Neigung zu autoimmunbedingten Schilddrüsenerkrankungen
Verschiedenen genetische Loci sind identifiziert worden, die mit autoimmunbedingten Schilddrüsenerkrankungen, wie Hashimoto-Thyreoiditid und Morbus Basedow assoziiert sind.
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. |
Caturegli P et. al. (2000) Hypothyroidism in transgenic mice expressing IFN-gamma in the thyroid. [^] |
| 4. |
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. [^] |
| 5. |
Shirasawa S et. al. (2004) SNPs in the promoter of a B cell-specific antisense transcript, SAS-ZFAT, determine susceptibility to autoimmune thyroid disease. [^] |
| 6. |
Hodge SE et. al. (1981) Close genetic linkage between diabetes mellitus and kidd blood group. [^] |
| 7. |
Merriman T et. al. (1997) Evidence by allelic association-dependent methods for a type 1 diabetes polygene (IDDM6) on chromosome 18q21. [^] |
| 8. |
Vaidya B et. al. (2000) Evidence for a new Graves disease susceptibility locus at chromosome 18q21. [^] |
| 9. |
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. [^] |
| 10. |
Collins JE et. al. (2003) Association of a rare thyroglobulin gene microsatellite variant with autoimmune thyroid disease. [^] |
| 11. |
Tomer Y et. al. (1999) Mapping the major susceptibility loci for familial Graves' and Hashimoto's diseases: evidence for genetic heterogeneity and gene interactions. [^] |
| 12. |
Klintschar M et. al. (2001) Evidence of fetal microchimerism in Hashimoto's thyroiditis. [^] |
| 13. |
Alkhateeb A et. al. (2002) Mapping of an autoimmunity susceptibility locus (AIS1) to chromosome 1p31.3-p32.2. [^] |
| 14. |
Ochi H et. al. (2002) Proteomic analysis of human brain identifies alpha-enolase as a novel autoantigen in Hashimoto's encephalopathy. [^] |
| 15. |
Vaidya B et. al. (2002) The genetics of autoimmune thyroid disease. [^] |
| 16. |
Allen EM et. al. (2003) A genome-wide scan for autoimmune thyroiditis in the Old Order Amish: replication of genetic linkage on chromosome 5q11.2-q14.3. [^] |
| 17. |
Ueda H et. al. (2003) Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease. [^] |
| 18. |
Akamizu T et. al. (2003) Association study of autoimmune thyroid disease at 5q23-q33 in Japanese patients. [^] |
| 19. |
HALL R et. al. (1962) A study of the parents of patients with Hashimoto's disease. [^] |
| 20. |
VOLPE R et. al. (1963) Genetic factors in Hashimoto's struma. [^] |
| 21. |
HALL R et. al. (1964) PATERNAL TRANSMISSION OF THYROID AUTOIMMUNITY. [^] |
| 22. |
MASI AT et. al. (1965) HASHIMOTO'S DISEASE. AN EPIDEMIOLOGICAL CRITIQUE. [^] |
| 23. |
Barbero P et. al. (2004) Choanal atresia associated with prenatal methimazole exposure: three new patients. [^] |
| 24. |
Criswell LA et. al. (2005) Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes. [^] |
| 25. |
Invernizzi P et. al. (2005) X chromosome monosomy: a common mechanism for autoimmune diseases. [^] |
