Citations for
1TPO, TSHR
The coexistence of a novel inactivating mutant thyrotropin receptor allele with two thyroid peroxidase mutations: a genotype-phenotype correlation.
Sriphrapradang C, Tenenbaum-Rakover Y, Weiss M, Barkoff MS, Admoni O, Kawthar D, Caltabiano G, Pardo L, Dumitrescu AM, Refetoff S.
J Clin Endocrinol Metab 96(6):E1001-6. Epub 2011 Apr 13. 2011
2TIOD, TPO
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 37(1):124-8. Epub 2009 Nov 17. 2010
3DUOX1, DUOX2, TPO
Functional consequences of dual oxidase-thyroperoxidase interaction at the plasma membrane.
Fortunato RS, Lima de Souza EC, Ameziane-el Hassani R, Boufraqech M, Weyemi U, Talbot M, Lagente-Chevallier O, de Carvalho DP, Bidart JM, Schlumberger M, Dupuy C.
J Clin Endocrinol Metab 95(12):5403-11. Epub 2010 Sep 8. 2010
4DUOX1, DUOX2, TPO
Association of duoxes with thyroid peroxidase and its regulation in thyrocytes.
Song Y, Ruf J, Lothaire P, Dequanter D, Andry G, Willemse E, Dumont JE, Van Sande J, De Deken X.
J Clin Endocrinol Metab 95(1):375-82. Epub 2009 Dec 1. 2010
5TIOD, TPO
Thyroid peroxidase gene mutations causing congenital hypothyroidism in three Turkish families.
Ozbek MN, Uslu AB, Onenli-Mungan N, Yuksel B, Pohlenz J, Topaloglu AK.
J Pediatr Endocrinol Metab 22(11):1033-9. 2009
6TPO
Thyroid peroxidase forms thionamide-sensitive homodimers: relevance for immunomodulation of thyroid autoimmunity.
McDonald DO, Pearce SH.
J Mol Med (Berl) 87(10):971-80. Epub 2009 Aug 8. 2009
7TIOD, TPO
Congenital hypothyroidism caused by a novel homozygous mutation in the thyroid peroxidase gene.
Fuchs O, Pfarr N, Pohlenz J, Thanner F, Schmidt H.
J Pediatr Endocrinol Metab 21(11):1093-7. 2008
8TPO
Thyroid peroxidase and galectin-3 immunostaining in differentiated thyroid carcinoma with clinicopathologic correlation.
Savin S, Cvejic D, Isic T, Paunovic I, Tatic S, Havelka M.
Hum Pathol 39(11):1656-63. Epub 2008 Jul 26. 2008
9TIOD, TPO
High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis.
Avbelj M, Tahirovic H, Debeljak M, Kusekova M, Toromanovic A, Krzisnik C, Battelino T.
Eur J Endocrinol 156(5):511-9. 2007
10TPO
Detection of abnormalities of PRV-1, TPO, and c-MPL genes detected by fluorescence in situ hybridization in essential thrombocythemia.
Puigdecanet E, Espinet B, Villa O, Florensa L, Besses C, Serrano S, Sole F.
Cancer Genet Cytogenet 167(1):39-42. 2006
11TPO, SLC26A4, PDS, TIOD
Goitrous congenital hypothyroidism and hearing impairment associated with mutations in the TPO and SLC26A4/PDS genes.
Pfarr N, Borck G, Turk A, Napiontek U, Keilmann A, MŸller-Forell W, Kopp P, Pohlenz J.
J Clin Endocrinol Metab 91(7):2678-81. Epub 2006 May 9. 2006
12TPO, TIOD
A novel mutation in the human thyroid peroxidase gene resulting in a total iodide organification defect.
Kotani T, et al.
J Endocrinol 160(2):267-73. 1999
13TPO, TIOD
Two different mutations in the thyroid peroxidase gene of a large inbred Amish kindred: power and limits of homozygosity mapping.
Pannain S, et al.
J Clin Endocrinol Metab 84(3):1061-71. 1999
14TPO, TIOD
A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect.
Santos CL, Bikker H, Rego KG, Nascimento AC, Tambascia M, De Vijlder JJ, Medeiros-Neto G.
Clin Endocrinol (Oxf) 51(2):165-172 1999
15FGA, TH, TPO
The short tandem repeat loci hTPO, THO1 and FGA.
Poltl R, Luckenbach C, Hixson J, Ritter H.
Hum Hered 48 : 318-324. 1998
16TPO, SLC26A4
Thyroid peroxidase : evidence for disease gene exclusion in Pendred's syndrome.
Gausden E, et al.
Clin Endocrinol 44 : 441-446. 1996
17TPO
Regional localization of the gene for thyroid peroxidase to human chromosome 2p25 and mouse chromosome 12C.
Endo Y, et al.
Genomics 25 : 760-761. 1995
18TPO, TIOD
Identification of five novel inactivating mutations in the human thyroid peroxidase gene by denaturing gradient gel electrophoresis.
Bikker H, et al.
Hum Mutat 6 : 9-16. 1995
19TPO
Regional sublocalization of the human thyroid peroxidase gene (TPO) by tritium and fluorescence in situ hybridization to chromosome 2p25-p24.
Barnett PS, et al.
Cytogenet Cell Genet 62 : 188-189. 1993
20TPO
The first genetic marker detected in the promoter region of the thyroid peroxidase gene by single-strand conformational polymorphism analysis.
Rose G, et al.
Hum Mutat 2 : 418-419. 1993
21TPO
Acyl-RFLP in intron 8 of hTPO gene.
Rose G, et al.
Nucleic Acids Res 20 : 1162. 1992
22TPO
Tetranucleotide repeat polymorphism at the human thyroid peroxidase (hTPO) locus.
Anker R, et al.
Hum Mol Genet 1 : 137. 1992
23TPO, TIOD
Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter.
Abramowicz MJ, et al.
J Clin Invest 90 : 1200-1204. 1992
24TPO, TIOD
Genetic linkage studies of thyroid peroxidase (TPO) gene in families with TPO deficiency.
Mangklabruks A, et al.
J Clin Endocrinol Metab 72 : 471-476. 1991
25TPO
Acyl-RFLP identified on an amplified region of the TPO gene.
Rose G, et al.
Nucleic Acids Res 19 : 4021. 1991
26TPO
EcoRI RFLP in the human thyroid peroxidase (TPO) gene on chromosome 2.
Bikker H, Bolhuis PA, Vassart G, Libert F, Massaro G, de Vijlder JJ.
Hum Genet 82 : 95. 1989
27TPO
RFLPs detected at 2 pter-p12 with a thyroid peroxidase cDNA probe, TPO3 (McKusick no. 27450).
Massaro G, Libert F, Vassart G, Dinsart C.
Nucleic Acids Res 17 : 2155. 1989
28TPO
Regional localization of the gene for thyroid peroxidase to human chromosome 2pter-p12.
de Vijlder JJM, et al.
Cytogenet Cell Genet 47 : 170-172. 1988
29TPO
Human thyroid peroxidase : complete cDNA and protein sequence, chromosome mapping, and identification ot two alternately spliced mRNAs.
Kimura S, et al.
Proc Natl Acad Sci U S A 84 : 5555-5559. 1987
30TPO
Thyroid iodine organification defects.
Pommier J, et al.
J Clin Endocrinol Metab 42 : 319-329. 1976