메뉴 건너뛰기




Volumn 10, Issue 7, 2004, Pages 302-305

The thyroglobulin gene: The third locus for autoimmune thyroid disease or a false dawn?

Author keywords

[No Author keywords available]

Indexed keywords

AUTOANTIGEN; CYTOTOXIC T LYMPHOCYTE ANTIGEN 4; HLA DQA1 ANTIGEN; HLA DQB1 ANTIGEN; HLA DR ANTIGEN;

EID: 3042835169     PISSN: 14714914     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molmed.2004.05.001     Document Type: Short Survey
Times cited : (6)

References (32)
  • 1
    • 0017757504 scopus 로고
    • The spectrum of thyroid disease in a community: The Whickham Survey
    • Tunbridge W.M.G., et al. The spectrum of thyroid disease in a community: The Whickham Survey. Clin. Endocrinol. (Oxf.). 7:1977;481-493
    • (1977) Clin. Endocrinol. (Oxf.) , vol.7 , pp. 481-493
    • Tunbridge, W.M.G.1
  • 2
    • 0034718938 scopus 로고    scopus 로고
    • Graves' disease
    • Weetman A.P. Graves' disease. N. Engl. J. Med. 343:2000;1236-1248
    • (2000) N. Engl. J. Med. , vol.343 , pp. 1236-1248
    • Weetman, A.P.1
  • 3
    • 0032510388 scopus 로고    scopus 로고
    • Mortality after the treatment of hyperthyroidism with radioactive iodine
    • Franklyn J.A., et al. Mortality after the treatment of hyperthyroidism with radioactive iodine. N. Engl. J. Med. 338:1998;712-718
    • (1998) N. Engl. J. Med. , vol.338 , pp. 712-718
    • Franklyn, J.A.1
  • 4
    • 0035883894 scopus 로고    scopus 로고
    • Prediction of all-cause and cardiovascular mortality in elderly people from one low serum thyrotropin result: A 10-year cohort study
    • Parle J.V., et al. Prediction of all-cause and cardiovascular mortality in elderly people from one low serum thyrotropin result: a 10-year cohort study. Lancet. 358:2001;861-865
    • (2001) Lancet , vol.358 , pp. 861-865
    • Parle, J.V.1
  • 6
    • 0037648405 scopus 로고    scopus 로고
    • Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease
    • Ueda H., et al. Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease. Nature. 423:2003;506-511
    • (2003) Nature , vol.423 , pp. 506-511
    • Ueda, H.1
  • 7
    • 0035875097 scopus 로고    scopus 로고
    • 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
    • Sakai K., et al. 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. Hum. Mol. Genet. 10:2001;1379-1386
    • (2001) Hum. Mol. Genet. , vol.10 , pp. 1379-1386
    • Sakai, K.1
  • 8
    • 0142059659 scopus 로고    scopus 로고
    • Common and unique susceptibility loci in Graves and Hashimoto diseases: Results of whole-genome screening in a data set of 102 multiplex families
    • Tomer Y., et al. Common and unique susceptibility loci in Graves and Hashimoto diseases: results of whole-genome screening in a data set of 102 multiplex families. Am. J. Hum. Genet. 73:2003;736-747
    • (2003) Am. J. Hum. Genet. , vol.73 , pp. 736-747
    • Tomer, Y.1
  • 9
    • 0036149916 scopus 로고    scopus 로고
    • Thyroglobulin is a thyroid specific gene for the familial autoimmune thyroid diseases
    • Tomer Y., et al. Thyroglobulin is a thyroid specific gene for the familial autoimmune thyroid diseases. J. Clin. Endocrinol. Metab. 87:2002;404-407
    • (2002) J. Clin. Endocrinol. Metab. , vol.87 , pp. 404-407
    • Tomer, Y.1
  • 10
    • 0344303638 scopus 로고    scopus 로고
    • Amino acid substitutions in the thyroglobulin gene are associated with susceptibility to human and murine autoimmune thyroid disease
    • Ban Y., et al. Amino acid substitutions in the thyroglobulin gene are associated with susceptibility to human and murine autoimmune thyroid disease. Proc. Natl. Acad. Sci. U. S. A. 100:2003;15119-15124
    • (2003) Proc. Natl. Acad. Sci. U. S. A. , vol.100 , pp. 15119-15124
