Takagishi Y - Search Results

1

Remodeling of hepatic metabolism and hyperaminoacidemia in mice deficient in proglucagon-derived peptides.

Watanabe C, Seino Y, Miyahira H, Yamamoto M, Fukami A, Ozaki N, Takagishi Y, Sato J, Fukuwatari T, Shibata K, Oiso Y, Murata Y, Hayashi Y. Watanabe C, et al. Among authors: takagishi y. Diabetes. 2012 Jan;61(1):74-84. doi: 10.2337/db11-0739. Diabetes. 2012. PMID: 22187375 Free PMC article.

2

Ectopic expression of GIP in pancreatic β-cells maintains enhanced insulin secretion in mice with complete absence of proglucagon-derived peptides.

Fukami A, Seino Y, Ozaki N, Yamamoto M, Sugiyama C, Sakamoto-Miura E, Himeno T, Takagishi Y, Tsunekawa S, Ali S, Drucker DJ, Murata Y, Seino Y, Oiso Y, Hayashi Y. Fukami A, et al. Among authors: takagishi y. Diabetes. 2013 Feb;62(2):510-8. doi: 10.2337/db12-0294. Epub 2012 Oct 25. Diabetes. 2013. PMID: 23099862 Free PMC article.

3

Xu S, Hayashi Y, Takagishi Y, Itoh M, Murata Y. Xu S, et al. Among authors: takagishi y. PLoS One. 2013 May 9;8(5):e64415. doi: 10.1371/journal.pone.0064415. Print 2013. PLoS One. 2013. PMID: 23671715 Free PMC article.

4

Pancreatic Neuroendocrine Tumors in Mice Deficient in Proglucagon-Derived Peptides.

Takano Y, Kasai K, Takagishi Y, Kikumori T, Imai T, Murata Y, Hayashi Y. Takano Y, et al. Among authors: takagishi y. PLoS One. 2015 Jul 20;10(7):e0133812. doi: 10.1371/journal.pone.0133812. eCollection 2015. PLoS One. 2015. PMID: 26192435 Free PMC article.

5

Myosin Va mutation in rats is an animal model for the human hereditary neurological disease, Griscelli syndrome type 1.

Takagishi Y, Murata Y. Takagishi Y, et al. Ann N Y Acad Sci. 2006 Nov;1086:66-80. doi: 10.1196/annals.1377.006. Ann N Y Acad Sci. 2006. PMID: 17185506 Review.

6

Inactivation of the Rcan2 gene in mice ameliorates the age- and diet-induced obesity by causing a reduction in food intake.

Sun XY, Hayashi Y, Xu S, Kanou Y, Takagishi Y, Tang YP, Murata Y. Sun XY, et al. Among authors: takagishi y. PLoS One. 2011 Jan 27;6(1):e14605. doi: 10.1371/journal.pone.0014605. PLoS One. 2011. PMID: 21298050 Free PMC article.

7

Insertion of an intracisternal A particle retrotransposon element in plasma membrane calcium ATPase 2 gene attenuates its expression and produces an ataxic phenotype in joggle mutant mice.

Sun XY, Chen ZY, Hayashi Y, Kanou Y, Takagishi Y, Oda S, Murata Y. Sun XY, et al. Among authors: takagishi y. Gene. 2008 Mar 31;411(1-2):94-102. doi: 10.1016/j.gene.2008.01.013. Epub 2008 Jan 26. Gene. 2008. PMID: 18280673

8

Prevention of neural tube defects by loss of function of inducible nitric oxide synthase in fetuses of a mouse model of streptozotocin-induced diabetes.

Sugimura Y, Murase T, Oyama K, Uchida A, Sato N, Hayasaka S, Kano Y, Takagishi Y, Hayashi Y, Oiso Y, Murata Y. Sugimura Y, et al. Among authors: takagishi y. Diabetologia. 2009 May;52(5):962-71. doi: 10.1007/s00125-009-1312-0. Epub 2009 Mar 13. Diabetologia. 2009. PMID: 19283362

9

Mapping of jog locus to the region between D6Mit104 and D6Mit336 on mouse chromosome 6.

Sun XY, Chen ZY, Kanou Y, Takagishi Y, Hayashi Y, Ohno T, Murata Y, Oda S. Sun XY, et al. Among authors: takagishi y. Exp Anim. 2007 Oct;56(5):389-92. doi: 10.1538/expanim.56.389. Exp Anim. 2007. PMID: 18075201 Free article.

10

A novel Caspr mutation causes the shambling mouse phenotype by disrupting axoglial interactions of myelinated nerves.

Sun XY, Takagishi Y, Okabe E, Chishima Y, Kanou Y, Murase S, Mizumura K, Inaba M, Komatsu Y, Hayashi Y, Peles E, Oda S, Murata Y. Sun XY, et al. Among authors: takagishi y. J Neuropathol Exp Neurol. 2009 Nov;68(11):1207-18. doi: 10.1097/NEN.0b013e3181be2e96. J Neuropathol Exp Neurol. 2009. PMID: 19816196

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