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  • Digitale Medien  (4)
  • Blutgruppen, Plasminogen (PLG)  (2)
  • 42.20  (1)
  • Biotin  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Plasminogen (PLG) polymorphism in northern Japanese: Confirmation of PLG*M6 allele (1989)
    Springer
    International journal of legal medicine 103 (1989), S. 43-45 
    Details
    ISSN: 1437-1596
    Schlagwort(e): Blood groups, plasminogen (PLG) polymorphism ; Plasminogen polymorphism in northern Japanese ; Blutgruppen, Plasminogen (PLG) ; Plasminogen-Polymorphismus, Nord-Japan
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin , Rechtswissenschaft
    Beschreibung / Inhaltsverzeichnis: Zusammenfassung Der genetische Polymorphismus des Plasminogen (PLG) wurde mit Hilfe der Isoelektrofokussierung und des Immunoblotting in einer Stichprobe von 450 nicht verwandten Personen aus der nördlichen Region Japans untersucht. Die folgende Allelfrequenzen wurden ermittelt: PLG*A =0.961, PLG*A3=0.009, PLG*M2=0.001, PLG*M5=0.016, PLG*M6= 0.001, PLG*B=0.003 and PLG*B2=0.009.
    Notizen: Summary Plasminogen (PLG) phenotyping has been performed on 450 unrelated individuals from northern Japan, using wide-scale ultrathin layer polyacrylamide gel isoelectric focusing combined with immunoblotting. One common phenotype and six rare ones were observed. The rare phenotypes included the recently detected allele PLG*M6 in a new combination with PLG*M5 allele. The estimated allele frequencies for PLG*A, PLG*A3, PLG*M2, PLG*M5, PLG*M6, PLG*B, and PLG*B2 were 0.961, 0.009, 0.001, 0.016, 0.001, 0.003, and 0.009, respectively.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/BF01255845
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Mechanism of speckle reduction in laser-microscope images using a rotating optical fiber (1985)
    Springer
    Applied physics 38 (1985), S. 71-78 
    Details
    ISSN: 1432-0649
    Schlagwort(e): 42.20 ; 42.30 ; 42.80
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract The reduction mechanism of speckles appearing in laser-microscope images is studied theoretically and experimentally when an object is illuminated by laser light through a rotating multimode optical fiber. The principle of the speckle reduction is based on independent addition of microscope images with boiling-like speckles as a result of the rotational motion of the optical fiber used for illumination. Especially, the speckle reduction is evaluated from first-order statistics of the speckle intensity in which its saturation effect is taken into consideration.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/BF00691773
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Plasminogen (PLG) polymorphism in northern Japanese: Confirmation of PLG*M6 allele (1989)
    Springer
    International journal of legal medicine 103 (1989), S. 43-45 
    Details
    ISSN: 1437-1596
    Schlagwort(e): Blood groups, plasminogen (PLG) polymorphism ; Plasminogen polymorphism in northern Japanese ; Blutgruppen, Plasminogen (PLG) ; Plasminogen-Polymorphismus, Nord-Japan
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin , Rechtswissenschaft
    Beschreibung / Inhaltsverzeichnis: Zusammenfassung Der genetische Polymorphismus des Plasminogen (PLG) wurde mit Hilfe der Isoelektrofokussierung und des Immunoblotting in einer Stichprobe von 450 nicht verwandten Personen aus der nördlichen Region Japans untersucht. Die folgende Allelfrequenzen wurden ermittelt: PLG*A = 0.961, PLG*A3 = 0.009, PLG*M2 = 0.001, PLG*M5 = 0.016, PLG*M6 = 0.001, PLG*B = 0.003 und PLG*B2 = 0.009.
    Notizen: Summary Plasminogen (PLG) phenotyping has been performed on 450 unrelated individuals from northern Japan, using wide-scale ultrathin layer polyacrylamide gel isoelectric focusing combined with immunoblotting. One common phenotype and six rare ones were observed. The rare phenotypes included the recently detected allele PLG*M6 in a new combination with PLG*M5 allele. The estimated allele frequencies for PLG*A, PLG*A3, PLG*M2, PLG*M5, PLG*M6, PLG*B, and PLG*B2 were 0.961, 0.009, 0.001, 0.016, 0.001, 0.003, and 0.009, respectively.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/BF00203942
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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    Artikel (Nationallizenzen)
    Volltext
  • 4
    Digitale Medien
    Digitale Medien
    Haplotype analysis suggests that the two predominant mutations in Japanese patients with holocarboxylase synthetase deficiency are founder mutations (2000)
    Springer
    Journal of human genetics 45 (2000), S. 358-362 
    Details
    ISSN: 1435-232X
    Schlagwort(e): Key words Holocarboxylase synthetase ; Multiple carboxylase deficiency ; Biotin ; Mutation ; Microsatellite markers ; Haplotype
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Abstract Holocarboxylase synthetase (HCS) deficiency is a rare autosomal recessive disorder of biotin metabolism. Including three new Japanese patients we diagnosed in this study, ten Japanese families have, so far, been accumulated. In these families, the mutations 237Leu 〉 Pro (sevenalleles) and 1067delG (five alleles) were predominant; 508Arg 〉 Trp and 550Val 〉 Met mutations were identified in three families in the heterozygous form and in one patient in the homozygous form, respectively. To determine the origin of these mutations, we identified new polymorphic microsatellite markers in the HCS gene and analyzed the haplotypes of the patients. All the 237Leu 〉 Pro and the 1067delG alleles were associated with haplotype 2-2. This finding is consistent with the notion that these mutations are founder mutations in the Japanese population. Three Japanese 508Arg 〉 Trp alleles were associated with several haplotypes, including 2-3 and 1-4. The haplotype of a Taiwanese patient homozygous for the 508Arg 〉 Trp mutation was 2-3/2-3. The haplotype of one Japanese patient homozygous for the 550Val 〉 Met mutation was 1-4/1-4, whereas that of a Jewish patient with the same homozygous mutation was 2-3/2-3. Both mutations were associated with at least two haplotypes and were found in several ethnic groups. The changes 508Arg 〉 Trp and 550Val 〉 Met occurred at CpG dinucleotide. The data suggest that these two mutations represent a mutational hot-spot.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/s100380070008
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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