Fujiki Y - 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. J Cell Sci. 2020 May 11;133(9):jcs236943. doi: 10.1242/jcs.236943. J Cell Sci. 2020. PMID: 32393673 Review.

2

A human gene responsible for Zellweger syndrome that affects peroxisome assembly.

Shimozawa N, Tsukamoto T, Suzuki Y, Orii T, Shirayoshi Y, Mori T, Fujiki Y. Shimozawa N, et al. Among authors: fujiki y. Science. 1992 Feb 28;255(5048):1132-4. doi: 10.1126/science.1546315. Science. 1992. PMID: 1546315

3

Isolation of a new peroxisome-deficient CHO cell mutant defective in peroxisome targeting signal-1 receptor.

Tsukamoto T, Bogaki A, Okumoto K, Tateishi K, Fujiki Y, Shimozawa N, Suzuki Y, Kondo N, Osumi T. Tsukamoto T, et al. Among authors: fujiki y. Biochem Biophys Res Commun. 1997 Jan 13;230(2):402-6. doi: 10.1006/bbrc.1996.5971. Biochem Biophys Res Commun. 1997. PMID: 9016792

4

Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III.

Okumoto K, Bogaki A, Tateishi K, Tsukamoto T, Osumi T, Shimozawa N, Suzuki Y, Orii T, Fujiki Y. Okumoto K, et al. Among authors: fujiki y. Exp Cell Res. 1997 May 25;233(1):11-20. doi: 10.1006/excr.1997.3552. Exp Cell Res. 1997. PMID: 9184070

5

Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammals.

Tateishi K, Okumoto K, Shimozawa N, Tsukamoto T, Osumi T, Suzuki Y, Kondo N, Okano I, Fujiki Y. Tateishi K, et al. Among authors: fujiki y. Eur J Cell Biol. 1997 Aug;73(4):352-9. Eur J Cell Biol. 1997. PMID: 9270878

6

PEX12 encodes an integral membrane protein of peroxisomes.

Okumoto K, Fujiki Y. Okumoto K, et al. Among authors: fujiki y. Nat Genet. 1997 Nov;17(3):265-6. doi: 10.1038/ng1197-265. Nat Genet. 1997. PMID: 9354782 No abstract available.

7

Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants.

Otera H, Okumoto K, Tateishi K, Ikoma Y, Matsuda E, Nishimura M, Tsukamoto T, Osumi T, Ohashi K, Higuchi O, Fujiki Y. Otera H, et al. Among authors: fujiki y. Mol Cell Biol. 1998 Jan;18(1):388-99. doi: 10.1128/MCB.18.1.388. Mol Cell Biol. 1998. PMID: 9418886 Free PMC article.

8

Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13.

Shimozawa N, Suzuki Y, Zhang Z, Imamura A, Tsukamoto T, Osumi T, Tateishi K, Okumoto K, Fujiki Y, Orii T, Barth PG, Wanders RJ, Kondo N. Shimozawa N, et al. Among authors: fujiki y. Biochem Biophys Res Commun. 1998 Feb 13;243(2):368-71. doi: 10.1006/bbrc.1997.8067. Biochem Biophys Res Commun. 1998. PMID: 9480815

9

Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I.

Tamura S, Okumoto K, Toyama R, Shimozawa N, Tsukamoto T, Suzuki Y, Osumi T, Kondo N, Fujiki Y. Tamura S, et al. Among authors: fujiki y. Proc Natl Acad Sci U S A. 1998 Apr 14;95(8):4350-5. doi: 10.1073/pnas.95.8.4350. Proc Natl Acad Sci U S A. 1998. PMID: 9539740 Free PMC article.

10

A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6p.

Tamura S, Shimozawa N, Suzuki Y, Tsukamoto T, Osumi T, Fujiki Y. Tamura S, et al. Among authors: fujiki y. Biochem Biophys Res Commun. 1998 Apr 28;245(3):883-6. doi: 10.1006/bbrc.1998.8522. Biochem Biophys Res Commun. 1998. PMID: 9588209

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