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  • 1
    ISSN: 1432-0584
    Keywords: an auto-anti-B in a regular A1B blood group ; no hemolytic disease
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Das Serum eines Patienten (Mr. Lat) mit der normalen Blutgruppe A1B enthält Anti-B, das mit allen Zellen reagiert, die ein B-Antigen aufweisen, ausgenommen Bx und cis AB. Das Anti-B reagiert bei 4° C und gelegentlich bei Zimmertemperatur, was durch Agglutination, Absorption-Elution und durch thermodynamische Unter-suchungen gezeigt wurde. Der Antikörper wird als irregulärer Autoantikörper angesehen, der zur Gruppe der „supprimierten“ oder „latenten“ Antikörper gehört.
    Notes: Summary The serum of a patient (Mr. Lat) with the regular blood group A1B contains an anti-B reacting with all cells having a B antigen except bx and cis AB. The anti-B reacts at 4° C and occasionally at room temperature as shown by agglutination, absorption-elution and by thermo-dynamic assays. The antibody is regarded as an irregular autoantibody belonging to the group of the so called “suppressed” or “latent” antibodies.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Human genetics 〈Berlin〉 58 (1981), S. 411-413 
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A new variant of the PGM a 1 erythrocyte enzyme system not identical with the known variants of the system has been detected in the hemolyzed red blood cells of a healthy blood donor by isoelectric focusing. Using this technique the variant is represented by two bands, a strong and slow one more cathodically located than the a3 band and a weak one in the position of the a2 band. Using agarose thinlayer or acetate foil electrophoresis the variant is represented only by a minimal cathodic broadening of the PGM1 1 band and therefore it is easily overlooked. Investigation of the propositus' family shows that the variant occurs combined with the common alleles PGM 1 a1 , PGM 1 a2 , and PGM 1 a3 and that it has an autosomal dominant inheritance. Obviously the variant has a very low frequency.
    Type of Medium: Electronic Resource
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