5), 1996, pp. 1208-1208
DISTRIBUTION OF ABNORMALLY PHOSPHORYLATED-TAU IN GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE WITH MUTATION AT CODON-198 OF THE PRION PROTEIN GENE
Authors: GHETTI B PICCARDO P FARLOW MR DLOUHY SR TAGLIAVINI F GIACCONE G BUGIANI O
Citation: B. Ghetti et al., DISTRIBUTION OF ABNORMALLY PHOSPHORYLATED-TAU IN GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE WITH MUTATION AT CODON-198 OF THE PRION PROTEIN GENE, Neurology, 46(2), 1996, pp. 2065-2065
FAMILIAL AND SPORADIC ALZHEIMERS-DISEASE - NEUROPATHOLOGY CANNOT EXCLUDE A FINAL COMMON PATHWAY
Authors: LIPPA CF SAUNDERS AM SMITH TW SWEARER JM DRACHMAN DA GHETTI B NEE L PULASKISALO D DICKSON D ROBITAILLE Y BERGERON C CRAIN B BENSON MD FARLOW M HYMAN BT STGEORGEHYSLOP P ROSES AD POLLEN DA
Citation: Cf. Lippa et al., FAMILIAL AND SPORADIC ALZHEIMERS-DISEASE - NEUROPATHOLOGY CANNOT EXCLUDE A FINAL COMMON PATHWAY, Neurology, 46(2), 1996, pp. 406-412
VASCULAR VARIANT OF PRION PROTEIN CEREBRAL AMYLOIDOSIS WITH TAU-POSITIVE NEUROFIBRILLARY TANGLES - THE PHENOTYPE OF THE STOP CODON-145 MUTATION IN PRNP
Authors: GHETTI B PICCARDO P SPILLANTINI MG ICHIMIYA Y PORRO M PERINI F KITAMOTO T TATEISHI J SEILER C FRANGIONE B BUGIANI O GIACCONE G PRELLI F GOEDERT M DLOUHY SR TAGLIAVINI F
Citation: B. Ghetti et al., VASCULAR VARIANT OF PRION PROTEIN CEREBRAL AMYLOIDOSIS WITH TAU-POSITIVE NEUROFIBRILLARY TANGLES - THE PHENOTYPE OF THE STOP CODON-145 MUTATION IN PRNP, Proceedings of the National Academy of Sciences of the United Statesof America, 93(2), 1996, pp. 744-748
HEREDITARY MULTIPLE SYSTEM DEGENERATION WITH PRESENILE-DEMENTIA - TAU(TAU)-ABNORMALITIES IN NERVE-CELLS AND OLIGODENDROGLIA
Authors: GHETTI B FARLOW MR CROWTHER RA GOEDERT M SPILLANTINI MG
Citation: B. Ghetti et al., HEREDITARY MULTIPLE SYSTEM DEGENERATION WITH PRESENILE-DEMENTIA - TAU(TAU)-ABNORMALITIES IN NERVE-CELLS AND OLIGODENDROGLIA, Journal of neuropathology and experimental neurology, 55(5), 1996, pp. 12-12
THE MURINE GENE TIAM1 IS DIFFERENTIALLY EXPRESSED IN MOUSE-BRAIN AND DEVELOPMENTALLY-REGULATED IN CEREBELLAR GRANULE NEURONS
Authors: DLOUHY S WEI J FENG Y WANG Y GHETTI B HODES M
Citation: S. Dlouhy et al., THE MURINE GENE TIAM1 IS DIFFERENTIALLY EXPRESSED IN MOUSE-BRAIN AND DEVELOPMENTALLY-REGULATED IN CEREBELLAR GRANULE NEURONS, Journal of neuropathology and experimental neurology, 55(5), 1996, pp. 41-41
MULTIPLE ISOFORMS OF ALTERNATIVELY-SPLICED GIRK2 TRANSCRIPTS ARE DIFFERENTIALLY EXPRESSED IN MURINE CNS AND TESTIS
Authors: WEI J HODES M PIVA R WANG Y FENG Y GHETTI B DLOUHY S
