Kobayashi K - Search Results

1

Psychosocial Twin Cohort Studies in Japan: The Keio Twin Research Center (KoTReC).

Ando J, Fujisawa KK, Hiraishi K, Shikishima C, Kawamoto T, Nozaki M, Yamagata S, Takahashi Y, Suzuki K, Someya Y, Ozaki K, Deno M, Tanaka M, Sasaki S, Toda T, Kobayashi K, Sakagami M, Okada M, Kijima N, Takizawa R, Murayama K. Ando J, et al. Among authors: kobayashi k. Twin Res Hum Genet. 2019 Dec;22(6):591-596. doi: 10.1017/thg.2019.109. Epub 2020 Jan 15. Twin Res Hum Genet. 2019. PMID: 31937382

2

Association studies of multiple candidate genes for Parkinson's disease using single nucleotide polymorphisms.

Momose Y, Murata M, Kobayashi K, Tachikawa M, Nakabayashi Y, Kanazawa I, Toda T. Momose Y, et al. Among authors: kobayashi k. Ann Neurol. 2002 Jan;51(1):133-6. doi: 10.1002/ana.10079. Ann Neurol. 2002. PMID: 11782995

3

Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseases.

Tachikawa M, Nagai Y, Nakamura K, Kobayashi K, Fujiwara T, Han HJ, Nakabayashi Y, Ichikawa Y, Goto J, Kanazawa I, Nakamura Y, Toda T. Tachikawa M, et al. Among authors: kobayashi k. J Hum Genet. 2002;47(6):275-8. doi: 10.1007/s100380200039. J Hum Genet. 2002. PMID: 12111376

4

Structure-function analysis of human protein O-linked mannose beta1,2-N-acetylglucosaminyltransferase 1, POMGnT1.

Akasaka-Manya K, Manya H, Kobayashi K, Toda T, Endo T. Akasaka-Manya K, et al. Among authors: kobayashi k. Biochem Biophys Res Commun. 2004 Jul 16;320(1):39-44. doi: 10.1016/j.bbrc.2004.05.129. Biochem Biophys Res Commun. 2004. PMID: 15207699

5

[Fukuyama-type congenital muscular dystrophy and alpha-dystroglycanopathy].

Kobayashi K, Toda T. Kobayashi K, et al. Tanpakushitsu Kakusan Koso. 2004 Nov;49(15 Suppl):2457-62. Tanpakushitsu Kakusan Koso. 2004. PMID: 15553001 Review. Japanese. No abstract available.

6

Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia.

Amino T, Ishikawa K, Toru S, Ishiguro T, Sato N, Tsunemi T, Murata M, Kobayashi K, Inazawa J, Toda T, Mizusawa H. Amino T, et al. Among authors: kobayashi k. J Hum Genet. 2007;52(8):643-649. doi: 10.1007/s10038-007-0154-1. Epub 2007 Jul 5. J Hum Genet. 2007. PMID: 17611710

7

Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy.

Kanagawa M, Nishimoto A, Chiyonobu T, Takeda S, Miyagoe-Suzuki Y, Wang F, Fujikake N, Taniguchi M, Lu Z, Tachikawa M, Nagai Y, Tashiro F, Miyazaki J, Tajima Y, Takeda S, Endo T, Kobayashi K, Campbell KP, Toda T. Kanagawa M, et al. Among authors: kobayashi k. Hum Mol Genet. 2009 Feb 15;18(4):621-31. doi: 10.1093/hmg/ddn387. Epub 2008 Nov 18. Hum Mol Genet. 2009. PMID: 19017726 Free PMC article.

8

Post-translational maturation of dystroglycan is necessary for pikachurin binding and ribbon synaptic localization.

Kanagawa M, Omori Y, Sato S, Kobayashi K, Miyagoe-Suzuki Y, Takeda S, Endo T, Furukawa T, Toda T. Kanagawa M, et al. Among authors: kobayashi k. J Biol Chem. 2010 Oct 8;285(41):31208-16. doi: 10.1074/jbc.M110.116343. Epub 2010 Aug 3. J Biol Chem. 2010. PMID: 20682766 Free PMC article.

9

Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy.

Taniguchi-Ikeda M, Kobayashi K, Kanagawa M, Yu CC, Mori K, Oda T, Kuga A, Kurahashi H, Akman HO, DiMauro S, Kaji R, Yokota T, Takeda S, Toda T. Taniguchi-Ikeda M, et al. Among authors: kobayashi k. Nature. 2011 Oct 5;478(7367):127-31. doi: 10.1038/nature10456. Nature. 2011. PMID: 21979053 Free PMC article.

10

Mislocalization of fukutin protein by disease-causing missense mutations can be rescued with treatments directed at folding amelioration.

Tachikawa M, Kanagawa M, Yu CC, Kobayashi K, Toda T. Tachikawa M, et al. Among authors: kobayashi k. J Biol Chem. 2012 Mar 9;287(11):8398-406. doi: 10.1074/jbc.M111.300905. Epub 2012 Jan 24. J Biol Chem. 2012. PMID: 22275357 Free PMC article.

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