Manya H - Search Results

1

CDP-ribitol prodrug treatment ameliorates ISPD-deficient muscular dystrophy mouse model.

Tokuoka H, Imae R, Nakashima H, Manya H, Masuda C, Hoshino S, Kobayashi K, Lefeber DJ, Matsumoto R, Okada T, Endo T, Kanagawa M, Toda T. Tokuoka H, et al. Among authors: manya h. Nat Commun. 2022 Apr 14;13(1):1847. doi: 10.1038/s41467-022-29473-4. Nat Commun. 2022. PMID: 35422047 Free PMC article.

2

Comparative study of the asparagine-linked sugar chains of human lipocalin-type prostaglandin D synthase purified from urine and amniotic fluid, and recombinantly expressed in Chinese hamster ovary cells.

Manya H, Sato Y, Eguchi N, Seiki K, Oda H, Nakajima H, Urade Y, Endo T. Manya H, et al. J Biochem. 2000 Jun;127(6):1001-11. doi: 10.1093/oxfordjournals.jbchem.a022691. J Biochem. 2000. PMID: 10833268 Free article.

3

Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1.

Yoshida A, Kobayashi K, Manya H, Taniguchi K, Kano H, Mizuno M, Inazu T, Mitsuhashi H, Takahashi S, Takeuchi M, Herrmann R, Straub V, Talim B, Voit T, Topaloglu H, Toda T, Endo T. Yoshida A, et al. Among authors: manya h. Dev Cell. 2001 Nov;1(5):717-24. doi: 10.1016/s1534-5807(01)00070-3. Dev Cell. 2001. PMID: 11709191 Free article.

4

Deficiency of alpha-dystroglycan in muscle-eye-brain disease.

Kano H, Kobayashi K, Herrmann R, Tachikawa M, Manya H, Nishino I, Nonaka I, Straub V, Talim B, Voit T, Topaloglu H, Endo T, Yoshikawa H, Toda T. Kano H, et al. Among authors: manya h. Biochem Biophys Res Commun. 2002 Mar 15;291(5):1283-6. doi: 10.1006/bbrc.2002.6608. Biochem Biophys Res Commun. 2002. PMID: 11883957

5

Klotho protein deficiency leads to overactivation of mu-calpain.

Manya H, Inomata M, Fujimori T, Dohmae N, Sato Y, Takio K, Nabeshima Y, Endo T. Manya H, et al. J Biol Chem. 2002 Sep 20;277(38):35503-8. doi: 10.1074/jbc.M206033200. Epub 2002 Jul 15. J Biol Chem. 2002. PMID: 12119304 Free article.

6

Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease.

Taniguchi K, Kobayashi K, Saito K, Yamanouchi H, Ohnuma A, Hayashi YK, Manya H, Jin DK, Lee M, Parano E, Falsaperla R, Pavone P, Van Coster R, Talim B, Steinbrecher A, Straub V, Nishino I, Topaloglu H, Voit T, Endo T, Toda T. Taniguchi K, et al. Among authors: manya h. Hum Mol Genet. 2003 Mar 1;12(5):527-34. doi: 10.1093/hmg/ddg043. Hum Mol Genet. 2003. PMID: 12588800

7

Loss-of-function of an N-acetylglucosaminyltransferase, POMGnT1, in muscle-eye-brain disease.

Manya H, Sakai K, Kobayashi K, Taniguchi K, Kawakita M, Toda T, Endo T. Manya H, et al. Biochem Biophys Res Commun. 2003 Jun 20;306(1):93-7. doi: 10.1016/s0006-291x(03)00924-0. Biochem Biophys Res Commun. 2003. PMID: 12788071

8

Galectin-1 induces astrocyte differentiation, which leads to production of brain-derived neurotrophic factor.

Sasaki T, Hirabayashi J, Manya H, Kasai K, Endo T. Sasaki T, et al. Among authors: manya h. Glycobiology. 2004 Apr;14(4):357-63. doi: 10.1093/glycob/cwh043. Epub 2003 Dec 23. Glycobiology. 2004. PMID: 14693917

9

Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity.

Manya H, Chiba A, Yoshida A, Wang X, Chiba Y, Jigami Y, Margolis RU, Endo T. Manya H, et al. Proc Natl Acad Sci U S A. 2004 Jan 13;101(2):500-5. doi: 10.1073/pnas.0307228101. Epub 2003 Dec 29. Proc Natl Acad Sci U S A. 2004. PMID: 14699049 Free PMC article.

10

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: manya h. 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

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