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