Miyata N - Search Results

1

Recent insights into peroxisome biogenesis and associated diseases.

Fujiki Y, Abe Y, Imoto Y, Tanaka AJ, Okumoto K, Honsho M, Tamura S, Miyata N, Yamashita T, Chung WK, Kuroiwa T. Fujiki Y, et al. Among authors: miyata n. J Cell Sci. 2020 May 11;133(9):jcs236943. doi: 10.1242/jcs.236943. J Cell Sci. 2020. PMID: 32393673 Review.

2

Shuttling mechanism of peroxisome targeting signal type 1 receptor Pex5: ATP-independent import and ATP-dependent export.

Miyata N, Fujiki Y. Miyata N, et al. Mol Cell Biol. 2005 Dec;25(24):10822-32. doi: 10.1128/MCB.25.24.10822-10832.2005. Mol Cell Biol. 2005. PMID: 16314507 Free PMC article.

3

Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p involved in shuttling of the PTS1 receptor Pex5p in peroxisome biogenesis.

Fujiki Y, Miyata N, Matsumoto N, Tamura S. Fujiki Y, et al. Among authors: miyata n. Biochem Soc Trans. 2008 Feb;36(Pt 1):109-13. doi: 10.1042/BST0360109. Biochem Soc Trans. 2008. PMID: 18208396 Review.

4

New insights into dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p in shuttling of PTS1-receptor Pex5p during peroxisome biogenesis.

Fujiki Y, Nashiro C, Miyata N, Tamura S, Okumoto K. Fujiki Y, et al. Among authors: miyata n. Biochim Biophys Acta. 2012 Jan;1823(1):145-9. doi: 10.1016/j.bbamcr.2011.10.012. Epub 2011 Nov 4. Biochim Biophys Acta. 2012. PMID: 22079764 Free article. Review.

5

The VDAC2-BAK axis regulates peroxisomal membrane permeability.

Hosoi KI, Miyata N, Mukai S, Furuki S, Okumoto K, Cheng EH, Fujiki Y. Hosoi KI, et al. Among authors: miyata n. J Cell Biol. 2017 Mar 6;216(3):709-722. doi: 10.1083/jcb.201605002. Epub 2017 Feb 7. J Cell Biol. 2017. PMID: 28174205 Free PMC article.

6

Identification of Peroxisomal Protein Complexes with PTS Receptors, Pex5 and Pex7, in Mammalian Cells.

Okumoto K, Miyata N, Fujiki Y. Okumoto K, et al. Among authors: miyata n. Subcell Biochem. 2018;89:287-298. doi: 10.1007/978-981-13-2233-4_12. Subcell Biochem. 2018. PMID: 30378028

7

Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.

Matsumoto N, Tamura S, Furuki S, Miyata N, Moser A, Shimozawa N, Moser HW, Suzuki Y, Kondo N, Fujiki Y. Matsumoto N, et al. Among authors: miyata n. Am J Hum Genet. 2003 Aug;73(2):233-46. doi: 10.1086/377004. Epub 2003 Jul 8. Am J Hum Genet. 2003. PMID: 12851857 Free PMC article.

8

Mutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p x Pex6p complex.

Furuki S, Tamura S, Matsumoto N, Miyata N, Moser A, Moser HW, Fujiki Y. Furuki S, et al. Among authors: miyata n. J Biol Chem. 2006 Jan 20;281(3):1317-23. doi: 10.1074/jbc.M510044200. Epub 2005 Oct 27. J Biol Chem. 2006. PMID: 16257970 Free article.

9

In vitro import of peroxisome-targeting signal type 2 (PTS2) receptor Pex7p into peroxisomes.

Miyata N, Hosoi K, Mukai S, Fujiki Y. Miyata N, et al. Biochim Biophys Acta. 2009 May;1793(5):860-70. doi: 10.1016/j.bbamcr.2009.02.007. Epub 2009 Mar 2. Biochim Biophys Acta. 2009. PMID: 19264098 Free article.

10

Cysteine ubiquitination of PTS1 receptor Pex5p regulates Pex5p recycling.

Okumoto K, Misono S, Miyata N, Matsumoto Y, Mukai S, Fujiki Y. Okumoto K, et al. Among authors: miyata n. Traffic. 2011 Aug;12(8):1067-83. doi: 10.1111/j.1600-0854.2011.01217.x. Epub 2011 Jun 13. Traffic. 2011. PMID: 21554508 Free article.

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