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Volumn 216, Issue 5, 2011, Pages 571-578

SLC26A4 expression among autoimmune thyroid tissues

Author keywords

Autoimmune thyroid diseases; Graves' disease; Hashimoto thyroiditis; Immunofluorescence; Pendrin; Real time PCR

Indexed keywords

PENDRIN; THYROGLOBULIN; THYROTROPIN;

EID: 79953274323     PISSN: 01712985     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.imbio.2010.09.015     Document Type: Article
Times cited : (8)

References (59)
  • 1
    • 48249155076 scopus 로고    scopus 로고
    • Molecular mechanisms of epithelial cell-specific expression and regulation of the human anion exchanger (pendrin) gene
    • Adler L., Efrati E., Zelikovic I. Molecular mechanisms of epithelial cell-specific expression and regulation of the human anion exchanger (pendrin) gene. Am. J. Physiol. Cell. Physiol. 2008, 294:1261-1276.
    • (2008) Am. J. Physiol. Cell. Physiol. , vol.294 , pp. 1261-1276
    • Adler, L.1    Efrati, E.2    Zelikovic, I.3
  • 3
    • 0034904523 scopus 로고    scopus 로고
    • Expression pattern of the pendrin and sodium/iodide symporter genes in human thyroid carcinoma cell lines and human thyroid tumors
    • Arturi F., Russo D., Bidart J.M., Scarpelli D., Schlumberger M., Filetti S. Expression pattern of the pendrin and sodium/iodide symporter genes in human thyroid carcinoma cell lines and human thyroid tumors. Eur. J. Endocrinol. 2001, 145:129-135.
    • (2001) Eur. J. Endocrinol. , vol.145 , pp. 129-135
    • Arturi, F.1    Russo, D.2    Bidart, J.M.3    Scarpelli, D.4    Schlumberger, M.5    Filetti, S.6
  • 6
    • 67649836744 scopus 로고    scopus 로고
    • Minireview: the sodium-iodide symporter NIS and pendrin in iodide homeostasis of the thyroid
    • Bizhanova A., Kopp P. Minireview: the sodium-iodide symporter NIS and pendrin in iodide homeostasis of the thyroid. Endocrinology 2009, 150:1084-1090.
    • (2009) Endocrinology , vol.150 , pp. 1084-1090
    • Bizhanova, A.1    Kopp, P.2
  • 9
    • 79953278430 scopus 로고    scopus 로고
    • Response to: the c.-103T>C variant in the 5'-UTR of SLC26A4 gene: a pathogenic mutation or coincidental polymorphism?
    • Choi B.Y., Alper S.L., Griffith A.J. Response to: the c.-103T>C variant in the 5'-UTR of SLC26A4 gene: a pathogenic mutation or coincidental polymorphism?. Hum. Mutat. 2009, 30:1471.
    • (2009) Hum. Mutat. , vol.30 , pp. 1471
    • Choi, B.Y.1    Alper, S.L.2    Griffith, A.J.3
  • 11
    • 0033999085 scopus 로고    scopus 로고
    • In situ hybridization and immunohistochemistry study of thyroid peroxidase expression in thyroid tumors
    • De Micco C., Kopp F., Vassko V., Grino M. In situ hybridization and immunohistochemistry study of thyroid peroxidase expression in thyroid tumors. Thyroid 2000, 10:109-115.
    • (2000) Thyroid , vol.10 , pp. 109-115
    • De Micco, C.1    Kopp, F.2    Vassko, V.3    Grino, M.4
  • 12
    • 0025732156 scopus 로고
    • Immunohistochemical study of thyroid peroxidase in normal, hyperplastic, and neoplastic human thyroid tissues
    • De Micco C., Ruf J., Chrestian M.A., Gros N., Henry J.F., Carayon P. Immunohistochemical study of thyroid peroxidase in normal, hyperplastic, and neoplastic human thyroid tissues. Cancer 1991, 67:3036-3041.
    • (1991) Cancer , vol.67 , pp. 3036-3041
    • De Micco, C.1    Ruf, J.2    Chrestian, M.A.3    Gros, N.4    Henry, J.F.5    Carayon, P.6
  • 14
    • 0036317991 scopus 로고    scopus 로고
    • Androgen-dependent expression of FcgammaRIIB2 by thyrocytes from patients with autoimmune Graves' disease: a possible molecular clue for sex dependence of autoimmune disease
    • Estienne V., Duthoit C., Reichert M., Praetor A., Carayon P., Hunziker W., Ruf J. Androgen-dependent expression of FcgammaRIIB2 by thyrocytes from patients with autoimmune Graves' disease: a possible molecular clue for sex dependence of autoimmune disease. FASEB J. 2002, 16:1087-1092.
    • (2002) FASEB J. , vol.16 , pp. 1087-1092
    • Estienne, V.1    Duthoit, C.2    Reichert, M.3    Praetor, A.4    Carayon, P.5    Hunziker, W.6    Ruf, J.7
  • 16
    • 0033578352 scopus 로고    scopus 로고
    • Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear
