54 results on '"Ghetti, B"'
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2. Intracellular Ferritin Accumulation in Neural and Extraneural Tissue Characterizes a Neurodegenerative Disease Associated with a Mutation in theFerritin Light PolypeptideGene
3. NEUROPATHOLOGICAL CHANGES AND APOLIPOPROTEIN E GENOTYPE IN ALZHEIMERʼS DISEASE (AD) WITH CONCOMITANT LEWY BODIES
4. CREUTZFELDT JAKOB DISEASE (CJD) WITH PRION PROTEIN GENE (PRNP) V2101 MUTATION
5. A CELL CYCLE ALTERATION PRECEDES APOPTOSIS OF GRANULE CELL PRECURSORS IN THE WEAVER MOUSE CEREBELLUM
6. PICK DISEASE WITH GLIAL TAU INCLUSIONS IN THE WHITE MATTER
7. AN INTRON MUTATION IN THE PRION PROTEIN GENE (PRNP)
8. INSOMNIA IN FAMILIAL CREUTZFELDT JAKOB DISEASE (FCJD), E200K, WITH THALAMIC INVOLVEMENT
9. NEUROPATHOLOGICAL CHANGES AND APOLIPOPROTEIN E GENOTYPE IN ALZHEIMERʼS DISEASE (AD) WITH CONCOMITANT LEWY BODIES
10. NEUROLOGICAL ILLNESS IN TRANSGENIC MICE EXPRESSING A PRION PROTEIN WITH AN INSERTIONAL MUTATION
11. GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE (GSS) WITH A MUTATION AT PRION PROTEIN (PrP) RESIDUE 212
12. LACK OF apoE GENE REDUCES AMYLOID FORMATION IN TRANSGENIC MICE OVEREXPRESSING APPV717F
13. PRION PROTEIN ISOFORMS IN THE NEW VARIANT OF GERSTMAN-STRÄUSSLER-SCHEINKER DISEASE Q212P
14. DISTINCTIVE PrP ISOFOMS IN GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE WITH TANGLES
15. GENOMIC ORGANIZATION OF Girk2, A POTASSIUM CHANNEL GENE IN MICE
16. GENETIC STRAIN BACKGROUND INFLUENCES THE PHENOTYPIC EFFECTS OF THE MOUSE WEAVER GENE
17. AN ANTISERUM TO RESIDUES 95–108 OF HUMAN PRP DETECTS PRPres IN A VARIETY OF HUMAN AND ANIMAL PRION DISEASES
18. GERSTMANN-STRÄUSSLER-SCHEINKER (GSS) DISEASE WITH THE PRION PROTEIN GENE (PRNP) P102L MUTATION AND LOWER MOTOR NEURON DEGENERATION
19. TOPOGRAPHY OF AT8 IMMUNOREACTIVITY IN GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE, INDIANA KINDRED
20. SPECIFIC. NON-POLYADENYLATED TRANSCRIPTS OF Girk2 AND Tiam1 ARE PRESENT DURING MURINE CNS DEVELOPMENT
21. PRION PROTEIN (PrP) AMYLOID COEXISTS WITH NEUROFIBRILLARY TANGLES AND LEWY BODIES IN A PATIENT FROM A NEW FAMILY OF GERSTMANN STRÄUSSLER SCHEINKER DISEASE (GSS)
22. GENE MAP OF THE MSTD (MULTIPLE SYSTEM TAUOPATHY WITH PRESENILE DEMENTIA) REGION ON HUMAN CHROMOSOME 17q21–22
23. PROTEINASE K (PK) RESISTANT PRION PROTEIN (PRP) ISOFORMS IN GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE (GSS) F198S
24. MULTIPLE ISOFORMS OF ALTERNATIVELY-SPLICED GIRK2 TRANSCRIPTS ARE DIFFERENTIALLY EXPRESSED IN MURINE CNS AND TESTIS
