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121 related items for PubMed ID: 3392390
1. Ultrastructural aspects of the goiter in cog/cog mice. Mayerhofer A, Amador AG, Beamer WG, Bartke A. J Hered; 1988; 79(3):200-3. PubMed ID: 3392390 [Abstract] [Full Text] [Related]
2. Mutant gene-induced disorders of structure, function and thyroglobulin synthesis in congenital goitre (cog/cog) in mice. Adkison LR, Taylor S, Beamer WG. J Endocrinol; 1990 Jul; 126(1):51-8. PubMed ID: 1696305 [Abstract] [Full Text] [Related]
5. Evaluation and characterization of the hyt/hyt hypothyroid mouse. II. Abnormalities of TSH and the thyroid gland. Stein SA, Shanklin DR, Krulich L, Roth MG, Chubb CM, Adams PM. Neuroendocrinology; 1989 May; 49(5):509-19. PubMed ID: 2725843 [Abstract] [Full Text] [Related]
6. A single amino acid change in the acetylcholinesterase-like domain of thyroglobulin causes congenital goiter with hypothyroidism in the cog/cog mouse: a model of human endoplasmic reticulum storage diseases. Kim PS, Hossain SA, Park YN, Lee I, Yoo SE, Arvan P. Proc Natl Acad Sci U S A; 1998 Aug 18; 95(17):9909-13. PubMed ID: 9707574 [Abstract] [Full Text] [Related]
7. Defective thyroglobulin export as a cause of congenital goitre. Lissitzky S, Torresani J, Burrow GN, Bouchilloux S, Chabaud O. Clin Endocrinol (Oxf); 1975 Jul 18; 4(4):363-92. PubMed ID: 1157342 [Abstract] [Full Text] [Related]
8. Maintaining the thyroid gland in mutant thyroglobulin-induced hypothyroidism requires thyroid cell proliferation that must continue in adulthood. Zhang X, Malik B, Young C, Zhang H, Larkin D, Liao XH, Refetoff S, Liu M, Arvan P. J Biol Chem; 2022 Jul 18; 298(7):102066. PubMed ID: 35618019 [Abstract] [Full Text] [Related]
9. Congenital hypothyroid goiter with deficient thyroglobulin. Identification of an endoplasmic reticulum storage disease with induction of molecular chaperones. Medeiros-Neto G, Kim PS, Yoo SE, Vono J, Targovnik HM, Camargo R, Hossain SA, Arvan P. J Clin Invest; 1996 Dec 15; 98(12):2838-44. PubMed ID: 8981932 [Abstract] [Full Text] [Related]
10. [Ultrastructural aspects and synthesis of thyroglobulin in thyroid cultures before and after transplantation in hypophysectomized rats]. Denys H, Pavlović-Hournac M. Exp Cell Res; 1975 May 15; 92(2):485-96. PubMed ID: 1132439 [No Abstract] [Full Text] [Related]
11. Abnormal properties of thyroglobulin in mice with inherited congenital goiter (cog/cog). Basche M, Beamer WG, Schneider AB. Endocrinology; 1989 Apr 15; 124(4):1822-9. PubMed ID: 2924725 [Abstract] [Full Text] [Related]
12. Qualitative and quantitative defects of thyroglobulin resulting in congenital goiter. Absence of gross gene deletion of coding sequences in the TG gene structure. Medeiros-Neto G, Targovnik H, Knobel M, Propato F, Varela V, Alkmin M, Barbosa S, Wajchenberg BL. J Endocrinol Invest; 1989 Dec 15; 12(11):805-13. PubMed ID: 2614017 [Abstract] [Full Text] [Related]
13. Missing secretory granules, dilated endoplasmic reticulum, and nuclear dislocation in the thyroid gland of rdw rats with hereditary dwarfism. Sakai Y, Yamashina S, Furudate SI. Anat Rec; 2000 May 01; 259(1):60-6. PubMed ID: 10760744 [Abstract] [Full Text] [Related]
15. Low-molecular-weight iodoproteins in the congenital goiters of cog/cog mice. Fogelfeld L, Harel G, Beamer WG, Schneider AB. Thyroid; 1992 Feb 01; 2(4):329-35. PubMed ID: 1493376 [Abstract] [Full Text] [Related]
16. The effect of oral administration of iodine to patients with goiter and hypothyroidism due to defective synthesis of thyroglobulin. Vono J, Lima N, Knobel M, Medeiros-Neto G. Thyroid; 1996 Feb 01; 6(1):11-5. PubMed ID: 8777378 [Abstract] [Full Text] [Related]
17. Biallelic p.R2223H mutation in the thyroglobulin gene causes thyroglobulin retention and severe hypothyroidism with subsequent development of thyroid carcinoma. Raef H, Al-Rijjal R, Al-Shehri S, Zou M, Al-Mana H, Baitei EY, Parhar RS, Al-Mohanna FA, Shi Y. J Clin Endocrinol Metab; 2010 Mar 01; 95(3):1000-6. PubMed ID: 20089614 [Abstract] [Full Text] [Related]
18. Endocytosis of human thyroglobulin (TG) in adenomatous goiter studied by an immuno-electron microscopic procedure. Nakayama I, Noguchi S, Mochizuki Y, Murakami N, Yamashita H, Moriuchi A, Yokoyama S, Noguchi A. Acta Pathol Jpn; 1984 Jan 01; 34(1):19-28. PubMed ID: 6428159 [Abstract] [Full Text] [Related]
19. Congenital euthyroid goitre with impaired thyroglobulin transport. Ohyama Y, Hosoya T, Kameya T, Suzuki N, Nakamura S, Kazahari K, Shibayama K, Yokota Y, Matsuura N. Clin Endocrinol (Oxf); 1994 Jul 01; 41(1):129-35. PubMed ID: 8050126 [Abstract] [Full Text] [Related]
20. The congenital goiter mutation is linked to the thyroglobulin gene in the mouse. Taylor BA, Rowe L. Proc Natl Acad Sci U S A; 1987 Apr 01; 84(7):1986-90. PubMed ID: 2882514 [Abstract] [Full Text] [Related] Page: [Next] [New Search]