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Items: 38

1.

Plasmalogen mediates integration of adherens junction.

Takahashi T, Honsho M, Abe Y, Fujiki Y.

J Biochem. 2019 Nov 1;166(5):423-432. doi: 10.1093/jb/mvz049.

PMID:
31236591
2.

Impaired plasmalogen synthesis dysregulates liver X receptor-dependent transcription in cerebellum.

Honsho M, Dorninger F, Abe Y, Setoyama D, Ohgi R, Uchiumi T, Kang D, Berger J, Fujiki Y.

J Biochem. 2019 May 28. pii: mvz043. doi: 10.1093/jb/mvz043. [Epub ahead of print]

PMID:
31135054
3.

An alternative membrane topology permits lipid droplet localization of peroxisomal fatty acyl-CoA reductase 1.

Exner T, Romero-Brey I, Yifrach E, Rivera-Monroy J, Schrul B, Zouboulis CC, Stremmel W, Honsho M, Bartenschlager R, Zalckvar E, Poppelreuther M, Füllekrug J.

J Cell Sci. 2019 Mar 18;132(6). pii: jcs223016. doi: 10.1242/jcs.223016.

4.

Peroxisome biogenesis deficiency attenuates the BDNF-TrkB pathway-mediated development of the cerebellum.

Abe Y, Honsho M, Itoh R, Kawaguchi R, Fujitani M, Fujiwara K, Hirokane M, Matsuzaki T, Nakayama K, Ohgi R, Marutani T, Nakayama KI, Yamashita T, Fujiki Y.

Life Sci Alliance. 2018 Dec 3;1(6):e201800062. doi: 10.26508/lsa.201800062. eCollection 2018 Dec.

5.

Onsite GTP fuelling via DYNAMO1 drives division of mitochondria and peroxisomes.

Imoto Y, Abe Y, Honsho M, Okumoto K, Ohnuma M, Kuroiwa H, Kuroiwa T, Fujiki Y.

Nat Commun. 2018 Nov 6;9(1):4634. doi: 10.1038/s41467-018-07009-z.

6.

Plasmalogen homeostasis - regulation of plasmalogen biosynthesis and its physiological consequence in mammals.

Honsho M, Fujiki Y.

FEBS Lett. 2017 Sep;591(18):2720-2729. doi: 10.1002/1873-3468.12743. Epub 2017 Jul 28. Review.

7.

Peroxisomal Membrane and Matrix Protein Import Using a Semi-Intact Mammalian Cell System.

Okumoto K, Honsho M, Liu Y, Fujiki Y.

Methods Mol Biol. 2017;1595:213-219. doi: 10.1007/978-1-4939-6937-1_20.

PMID:
28409465
8.

In Vitro PMP Import Analysis Using Cell-Free Synthesized PMP and Isolated Peroxisomes.

Liu Y, Honsho M, Fujiki Y.

Methods Mol Biol. 2017;1595:207-212. doi: 10.1007/978-1-4939-6937-1_19.

PMID:
28409464
9.

Analysis of Plasmalogen Synthesis in Cultured Cells.

Honsho M, Fujiki Y.

Methods Mol Biol. 2017;1595:55-61. doi: 10.1007/978-1-4939-6937-1_6.

PMID:
28409451
10.

Reduction of Ether-Type Glycerophospholipids, Plasmalogens, by NF-κB Signal Leading to Microglial Activation.

Hossain MS, Abe Y, Ali F, Youssef M, Honsho M, Fujiki Y, Katafuchi T.

J Neurosci. 2017 Apr 12;37(15):4074-4092. doi: 10.1523/JNEUROSCI.3941-15.2017. Epub 2017 Mar 14.

11.
12.

Defining the dynamin-based ring organizing center on the peroxisome-dividing machinery isolated from Cyanidioschyzon merolae.

Imoto Y, Abe Y, Okumoto K, Honsho M, Kuroiwa H, Kuroiwa T, Fujiki Y.

J Cell Sci. 2017 Mar 1;130(5):853-867. doi: 10.1242/jcs.199182. Epub 2017 Jan 23.

13.

Dysregulation of Plasmalogen Homeostasis Impairs Cholesterol Biosynthesis.

Honsho M, Abe Y, Fujiki Y.

J Biol Chem. 2015 Nov 27;290(48):28822-33. doi: 10.1074/jbc.M115.656983. Epub 2015 Oct 13.

14.

Peroxisome homeostasis: Mechanisms of division and selective degradation of peroxisomes in mammals.

Honsho M, Yamashita S, Fujiki Y.

Biochim Biophys Acta. 2016 May;1863(5):984-91. doi: 10.1016/j.bbamcr.2015.09.032. Epub 2015 Oct 3. Review.

15.

Pex11mediates peroxisomal proliferation by promoting deformation of the lipid membrane.

Yoshida Y, Niwa H, Honsho M, Itoyama A, Fujiki Y.

Biol Open. 2015 Apr 24;4(6):710-21. doi: 10.1242/bio.201410801.

16.

Peroxisome biogenesis in mammalian cells.

Fujiki Y, Okumoto K, Mukai S, Honsho M, Tamura S.

Front Physiol. 2014 Aug 15;5:307. doi: 10.3389/fphys.2014.00307. eCollection 2014. Review.

