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 *

169 related articles for article (PubMed ID: 34915750)

  • 1. Pathogenesis of Multinodular Goiter in Elderly XB130-Deficient Mice: Alteration of Thyroperoxidase Affinity with Iodide and Hydrogen Peroxide.
    Cho HR; Sugihara J; Shimizu H; Xiang YY; Bai X; Wang Y; Liao XH; Asa SL; Refetoff S; Liu M
    Thyroid; 2022 Apr; 32(4):385-396. PubMed ID: 34915750
    [No Abstract]   [Full Text] [Related]  

  • 2. XB130 Deficiency Causes Congenital Hypothyroidism in Mice due to Disorganized Apical Membrane Structure and Function of Thyrocytes.
    Wang Y; Shimizu H; Xiang YY; Sugihara J; Lu WY; Liao XH; Cho HR; Toba H; Bai XH; Asa SL; Arvan P; Refetoff S; Liu M
    Thyroid; 2021 Nov; 31(11):1650-1661. PubMed ID: 34470464
    [No Abstract]   [Full Text] [Related]  

  • 3. Thyroidal Transcriptomic Profiles of Pathoadaptive Responses to Congenital Hypothyroidism in XB130 Knockout Mice.
    Sugihara J; Wong A; Shimizu H; Zhao J; Cho HR; Wang Y; Refetoff S; Arvan P; Liu M
    Cells; 2022 Mar; 11(6):. PubMed ID: 35326426
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect.
    Nascimento AC; Guedes DR; Santos CS; Knobel M; Rubio IG; Medeiros-Neto G
    Thyroid; 2003 Dec; 13(12):1145-51. PubMed ID: 14751036
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Defective organification of iodide causing congenital goitrous hypothyroidism.
    Ishikawa N; Eguchi K; Ohmori T; Momotani N; Nagayama Y; Hosoya T; Oguchi H; Mimura T; Kimura S; Nagataki S; Ito K
    J Clin Endocrinol Metab; 1996 Jan; 81(1):376-83. PubMed ID: 8550781
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dissociation of thyrotropin-dependent enzyme activities, reduced iodide transport, and preserved iodide organification in nonfunctioning thyroid adenoma and multinodular goiter.
    Masini-Repiso AM; Cabanillas AM; Bonaterra M; Coleoni AH
    J Clin Endocrinol Metab; 1994 Jul; 79(1):39-44. PubMed ID: 8027249
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Iodide handling disorders (NIS, TPO, TG, IYD).
    Targovnik HM; Citterio CE; Rivolta CM
    Best Pract Res Clin Endocrinol Metab; 2017 Mar; 31(2):195-212. PubMed ID: 28648508
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Negative correlation between thyroperoxidase and dual oxidase H2O2-generating activities in thyroid nodular lesions.
    Ginabreda MG; Cardoso LC; Nobrega FM; Ferreira AC; Gonçalves MD; Vaisman M; Carvalho DP
    Eur J Endocrinol; 2008 Feb; 158(2):223-7. PubMed ID: 18230830
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial iodide organification defect caused by a novel mutation of the thyroid peroxidase gene in three siblings.
    Kotani T; Umeki K; Kawano J; Suganuma T; Hishinuma A; Ieiri T; Harada S
    Clin Endocrinol (Oxf); 2003 Aug; 59(2):198-206. PubMed ID: 12864797
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. Thyroid iodine organification defects: a case with lack of thyroglobulin iodination and a case without any peroxidase activity.
    Pommier J; Tourniaire J; Rahmoun B; Déme D; Pallo D; Bornet H; Nunez J
    J Clin Endocrinol Metab; 1976 Feb; 42(2):319-29. PubMed ID: 1262432
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Defective organification of iodide causing hereditary goitrous hypothyroidism.
    Medeiros-Neto GA; Billerbeck AE; Wajchenberg BL; Targovnik HM
    Thyroid; 1993; 3(2):143-59. PubMed ID: 8369653
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two compound heterozygous mutations (c.215delA/c.2422T-->C and c.387delC/c.1159G-->A) in the thyroid peroxidase gene responsible for congenital goitre and iodide organification defect.
    Rivolta CM; Louis-Tisserand M; Varela V; Gruñeiro-Papendieck L; Chiesa A; González-Sarmiento R; Targovnik HM
    Clin Endocrinol (Oxf); 2007 Aug; 67(2):238-46. PubMed ID: 17547680
    [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. Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis.
    Tenenbaum-Rakover Y; Mamanasiri S; Ris-Stalpers C; German A; Sack J; Allon-Shalev S; Pohlenz J; Refetoff S
    Clin Endocrinol (Oxf); 2007 May; 66(5):695-702. PubMed ID: 17381485
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. XB130 Plays an Essential Role in Folliculogenesis Through Mediating Interactions Between Microfilament and Microtubule Systems in Thyrocytes.
    Wang Y; Xiang YY; Sugihara J; Lu WY; Liao XH; Arvan P; Refetoff S; Liu M
    Thyroid; 2022 Feb; 32(2):128-137. PubMed ID: 34652970
    [No Abstract]   [Full Text] [Related]  

  • 18. DUOXS defects: Genotype-phenotype correlations.
    Fugazzola L; Muzza M; Weber G; Beck-Peccoz P; Persani L
    Ann Endocrinol (Paris); 2011 Apr; 72(2):82-6. PubMed ID: 21511237
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of TPO gene in Turkish children with iodide organification defect: identification of a novel mutation.
    Turkkahraman D; Alper OM; Pehlivanoglu S; Aydin F; Yildiz A; Luleci G; Akcurin S; Bircan I
    Endocrine; 2010 Feb; 37(1):124-8. PubMed ID: 20963560
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel mutation in the human thyroid peroxidase gene resulting in a total iodide organification defect.
    Kotani T; Umeki K; Yamamoto I; Maesaka H; Tachibana K; Ohtaki S
    J Endocrinol; 1999 Feb; 160(2):267-73. PubMed ID: 9924196
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.