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 *

105 related articles for article (PubMed ID: 1696305)

  • 1. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Abnormal properties of thyroglobulin in mice with inherited congenital goiter (cog/cog).
    Basche M; Beamer WG; Schneider AB
    Endocrinology; 1989 Apr; 124(4):1822-9. PubMed ID: 2924725
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inherited congenital goiter in mice.
    Beamer WG; Maltais LJ; DeBaets MH; Eicher EM
    Endocrinology; 1987 Feb; 120(2):838-40. PubMed ID: 3803305
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Relationship between serum thyroglobulin and intrathyroidal stable iodine in human simple goitre.
    Unger J; de Maertelaer V; Golstein J; Decoster C; Jonckheer MH
    Clin Endocrinol (Oxf); 1985 Jul; 23(1):1-6. PubMed ID: 4028462
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial goitre with absence of thyroglobulin and synthesis of thyroid hormones from thyroidal albumin.
    Desai KB; Mehta MN; Patel MC; Sharma SM; Ramanna L; Ganatra RD
    J Endocrinol; 1974 Mar; 60(3):389-97. PubMed ID: 4823248
    [No Abstract]   [Full Text] [Related]  

  • 8. Low-molecular-weight iodoproteins in the congenital goiters of cog/cog mice.
    Fogelfeld L; Harel G; Beamer WG; Schneider AB
    Thyroid; 1992; 2(4):329-35. PubMed ID: 1493376
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 6(1):11-5. PubMed ID: 8777378
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 95(17):9909-13. PubMed ID: 9707574
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Increased serum thyroglobulin levels in patients with nontoxic goiter.
    Pezzino V; Vigneri R; Squatrito S; Filetti S; Camus M; Polosa P
    J Clin Endocrinol Metab; 1978 Apr; 46(4):653-7. PubMed ID: 755050
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 298(7):102066. PubMed ID: 35618019
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 84(7):1986-90. PubMed ID: 2882514
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The hormone synthesis of hyperfunctioning thyroid nodules in euthyroid patients.
    Agerbaek H
    Acta Endocrinol (Copenh); 1974 Sep; 77(1):53-63. PubMed ID: 4137272
    [No Abstract]   [Full Text] [Related]  

  • 15. An endoplasmic reticulum storage disease causing congenital goiter with hypothyroidism.
    Kim PS; Kwon OY; Arvan P
    J Cell Biol; 1996 May; 133(3):517-27. PubMed ID: 8636228
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Serum thyrotrophin and circulating thyroglobulin antibodies in subjects with non-toxic goitre and in euthyroid subjects who had undergone subtotal thyroidectomy or radioiodine therapy.
    Gordin A
    Acta Endocrinol (Copenh); 1973 Oct; 74(2):283-95. PubMed ID: 4126377
    [No Abstract]   [Full Text] [Related]  

  • 17. 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; 12(11):805-13. PubMed ID: 2614017
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Normal thyroglobulin and thyroperoxidase gene expression in thyroid congenital defective thyroglobulin synthesis.
    Targovnik HM; Varela V; Abatangelo C; Wajchenberg BL; Medeiros-Neto G
    Thyroid; 1991; 1(4):339-45. PubMed ID: 1726786
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Differential levels of thyroid peroxidase and thyroglobulin messenger ribonucleic acids in congenital goiter with defective thyroglobulin synthesis.
    Targovnik HM; Varela V; Juvenal GJ; Propato F; Chester HA; Krawiec L; Frechtel G; Moran DH; Perinetti HA; Pisarev MA
    J Endocrinol Invest; 1990 Nov; 13(10):797-806. PubMed ID: 2096156
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The loss of the chloride channel, ClC-5, delays apical iodide efflux and induces a euthyroid goiter in the mouse thyroid gland.
    van den Hove MF; Croizet-Berger K; Jouret F; Guggino SE; Guggino WB; Devuyst O; Courtoy PJ
    Endocrinology; 2006 Mar; 147(3):1287-96. PubMed ID: 16306076
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.