Kunieda T - Search Results

1

Skeletal analysis of the long bone abnormality (lbab/lbab) mouse, a novel chondrodysplastic C-type natriuretic peptide mutant.

Kondo E, Yasoda A, Tsuji T, Fujii T, Miura M, Kanamoto N, Tamura N, Arai H, Kunieda T, Nakao K. Kondo E, et al. Among authors: kunieda t. Calcif Tissue Int. 2012 Apr;90(4):307-18. doi: 10.1007/s00223-011-9567-0. Epub 2012 Jan 25. Calcif Tissue Int. 2012. PMID: 22271248 Free article.

2

Hypomorphic mutation in mouse Nppc gene causes retarded bone growth due to impaired endochondral ossification.

Tsuji T, Kondo E, Yasoda A, Inamoto M, Kiyosu C, Nakao K, Kunieda T. Tsuji T, et al. Among authors: kunieda t. Biochem Biophys Res Commun. 2008 Nov 7;376(1):186-90. doi: 10.1016/j.bbrc.2008.08.139. Epub 2008 Sep 4. Biochem Biophys Res Commun. 2008. PMID: 18775416

3

A loss-of-function mutation in natriuretic peptide receptor 2 (Npr2) gene is responsible for disproportionate dwarfism in cn/cn mouse.

Tsuji T, Kunieda T. Tsuji T, et al. Among authors: kunieda t. J Biol Chem. 2005 Apr 8;280(14):14288-92. doi: 10.1074/jbc.C500024200. Epub 2005 Feb 18. J Biol Chem. 2005. PMID: 15722353 Free article.

4

Characterization of the dwg mutations: dwg and dwg(Bayer) are new mutant alleles of the Ggt1 gene.

Tsuji T, Yamada K, Kunieda T. Tsuji T, et al. Among authors: kunieda t. Mamm Genome. 2009 Nov-Dec;20(11-12):711-9. doi: 10.1007/s00335-009-9221-6. Epub 2009 Sep 16. Mamm Genome. 2009. PMID: 19760322

5

Gastrointestinal tract disorder in natriuretic peptide receptor B gene mutant mice.

Sogawa C, Abe A, Tsuji T, Koizumi M, Saga T, Kunieda T. Sogawa C, et al. Among authors: kunieda t. Am J Pathol. 2010 Aug;177(2):822-8. doi: 10.2353/ajpath.2010.091278. Epub 2010 Jul 8. Am J Pathol. 2010. PMID: 20616347 Free PMC article.

6

New mutant mouse with skeletal deformities caused by mutation in delta like 3 (Dll3) gene.

Shinkai Y, Tsuji T, Kawamoto Y, Kunieda T. Shinkai Y, et al. Among authors: kunieda t. Exp Anim. 2004 Apr;53(2):129-36. doi: 10.1538/expanim.53.129. Exp Anim. 2004. PMID: 15153675 Free article.

7

Short-limbed dwarfism: slw is a new allele of Npr2 causing chondrodysplasia.

Sogawa C, Tsuji T, Shinkai Y, Katayama K, Kunieda T. Sogawa C, et al. Among authors: kunieda t. J Hered. 2007 Sep-Oct;98(6):575-80. doi: 10.1093/jhered/esm065. Epub 2007 Aug 28. J Hered. 2007. PMID: 17728275

8

Characterization and linkage mapping of an ENU-induced mutant mouse with defective spermatogenesis.

Asano Y, Akiyama K, Tsuji T, Takahashi S, Noguchi J, Kunieda T. Asano Y, et al. Among authors: kunieda t. Exp Anim. 2009 Oct;58(5):525-32. doi: 10.1538/expanim.58.525. Exp Anim. 2009. PMID: 19897936 Free article.

9

NPPC/NPR2 signaling is essential for oocyte meiotic arrest and cumulus oophorus formation during follicular development in the mouse ovary.

Kiyosu C, Tsuji T, Yamada K, Kajita S, Kunieda T. Kiyosu C, et al. Among authors: kunieda t. Reproduction. 2012 Aug;144(2):187-93. doi: 10.1530/REP-12-0050. Epub 2012 Jun 13. Reproduction. 2012. PMID: 22696190

10

Phenotypic characterization of Ggt1(dwg/dwg) mice,a mouse model for hereditary γ-glutamyltransferase deficiency.

Yamada K, Tsuji T, Kunieda T. Yamada K, et al. Among authors: kunieda t. Exp Anim. 2013;62(2):151-7. doi: 10.1538/expanim.62.151. Exp Anim. 2013. PMID: 23615310 Free article.

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