PubMed for id: 22018

Year	Number of Results
1973	1
1989	1
1992	1
1993	2
1994	3
1995	1
1996	1
1998	1
1999	2
2000	2
2001	2
2002	3
2003	3
2004	2
2005	4
2006	1
2010	2
2011	6
2013	4
2014	3
2017	2
2018	2
2022	1
2023	1
2024	0

1

Hearing impairment in hypothyroid dwarf mice caused by mutations of the thyroid peroxidase gene.

Johnson KR, Gagnon LH, Longo-Guess CM, Harris BS, Chang B. Johnson KR, et al. J Assoc Res Otolaryngol. 2014 Feb;15(1):45-55. doi: 10.1007/s10162-013-0427-7. Epub 2013 Dec 3. J Assoc Res Otolaryngol. 2014. PMID: 24297261 Free PMC article.

2

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. Takabayashi S, et al. Mol Endocrinol. 2006 Oct;20(10):2584-90. doi: 10.1210/me.2006-0099. Epub 2006 Jun 8. Mol Endocrinol. 2006. PMID: 16762971

3

Ascidian homologs of mammalian thyroid peroxidase genes are expressed in the thyroid-equivalent region of the endostyle.

Ogasawara M, Di Lauro R, Satoh N. Ogasawara M, et al. J Exp Zool. 1999 Aug 15;285(2):158-69. doi: 10.1002/(sici)1097-010x(19990815)285:2<158::aid-jez8>3.0.co;2-0. J Exp Zool. 1999. PMID: 10440727

4

Nucleotide sequence of the cDNA encoding mouse thyroid peroxidase.

Kotani T, Umeki K, Yamamoto I, Takeuchi M, Takechi S, Nakayama T, Ohtaki S. Kotani T, et al. Gene. 1993 Jan 30;123(2):289-90. doi: 10.1016/0378-1119(93)90141-o. Gene. 1993. PMID: 7916704

5

Normal peroxidase activity in Pendred's syndrome.

Burrow GN, Spaulding SW, Alexander NM, Bower BF. Burrow GN, et al. J Clin Endocrinol Metab. 1973 Mar;36(3):522-30. doi: 10.1210/jcem-36-3-522. J Clin Endocrinol Metab. 1973. PMID: 4346605 No abstract available.

6

Hematopoietic stem cells temporally transition to thrombopoietin dependence in the fetal liver.

Lee Y, DiMaulo-Milk E, Leslie J, Ding L. Lee Y, et al. Sci Adv. 2022 Mar 18;8(11):eabm7688. doi: 10.1126/sciadv.abm7688. Epub 2022 Mar 16. Sci Adv. 2022. PMID: 35294228 Free PMC article.

7

Lnk Deficiency Leads to TPO-Mediated Osteoclastogenesis and Increased Bone Mass Phenotype.

Olivos DJ 3rd, Alvarez M, Cheng YH, Hooker RA, Ciovacco WA, Bethel M, McGough H, Yim C, Chitteti BR, Eleniste PP, Horowitz MC, Srour EF, Bruzzaniti A, Fuchs RK, Kacena MA. Olivos DJ 3rd, et al. J Cell Biochem. 2017 Aug;118(8):2231-2240. doi: 10.1002/jcb.25874. Epub 2017 Apr 18. J Cell Biochem. 2017. PMID: 28067429 Free PMC article.

8

Transgenic mice overexpressing murine thrombopoietin develop myelofibrosis and osteosclerosis.

Kakumitsu H, Kamezaki K, Shimoda K, Karube K, Haro T, Numata A, Shide K, Matsuda T, Oshima K, Harada M. Kakumitsu H, et al. Leuk Res. 2005 Jul;29(7):761-9. doi: 10.1016/j.leukres.2004.12.009. Epub 2005 Mar 2. Leuk Res. 2005. PMID: 15927672

9

A 20-basepair duplication in the human thyroid peroxidase gene results in a total iodide organification defect and congenital hypothyroidism.

Bikker H, den Hartog MT, Baas F, Gons MH, Vulsma T, de Vijlder JJ. Bikker H, et al. J Clin Endocrinol Metab. 1994 Jul;79(1):248-52. doi: 10.1210/jcem.79.1.8027236. J Clin Endocrinol Metab. 1994. PMID: 8027236

10

Regional localization of the gene for thyroid peroxidase to human chromosome 2p25 and mouse chromosome 12C.

Endo Y, Onogi S, Umeki K, Yamamoto I, Kotani T, Ohtaki S, Fujita T. Endo Y, et al. Genomics. 1995 Feb 10;25(3):760-1. doi: 10.1016/0888-7543(95)80028-k. Genomics. 1995. PMID: 7759120 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

47 results

Results by year