Okumoto K - 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: okumoto k. 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

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. Exp Cell Res. 1997 May 25;233(1):11-20. doi: 10.1006/excr.1997.3552. Exp Cell Res. 1997. PMID: 9184070

3

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: okumoto k. Eur J Cell Biol. 1997 Aug;73(4):352-9. Eur J Cell Biol. 1997. PMID: 9270878

4

PEX12 encodes an integral membrane protein of peroxisomes.

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

5

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: okumoto k. 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.

6

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: okumoto k. 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.

7

PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p.

Okumoto K, Shimozawa N, Kawai A, Tamura S, Tsukamoto T, Osumi T, Moser H, Wanders RJ, Suzuki Y, Kondo N, Fujiki Y. Okumoto K, et al. Mol Cell Biol. 1998 Jul;18(7):4324-36. doi: 10.1128/MCB.18.7.4324. Mol Cell Biol. 1998. PMID: 9632816 Free PMC article.

Rat PEX12 cDNA was isolated by functional complementation of peroxisome deficiency of a mutant CHO cell line, ZP109 (K. Okumoto, A. Bogaki, K. Tateishi, T. Tsukamoto, T. Osumi, N. Shimozawa, Y. Suzuki, T. ...

Rat PEX12 cDNA was isolated by functional complementation of peroxisome deficiency of a mutant CHO cell line, ZP109 (K. Okumoto …

8

Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.

Okumoto K, Itoh R, Shimozawa N, Suzuki Y, Tamura S, Kondo N, Fujiki Y. Okumoto K, et al. Hum Mol Genet. 1998 Sep;7(9):1399-405. doi: 10.1093/hmg/7.9.1399. Hum Mol Genet. 1998. PMID: 9700193

9

Clofibrate-inducible, 28-kDa peroxisomal integral membrane protein is encoded by PEX11.

Abe I, Okumoto K, Tamura S, Fujiki Y. Abe I, et al. Among authors: okumoto k. FEBS Lett. 1998 Jul 24;431(3):468-72. doi: 10.1016/s0014-5793(98)00815-1. FEBS Lett. 1998. PMID: 9714566 Free article.

10

Newly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (Peroxisomal ghosts), representing a novel complementation group in mammals.

Kinoshita N, Ghaedi K, Shimozawa N, Wanders RJ, Matsuzono Y, Imanaka T, Okumoto K, Suzuki Y, Kondo N, Fujiki Y. Kinoshita N, et al. Among authors: okumoto k. J Biol Chem. 1998 Sep 11;273(37):24122-30. doi: 10.1074/jbc.273.37.24122. J Biol Chem. 1998. PMID: 9727033 Free article.

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