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Journal Abstract Search

212 related items for PubMed ID: 12907760

  • 1. Hypothyroidism in thyroid transcription factor 1 haploinsufficiency is caused by reduced expression of the thyroid-stimulating hormone receptor.
    Moeller LC, Kimura S, Kusakabe T, Liao XH, Van Sande J, Refetoff S.
    Mol Endocrinol; 2003 Nov; 17(11):2295-302. PubMed ID: 12907760
    [Abstract] [Full Text] [Related]

  • 2. Role of the thyroid-stimulating hormone receptor signaling in development and differentiation of the thyroid gland.
    Postiglione MP, Parlato R, Rodriguez-Mallon A, Rosica A, Mithbaokar P, Maresca M, Marians RC, Davies TF, Zannini MS, De Felice M, Di Lauro R.
    Proc Natl Acad Sci U S A; 2002 Nov 26; 99(24):15462-7. PubMed ID: 12432093
    [Abstract] [Full Text] [Related]

  • 3. Partial deficiency of thyroid transcription factor 1 produces predominantly neurological defects in humans and mice.
    Pohlenz J, Dumitrescu A, Zundel D, Martiné U, Schönberger W, Koo E, Weiss RE, Cohen RN, Kimura S, Refetoff S.
    J Clin Invest; 2002 Feb 26; 109(4):469-73. PubMed ID: 11854318
    [Abstract] [Full Text] [Related]

  • 4. Thyroid transcription factor 1 activates the promoter of the thyrotropin receptor gene.
    Civitareale D, Castelli MP, Falasca P, Saiardi A.
    Mol Endocrinol; 1993 Dec 26; 7(12):1589-95. PubMed ID: 8145764
    [Abstract] [Full Text] [Related]

  • 5. A novel mutation (Q40P) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia: evidence for phenotypic variability in mother and child.
    Congdon T, Nguyen LQ, Nogueira CR, Habiby RL, Medeiros-Neto G, Kopp P.
    J Clin Endocrinol Metab; 2001 Aug 26; 86(8):3962-7. PubMed ID: 11502839
    [Abstract] [Full Text] [Related]

  • 6. The site of the molecular defect in the thyroid gland of the hyt/hyt mouse: abnormalities in the TSH receptor-G protein complex.
    Stein SA, Zakarija M, McKenzie JM, Shanklin DR, Palnitkar MB, Adams PM.
    Thyroid; 1991 Aug 26; 1(3):257-66. PubMed ID: 1668617
    [Abstract] [Full Text] [Related]

  • 7. Germline mutations of TSH receptor gene as cause of nonautoimmune subclinical hypothyroidism.
    Alberti L, Proverbio MC, Costagliola S, Romoli R, Boldrighini B, Vigone MC, Weber G, Chiumello G, Beck-Peccoz P, Persani L.
    J Clin Endocrinol Metab; 2002 Jun 26; 87(6):2549-55. PubMed ID: 12050212
    [Abstract] [Full Text] [Related]

  • 8. Modulation of thyroid-specific gene expression in normal and nodular human thyroid tissues from adults: an in vivo effect of thyrotropin.
    Bruno R, Ferretti E, Tosi E, Arturi F, Giannasio P, Mattei T, Scipioni A, Presta I, Morisi R, Gulino A, Filetti S, Russo D.
    J Clin Endocrinol Metab; 2005 Oct 26; 90(10):5692-7. PubMed ID: 16076943
    [Abstract] [Full Text] [Related]

  • 9. Congenital hypothyroidism and apparent athyreosis with compound heterozygosity or compensated hypothyroidism with probable hemizygosity for inactivating mutations of the TSH receptor.
    Park SM, Clifton-Bligh RJ, Betts P, Chatterjee VK.
    Clin Endocrinol (Oxf); 2004 Feb 26; 60(2):220-7. PubMed ID: 14725684
    [Abstract] [Full Text] [Related]

  • 10. Congenital hypothyroidism with impaired thyroid response to thyrotropin (TSH) and absent circulating thyroglobulin: evidence for a new inactivating mutation of the TSH receptor gene.
    Tonacchera M, Agretti P, Pinchera A, Rosellini V, Perri A, Collecchi P, Vitti P, Chiovato L.
    J Clin Endocrinol Metab; 2000 Mar 26; 85(3):1001-8. PubMed ID: 10720030
    [Abstract] [Full Text] [Related]

