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 *

150 related articles for article (PubMed ID: 18434655)

  • 1. Reduce, recycle, reuse--iodotyrosine deiodinase in thyroid iodide metabolism.
    Kopp PA
    N Engl J Med; 2008 Apr; 358(17):1856-9. PubMed ID: 18434655
    [No Abstract]   [Full Text] [Related]  

  • 2. Mutations in the iodotyrosine deiodinase gene and hypothyroidism.
    Moreno JC; Klootwijk W; van Toor H; Pinto G; D'Alessandro M; Lèger A; Goudie D; Polak M; Grüters A; Visser TJ
    N Engl J Med; 2008 Apr; 358(17):1811-8. PubMed ID: 18434651
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetics and phenomics of hypothyroidism and goiter due to iodotyrosine deiodinase (DEHAL1) gene mutations.
    Moreno JC; Visser TJ
    Mol Cell Endocrinol; 2010 Jun; 322(1-2):91-8. PubMed ID: 20298747
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetics and phenomics of hypothyroidism and goiter due to TPO mutations.
    Ris-Stalpers C; Bikker H
    Mol Cell Endocrinol; 2010 Jun; 322(1-2):38-43. PubMed ID: 20153806
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Disorder of thyroid hormone synthesis].
    Kotani T; Ohtaki S
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):909-11. PubMed ID: 3270908
    [No Abstract]   [Full Text] [Related]  

  • 6. Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defect.
    Rivolta CM; Esperante SA; Gruñeiro-Papendieck L; Chiesa A; Moya CM; Domené S; Varela V; Targovnik HM
    Hum Mutat; 2003 Sep; 22(3):259. PubMed ID: 12938097
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Iodotyrosine deiodinase defect identified via genome-wide approach.
    Burniat A; Pirson I; Vilain C; Kulik W; Afink G; Moreno-Reyes R; Corvilain B; Abramowicz M
    J Clin Endocrinol Metab; 2012 Jul; 97(7):E1276-83. PubMed ID: 22535972
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Molecular genetics of hereditary thyroid disease].
    Targovnik HM
    Medicina (B Aires); 2000; 60(5 Pt 2):703-6. PubMed ID: 11188886
    [No Abstract]   [Full Text] [Related]  

  • 9. Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter.
    Abramowicz MJ; Targovnik HM; Varela V; Cochaux P; Krawiec L; Pisarev MA; Propato FV; Juvenal G; Chester HA; Vassart G
    J Clin Invest; 1992 Oct; 90(4):1200-4. PubMed ID: 1401057
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Congenital primary hypothyroidism with subsequent adenomatous goiter in a Turkish patient caused by a homozygous 10-bp deletion in the thyroid peroxidase (TPO) gene.
    Pfarr N; Musholt TJ; Musholt PB; Brzezinska R; Pohlenz J
    Clin Endocrinol (Oxf); 2006 May; 64(5):514-8. PubMed ID: 16649969
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Intrauterine therapy of goitrous hypothyroidism in a boy with a new compound heterozygous mutation (Y453D and C800R) in the thyroid peroxidase gene. A long-term follow-up.
    Börgel K; Pohlenz J; Holzgreve W; Bramswig JH
    Am J Obstet Gynecol; 2005 Sep; 193(3 Pt 1):857-8. PubMed ID: 16150286
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel hypothyroid dwarfism due to the missense mutation Arg479Cys of the thyroid peroxidase gene in the mouse.
    Takabayashi S; Umeki K; Yamamoto E; Suzuki T; Okayama A; Katoh H
    Mol Endocrinol; 2006 Oct; 20(10):2584-90. PubMed ID: 16762971
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [The thyroid as a model for molecular mechanisms in genetic diseases].
    Rivolta CM; Moya CM; Esperante SA; Gutnisky VJ; Varela V; Targovnik HM
    Medicina (B Aires); 2005; 65(3):257-67. PubMed ID: 16042141
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism.
    Umeki K; Kotani T; Kawano J; Suganuma T; Yamamoto I; Aratake Y; Furujo M; Ichiba Y
    Eur J Endocrinol; 2002 Apr; 146(4):491-8. PubMed ID: 11916616
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Screening for mutations of the human thyroid peroxidase gene in patients with congenital hypothyroidism.
    Grüters A; Köhler B; Wolf A; Söling A; de Vijlder L; Krude H; Biebermann H
    Exp Clin Endocrinol Diabetes; 1996; 104 Suppl 4():121-3. PubMed ID: 8981018
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [On 3 cases of familial goiter due to probable congenital defect of hormonogenesis].
    Torino G; Esposito V
    Pediatria (Napoli); 1972; 80(4):388-97. PubMed ID: 4646632
    [No Abstract]   [Full Text] [Related]  

  • 17. [Goiter and hypothyroidism due to a familial defect o deiodation of iodotyrosine].
    Bigozzi U; Bigazzi M; Guazzelli R; Melani F
    Acta Genet Med Gemellol (Roma); 1967 Oct; 16(4):410-6. PubMed ID: 4173309
    [No Abstract]   [Full Text] [Related]  

  • 18. [Iodide organification defect].
    Hishinuma A; Ieiri T; Fukata S; Nishi Y; Kiwaki K
    Nihon Rinsho; 2006 May; Suppl 1():360-2. PubMed ID: 16776165
    [No Abstract]   [Full Text] [Related]  

  • 19. [Congenital hypothyroidism due to a type I hormonogenesis disorder. (3 cases in the same family and literature review)].
    Marie J; Rivière R; Hennequet A; Desbois JC; Seince JM
    Ann Pediatr (Paris); 1969; 16(6):424-36. PubMed ID: 4184994
    [No Abstract]   [Full Text] [Related]  

  • 20. Congenital Hypothyroidism in Two Sudanese Families Harboring a Novel Iodotyrosine Deiodinase Mutation (IYD R279C).
    Shareef R; Furman A; Watanabe Y; Bruellman R; Abdullah MA; Dumitresu AM; Refetoff S; Bertolini A; Borsò M; Saba A; Zucchi R; Weiss RE
    Thyroid; 2023 Feb; 33(2):261-266. PubMed ID: 36633921
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.