25. TOPOGRAPHY OF PHOSPHORYLATED TAU IMMUNOREACTIVITY IN ALZHEIMER DISEASE, PROGRESSIVE SUPRANUCLEAR PALSY AND PICK DISEASE
26. THE MURINE GENE TIAMI IS DIFFERENTIALLY EXPRESSED IN MOUSE BRAIN AND DEVELOPMENTALLY REGULATED IN CEREBELLAR GRANULE NEURONS
27. MODALITIES OF CELL DEATH IN WEAVER MUTANT MICE
28. HEREDITARY MULTIPLE SYSTEM DEGENERATION WITH PRESENILE DEMENTIA
29. PROTEASE-RESISTANT PRION PROTEIN IN SPORADIC CREUTZFELDT-JAKOB DISEASE (CJD)
30. ONLY MUTANT PRP PARTICIPATES IN AMYLOID FORMATION IN GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE WITH ALA>VAL SUBSTITUTION AT CODON 117
31. GERSTMANN-STRÄUSSLER-SCHEINKER (GSS) DISEASE WITH SPINAL ATROPHY
32. LATE-GENERATED MIDBRAIN DOPAMINERGIC NEURONS ARE TARGETS OF LETHAL WEAVER GENE ACTION
33. GENETIC MAPPING OF GENOMIC MARKERS DERIVED BY MICRO-DISSECTION OP THE DISTAL PORTION OF MOUSE CHROMOSOME 16
34. JUVENILE ALZHEIMER DISEASE WITH ATAXIA
35. MOLECULAR CHARACTERIZATION OF TWO NOVEL cDNAS OBTAINED BY ANTIBODY SCREENING OF A HOUSE CEREBELLAR cDNA EXPRESSION LIBRARY
36. MONOAMINERGIC INTERACTIONS IN THE WEAVER MOUSE NEO-STRIATUM
37. 79 CEREBELLAR ATROPHY IN ALUMINUM ENCEPHALOPATHY
38. STUDIES ON THE PURKINJE CELL DEGENERATION (pcd) MUTANT: PRIMARY PATHOLOGY AND TRANSNEURONAL CHANGES
39. A FAMILIAL PARKINSON-DEMENTIA-ATAXIA SYNDROME WITH KURU-LIKE PLAQUES IN THE CEREBELLUM
40. UP-REGULATION OF B2 RECEPTORS IN THE STRIATUM OF WEAVER MUTANT MICE.
41. PROGRESSIVE SUPRANUCLEAR PALSY (PSP)
42. NERVE CELL ATROPHY AND LOSS IN THE INFERIOR OLIVARY COMPLEX OF PURKINJE CELL DEGENERATION (ved) MUTANT MICE
43. MONOAMINERGIC NERVE TERMINALS SURVIVE THE LOSS OF THEIR TARGET PURKINJE CELLS IN THE CEREBELLAR CORTEX OF PURKINJE CELL DEGENERATION (pcd) MUTANT MICE
44. CATECHOLAMINE CONCENTRATION IN THE CEREBELLUM OF PURKINJE CELL DEGENERATION (pcd) MUTANT MICE
45. ASYMMETRIC CEREBRAL ATROPHY IN ALZHEIMERʼS DISEASE
46. ABNORMAL PHOSPHORYLATION OF NEUROFILAMENTS FOLLOWING ADMINISTRATION OF ANTIMITOTIC DRUGS
47. LONG-TERM SURVIVAL OF VENTRAL MESENCEPHALIC GRAFTS REINNERVATING THE NEOSTRIATUM OF ADULT WEAVER MUTANT MICE.
48. ALUMINUM (Al) POWDER INDUCES A SLOWLY PROGRESSING ENCEPHALOMYELOPATHY IN ADULT RABBITS
49. NEUROCHEMICAL STUDIES ON THE CEREBELLUM OF THE PURKINJE CELL DEGENERATION (pcd) MUTANT
50. 44 IMMUNOCYTOCHEMICAL CHARACTERIZATION OF THE NEUROFIBRILLARY TANGLES IN MAYTANSINE ENCEPHALOPATHY
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