Vitamin D receptor gene polymorphism is associated with Graves' disease in the Japanese population

Journal of Clinical Endocrinology and Metabolism

Volumn 85, Issue 12, 2000, Pages 4639-4643

  Ban, Y ^a   Taniyama, M ^a  

^a SHOWA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOTOXIC T LYMPHOCYTE ANTIGEN 4; ENDONUCLEASE; HLA ANTIGEN; VITAMIN D RECEPTOR;

3' UNTRANSLATED REGION; ADULT; AGED; ARTICLE; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETIC RISK; GENOTYPE; GRAVES DISEASE; HUMAN; JAPAN; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RECEPTOR GENE;

AGED; ALLELES; BONE AND BONES; CALCITRIOL; DEOXYRIBONUCLEASES, TYPE II SITE-SPECIFIC; EXONS; FEMALE; GENOTYPE; GRAVES DISEASE; HUMANS; JAPAN; MALE; MIDDLE AGED; POLYMORPHISM, GENETIC; RECEPTORS, CALCITRIOL; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;

EID: 0034489819     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.85.12.4639     Document Type: Article

References (40)

1. The causes of autoimmune thyroid disease
2. Hyperthyroidism
3. Graves' disease
4. Human histocompatibility leukocyte antigen DQA1 *0501 allele associated with genetic susceptibility to Graves' disease in a Caucasian population
5. Susceptibility and resistance alleles of human leukocyte antigen (HLA) DQA1 and HLA DQB1 are shared in endocrine automunune disease
6. The cytotoxic T lymphocyte antigen-4 is a major Graves' disease locus
7. CTLA-4 gene polymorphism associated with Graves' disease in a Caucasian population
8. The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes
9. CTLA-4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus
10. CTLA-4 gene polymorphism confers susceptibility to Graves' disease in Japanese
11. Vitamin D receptor initiation codon polymorphism in Japanese patients with Graves' disease
12. Prediction of bone density from vitamin D receptor alleles
13. The RXR heterodimers and orphan receptors
14. A vitamin D receptor gene polymorphism in the translation initiation codon: Effect on protein activity and relation to bone mineral density in Japanese women
15. Vitamin D receptor alleles, bone mineral density and turnover in premenopausal Japanese women J Bone Miner Res
16. Strength of linkage disequilibrium between two vitamin D receptor markers in five ethnic groups: Implications for association studies
17. Association of prostate cancer risk with genetic polymorphisms in vitamin D receptor and androgen receptor
18. The presence of a polymorphism at the translation initiation site of the vitamin D receptor is associated with low bone mineral density in postmenopausal Mexican-American women
19. Lack of correlation between start codon polymorphism of the vitamin D receptor gene and bone mineral density in premenopausal French women: The OFELY study
20. The vitamin D receptor start codon polymorphism (FokI) and bone mineral density in premenopausal American black and white women
21. Vitamin D receptor genotypes in primary hyperparathyroidism
22. Vitamin D receptor (VDR) and parathyroid hormone mRNA levels correspond to polymorphic VDR alleles in human parathyroid tumors
23. Allelic variation in the vitamin D receptor influences susceptibility to IDDM in Indian Asians
24. Association of vitamin D receptor gene polymorphism with multiple sclerosis in Japanese
25. On estimating the relation between blood group and disease
26. Genetic influences on bone density: Physiological correlates of vitamin D receptor gene alleles in premenopausal women
27. The genetic basis of autoimmune thyroid disease: Time to focus on chromosomal loci other than the major histocompatibility complex
28. Genetics of autoimmune thyroid disease: Lack of evidence for linkage to HLA within families
29. No evidence for allelic association of human CTLA-4 promoter polymorphism with autoimmune thyroid disease in either population-based case-control or family-based studies
30. 3
31. The role of IL-12 in the induction of organ-specific autoimmune diseases
32. 3 on serum levels of thyroid hormones in hyperthyroid patients with untreated Graves' disease
33. Contribution of transacting factor alleles to normal physiological variability: Vitamin D receptor gene polymorphism and circulating osteocalcin
34. Vitamin D receptor genotypes and bone mineral density
35. Vitamin D receptor gene polymorphism and bone mineral density in healthy Japanese women
36. Mapping the major susceptibility loci for familial Graves' and Hashimoto's diseases: Evidence for genetic heterogeneity and gene interactions
37. Linkage analysis of candidate genes in autoimmune thyroid disease. III. Detailed analysis of chromosome 14 localizes GD-1 dose to MNG-1
38. A Graves' disease-susceptibility locus maps to chromosome 20q11.2
39. Linkage analysis of candidate genes in autoimmune thyroid disease. II. Selected gender-related genes and the X-chromosome
40. Linkage analysis of candidate genes in autoimmune thyroid disease. I. Selected immunoregulatory genes