Citation: J. Wei et al., MULTIPLE ISOFORMS OF ALTERNATIVELY-SPLICED GIRK2 TRANSCRIPTS ARE DIFFERENTIALLY EXPRESSED IN MURINE CNS AND TESTIS, Journal of neuropathology and experimental neurology, 55(5), 1996, pp. 42-42
MODALITIES OF CELL-DEATH IN WEAVER MUTANT MICE
Authors: MIGHELI A ATTANASIO A PIVA R WEI JJ HODES ME DLOUHY S GHETTI B
Citation: A. Migheli et al., MODALITIES OF CELL-DEATH IN WEAVER MUTANT MICE, Journal of neuropathology and experimental neurology, 55(5), 1996, pp. 63-63
TOPOGRAPHY OF PHOSPHORYLATED TAU-IMMUNOREACTIVITY IN ALZHEIMER-DISEASE, PROGRESSIVE SUPRANUCLEAR PALSY AND PICK DISEASE
Authors: GIACCONE G FRIGERIO L POLLO B GHETTI B TAGLIAVINI F BUGIANI O
Citation: G. Giaccone et al., TOPOGRAPHY OF PHOSPHORYLATED TAU-IMMUNOREACTIVITY IN ALZHEIMER-DISEASE, PROGRESSIVE SUPRANUCLEAR PALSY AND PICK DISEASE, Journal of neuropathology and experimental neurology, 55(5), 1996, pp. 118-118
PROTEINASE-K (PK) RESISTANT PRION PROTEIN (PRP) ISOFORMS IN GERSTMANN-STRAUSSLER-SCHEINKER DISEASE (GSS) F198S
Authors: PICCARDO P SEILER C DLOUHY S YOUNG K FARLOW M PRELLI F FRANGIONE B BUGIANI O TAGLIAVINI F GHETTI B
Citation: P. Piccardo et al., PROTEINASE-K (PK) RESISTANT PRION PROTEIN (PRP) ISOFORMS IN GERSTMANN-STRAUSSLER-SCHEINKER DISEASE (GSS) F198S, Journal of neuropathology and experimental neurology, 55(5), 1996, pp. 125-125
PROTEINASE-K-RESISTANT PRION PROTEIN ISOFORMS IN GERSTMANN-STRAUSSLER-SCHEINKER DISEASE (INDIANA KINDRED)
Authors: PICCARDO P SEILER C DLOUHY SR YOUNG K FARLOW MR PRELLI F FRANGIONE B BUGIANI O TAGLIAVINI F GHETTI B
Citation: P. Piccardo et al., PROTEINASE-K-RESISTANT PRION PROTEIN ISOFORMS IN GERSTMANN-STRAUSSLER-SCHEINKER DISEASE (INDIANA KINDRED), Journal of neuropathology and experimental neurology, 55(11), 1996, pp. 1157-1163
THE WEAVER MUTATION CHANGES THE ION SELECTIVITY OF THE AFFECTED INWARDLY RECTIFYING POTASSIUM CHANNEL GIRK2
Authors: TONG YH WEI JJ ZHANG SW STRONG JA DLOUHY SR HODES ME GHETTI B YU L
Citation: Yh. Tong et al., THE WEAVER MUTATION CHANGES THE ION SELECTIVITY OF THE AFFECTED INWARDLY RECTIFYING POTASSIUM CHANNEL GIRK2, FEBS letters, 390(1), 1996, pp. 63-68
PRP(27-30) IS A NORMAL SOLUBLE PRION PROTEIN-FRAGMENT RELEASED BY HUMAN PLATELETS
Authors: PERINI F VIDAL R GHETTI B TAGLIAVINI F FRANGIONE B PRELLI F
Citation: F. Perini et al., PRP(27-30) IS A NORMAL SOLUBLE PRION PROTEIN-FRAGMENT RELEASED BY HUMAN PLATELETS, Biochemical and biophysical research communications, 223(3), 1996, pp. 572-577
GERSTMANN-STRAUSSLER-SCHEINKER DISEASE AND THE INDIANA KINDRED
Authors: GHETTI B DLOUHY SR GIACCONE G BUGIANI O FRANGIONE B FARLOW MR TAGLIAVINI F
Citation: B. Ghetti et al., GERSTMANN-STRAUSSLER-SCHEINKER DISEASE AND THE INDIANA KINDRED, Brain pathology, 5(1), 1995, pp. 61-75
