These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

213 related articles for article (PubMed ID: 16079263)

  • 61. Sporadic congenital hyperthyroidism due to a spontaneous germline mutation in the thyrotropin receptor gene.
    Holzapfel HP; Wonerow P; von Petrykowski W; Henschen M; Scherbaum WA; Paschke R
    J Clin Endocrinol Metab; 1997 Nov; 82(11):3879-84. PubMed ID: 9360555
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Lysine 183 and glutamic acid 157 of the TSH receptor: two interacting residues with a key role in determining specificity toward TSH and human CG.
    Smits G; Govaerts C; Nubourgh I; Pardo L; Vassart G; Costagliola S
    Mol Endocrinol; 2002 Apr; 16(4):722-35. PubMed ID: 11923469
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Thyroid gene expression in familial nonautoimmune hyperthyroidism shows common characteristics with hyperfunctioning autonomous adenomas.
    Hébrant A; Van Sande J; Roger PP; Patey M; Klein M; Bournaud C; Savagner F; Leclère J; Dumont JE; van Staveren WC; Maenhaut C
    J Clin Endocrinol Metab; 2009 Jul; 94(7):2602-9. PubMed ID: 19383781
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Identification of the first germline mutation in the extracellular domain of the follitropin receptor responsible for spontaneous ovarian hyperstimulation syndrome.
    De Leener A; Caltabiano G; Erkan S; Idil M; Vassart G; Pardo L; Costagliola S
    Hum Mutat; 2008 Jan; 29(1):91-8. PubMed ID: 17721928
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Thyrotropin receptor gene alterations in thyroid hyperfunctioning adenomas.
    Russo D; Arturi F; Suarez HG; Schlumberger M; Du Villard JA; Crocetti U; Filetti S
    J Clin Endocrinol Metab; 1996 Apr; 81(4):1548-51. PubMed ID: 8636365
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Multiple relapses of hyperthyroidism after thyroid surgeries in a patient with long term follow-up of sporadic non-autoimmune hyperthyroidism.
    Bircan R; Miehle K; Mladenova G; Ivanova R; Ivanova R; Sarafova A; Borissova AM; Lüblinghoff J; Paschke R
    Exp Clin Endocrinol Diabetes; 2008 Jun; 116(6):341-6. PubMed ID: 18528812
    [TBL] [Abstract][Full Text] [Related]  

  • 67. A novel thyrotropin receptor germline mutation (Asp617Tyr) causing hereditary hyperthyroidism.
    Nishihara E; Nagayama Y; Amino N; Hishinuma A; Takano T; Yoshida H; Kubota S; Fukata S; Kuma K; Miyauchi A
    Endocr J; 2007 Dec; 54(6):927-34. PubMed ID: 18025759
    [TBL] [Abstract][Full Text] [Related]  

  • 68. A neomutation of the thyroid-stimulating hormone receptor in a severe neonatal hyperthyroidism.
    de Roux N; Polak M; Couet J; Leger J; Czernichow P; Milgrom E; Misrahi M
    J Clin Endocrinol Metab; 1996 Jun; 81(6):2023-6. PubMed ID: 8964822
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Mild congenital primary hypothyroidism in a Turkish family caused by a homozygous missense thyrotropin receptor (TSHR) gene mutation (A593 V).
    Fricke-Otto S; Pfarr N; Mühlenberg R; Pohlenz J
    Exp Clin Endocrinol Diabetes; 2005 Dec; 113(10):582-5. PubMed ID: 16320156
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Familial thyrotoxicocis in five Nigerians.
    Afolabi AO; Akute OO
    Niger J Clin Pract; 2005 Dec; 8(2):133-5. PubMed ID: 16477871
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Congenital nonautoimmune hyperthyroidism in a nonidentical twin caused by a sporadic germline mutation in the thyrotropin receptor gene.
    Kopp P; Jameson JL; Roe TF
    Thyroid; 1997 Oct; 7(5):765-70. PubMed ID: 9349581
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Expanding clinical spectrum of non-autoimmune hyperthyroidism due to an activating germline mutation, p.M453T, in the thyrotropin receptor gene.
    Supornsilchai V; Sahakitrungruang T; Wongjitrat N; Wacharasindhu S; Suphapeetiporn K; Shotelersuk V
    Clin Endocrinol (Oxf); 2009 Apr; 70(4):623-8. PubMed ID: 18681856
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Subclinical nonautoimmune hyperthyroidism in a family segregates with a thyrotropin receptor mutation with weakly increased constitutive activity.
    Nishihara E; Chen CR; Higashiyama T; Mizutori-Sasai Y; Ito M; Kubota S; Amino N; Miyauchi A; Rapoport B
    Thyroid; 2010 Nov; 20(11):1307-14. PubMed ID: 20929407
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Subclinical hyperthyroidism due to a thyrotropin receptor (TSHR) gene mutation (S505R).
    Pohlenz J; Pfarr N; Krüger S; Hesse V
    Acta Paediatr; 2006 Dec; 95(12):1685-7. PubMed ID: 17129985
    [TBL] [Abstract][Full Text] [Related]  

  • 75. A new case of familial nonautoimmune hyperthyroidism caused by the M463V mutation in the TSH receptor with anticipation of the disease across generations: a possible role of iodine supplementation.
    Ferrara AM; Capalbo D; Rossi G; Capuano S; Del Prete G; Esposito V; Montesano G; Zampella E; Fenzi G; Salerno M; Macchia PE
    Thyroid; 2007 Jul; 17(7):677-80. PubMed ID: 17696839
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Sporadic nonautoimmune congenital hyperthyroidism due to a strong activating mutation of the thyrotropin receptor gene.
    Tonacchera M; Agretti P; Rosellini V; Ceccarini G; Perri A; Zampolli M; Longhi R; Larizza D; Pinchera A; Vitti P; Chiovato L
    Thyroid; 2000 Oct; 10(10):859-63. PubMed ID: 11081252
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Point mutations in the thyrotropin receptor in human thyroid tumors.
    Ohno M; Endo T; Ohta K; Gunji K; Onaya T
    Thyroid; 1995 Apr; 5(2):97-100. PubMed ID: 7647578
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Follicular carcinoma presenting as autonomous functioning thyroid nodule and containing an activating mutation of the TSH receptor (T620I) and a mutation of the Ki-RAS (G12C) genes.
    Niepomniszcze H; Suárez H; Pitoia F; Pignatta A; Danilowicz K; Manavela M; Elsner B; Bruno OD
    Thyroid; 2006 May; 16(5):497-503. PubMed ID: 16756473
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Novel mutations of thyrotropin receptor gene in thyroid hyperfunctioning adenomas. Rapid identification by fine needle aspiration biopsy.
    Porcellini A; Ciullo I; Laviola L; Amabile G; Fenzi G; Avvedimento VE
    J Clin Endocrinol Metab; 1994 Aug; 79(2):657-61. PubMed ID: 8045989
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Cysteine 390 mutation of the TSH receptor modulates its ectodomain as an inverse agonist on the serpentine domain with decrease in basal constitutive activity.
    Ho SC; Goh SS; Su Q; Khoo DH
    Mol Cell Endocrinol; 2005 Dec; 245(1-2):158-68. PubMed ID: 16364538
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.