    • Everett L.A., Morsli H., Wu D.K., Green E.D. Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear. Proc. Natl. Acad. Sci. U. S. A. 1999, 96:9727-9732.
    • (1999) Proc. Natl. Acad. Sci. U. S. A. , vol.96 , pp. 9727-9732
    • Everett, L.A.1    Morsli, H.2    Wu, D.K.3    Green, E.D.4
  • 17
    • 0346154518 scopus 로고
    • Association of congenital deafness with goitre (Pendred's syndrome): a study of 207 families
    • Fraser G.R. Association of congenital deafness with goitre (Pendred's syndrome): a study of 207 families. Ann. Hum. Genet. 1965, 28:201-249.
    • (1965) Ann. Hum. Genet. , vol.28 , pp. 201-249
    • Fraser, G.R.1
  • 20
    • 1842581804 scopus 로고    scopus 로고
    • Functional characterization of pendrin in a polarized cell system: evidence for pendrin-mediated apical iodide efflux
    • Gillam M.P., Sidhaye A.R., Lee E.J., Rutishauser J., Stephan C.W., Kopp P. Functional characterization of pendrin in a polarized cell system: evidence for pendrin-mediated apical iodide efflux. J. Biol. Chem. 2004, 279:13004-13010.
    • (2004) J. Biol. Chem. , vol.279 , pp. 13004-13010
    • Gillam, M.P.1    Sidhaye, A.R.2    Lee, E.J.3    Rutishauser, J.4    Stephan, C.W.5    Kopp, P.6
  • 21
  • 22
    • 0024514347 scopus 로고
    • The WHO histological classification of thyroid tumors: a commentary on the second edition
    • Hedinger C., Williams E.D., Sobin L.H. The WHO histological classification of thyroid tumors: a commentary on the second edition. Cancer 1989, 63:908-911.
    • (1989) Cancer , vol.63 , pp. 908-911
    • Hedinger, C.1    Williams, E.D.2    Sobin, L.H.3
  • 30
    • 73149096698 scopus 로고    scopus 로고
    • Thyroglobulin (Tg) induces thyroid cell growth in a concentration-specific manner by a mechanism other than thyrotropin/cAMP stimulation
    • Noguchi Y., Harii N., Giuliani C., Tatsuno I., Suzuki K., Kohn L.D. Thyroglobulin (Tg) induces thyroid cell growth in a concentration-specific manner by a mechanism other than thyrotropin/cAMP stimulation. Biochem. Biophys. Res. Commun. 2009, 391:890-894.
    • (2009) Biochem. Biophys. Res. Commun. , vol.391 , pp. 890-894
    • Noguchi, Y.1    Harii, N.2    Giuliani, C.3    Tatsuno, I.4    Suzuki, K.5    Kohn, L.D.6
  • 31
    • 50549149000 scopus 로고
    • Deaf mutism and goitre
    • Pendred V. Deaf mutism and goitre. Lancet 1896, 11:532.
    • (1896) Lancet , vol.11 , pp. 532
    • Pendred, V.1
  • 32
    • 17344392308 scopus 로고    scopus 로고
    • A new mathematical model for relative quantification in real-time RT-PCR
    • Pfaffl M.W. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 2001, 29(9):e45.
    • (2001) Nucleic Acids Res. , vol.29 , Issue.9
    • Pfaffl, M.W.1
  • 33
    • 0036581160 scopus 로고    scopus 로고
    • ©) for group-wise comparison and statistical analysis of relative expression results in real-time PCR
    • ©) for group-wise comparison and statistical analysis of relative expression results in real-time PCR. Nucleic Acids Res. 2002, 30(9):e36.
    • (2002) Nucleic Acids Res. , vol.30 , Issue.9
    • Pfaffl, M.W.1    Horgan, G.W.2    Dempfle, L.3
  • 39
    • 0037225536 scopus 로고    scopus 로고
    • Prolactin regulation of the pendrin-iodide transporter in the mammary gland
    • Rillema J.A., Hill M.A. Prolactin regulation of the pendrin-iodide transporter in the mammary gland. Am. J. Physiol. Endocrinol. Metab. 2003, 284:E25-E28.
    • (2003) Am. J. Physiol. Endocrinol. Metab. , vol.284
    • Rillema, J.A.1    Hill, M.A.2
  • 42
    • 0141729459 scopus 로고    scopus 로고
    • Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in Pendred syndrome
    • Royaux I.E., Belyantseva I.A., Wu T., Kachar B., Everett L.A., Marcus D.C., Green E.D. Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in Pendred syndrome. J. Assoc. Res. Otolaryngol. 2003, 4:394-404.
    • (2003) J. Assoc. Res. Otolaryngol. , vol.4 , pp. 394-404
    • Royaux, I.E.1    Belyantseva, I.A.2    Wu, T.3    Kachar, B.4    Everett, L.A.5    Marcus, D.C.6    Green, E.D.7
  • 43
    • 0034463973 scopus 로고    scopus 로고
    • Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells
    • Royaux I.E., Suzuki K., Mori A., Katoh R., Everett L.A., Kohn L.D., Green E.D. Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells. Endocrinology 2000, 141:839-845.
    • (2000) Endocrinology , vol.141 , pp. 839-845
    • Royaux, I.E.1    Suzuki, K.2    Mori, A.3    Katoh, R.4    Everett, L.A.5    Kohn, L.D.6    Green, E.D.7
  • 44
    • 0035957363 scopus 로고    scopus 로고
    • Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion
    • Royaux I.E., Wall S.M., Karniski L.P., Everett L.A., Suzuki K., Knepper M.A., Green E.D. Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion. Proc. Natl. Acad. Sci. U. S. A. 2001, 98:4221-4226.
    • (2001) Proc. Natl. Acad. Sci. U. S. A. , vol.98 , pp. 4221-4226
    • Royaux, I.E.1    Wall, S.M.2    Karniski, L.P.3    Everett, L.A.4    Suzuki, K.5    Knepper, M.A.6    Green, E.D.7
  • 45
    • 0033990048 scopus 로고    scopus 로고
    • Primer 3 on the WWW for general users and for biologist programmers
    • Humana Press, Totowa, NJ, S. Krawetz, S. Misener (Eds.)
    • Rozen S., Skaletsky H.J. Primer 3 on the WWW for general users and for biologist programmers. Bioinformatics Methods and Protocols: Methods in Molecular Biology 2000, 365-386. Humana Press, Totowa, NJ. S. Krawetz, S. Misener (Eds.).
    • (2000) Bioinformatics Methods and Protocols: Methods in Molecular Biology , pp. 365-386
    • Rozen, S.1    Skaletsky, H.J.2
  • 46
    • 0024430122 scopus 로고
    • Relationship between immunological structure and biochemical properties of human thyroid peroxidase
    • Ruf J., Toubert M.E., Czarnocka B., Durand-Gorde J.M., Ferrand M., Carayon P. Relationship between immunological structure and biochemical properties of human thyroid peroxidase. Endocrinology 1989, 125:1211-1218.
    • (1989) Endocrinology , vol.125 , pp. 1211-1218
    • Ruf, J.1    Toubert, M.E.2    Czarnocka, B.3    Durand-Gorde, J.M.4    Ferrand, M.5    Carayon, P.6
  • 48
    • 0034235222 scopus 로고    scopus 로고
    • Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4)
    • Scott D.A., Wang R., Kreman T.M., Andrews M., McDonald J.M., Bishop J.R., Smith R.J., Karniski L.P., Sheffield V.C. Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4). Hum. Mol. Genet. 2000, 9:1709-1715.
    • (2000) Hum. Mol. Genet. , vol.9 , pp. 1709-1715
    • Scott, D.A.1    Wang, R.2    Kreman, T.M.3    Andrews, M.4    McDonald, J.M.5    Bishop, J.R.6    Smith, R.J.7    Karniski, L.P.8    Sheffield, V.C.9
  • 51
    • 33646811842 scopus 로고    scopus 로고
    • Differential regulation of apical and basal iodide transporters in the thyroid by thyroglobulin
    • Suzuki K., Kohn L.D. Differential regulation of apical and basal iodide transporters in the thyroid by thyroglobulin. J. Endocrinol. 2006, 189:247-255.
    • (2006) J. Endocrinol. , vol.189 , pp. 247-255
    • Suzuki, K.1    Kohn, L.D.2
  • 53
    • 0036283790 scopus 로고    scopus 로고
    • Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome
    • Taylor J.P., Metcalfe R.A., Watson P.F., Weetman A.P., Trembath R.C. Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome. J. Clin. Endocrinol. Metab. 2002, 87:1778-1784.
    • (2002) J. Clin. Endocrinol. Metab. , vol.87 , pp. 1778-1784
    • Taylor, J.P.1    Metcalfe, R.A.2    Watson, P.F.3    Weetman, A.P.4    Trembath, R.C.5
  • 56
    • 73349102851 scopus 로고    scopus 로고
    • The c.-103T>C variant in the 5'-UTR of SLC26A4 gene: a pathogenic mutation or coincidental polymorphism?
    • Yang T., Smith R.J. The c.-103T>C variant in the 5'-UTR of SLC26A4 gene: a pathogenic mutation or coincidental polymorphism?. Hum. Mutat. 2009, 30:1469-1470.
    • (2009) Hum. Mutat. , vol.30 , pp. 1469-1470
    • Yang, T.1    Smith, R.J.2
  • 57
    • 34250803246 scopus 로고    scopus 로고
    • Transcriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4)
    • Yang T., Vidarsson H., Rodrigo-Blomqvist S., Rosengren S.S., Enerback S., Smith R.J. Transcriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4). Am. J. Hum. Genet. 2007, 80:1055-1063.
    • (2007) Am. J. Hum. Genet. , vol.80 , pp. 1055-1063
    • Yang, T.1    Vidarsson, H.2    Rodrigo-Blomqvist, S.3    Rosengren, S.S.4    Enerback, S.5    Smith, R.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.