VENTRAL MESENCEPHALIC GRAFTS IN THE NEOSTRIATUM OF THE WEAVER MUTANT MOUSE - STRUCTURAL-MOLECULE AND RECEPTOR STUDIES
Authors: TRIARHOU LC SOLA C MENGOD G GARCIALADONA FJ LANDWEHRMEYER B GHETTI B PALACIOS JM
Citation: Lc. Triarhou et al., VENTRAL MESENCEPHALIC GRAFTS IN THE NEOSTRIATUM OF THE WEAVER MUTANT MOUSE - STRUCTURAL-MOLECULE AND RECEPTOR STUDIES, Cell transplantation, 4(1), 1995, pp. 39-48
ENDOGENOUS SEROTONIN RELEASE FROM THE DOPAMINE-DEFICIENT STRIATUM OF THE WEAVER MUTANT MOUSE
Authors: STOTZPOTTER EH GHETTI B SIMON JR
Citation: Eh. Stotzpotter et al., ENDOGENOUS SEROTONIN RELEASE FROM THE DOPAMINE-DEFICIENT STRIATUM OF THE WEAVER MUTANT MOUSE, Neurochemical research, 20(7), 1995, pp. 821-826
DOPAMINERGIC PARAMETERS IN THE STRIATUM AND SUBSTANTIA-NIGRA OF 7 STRAINS OF MICE - HIGHER DENSITY IN STRIATUM OF CAST COMPARED TO BALB MICE
Authors: RICHTER JA BRENNEMAN MG DLOUHY SR GHETTI B
Citation: Ja. Richter et al., DOPAMINERGIC PARAMETERS IN THE STRIATUM AND SUBSTANTIA-NIGRA OF 7 STRAINS OF MICE - HIGHER DENSITY IN STRIATUM OF CAST COMPARED TO BALB MICE, Neurochemical research, 20(4), 1995, pp. 395-400
DETECTION OF APOPTOSIS IN WEAVER CEREBELLUM BY ELECTRON-MICROSCOPIC IN-SITU END-LABELING OF FRAGMENTED DNA
Authors: MIGHELI A ATTANASIO A LEE WH BAYER SA GHETTI B
Citation: A. Migheli et al., DETECTION OF APOPTOSIS IN WEAVER CEREBELLUM BY ELECTRON-MICROSCOPIC IN-SITU END-LABELING OF FRAGMENTED DNA, Neuroscience letters, 199(1), 1995, pp. 53-56
ALTERED IGFBP5 GENE-EXPRESSION IN THE CEREBELLAR EXTERNAL GERMINAL LAYER OF WEAVER MUTANT MICE
Authors: LEE WH WANG GM LO T TRIARHOU LC GHETTI B
Citation: Wh. Lee et al., ALTERED IGFBP5 GENE-EXPRESSION IN THE CEREBELLAR EXTERNAL GERMINAL LAYER OF WEAVER MUTANT MICE, Molecular brain research, 30(2), 1995, pp. 259-268
DEGENERATION OF SERTOLI AND SPERMATOGENIC CELLS IN HOMOZYGOUS AND HETEROZYGOUS WEAVER MICE
Authors: VERINA T TANG X FITZPATRICK L NORTON J VOGELWEID C GHETTI B
Citation: T. Verina et al., DEGENERATION OF SERTOLI AND SPERMATOGENIC CELLS IN HOMOZYGOUS AND HETEROZYGOUS WEAVER MICE, Journal of neurogenetics, 9(4), 1995, pp. 251-265
GERSTMANN-STRAUSSLER-SCHEINKER DISEASE WITH MUTATION AT CODON-102 ANDMETHIONINE AT CODON-129 OF PRNP IN PREVIOUSLY UNREPORTED PATIENTS
Authors: YOUNG K JONES CK PICCARDO P LAZZARINI A GOLBE LI ZIMMERMAN TR DICKSON DW MCLACHLAN DC STGEORGEHYSLOP P LENNOX A PERLMAN S VINTERS HV HODES ME DLOUHY S GHETTI B
Citation: K. Young et al., GERSTMANN-STRAUSSLER-SCHEINKER DISEASE WITH MUTATION AT CODON-102 ANDMETHIONINE AT CODON-129 OF PRNP IN PREVIOUSLY UNREPORTED PATIENTS, Neurology, 45(6), 1995, pp. 1127-1134
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