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309 related items for PubMed ID: 8345041

  • 1. Thyroxine interactions with transthyretin: a comparison of 10 different naturally occurring human transthyretin variants.
    Rosen HN, Moses AC, Murrell JR, Liepnieks JJ, Benson MD.
    J Clin Endocrinol Metab; 1993 Aug; 77(2):370-4. PubMed ID: 8345041
    [Abstract] [Full Text] [Related]

  • 2. Threonine for alanine substitution at position 109 of transthyretin differentially alters human transthyretin's affinity for iodothyronines.
    Rosen HN, Murrell JR, Liepnieks JJ, Benson MD, Cody V, Moses AC.
    Endocrinology; 1994 Jan; 134(1):27-34. PubMed ID: 8275943
    [Abstract] [Full Text] [Related]

  • 3. A new family with hyperthyroxinemia caused by transthyretin Val109 misdiagnosed as thyrotoxicosis and resistance to thyroid hormone--a clinical research center study.
    Refetoff S, Marinov VS, Tunca H, Byrne MM, Sunthornthepvarakul T, Weiss RE.
    J Clin Endocrinol Metab; 1996 Sep; 81(9):3335-40. PubMed ID: 8784093
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  • 4. Thyroxine binding in a TTR Met 119 kindred.
    Alves IL, Divino CM, Schussler GC, Altland K, Almeida MR, Palha JA, Coelho T, Costa PP, Saraiva MJ.
    J Clin Endocrinol Metab; 1993 Aug; 77(2):484-8. PubMed ID: 8102146
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  • 5. [Thyroxine-binding proteins--familial euthyroid hyperthyroxinemia due to point mutations of transthyretin].
    Hishinuma A, Mochizuki Y, Kasai K, Shimoda S.
    Nihon Rinsho; 1994 Apr; 52(4):886-9. PubMed ID: 8196175
    [Abstract] [Full Text] [Related]

  • 6. Drug competition for thyroxine binding to transthyretin (prealbumin): comparison with effects on thyroxine-binding globulin.
    Munro SL, Lim CF, Hall JG, Barlow JW, Craik DJ, Topliss DJ, Stockigt JR.
    J Clin Endocrinol Metab; 1989 Jun; 68(6):1141-7. PubMed ID: 2498384
    [Abstract] [Full Text] [Related]

  • 7. Production and functional analysis of normal and variant recombinant human transthyretin proteins.
    Murrell JR, Schoner RG, Liepnieks JJ, Rosen HN, Moses AC, Benson MD.
    J Biol Chem; 1992 Aug 15; 267(23):16595-600. PubMed ID: 1644839
    [Abstract] [Full Text] [Related]

  • 8. Chromium(III) ion and thyroxine cooperate to stabilize the transthyretin tetramer and suppress in vitro amyloid fibril formation.
    Sato T, Ando Y, Susuki S, Mikami F, Ikemizu S, Nakamura M, Suhr O, Anraku M, Kai T, Suico MA, Shuto T, Mizuguchi M, Yamagata Y, Kai H.
    FEBS Lett; 2006 Jan 23; 580(2):491-6. PubMed ID: 16386248
    [Abstract] [Full Text] [Related]

  • 9. Reduced affinity for thyroxine in two of three structural thyroxine-binding prealbumin variants associated with familial amyloidotic polyneuropathy.
    Refetoff S, Dwulet FE, Benson MD.
    J Clin Endocrinol Metab; 1986 Dec 23; 63(6):1432-7. PubMed ID: 3097057
    [Abstract] [Full Text] [Related]

  • 10. A point mutation in transthyretin increases affinity for thyroxine and produces euthyroid hyperthyroxinemia.
    Moses AC, Rosen HN, Moller DE, Tsuzaki S, Haddow JE, Lawlor J, Liepnieks JJ, Nichols WC, Benson MD.
    J Clin Invest; 1990 Dec 23; 86(6):2025-33. PubMed ID: 1979335
    [Abstract] [Full Text] [Related]

  • 11. Thyroxine binding to transthyretin (TTR) variants--two variants (TTR Pro 55 and TTR Met 111) with a particularly low binding affinity.
    Almeida MR, Saraiva MJ.
    Eur J Endocrinol; 1996 Aug 23; 135(2):226-30. PubMed ID: 8810738
    [Abstract] [Full Text] [Related]

  • 12. Thyroxine binding by human transthyretin variants: mutations at position 119, but not position 54, increase thyroxine binding affinity.
    Curtis AJ, Scrimshaw BJ, Topliss DJ, Stockigt JR, George PM, Barlow JW.
    J Clin Endocrinol Metab; 1994 Feb 23; 78(2):459-62. PubMed ID: 7906282
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  • 17. Homozygosity for the transthyretin-Met30 gene in three Japanese siblings with type I familial amyloidotic polyneuropathy.
    Yoshinaga T, Nakazato M, Ikeda S, Ohnishi A.
    Neurology; 1992 Oct 23; 42(10):2045-7. PubMed ID: 1407590
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  • 18. Change in structure of the N-terminal region of transthyretin produces change in affinity of transthyretin to T4 and T3.
    Prapunpoj P, Leelawatwatana L, Schreiber G, Richardson SJ.
    FEBS J; 2006 Sep 23; 273(17):4013-23. PubMed ID: 16879610
    [Abstract] [Full Text] [Related]

  • 19. Comparative studies of two transthyretin variants with protective effects on familial amyloidotic polyneuropathy: TTR R104H and TTR T119M.
    Almeida MR, Alves IL, Terazaki H, Ando Y, Saraiva MJ.
    Biochem Biophys Res Commun; 2000 Apr 21; 270(3):1024-8. PubMed ID: 10772944
    [Abstract] [Full Text] [Related]

  • 20. Novel mutation p.A64D in the Serpina7 gene as a cause of partial thyroxine-binding globulin deficiency associated with increases affinity in transthyretin by a known p.A109T mutation in the TTR gene.
    Sklate RT, Olcese MC, Maccallini GC, Sarmiento RG, Targovnik HM, Rivolta CM.
    Horm Metab Res; 2014 Feb 21; 46(2):100-8. PubMed ID: 24356794
    [Abstract] [Full Text] [Related]

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