Noda T - Search Results

1

Analysis on the phenotype of E-FABP-gene knockout mice.

Owada Y, Suzuki I, Noda T, Kondo H. Owada Y, et al. Among authors: noda t. Mol Cell Biochem. 2002 Oct;239(1-2):83-6. Mol Cell Biochem. 2002. PMID: 12479572

2

Altered water barrier function in epidermal-type fatty acid binding protein-deficient mice.

Owada Y, Takano H, Yamanaka H, Kobayashi H, Sugitani Y, Tomioka Y, Suzuki I, Suzuki R, Terui T, Mizugaki M, Tagami H, Noda T, Kondo H. Owada Y, et al. Among authors: noda t. J Invest Dermatol. 2002 Mar;118(3):430-5. doi: 10.1046/j.0022-202x.2001.01616.x. J Invest Dermatol. 2002. PMID: 11874481 Free article.

3

Altered emotional behavioral responses in mice lacking brain-type fatty acid-binding protein gene.

Owada Y, Abdelwahab SA, Kitanaka N, Sakagami H, Takano H, Sugitani Y, Sugawara M, Kawashima H, Kiso Y, Mobarakeh JI, Yanai K, Kaneko K, Sasaki H, Kato H, Saino-Saito S, Matsumoto N, Akaike N, Noda T, Kondo H. Owada Y, et al. Among authors: noda t. Eur J Neurosci. 2006 Jul;24(1):175-87. doi: 10.1111/j.1460-9568.2006.04855.x. Eur J Neurosci. 2006. PMID: 16882015

4

Deficiency of zonula occludens-1 causes embryonic lethal phenotype associated with defected yolk sac angiogenesis and apoptosis of embryonic cells.

Katsuno T, Umeda K, Matsui T, Hata M, Tamura A, Itoh M, Takeuchi K, Fujimori T, Nabeshima Y, Noda T, Tsukita S, Tsukita S. Katsuno T, et al. Among authors: noda t. Mol Biol Cell. 2008 Jun;19(6):2465-75. doi: 10.1091/mbc.e07-12-1215. Epub 2008 Mar 19. Mol Biol Cell. 2008. PMID: 18353970 Free PMC article.

5

Late-onset hearing loss in a mouse model of DFN3 non-syndromic deafness: morphologic and immunohistochemical analyses.

Xia AP, Kikuchi T, Minowa O, Katori Y, Oshima T, Noda T, Ikeda K. Xia AP, et al. Among authors: noda t. Hear Res. 2002 Apr;166(1-2):150-8. doi: 10.1016/s0378-5955(02)00309-x. Hear Res. 2002. PMID: 12062767

6

A monogenic dominant mutation in Rom1 generated by N-ethyl-N-nitrosourea mutagenesis causes retinal degeneration in mice.

Sato H, Suzuki T, Ikeda K, Masuya H, Sezutsu H, Kaneda H, Kobayashi K, Miura I, Kurihara Y, Yokokura S, Nishida K, Tamai M, Gondo Y, Noda T, Wakana S. Sato H, et al. Among authors: noda t. Mol Vis. 2010 Mar 10;16:378-91. Mol Vis. 2010. PMID: 20300562 Free PMC article.

7

Biphasic response of pancreatic beta-cell mass to ablation of tuberous sclerosis complex 2 in mice.

Shigeyama Y, Kobayashi T, Kido Y, Hashimoto N, Asahara S, Matsuda T, Takeda A, Inoue T, Shibutani Y, Koyanagi M, Uchida T, Inoue M, Hino O, Kasuga M, Noda T. Shigeyama Y, et al. Among authors: noda t. Mol Cell Biol. 2008 May;28(9):2971-9. doi: 10.1128/MCB.01695-07. Epub 2008 Mar 3. Mol Cell Biol. 2008. PMID: 18316403 Free PMC article.

8

The corepressor mSin3A regulates phosphorylation-induced activation, intranuclear location, and stability of AML1.

Imai Y, Kurokawa M, Yamaguchi Y, Izutsu K, Nitta E, Mitani K, Satake M, Noda T, Ito Y, Hirai H. Imai Y, et al. Among authors: noda t. Mol Cell Biol. 2004 Feb;24(3):1033-43. doi: 10.1128/MCB.24.3.1033-1043.2004. Mol Cell Biol. 2004. PMID: 14729951 Free PMC article.

9

RNA-binding protein Musashi family: roles for CNS stem cells and a subpopulation of ependymal cells revealed by targeted disruption and antisense ablation.

Sakakibara S, Nakamura Y, Yoshida T, Shibata S, Koike M, Takano H, Ueda S, Uchiyama Y, Noda T, Okano H. Sakakibara S, et al. Among authors: noda t. Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):15194-9. doi: 10.1073/pnas.232087499. Epub 2002 Oct 29. Proc Natl Acad Sci U S A. 2002. PMID: 12407178 Free PMC article.

10

Targeted disruption of FSCN2 gene induces retinopathy in mice.

Yokokura S, Wada Y, Nakai S, Sato H, Yao R, Yamanaka H, Ito S, Sagara Y, Takahashi M, Nakamura Y, Tamai M, Noda T. Yokokura S, et al. Among authors: noda t. Invest Ophthalmol Vis Sci. 2005 Aug;46(8):2905-15. doi: 10.1167/iovs.04-0856. Invest Ophthalmol Vis Sci. 2005. PMID: 16043865

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