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Volumn 20, Issue 10, 2006, Pages 2584-2590

A novel hypothyroid dwarfism due to the missense mutation Arg479Cys of the thyroid peroxidase gene in the mouse

Author keywords

[No Author keywords available]

Indexed keywords

LIOTHYRONINE; PEROXIDASE; THYROID HORMONE; THYROID PEROXIDASE; THYROTROPIN; THYROXINE;

EID: 33749357065     PISSN: 08888809     EISSN: 08888809     Source Type: Journal    
DOI: 10.1210/me.2006-0099     Document Type: Article
Times cited : (15)

References (33)
  • 3
    • 24944524163 scopus 로고    scopus 로고
    • A mutant mouse with severe anemia and skin abnormalities controlled by a new allele of the flaky skin (fsn) locus
    • Takabayashi T, Katoh H 2005 A mutant mouse with severe anemia and skin abnormalities controlled by a new allele of the flaky skin (fsn) locus. Exp Anim 54:339-347
    • (2005) Exp Anim , vol.54 , pp. 339-347
    • Takabayashi, T.1    Katoh, H.2
  • 4
    • 0001560622 scopus 로고
    • Dwarf, a new Mendelian recessive character of the house mouse
    • Snell GD 1929 Dwarf, a new Mendelian recessive character of the house mouse. Proc Natl Acad Sci USA 15:733-734
    • (1929) Proc Natl Acad Sci USA , vol.15 , pp. 733-734
    • Snell, G.D.1
  • 5
    • 0019305553 scopus 로고
    • New mouse dw allele: Genetic location and effects on lifespan and growth hormone levels
    • Eicher EM, Beamer WG 1980 New mouse dw allele: genetic location and effects on lifespan and growth hormone levels. J Hered 71:187-190
    • (1980) J Hered , vol.71 , pp. 187-190
    • Eicher, E.M.1    Beamer, W.G.2
  • 7
    • 0025885764 scopus 로고
    • Localization of the panhypopituitary dwarf mutation (df) on mouse chromosome 11 in an intersubspecific backcross
    • Buckwalter MS, Katz RW, Camper SA 1991 Localization of the panhypopituitary dwarf mutation (df) on mouse chromosome 11 in an intersubspecific backcross. Genomics 10:515-526
    • (1991) Genomics , vol.10 , pp. 515-526
    • Buckwalter, M.S.1    Katz, R.W.2    Camper, S.A.3
  • 8
    • 0017078016 scopus 로고
    • Inherited ateliotic dwarfism in mice: Characteristics of the mutation, little, on chromosome 6
    • Eicher EM, Beamer WG 1976 Inherited ateliotic dwarfism in mice: characteristics of the mutation, little, on chromosome 6. J Hered 67:87-91
    • (1976) J Hered , vol.67 , pp. 87-91
    • Eicher, E.M.1    Beamer, W.G.2
  • 13
    • 0025242757 scopus 로고
    • The Pit-1 transcription factor gene is a candidate for the murine Snell dwarf mutation
    • Camper SA, Saunders TL, Katz RW, Reeves RH 1990 The Pit-1 transcription factor gene is a candidate for the murine Snell dwarf mutation. Genomics 8:586-590
    • (1990) Genomics , vol.8 , pp. 586-590
    • Camper, S.A.1    Saunders, T.L.2    Katz, R.W.3    Reeves, R.H.4
  • 15
    • 0025582645 scopus 로고
    • Tissuespecific expression of the growth hormone gene and its control by growth hormone factor-1
    • Karin M, Theill L, Castrillo J-L, McCormic A, Brady H 1990 Tissuespecific expression of the growth hormone gene and its control by growth hormone factor-1. Recent Prog Horm Res 46:43-58
    • (1990) Recent Prog Horm Res , vol.46 , pp. 43-58
    • Karin, M.1    Theill, L.2    Castrillo, J.-L.3    McCormic, A.4    Brady, H.5
  • 16
    • 0027236844 scopus 로고
    • Molecular basis of the little mouse phenotype and implications for cell type-specific growth
    • Lin SC, Lin CR, Gukovsky I, Lusis AJ, Sawchenko PE, Rosenfeld MG 1993 Molecular basis of the little mouse phenotype and implications for cell type-specific growth. Nature 364:208-213
    • (1993) Nature , vol.364 , pp. 208-213
    • Lin, S.C.1    Lin, C.R.2    Gukovsky, I.3    Lusis, A.J.4    Sawchenko, P.E.5    Rosenfeld, M.G.6
  • 18
    • 0026742738 scopus 로고
    • Linkage of the thyroid peroxidase locus (Tpo) to markers in the proximal part of chromosome 12 of the mouse
    • Taylor BA, Reifsnyder PC, DiLauro R 1992 Linkage of the thyroid peroxidase locus (Tpo) to markers in the proximal part of chromosome 12 of the mouse. Cytogenet Cell Genet 60:250-251
    • (1992) Cytogenet Cell Genet , vol.60 , pp. 250-251
    • Taylor, B.A.1    Reifsnyder, P.C.2    DiLauro, R.3
  • 20
    • 0029887742 scopus 로고    scopus 로고
