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Träfflista för sökning "WFRF:(Edström L) srt2:(1995-1999)"

Sökning: WFRF:(Edström L) > (1995-1999)

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1.
  • GHANDOUR, AM, et al. (författare)
  • FE-57 MOSSBAUER STUDIES OF BA2+-DOPED POTASSIUM FERRITE
  • 1995
  • Ingår i: JOURNAL OF PHYSICS-CONDENSED MATTER. - : IOP PUBLISHING LTD. - 0953-8984. ; 7:28, s. 5657-5663
  • Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
    • Mossbauer spectroscopic study of the hexagonal beta-ferrite Ba0.45K0.39Fe11O17 has been undertaken between 10 K and 743 K. Below the magnetic transition temperature (T-N = 713 +/- 5 K) six magnetically split Fe3+ components can be fitted to our experiment
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2.
  • Xiang, F, et al. (författare)
  • A Huntington disease-like neurodegenerative disorder maps to chromosome 20p.
  • 1998
  • Ingår i: American Journal of Human Genetics. - : Elsevier BV. - 0002-9297 .- 1537-6605. ; 63:5, s. 1431-8
  • Tidskriftsartikel (refereegranskat)abstract
    • Huntington disease (HD) is an autosomal dominant neurodegenerative disorder characterized by motor disturbance, cognitive loss, and psychiatric manifestations. The disease is associated with a CAG trinucleotide-repeat expansion in the Huntington gene (IT15) on chromosome 4p16.3. One family with a history of HD was referred to us initially for predictive testing using linkage analysis. However, the chromosome 4p region was completely excluded by polymorphic markers, and later no CAG-repeat expansion in the HD gene was detected. To map the disease trait segregating in this family, whole-genome screening with highly polymorphic dinucleotide-, trinucleotide-, and tetranucleotide-repeat DNA markers was performed. A positive LOD score of 3.01 was obtained for the marker D20S482 on chromosome 20p, by two-point LOD-score analysis with the MLINK program. Haplotype analysis indicated that the gene responsible for the disease is likely located in a 2.7-cM region between the markers D20S193 and D20S895. Candidate genes from the mapping region were screened for mutations.
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