17 results on '"Dlouhy, S R"'
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2. ALPHA-SYNUCLEIN DEPOSITS IN THE SUBSTANTIA NIGRA OF INDIVIDUALS WITH GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE (F198S-129V).
3. INSOMNIA IN FAMILIAL CREUTZFELDT JAKOB DISEASE (FCJD), E200K, WITH THALAMIC INVOLVEMENT.
4. A CELL CYCLE ALTERATION PRECEDES APOPTOSIS OF GRANULE CELL PRECURSORS IN THE WEAVER MOUSE CEREBELLUM.
5. CREUTZFELDT JAKOB DISEASE (CJD) WITH PRION PROTEIN GENE (PRNP) V2101 MUTATION.
6. Ahall polymorphism in human X-linked proteolipid protein gene (PLP).
7. PRION PROTEIN ISOFORMS IN THE NEW VARIANT OF GERSTMAN-STRÄUSSLER-SCHEINKER DISEASE Q212P.
8. GENOMIC ORGANIZATION OF Girk2, A POTASSIUM CHANNEL GENE IN MICE.
9. SPECIFIC. NON-POLYADENYLATED TRANSCRIPTS OF Girk2 AND Tiam1 ARE PRESENT DURING MURINE CNS DEVELOPMENT.
10. GERSTMANN-STRÄUSSLER-SCHEINKER (GSS) DISEASE WITH THE PRION PROTEIN GENE (PRNP) P102L MUTATION AND LOWER MOTOR NEURON DEGENERATION.
11. AN ANTISERUM TO RESIDUES 95-108 OF HUMAN PRP DETECTS PRPres IN A VARIETY OF HUMAN AND ANIMAL PRION DISEASES.
12. GENETIC STRAIN BACKGROUND INFLUENCES THE PHENOTYPIC EFFECTS OF THE MOUSE WEAVER GENE.
13. GENETIC MAPPING OF GENOMIC MARKERS DERIVED BY MICRO-DISSECTION OP THE DISTAL PORTION OF MOUSE CHROMOSOME 16.
14. GERSTMANN-STRÄUSSLER-SCHEINKER (GSS) DISEASE WITH SPINAL ATROPHY.
15. ONLY MUTANT PRP PARTICIPATES IN AMYLOID FORMATION IN GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE WITH ALA>VAL SUBSTITUTION AT CODON 117.
16. PELIZAEUS-MERZBACHER DISEASE CAUSED BY DE NOVO MUTATION.
17. MOLECULAR CHARACTERIZATION OF TWO NOVEL cDNAS OBTAINED BY ANTIBODY SCREENING OF A HOUSE CEREBELLAR cDNA EXPRESSION LIBRARY.
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