    • Ban, Y.1
  • 11
    • 0028877463 scopus 로고
    • Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
    • Lander E., et al. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat. Genet. 11:1995;241-247
    • (1995) Nat. Genet. , vol.11 , pp. 241-247
    • Lander, E.1
  • 12
    • 0035209177 scopus 로고    scopus 로고
    • Large upward bias in estimation of locus-specific effects from genomewide scans
    • Goring H.H., et al. Large upward bias in estimation of locus-specific effects from genomewide scans. Am. J. Hum. Genet. 69:2001;1357-1369
    • (2001) Am. J. Hum. Genet. , vol.69 , pp. 1357-1369
    • Goring, H.H.1
  • 13
    • 0033304849 scopus 로고    scopus 로고
    • Mapping the major susceptibility loci for familial Graves' and Hashimoto's diseases: Evidence for genetic heterogeneity and gene interactions
    • Tomer Y., et al. Mapping the major susceptibility loci for familial Graves' and Hashimoto's diseases: evidence for genetic heterogeneity and gene interactions. J. Clin. Endocrinol. Metab. 84:1999;4656-4664
    • (1999) J. Clin. Endocrinol. Metab. , vol.84 , pp. 4656-4664
    • Tomer, Y.1
  • 14
    • 0032952468 scopus 로고    scopus 로고
    • Freely associating
    • (1999) Freely associating. Nat Genet. 22, 1-2.
    • (1999) Nat Genet. , vol.22 , pp. 1-2
  • 15
    • 0037309889 scopus 로고    scopus 로고
    • In search of genetic precision
    • (2003) In search of genetic precision. Lancet 361, 357.
    • (2003) Lancet , vol.361 , pp. 357
  • 16
    • 18544380387 scopus 로고    scopus 로고
    • Parameters for reliable results in genetic association studies in common disease
    • Dahlman I., et al. Parameters for reliable results in genetic association studies in common disease. Nat. Genet. 30:2002;149-150
    • (2002) Nat. Genet. , vol.30 , pp. 149-150
    • Dahlman, I.1
  • 17
    • 0037426052 scopus 로고    scopus 로고
    • Problems of reporting genetic associations with complex outcomes
    • Colhoun H.M., et al. Problems of reporting genetic associations with complex outcomes. Lancet. 361:2003;865-872
    • (2003) Lancet , vol.361 , pp. 865-872
    • Colhoun, H.M.1
  • 18
    • 0242383308 scopus 로고    scopus 로고
    • Association of a rare thyroglobulin gene microsatellite variant with autoimmune thyroid disease
    • Collins J.E., et al. Association of a rare thyroglobulin gene microsatellite variant with autoimmune thyroid disease. J. Clin. Endocrinol. Metab. 88:2003;5039-5042
    • (2003) J. Clin. Endocrinol. Metab. , vol.88 , pp. 5039-5042
    • Collins, J.E.1
  • 19
    • 0030716833 scopus 로고    scopus 로고
    • Genetic susceptibility to the development of autoimmune disease
    • Heward J., et al. Genetic susceptibility to the development of autoimmune disease. Clin. Sci. (Lond.). 93:1997;479-491
    • (1997) Clin. Sci. (Lond.) , vol.93 , pp. 479-491
    • Heward, J.1
  • 20
    • 0036329099 scopus 로고    scopus 로고
    • Cathepsin S inhibitor prevents autoantigen presentation and autoimmunity
    • Saegusa K., et al. Cathepsin S inhibitor prevents autoantigen presentation and autoimmunity. J. Clin. Invest. 110:2002;361-369
    • (2002) J. Clin. Invest. , vol.110 , pp. 361-369
    • Saegusa, K.1
  • 21
    • 0031902882 scopus 로고    scopus 로고
    • Iodination of human thyroglobulin (Tg) alters its immunoreactivity. II. Fine specificity of a monoclonal antibody that recognizes iodinated Tg
    • Saboori A.M., et al. Iodination of human thyroglobulin (Tg) alters its immunoreactivity. II. Fine specificity of a monoclonal antibody that recognizes iodinated Tg. Clin. Exp. Immunol. 113:1998;303-308
    • (1998) Clin. Exp. Immunol. , vol.113 , pp. 303-308
    • Saboori, A.M.1
  • 22
    • 0031878623 scopus 로고    scopus 로고
