메뉴 건너뛰기




Volumn 230, Issue 1, 2005, Pages 65-71

A novel loss-of-function deletion in sodium/iodide symporter gene in follicular thyroid adenoma

Author keywords

I 125 uptake assay; Iodide transport defect; Sodium iodide symporter; Thyroid carcinoma

Indexed keywords

IODINE 125; SODIUM IODIDE SYMPORTER;

EID: 27144491086     PISSN: 03043835     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.canlet.2004.12.036     Document Type: Article
Times cited : (8)

References (13)
  • 1
    • 0033922682 scopus 로고    scopus 로고
    • Molecular analysis of the sodium/iodide symporter: Impact on thyroid and extrathyroid pathophysiology
    • A. De La Vieja, O. Dohan, O. Levy, and N. Carrasco Molecular analysis of the sodium/iodide symporter: impact on thyroid and extrathyroid pathophysiology Physiol. Rev. 80 2000 1083 1105
    • (2000) Physiol. Rev. , vol.80 , pp. 1083-1105
    • De La Vieja, A.1    Dohan, O.2    Levy, O.3    Carrasco, N.4
  • 3
    • 0002083634 scopus 로고    scopus 로고
    • Carcinoma of the follicular epithelium
    • L.E. Braverman R. Utiger eighth ed. Lippincott Philadephia
    • E.L. Mazaferri Carcinoma of the follicular epithelium L.E. Braverman R. Utiger The Thyroid: A Fundamental and Clinical Text eighth ed. 2000 Lippincott Philadephia 904 930
    • (2000) The Thyroid: A Fundamental and Clinical Text , pp. 904-930
    • Mazaferri, E.L.1
  • 4
    • 0023277545 scopus 로고
    • Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction
    • C. Piotr, and S. Nicoletta Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction Anal. Biochem. 162 1987 156 159
    • (1987) Anal. Biochem. , vol.162 , pp. 156-159
    • Piotr, C.1    Nicoletta, S.2
  • 5
    • 0030735539 scopus 로고    scopus 로고
    • A homozygous missense mutation of the sodium/iodide symporter gene causing iodide transport defect
    • A. Matsuda, and S. Kosugi A homozygous missense mutation of the sodium/iodide symporter gene causing iodide transport defect J. Clin. Endocrinol. Metab. 82 1997 3966 3971
    • (1997) J. Clin. Endocrinol. Metab. , vol.82 , pp. 3966-3971
    • Matsuda, A.1    Kosugi, S.2
  • 6
    • 0031763451 scopus 로고    scopus 로고
    • High prevalence of T354P sodium/iodide symporter gene mutation in Japanese patients with iodide transport defect who have heterogeneous clinical pictures
    • S. Kosugi, Y. Sato, A. Matsuda, Y. Ohyama, K. Fujieda, H. Inomata, T. Kameya, O. Isozaki, and S.M. Jhiang High prevalence of T354P sodium/iodide symporter gene mutation in Japanese patients with iodide transport defect who have heterogeneous clinical pictures J. Clin. Endocrinol. Metab. 83 1998 4123 4129
    • (1998) J. Clin. Endocrinol. Metab. , vol.83 , pp. 4123-4129
    • Kosugi, S.1    Sato, Y.2    Matsuda, A.3    Ohyama, Y.4    Fujieda, K.5    Inomata, H.6    Kameya, T.7    Isozaki, O.8    Jhiang, S.M.9
  • 8
    • 0033304901 scopus 로고    scopus 로고
    • A novel mutation in the sodium/iodide symporter gene in the largest family with iodide transport defect
    • S. Kosugi, S. Bhyayana, and H.J. Dean A novel mutation in the sodium/iodide symporter gene in the largest family with iodide transport defect J. Clin. Endocrinol. Metab. 84 1999 3248 3253
    • (1999) J. Clin. Endocrinol. Metab. , vol.84 , pp. 3248-3253
    • Kosugi, S.1    Bhyayana, S.2    Dean, H.J.3
  • 9
    • 0033917722 scopus 로고    scopus 로고
    • A novel V59E missense mutation in the sodium iodide symporter gene in a family with iodide transport defect
    • H. Fujiwara, K. Tatsumi, S. Tanaka, M. Kimura, O. Nose, and N. Amino A novel V59E missense mutation in the sodium iodide symporter gene in a family with iodide transport defect Thyroid 10 2000 471 474
    • (2000) Thyroid , vol.10 , pp. 471-474
    • Fujiwara, H.1    Tatsumi, K.2    Tanaka, S.3    Kimura, M.4    Nose, O.5    Amino, N.6
  • 10
    • 0031576397 scopus 로고    scopus 로고
    • Hypothyroidism in a Brazilian kindred due to iodide trapping defect caused by a homozygous mutation in the sodium/iodide symporter gene
    • J. Pohlenz, G. Medeiros-Neto, J.L. Gross, S.P. Silveiro, M. Knobel, and S. Refetoff Hypothyroidism in a Brazilian kindred due to iodide trapping defect caused by a homozygous mutation in the sodium/iodide symporter gene Biochem. Biophys. Res. Commun. 240 1997 488 491
    • (1997) Biochem. Biophys. Res. Commun. , vol.240 , pp. 488-491
    • Pohlenz, J.1    Medeiros-Neto, G.2    Gross, J.L.3    Silveiro, S.P.4    Knobel, M.5    Refetoff, S.6
  • 11
    • 0032031728 scopus 로고    scopus 로고
    • Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3′ splice site
    • J. Pohlenz, I.M. Rosenthal, R.E. Weiss, S.M. Jhiang, C. Burant, and S. Refetoff Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3′ splice site J. Clin. Invest. 101 1998 1028 1035
    • (1998) J. Clin. Invest. , vol.101 , pp. 1028-1035
    • Pohlenz, J.1    Rosenthal, I.M.2    Weiss, R.E.3    Jhiang, S.M.4    Burant, C.5    Refetoff, S.6
  • 12
    • 0030053759 scopus 로고    scopus 로고
    • Cloning and characterization of the thyroid iodide transporter
    • G. Dai, O. Levy, and N. Carrasco Cloning and characterization of the thyroid iodide transporter Nature 279 1996 458 460
    • (1996) Nature , vol.279 , pp. 458-460
    • Dai, G.1    Levy, O.2    Carrasco, N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.