  • 11. Sequence analysis of the thyrotropin (TSH) receptor gene in congenital primary hypothyroidism associated with TSH unresponsiveness.
    Takeshita A, Nagayama Y, Yamashita S, Takamatsu J, Ohsawa N, Maesaka H, Tachibana K, Tokuhiro E, Ashizawa K, Yokoyama N.
    Thyroid; 1994 Mar 26; 4(3):255-9. PubMed ID: 7833660
    [Abstract] [Full Text] [Related]

  • 12. Long-term outcome of loss-of-function mutations in thyrotropin receptor gene.
    Tenenbaum-Rakover Y, Almashanu S, Hess O, Admoni O, Hag-Dahood Mahameed A, Schwartz N, Allon-Shalev S, Bercovich D, Refetoff S.
    Thyroid; 2015 Mar 26; 25(3):292-9. PubMed ID: 25557138
    [Abstract] [Full Text] [Related]

  • 13. Analysis of the promoter of the thyrotropin receptor gene and the entire genomic sequence of thyroid transcription factor-1 in familial congenital hypothyroidism due to thyrotropin unresponsiveness.
    Hishinuma A, Takamatsu J, Kanno Y, Yoshida S, Ieiri T.
    Thyroid; 1998 Apr 26; 8(4):305-9. PubMed ID: 9588495
    [Abstract] [Full Text] [Related]

  • 14. Regulation of thyrotropin receptor gene expression in 3T3-L1 adipose cells is distinct from its regulation in FRTL-5 thyroid cells.
    Shimura H, Haraguchi K, Endo T, Onaya T.
    Endocrinology; 1997 Apr 26; 138(4):1483-90. PubMed ID: 9075706
    [Abstract] [Full Text] [Related]

  • 15. Subclinical hypothyroidism in early childhood: a frequent outcome of transient neonatal hyperthyrotropinemia.
    Calaciura F, Motta RM, Miscio G, Fichera G, Leonardi D, Carta A, Trischitta V, Tassi V, Sava L, Vigneri R.
    J Clin Endocrinol Metab; 2002 Jul 26; 87(7):3209-14. PubMed ID: 12107226
    [Abstract] [Full Text] [Related]

  • 16. Cloning of the single strand DNA-binding protein important for maximal expression and thyrotropin (TSH)-induced negative regulation of the TSH receptor.
    Ohmori M, Ohta M, Shimura H, Shimurat Y, Suzuki K, Kohn LD.
    Mol Endocrinol; 1996 Nov 26; 10(11):1407-24. PubMed ID: 8923467
    [Abstract] [Full Text] [Related]

  • 17. Defining thyrotropin-dependent and -independent steps of thyroid hormone synthesis by using thyrotropin receptor-null mice.
    Marians RC, Ng L, Blair HC, Unger P, Graves PN, Davies TF.
    Proc Natl Acad Sci U S A; 2002 Nov 26; 99(24):15776-81. PubMed ID: 12432094
    [Abstract] [Full Text] [Related]

  • 18. Pituitary-thyroid setpoint and thyrotropin receptor expression in consomic rats.
    Moeller LC, Alonso M, Liao X, Broach V, Dumitrescu A, Van Sande J, Montanelli L, Skjei S, Goodwin C, Grasberger H, Refetoff S, Weiss RE.
    Endocrinology; 2007 Oct 26; 148(10):4727-33. PubMed ID: 17640981
    [Abstract] [Full Text] [Related]

  • 19. Congenital hypothyroidism: etiologies, diagnosis, and management.
    LaFranchi S.
    Thyroid; 1999 Jul 26; 9(7):735-40. PubMed ID: 10447022
    [Abstract] [Full Text] [Related]

  • 20. Thyroid-specific expression and cyclic adenosine 3',5'-monophosphate autoregulation of the thyrotropin receptor gene involves thyroid transcription factor-1.
    Shimura H, Okajima F, Ikuyama S, Shimura Y, Kimura S, Saji M, Kohn LD.
    Mol Endocrinol; 1994 Aug 26; 8(8):1049-69. PubMed ID: 7997232
    [Abstract] [Full Text] [Related]

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