Kameya S - Search Results

1

CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina.

Mehalow AK, Kameya S, Smith RS, Hawes NL, Denegre JM, Young JA, Bechtold L, Haider NB, Tepass U, Heckenlively JR, Chang B, Naggert JK, Nishina PM. Mehalow AK, et al. Among authors: kameya s. Hum Mol Genet. 2003 Sep 1;12(17):2179-89. doi: 10.1093/hmg/ddg232. Epub 2003 Jul 15. Hum Mol Genet. 2003. PMID: 12915475

2

Mfrp, a gene encoding a frizzled related protein, is mutated in the mouse retinal degeneration 6.

Kameya S, Hawes NL, Chang B, Heckenlively JR, Naggert JK, Nishina PM. Kameya S, et al. Hum Mol Genet. 2002 Aug 1;11(16):1879-86. doi: 10.1093/hmg/11.16.1879. Hum Mol Genet. 2002. PMID: 12140190

3

Ocular abnormalities in Large(myd) and Large(vls) mice, spontaneous models for muscle, eye, and brain diseases.

Lee Y, Kameya S, Cox GA, Hsu J, Hicks W, Maddatu TP, Smith RS, Naggert JK, Peachey NS, Nishina PM. Lee Y, et al. Among authors: kameya s. Mol Cell Neurosci. 2005 Oct;30(2):160-72. doi: 10.1016/j.mcn.2005.07.009. Mol Cell Neurosci. 2005. PMID: 16111892

4

Dp260 disrupted mice revealed prolonged implicit time of the b-wave in ERG and loss of accumulation of beta-dystroglycan in the outer plexiform layer of the retina.

Kameya S, Araki E, Katsuki M, Mizota A, Adachi E, Nakahara K, Nonaka I, Sakuragi S, Takeda S, Nabeshima Y. Kameya S, et al. Hum Mol Genet. 1997 Dec;6(13):2195-203. doi: 10.1093/hmg/6.13.2195. Hum Mol Genet. 1997. PMID: 9361023

5

Reactive gliosis of astrocytes and Müller glial cells in retina of POMGnT1-deficient mice.

Takahashi H, Kanesaki H, Igarashi T, Kameya S, Yamaki K, Mizota A, Kudo A, Miyagoe-Suzuki Y, Takeda S, Takahashi H. Takahashi H, et al. Among authors: kameya s. Mol Cell Neurosci. 2011 Jun;47(2):119-30. doi: 10.1016/j.mcn.2011.03.006. Epub 2011 Apr 8. Mol Cell Neurosci. 2011. PMID: 21447391

6

Targeted disruption of exon 52 in the mouse dystrophin gene induced muscle degeneration similar to that observed in Duchenne muscular dystrophy.

Araki E, Nakamura K, Nakao K, Kameya S, Kobayashi O, Nonaka I, Kobayashi T, Katsuki M. Araki E, et al. Among authors: kameya s. Biochem Biophys Res Commun. 1997 Sep 18;238(2):492-7. doi: 10.1006/bbrc.1997.7328. Biochem Biophys Res Commun. 1997. PMID: 9299538

7

alpha1-syntrophin gene disruption results in the absence of neuronal-type nitric-oxide synthase at the sarcolemma but does not induce muscle degeneration.

Kameya S, Miyagoe Y, Nonaka I, Ikemoto T, Endo M, Hanaoka K, Nabeshima Y, Takeda S. Kameya S, et al. J Biol Chem. 1999 Jan 22;274(4):2193-200. doi: 10.1074/jbc.274.4.2193. J Biol Chem. 1999. PMID: 9890982 Free article.

8

The expression of dystrophin and alpha1-syntrophin during skeletal muscle regeneration.

Hoshino S, Ohkoshi N, Ishii A, Kameya S, Takeda S, Shoji S. Hoshino S, et al. Among authors: kameya s. J Muscle Res Cell Motil. 2001;22(2):185-91. doi: 10.1023/a:1010553104341. J Muscle Res Cell Motil. 2001. PMID: 11519741

9

A new mutation in the RP1L1 gene in a patient with occult macular dystrophy associated with a depolarizing pattern of focal macular electroretinograms.

Kabuto T, Takahashi H, Goto-Fukuura Y, Igarashi T, Akahori M, Kameya S, Iwata T, Mizota A, Yamaki K, Miyake Y, Takahashi H. Kabuto T, et al. Among authors: kameya s. Mol Vis. 2012;18:1031-9. Epub 2012 Apr 24. Mol Vis. 2012. PMID: 22605915 Free PMC article.

10

High-resolution en face images of microcystic macular edema in patients with autosomal dominant optic atrophy.

Gocho K, Kikuchi S, Kabuto T, Kameya S, Shinoda K, Mizota A, Yamaki K, Takahashi H. Gocho K, et al. Among authors: kameya s. Biomed Res Int. 2013;2013:676803. doi: 10.1155/2013/676803. Epub 2013 Nov 28. Biomed Res Int. 2013. PMID: 24369534 Free PMC article.

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