    • Iodination of human thyroglobulin (Tg) alters its immunoreactivity. I. Iodination alters multiple epitopes of human Tg
    • Saboori A.M., et al. Iodination of human thyroglobulin (Tg) alters its immunoreactivity. I. Iodination alters multiple epitopes of human Tg. Clin. Exp. Immunol. 113:1998;297-302
    • (1998) Clin. Exp. Immunol. , vol.113 , pp. 297-302
    • Saboori, A.M.1
  • 23
    • 0028871202 scopus 로고
    • Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus
    • Bennett S.T., et al. Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus. Nat. Genet. 9:1995;284-292
    • (1995) Nat. Genet. , vol.9 , pp. 284-292
    • Bennett, S.T.1
  • 24
    • 0028151819 scopus 로고
    • Negative selection of lymphocytes
    • Nossal G.J. Negative selection of lymphocytes. Cell. 76:1994;229-239
    • (1994) Cell , vol.76 , pp. 229-239
    • Nossal, G.J.1
  • 25
    • 0031018819 scopus 로고    scopus 로고
    • Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus
    • Vafiadis P., et al. Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus. Nat. Genet. 15:1997;289-292
    • (1997) Nat. Genet. , vol.15 , pp. 289-292
    • Vafiadis, P.1
  • 26
    • 0034454508 scopus 로고    scopus 로고
    • A heterozygous deletion of the autoimmune regulator (AIRE1) gene, autoimmune thyroid disease, and type 1 diabetes: No evidence for association
    • Nithiyananthan R., et al. A heterozygous deletion of the autoimmune regulator (AIRE1) gene, autoimmune thyroid disease, and type 1 diabetes: no evidence for association. J. Clin. Endocrinol. Metab. 85:2000;1320-1322
    • (2000) J. Clin. Endocrinol. Metab. , vol.85 , pp. 1320-1322
    • Nithiyananthan, R.1
  • 27
    • 1542374068 scopus 로고    scopus 로고
    • Assessing Whether an Allele Can Account in Part for a Linkage Signal: The Genotype-IBD Sharing Test (GIST)
    • Li C., et al. Assessing Whether an Allele Can Account in Part for a Linkage Signal: The Genotype-IBD Sharing Test (GIST). Am. J. Hum. Genet. 74:2004;418-431
    • (2004) Am. J. Hum. Genet. , vol.74 , pp. 418-431
    • Li, C.1
  • 28
    • 0022359205 scopus 로고
    • The genetics of Graves' disease: HLA and disease susceptibility
    • Stenszky V., et al. The genetics of Graves' disease: HLA and disease susceptibility. J. Clin. Endocrinol. Metab. 61:1985;735-740
    • (1985) J. Clin. Endocrinol. Metab. , vol.61 , pp. 735-740
    • Stenszky, V.1
  • 29
    • 0028873470 scopus 로고
    • CTLA-4 gene polymorphism associated with Graves' disease in a Caucasian population
    • Yanagawa T., et al. CTLA-4 gene polymorphism associated with Graves' disease in a Caucasian population. J. Clin. Endocrinol. Metab. 80:1995;41-45
    • (1995) J. Clin. Endocrinol. Metab. , vol.80 , pp. 41-45
    • Yanagawa, T.1
  • 30
    • 0037442092 scopus 로고    scopus 로고
    • Population stratification and spurious allelic association
    • Cardon L.R., et al. Population stratification and spurious allelic association. Lancet. 361:2003;598-604
    • (2003) Lancet , vol.361 , pp. 598-604
    • Cardon, L.R.1
  • 31
    • 85086950471 scopus 로고    scopus 로고
    • A call for accurate phenotype definition in the study of complex disorders
    • Funalot B., et al. A call for accurate phenotype definition in the study of complex disorders. Nat. Genet. 36:2004;3
    • (2004) Nat. Genet. , vol.36 , pp. 3
    • Funalot, B.1
  • 32
    • 0037312921 scopus 로고    scopus 로고
    • Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease
    • Lohmueller K.E., et al. Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease. Nat. Genet. 33:2003;177-182
    • (2003) Nat. Genet. , vol.33 , pp. 177-182
    • Lohmueller, K.E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.