Agui T - Search Results

1

A mutation in Tpst2 encoding tyrosylprotein sulfotransferase causes dwarfism associated with hypothyroidism.

Sasaki N, Hosoda Y, Nagata A, Ding M, Cheng JM, Miyamoto T, Okano S, Asano A, Miyoshi I, Agui T. Sasaki N, et al. Among authors: agui t. Mol Endocrinol. 2007 Jul;21(7):1713-21. doi: 10.1210/me.2007-0040. Epub 2007 Apr 24. Mol Endocrinol. 2007. PMID: 17456791 Free article.

2

Female infertility in grt mice is caused by thyroid hormone deficiency, not by insufficient TPST2 activity in the reproductive organs.

Hosoda Y, Sasaki N, Agui T. Hosoda Y, et al. Among authors: agui t. J Vet Med Sci. 2008 Oct;70(10):1043-9. doi: 10.1292/jvms.70.1043. J Vet Med Sci. 2008. PMID: 18981659 Free article.

3

Hypothyroid phenotype of the Tpst2 mutant mouse is dependent upon genetic background.

Hosoda Y, Sasaki N, Agui T. Hosoda Y, et al. Among authors: agui t. Biomed Res. 2010 Jun;31(3):207-11. doi: 10.2220/biomedres.31.207. Biomed Res. 2010. PMID: 20622471 Free article.

4

A missense mutation G2320R in the thyroglobulin gene causes non-goitrous congenital primary hypothyroidism in the WIC-rdw rat.

Kim PS, Ding M, Menon S, Jung CG, Cheng JM, Miyamoto T, Li B, Furudate S, Agui T. Kim PS, et al. Among authors: agui t. Mol Endocrinol. 2000 Dec;14(12):1944-53. doi: 10.1210/mend.14.12.0571. Mol Endocrinol. 2000. PMID: 11117525

5

Examination of the Lunatic fringe and Uncx4.1 expression by whole-mount in situ hybridization in the embryo of the CKH-Jsr (jumbled spine and ribs) mouse.

Okano S, Asano A, Sasaki N, Kon Y, Watanabe T, Agui T. Okano S, et al. Among authors: agui t. Jpn J Vet Res. 2005 Feb;52(4):145-9. Jpn J Vet Res. 2005. PMID: 15822856

6

Deficiency of the tensin2 gene in the ICGN mouse: an animal model for congenital nephrotic syndrome.

Cho AR, Uchio-Yamada K, Torigai T, Miyamoto T, Miyoshi I, Matsuda J, Kurosawa T, Kon Y, Asano A, Sasaki N, Agui T. Cho AR, et al. Among authors: agui t. Mamm Genome. 2006 May;17(5):407-16. doi: 10.1007/s00335-005-0167-z. Mamm Genome. 2006. PMID: 16688531

7

A deletion mutation of the protein tyrosine phosphatase kappa (Ptprk) gene is responsible for T-helper immunodeficiency (thid) in the LEC rat.

Asano A, Tsubomatsu K, Jung CG, Sasaki N, Agui T. Asano A, et al. Among authors: agui t. Mamm Genome. 2007 Nov;18(11):779-86. doi: 10.1007/s00335-007-9062-0. Epub 2007 Oct 2. Mamm Genome. 2007. PMID: 17909891 Free article.

8

Identifying quantitative trait loci affecting resistance to congenital hypothyroidism in 129/SvJcl strain mice.

Hosoda Y, Sasaki N, Kameda Y, Torigoe D, Agui T. Hosoda Y, et al. Among authors: agui t. PLoS One. 2012;7(1):e31035. doi: 10.1371/journal.pone.0031035. Epub 2012 Jan 27. PLoS One. 2012. PMID: 22299049 Free PMC article.

9

Mapping of the grt locus to mouse chromosome 5.

Agui T, Miyamoto T, Tsumura H, Yoshida T. Agui T, et al. Mamm Genome. 1997 Dec;8(12):944. doi: 10.1007/s003359900632. Mamm Genome. 1997. PMID: 9383300 No abstract available.

10

Exon skipping of exonuclease 1 in MRL/MpJ mice is caused by a nucleotide substitution of the branchpoint sequence in intron eight.

Namiki Y, Kon Y, Sasaki N, Agui T, Endoh D. Namiki Y, et al. Among authors: agui t. Jpn J Vet Res. 2004 Nov;52(3):125-34. Jpn J Vet Res. 2004. PMID: 15631010

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