Honsho M - Search Results

1

Systematic Identification of Regulators of Oxidative Stress Reveals Non-canonical Roles for Peroxisomal Import and the Pentose Phosphate Pathway.

Dubreuil MM, Morgens DW, Okumoto K, Honsho M, Contrepois K, Lee-McMullen B, Traber GM, Sood RS, Dixon SJ, Snyder MP, Fujiki Y, Bassik MC. Dubreuil MM, et al. Among authors: honsho m. Cell Rep. 2020 Feb 4;30(5):1417-1433.e7. doi: 10.1016/j.celrep.2020.01.013. Cell Rep. 2020. PMID: 32023459 Free PMC article.

2

Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

Honsho M, Tamura S, Shimozawa N, Suzuki Y, Kondo N, Fujiki Y. Honsho M, et al. Am J Hum Genet. 1998 Dec;63(6):1622-30. doi: 10.1086/302161. Am J Hum Genet. 1998. PMID: 9837814 Free PMC article.

3

The mammalian peroxin Pex5pL, the longer isoform of the mobile peroxisome targeting signal (PTS) type 1 transporter, translocates the Pex7p.PTS2 protein complex into peroxisomes via its initial docking site, Pex14p.

Otera H, Harano T, Honsho M, Ghaedi K, Mukai S, Tanaka A, Kawai A, Shimizu N, Fujiki Y. Otera H, et al. Among authors: honsho m. J Biol Chem. 2000 Jul 14;275(28):21703-14. doi: 10.1074/jbc.M000720200. J Biol Chem. 2000. PMID: 10767286 Free article.

4

PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.

Ghaedi K, Honsho M, Shimozawa N, Suzuki Y, Kondo N, Fujiki Y. Ghaedi K, et al. Among authors: honsho m. Am J Hum Genet. 2000 Oct;67(4):976-81. doi: 10.1086/303086. Epub 2000 Aug 31. Am J Hum Genet. 2000. PMID: 10968777 Free PMC article.

5

Topogenesis of peroxisomal membrane protein requires a short, positively charged intervening-loop sequence and flanking hydrophobic segments. study using human membrane protein PMP34.

Honsho M, Fujiki Y. Honsho M, et al. J Biol Chem. 2001 Mar 23;276(12):9375-82. doi: 10.1074/jbc.M003304200. Epub 2000 Dec 19. J Biol Chem. 2001. PMID: 11121399 Free article.

6

The membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assembly.

Honsho M, Hiroshige T, Fujiki Y. Honsho M, et al. J Biol Chem. 2002 Nov 15;277(46):44513-24. doi: 10.1074/jbc.M206139200. Epub 2002 Sep 9. J Biol Chem. 2002. PMID: 12223482 Free article.

7

Isolation and characterization of mutant animal cell line defective in alkyl-dihydroxyacetonephosphate synthase: localization and transport of plasmalogens to post-Golgi compartments.

Honsho M, Yagita Y, Kinoshita N, Fujiki Y. Honsho M, et al. Biochim Biophys Acta. 2008 Oct;1783(10):1857-65. doi: 10.1016/j.bbamcr.2008.05.018. Epub 2008 Jun 3. Biochim Biophys Acta. 2008. PMID: 18571506 Free article.

8

Posttranslational regulation of fatty acyl-CoA reductase 1, Far1, controls ether glycerophospholipid synthesis.

Honsho M, Asaoku S, Fujiki Y. Honsho M, et al. J Biol Chem. 2010 Mar 19;285(12):8537-42. doi: 10.1074/jbc.M109.083311. Epub 2010 Jan 13. J Biol Chem. 2010. PMID: 20071337 Free PMC article.

9

Interaction defect of the medium isoform of PTS1-receptor Pex5p with PTS2-receptor Pex7p abrogates the PTS2 protein import into peroxisomes in mammals.

Honsho M, Hashiguchi Y, Ghaedi K, Fujiki Y. Honsho M, et al. J Biochem. 2011 Feb;149(2):203-10. doi: 10.1093/jb/mvq130. Epub 2010 Nov 2. J Biochem. 2011. PMID: 21047816

10

Docosahexaenoic acid mediates peroxisomal elongation, a prerequisite for peroxisome division.

Itoyama A, Honsho M, Abe Y, Moser A, Yoshida Y, Fujiki Y. Itoyama A, et al. Among authors: honsho m. J Cell Sci. 2012 Feb 1;125(Pt 3):589-602. doi: 10.1242/jcs.087452. J Cell Sci. 2012. PMID: 22389399

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