    • Thyroid peroxidase: Experimental and clinical integration
    • Ohtaki S, Nakagawa H, Nakamura M, Kotani T 1996 Thyroid peroxidase: experimental and clinical integration. Endocr J 43:1-14
    • (1996) Endocr J , vol.43 , pp. 1-14
    • Ohtaki, S.1    Nakagawa, H.2    Nakamura, M.3    Kotani, T.4
  • 21
  • 22
    • 0033756917 scopus 로고    scopus 로고
    • Two decades of screening for congenital hypothyroidism in the Netherlands: TPO gene mutations in total iodide organification defects
    • Bakker B, Bikker H, Vulsma T, de Randamie JS, Wiedijk BM, De Vijlder JJ 2000 Two decades of screening for congenital hypothyroidism in The Netherlands: TPO gene mutations in total iodide organification defects. J Clin Endocrinol Metab 85:3708-3712
    • (2000) J Clin Endocrinol Metab , vol.85 , pp. 3708-3712
    • Bakker, B.1    Bikker, H.2    Vulsma, T.3    De Randamie, J.S.4    Wiedijk, B.M.5    De Vijlder, J.J.6
  • 23
    • 0036120080 scopus 로고    scopus 로고
    • Mutation analysis of thyroid peroxidase gene in Chinese patients with total iodide organification defect: Identification of five novel mutations
    • Wu JY, Shu SG, Yang CF, Lee CC, Tsai FJ 2002 Mutation analysis of thyroid peroxidase gene in Chinese patients with total iodide organification defect: identification of five novel mutations. J Endocrinol 172:627-635
    • (2002) J Endocrinol , vol.172 , pp. 627-635
    • Wu, J.Y.1    Shu, S.G.2    Yang, C.F.3    Lee, C.C.4    Tsai, F.J.5
  • 25
    • 0032974611 scopus 로고    scopus 로고
    • A novel mutation in the human thyroid peroxidase gene resulting in a total iodide organification defect
    • Kotani T, Umeki K, Yamamoto I, Maesaka H, Tachibana K, Ohtaki S 1999 A novel mutation in the human thyroid peroxidase gene resulting in a total iodide organification defect. J Endocrinol 160:267-273
    • (1999) J Endocrinol , vol.160 , pp. 267-273
    • Kotani, T.1    Umeki, K.2    Yamamoto, I.3    Maesaka, H.4    Tachibana, K.5    Ohtaki, S.6
  • 27
    • 0345647163 scopus 로고
    • Congenital hypothyroidism
    • 18-21:24-28
    • Gruters A 1992 Congenital hypothyroidism. Pediatr Ann 21:15, 18-21:24-28
    • (1992) Pediatr Ann , vol.21 , pp. 15
    • Gruters, A.1
  • 28
    • 0006862997 scopus 로고
    • Turnip peroxidase. II. The reaction mechanisms of turnip peroxidase A1, A2 and D
    • Hosoya T 1960 Turnip peroxidase. II. The reaction mechanisms of turnip peroxidase A1, A2 and D. J Biochem 47:794
    • (1960) J Biochem , vol.47 , pp. 794
    • Hosoya, T.1
  • 29
    • 0014077322 scopus 로고
    • A study of the hemoprotein of thyroid microsomes with emphasis on the thyroid peroxidase
    • Hosoya T, Morrison M 1967 A study of the hemoprotein of thyroid microsomes with emphasis on the thyroid peroxidase. Biochemistry 6:1021-1026
    • (1967) Biochemistry , vol.6 , pp. 1021-1026
    • Hosoya, T.1    Morrison, M.2
  • 30
    • 0021813042 scopus 로고
    • Characterization of a monoclonal antibody to hog thyroid peroxidase and its use for immuno-histochemical localization of the peroxidase in the thyroid gland
    • Nakagawa H, Kotani T, Ohtaki S, Kawano J, Aikawa E, Imagawa M, Hashida S, Ishikawa E 1985 Characterization of a monoclonal antibody to hog thyroid peroxidase and its use for immuno-histochemical localization of the peroxidase in the thyroid gland. J Biochem 97:1709-1718
    • (1985) J Biochem , vol.97 , pp. 1709-1718
    • Nakagawa, H.1    Kotani, T.2    Ohtaki, S.3    Kawano, J.4    Aikawa, E.5    Imagawa, M.6    Hashida, S.7    Ishikawa, E.8
  • 31
    • 0017184389 scopus 로고
    • A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
    • Bradford MM 1976 A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248-254
    • (1976) Anal Biochem , vol.72 , pp. 248-254
    • Bradford, M.M.1
  • 33
    • 0036231997 scopus 로고    scopus 로고
    • Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism
    • Umeki K, Kotani T, Kawano J, Suganuma T, Yamamoto I, Aratake Y, Furujo M, Ichiba Y 2002 Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism. Eur J Endocrinol 146:491-498
    • (2002) Eur J Endocrinol , vol.146 , pp. 491-498
    • Umeki, K.1    Kotani, T.2    Kawano, J.3    Suganuma, T.4    Yamamoto, I.5    Aratake, Y.6    Furujo, M.7    Ichiba, Y.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.