Neigung zu autoimmunbedingten Schilddrüsenerkrankungen 3
Der Typ 3 der Neigung zu autoimmunbedingten Schilddrüsenerkrankungen wird durch Polymorphismen im ZFAT- und TG-Gen verursacht.
Gliederung
Referenzen:
| 1. |
Ban Y et. al. (2003) Amino acid substitutions in the thyroglobulin gene are associated with susceptibility to human and murine autoimmune thyroid disease. [^] |
| 2. |
Collins JE et. al. (2004) Common allelic variants of exons 10, 12, and 33 of the thyroglobulin gene are not associated with autoimmune thyroid disease in the United Kingdom. [^] |
| 3. |
Sakai K et. al. (2001) Identification of susceptibility loci for autoimmune thyroid disease to 5q31-q33 and Hashimoto's thyroiditis to 8q23-q24 by multipoint affected sib-pair linkage analysis in Japanese. [^] |
| 4. |
Shirasawa S et. al. (2004) SNPs in the promoter of a B cell-specific antisense transcript, SAS-ZFAT, determine susceptibility to autoimmune thyroid disease. [^] |
| 5. |
Tomer Y et. al. (2003) Common and unique susceptibility loci in Graves and Hashimoto diseases: results of whole-genome screening in a data set of 102 multiplex families. [^] |
| 6. |
Collins JE et. al. (2003) Association of a rare thyroglobulin gene microsatellite variant with autoimmune thyroid disease. [^] |
| 7. |
Tomer Y et. al. (1999) Mapping the major susceptibility loci for familial Graves' and Hashimoto's diseases: evidence for genetic heterogeneity and gene interactions. [^] |
| 8. |
Tomer Y et. al. (2002) Thyroglobulin is a thyroid specific gene for the familial autoimmune thyroid diseases. [^] |
