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  • 1985-1989  (3)
  • 1985  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    International journal of legal medicine 94 (1985), S. 165-171 
    ISSN: 1437-1596
    Keywords: Plasminogen (PLG), Genetic polymorphism ; Paternity testing ; Plasminogen (PLG), Genetischer Polymorphismus ; Vaterschaftsuntersuchung
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Law
    Description / Table of Contents: Zusammenfassung Der genetisch determinierte Polymorphismus des Plasminogens (PLG) wurde mit der isoelektrischen Fokussierung auf Polyacrylamidgelen untersucht. Für die Untersuchungen wurden Neuraminidase behandelte Serumproben verwendet. Der PLG-Nachweis erfolgte funktionell durch Urokinaseaktivierung und darauffolgender Lyse von Casein im Agar-Overlay. Bei einer Stichprobe von 957 nichtverwandten, gesunden Personen aus dem süddeutschen Raum wurden drei häufige Phänotypen PLG1, 2-1 und 2 sowie fünf seltene Varianten gefunden. Folgende Allelfrequenzen wurden ermittelt: PLG*1=0,7174, PLG*2=0,2780 und PLG*Var=0,0046. Aufgrund unserer Untersuchungsergebnisse errechnet sich für das PLG-System eine theoretische Ausschlußchance von 16,5%.
    Notes: Summary The genetically determined polymorphism of plasminogen (PLG) was analyzed by isoelectric focusing on polyacrylamide gels. For analysis neuraminidase-pretreated sera were used. PLG was developed functionally by activation with urokinase and subsequent lysis of casein in an agar overlay. In a random sample of 957 unrelated healthy individuals from Southern Germany, three common phenotypes, PLG1, 2-1, and 2, and five rare variants were found. The allele frequencies were: PLG*1=0.7174, PLG*2=0.2780, and PLG*Var=0.0046. The theoretical exclusion rate in cases of disputed paternity is 16.5%.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Human genetics 〈Berlin〉 69 (1985), S. 284-286 
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Polyacrylamide gel isoelectric focusing (PAGIF) with carrier ampholytes was used for the determination of Tf phenotypes in a sample of 965 unrelated healthy blood donors from Tuscany (Italy). Thirteen rare variants in a heterozygote state were found (four Tf D, seven Tf B, and two rare Tf C subtypes). Among them two apparently new variants, tentatively called Tf C15 and Tf B4, were identified. The rare Tf B0 mutant was also observed.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Human genetics 〈Berlin〉 71 (1985), S. 27-29 
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The phenotypes of the protease inhibitor (PI) alpha-1-antitrypsin have been analyzed by isoelectric focusing on polyacrylamide gels. With improved resolution by a modified procedure it was possible to demonstrate a fifth PI*M suballele. The bands of PI M5 are located between PI M1 and PI M3. In addition, a further deficiency allele similar to PI*Z was found in a female patient with obstructive pulmonary disease. This variant was provisionally named PI Zaugsburg (PI Zaug). Family data confirm a simple codominant mode of inheritance for PI Zaug.
    Type of Medium: Electronic Resource
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