17.

Mild reduction of plasmalogens causes rhizomelic chondrodysplasia punctata: functional characterization of a novel mutation.

Noguchi M, Honsho M, Abe Y, Toyama R, Niwa H, Sato Y, Ghaedi K, Rahmanifar A, Shafeghati Y, Fujiki Y.

J Hum Genet. 2014 Jul;59(7):387-92. doi: 10.1038/jhg.2014.39. Epub 2014 May 22. Erratum in: J Hum Genet. 2014 Jul;59(7):417.

PMID:
24849933
18.

Very-long-chain polyunsaturated fatty acids accumulate in phosphatidylcholine of fibroblasts from patients with Zellweger syndrome and acyl-CoA oxidase1 deficiency.

Abe Y, Honsho M, Nakanishi H, Taguchi R, Fujiki Y.

Biochim Biophys Acta. 2014 Apr 4;1841(4):610-9. doi: 10.1016/j.bbalip.2014.01.001. Epub 2014 Jan 10.

PMID:
24418004
19.

Mff functions with Pex11pβ and DLP1 in peroxisomal fission.

Itoyama A, Michiyuki S, Honsho M, Yamamoto T, Moser A, Yoshida Y, Fujiki Y.

Biol Open. 2013 Aug 14;2(10):998-1006. doi: 10.1242/bio.20135298. eCollection 2013.

20.

Topogenesis and homeostasis of fatty acyl-CoA reductase 1.

Honsho M, Asaoku S, Fukumoto K, Fujiki Y.

J Biol Chem. 2013 Nov 29;288(48):34588-98. doi: 10.1074/jbc.M113.498345. Epub 2013 Oct 9.

21.

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

Itoyama A, Honsho M, Abe Y, Moser A, Yoshida Y, Fujiki Y.

J Cell Sci. 2012 Feb 1;125(Pt 3):589-602. doi: 10.1242/jcs.087452.

22.

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.

J Biochem. 2011 Feb;149(2):203-10. doi: 10.1093/jb/mvq130. Epub 2010 Nov 2.

PMID:
21047816
23.

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

Honsho M, Asaoku S, Fujiki Y.

J Biol Chem. 2010 Mar 19;285(12):8537-42. doi: 10.1074/jbc.M109.083311. Epub 2010 Jan 13.

24.

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.

Biochim Biophys Acta. 2008 Oct;1783(10):1857-65. doi: 10.1016/j.bbamcr.2008.05.018. Epub 2008 Jun 3.

25.

Flotillin-dependent clustering of the amyloid precursor protein regulates its endocytosis and amyloidogenic processing in neurons.

Schneider A, Rajendran L, Honsho M, Gralle M, Donnert G, Wouters F, Hell SW, Simons M.

J Neurosci. 2008 Mar 12;28(11):2874-82. doi: 10.1523/JNEUROSCI.5345-07.2008.

26.

Alzheimer's disease beta-amyloid peptides are released in association with exosomes.

Rajendran L, Honsho M, Zahn TR, Keller P, Geiger KD, Verkade P, Simons K.

Proc Natl Acad Sci U S A. 2006 Jul 25;103(30):11172-7. Epub 2006 Jul 12.

27.

Generation of single and double knockdowns in polarized epithelial cells by retrovirus-mediated RNA interference.

Schuck S, Manninen A, Honsho M, Füllekrug J, Simons K.

Proc Natl Acad Sci U S A. 2004 Apr 6;101(14):4912-7. Epub 2004 Mar 29.

28.

Dual subcellular distribution of cytochrome b5 in plant, cauliflower, cells.

Zhao J, Onduka T, Kinoshita JY, Honsho M, Kinoshita T, Shimazaki K, Ito A.

J Biochem. 2003 Jan;133(1):115-21.

29.

Resistance of cell membranes to different detergents.

Schuck S, Honsho M, Ekroos K, Shevchenko A, Simons K.

Proc Natl Acad Sci U S A. 2003 May 13;100(10):5795-800. Epub 2003 Apr 29.

30.

Involvement of caveolin-2 in caveolar biogenesis in MDCK cells.

Lahtinen U, Honsho M, Parton RG, Simons K, Verkade P.

FEBS Lett. 2003 Mar 13;538(1-3):85-8.

31.

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

Honsho M, Hiroshige T, Fujiki Y.

J Biol Chem. 2002 Nov 15;277(46):44513-24. Epub 2002 Sep 9.

33.

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.

Am J Hum Genet. 2000 Oct;67(4):976-81. Epub 2000 Aug 31.

34.
35.

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.

Am J Hum Genet. 1998 Dec;63(6):1622-30.

36.

Charged amino acids at the carboxyl-terminal portions determine the intracellular locations of two isoforms of cytochrome b5.

Kuroda R, Ikenoue T, Honsho M, Tsujimoto S, Mitoma JY, Ito A.

J Biol Chem. 1998 Nov 20;273(47):31097-102.

37.
38.

In situ topology of cytochrome b5 in the endoplasmic reticulum membrane.

Kuroda R, Kinoshita J, Honsho M, Mitoma J, Ito A.

J Biochem. 1996 Oct;120(4):828-33.

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