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  • Sjögren's syndrome  (1)
  • −α 4.2 Deletion  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Rheumatology international 10 (1990), S. 71-73 
    ISSN: 1437-160X
    Schlagwort(e): Complement receptor type 1 ; Ankylosing spondylitis ; Rheumatoid arthritis ; Gout ; Sjögren's syndrome ; Systemic lupus erythematosus
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary An investigation was conducted to measure the levels of erythrocyte complement receptor type 1 (CR1) in patients with various rheumatic diseases other than systemic lupus erythematosus, and to evaluate the clinical significance of this receptor in patients with ankylosing spondylitis (AS) and rheumatoid arthritis (RA). Erythrocyte CR1 was measured in 37 normal controls and 106 patients with various rheumatic diseases. The levels of erythrocyte CR1 decreased significantly in patients with AS, juvenile rheumatoid arthritis, Sjögren's syndrome, and RA, while there was no statistical difference in levels of erythrocyte CR1 between normal controls and patients with gouty arthritis. This suggests that erythrocyte CR1 deficiency may occur in immune-mediated rheumatic diseases, but not in nonimmune-mediated rheumatic diseases such as crystal-induced arthritis. In this study, we noted that the levels of erythrocyte CR1 were not related to the disease activity and severity of AS. The levels of erythrocyte CR1 were also not correlated with the clinical and laboratory parameters of disease activity in RA patients. However, there was a negative association between the levels of erythrocyte CR1 and titer of rheumtoid factor in RA patients. Further study is needed to determine whether or not the level of erythrocyte CR1 is related to prognosis in patients with RA.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1432-0584
    Schlagwort(e): −α 4.2 Deletion ; α-Thalassemia-2 ; −α G-Taichung
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary We sequenced part of the X boxes ofα-thalassemia-1 of Southeast Asia type (- -SEA) with−α 4.2,−α 3.7,−α G-Taichung, andα CSα. We found the X box of−α 3.7 belonged to the X box of α2 globin gene and the X box ofα csα contained X boxes of both al andα2 globin gene, whereas the X box of−α 4.2 and−α G-Taichung was a hybrid of X boxes of α2 and α1 globin gene. We also found there are two types of−α 4.2 deletion; type 1 is a common type of−α 4.2 deletion and type 2 is linkage to−α G-Taichung. We used a combination of two methods, the amplification refractory mutation system (ARMS) and the amplified created restriction sites (ACRS), to amplify the hybrids of X boxes specifically. The upstream primer for X box ofα2 globin gene was designed following the standard ARMS procedure to amplify the X segment of theα-globin gene. The downstream primer was designed according to the ACRS method to check the specificity of PCR products. Using this approach, we can diagnose the different types of−α 4.2 deletion. This kind of approach can also be used to amplify the specific region from the cluster of highly homologous genes.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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