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Items: 1 to 20 of 65

1.

Molecular characterization of thyroid peroxidase gene in porcine (Sus scrofa).

Wang Y, Zhao X, Jiang X, Hua X, Xu N.

J Genet Genomics. 2010 Jun;37(6):381-8. doi: 10.1016/S1673-8527(09)60056-4. Epub 2010 Jul 1.

PMID:
20621020
2.

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.

PMID:
12864797
4.

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. Epub 2007 Mar 23.

PMID:
17381485
5.

[Thyroid peroxidase (TPO) gene and pathogenic TPO mutation].

Asakawa H.

Nihon Rinsho. 1994 Apr;52(4):864-8. Review. Japanese.

PMID:
8196171
6.
7.

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.

8.

[Thyroid peroxidase].

Kotani T, Ohtaki S.

Rinsho Byori. 1990 Apr;38(4):442-5. Review. Japanese.

PMID:
2195199
9.

Activation of the thyroid peroxidase gene in human thyroid cells: effect of thyrotrophin, forskolin and phorbol ester.

Collison KS, Banga JP, Barnett PS, Kung AW, McGregor AM.

J Mol Endocrinol. 1989 Jul;3(1):1-5.

PMID:
2742742
10.
11.

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. 2009 Nov;22(11):1033-9.

PMID:
20101889
12.

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. Review.

PMID:
16649969
13.
14.

Isolation of a complementary DNA clone for thyroid microsomal antigen. Homology with the gene for thyroid peroxidase.

Seto P, Hirayu H, Magnusson RP, Gestautas J, Portmann L, DeGroot LJ, Rapoport B.

J Clin Invest. 1987 Oct;80(4):1205-8.

15.

The 4830C>A polymorphism within intron 5 affects the pattern of alternative splicing occurring within exon 6 of the thrombopoietin gene.

Webb KE, Martin JF, Cotton J, Erusalimsky JD, Humphries SE.

Exp Hematol. 2003 Jun;31(6):488-94.

PMID:
12829024
16.

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.

17.

Moderate doses of iodide in vivo inhibit cell proliferation and the expression of thyroperoxidase and Na+/I- symporter mRNAs in dog thyroid.

Uyttersprot N, Pelgrims N, Carrasco N, Gervy C, Maenhaut C, Dumont JE, Miot F.

Mol Cell Endocrinol. 1997 Aug 8;131(2):195-203.

PMID:
9296378
18.

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. Epub 2007 Jun 4.

PMID:
17547680
19.

Immunohistochemical loss of thyroid peroxidase in papillary thyroid carcinoma: strong suppression of peroxidase gene expression.

Tanaka T, Umeki K, Yamamoto I, Sugiyama S, Noguchi S, Ohtaki S.

J Pathol. 1996 May;179(1):89-94.

PMID:
8691351
20.

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.

PMID:
12938097

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