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2. 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 Eur J Cell Biol; 1997 Aug; 73(4):352-9. PubMed ID: 9270878 [TBL] [Abstract][Full Text] [Related]
3. 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 Exp Cell Res; 1997 May; 233(1):11-20. PubMed ID: 9184070 [TBL] [Abstract][Full Text] [Related]
4. Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans. Fukuda S; Shimozawa N; Suzuki Y; Zhang Z; Tomatsu S; Tsukamoto T; Hashiguchi N; Osumi T; Masuno M; Imaizumi K; Kuroki Y; Fujiki Y; Orii T; Kondo N Am J Hum Genet; 1996 Dec; 59(6):1210-20. PubMed ID: 8940266 [TBL] [Abstract][Full Text] [Related]
5. 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 Biochem Biophys Res Commun; 1998 Feb; 243(2):368-71. PubMed ID: 9480815 [TBL] [Abstract][Full Text] [Related]
6. Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals. Ghaedi K; Itagaki A; Toyama R; Tamura S; Matsumura T; Kawai A; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y Exp Cell Res; 1999 May; 248(2):482-8. PubMed ID: 10222139 [TBL] [Abstract][Full Text] [Related]
7. Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders. Portsteffen H; Beyer A; Becker E; Epplen C; Pawlak A; Kunau WH; Dodt G Nat Genet; 1997 Dec; 17(4):449-52. PubMed ID: 9398848 [TBL] [Abstract][Full Text] [Related]
8. 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 Biochem Biophys Res Commun; 1997 Jan; 230(2):402-6. PubMed ID: 9016792 [TBL] [Abstract][Full Text] [Related]
9. Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein. Ghaedi K; Kawai A; Okumoto K; Tamura S; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y Exp Cell Res; 1999 May; 248(2):489-97. PubMed ID: 10222140 [TBL] [Abstract][Full Text] [Related]
10. Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders. Zhang Z; Suzuki Y; Shimozawa N; Fukuda S; Imamura A; Tsukamoto T; Osumi T; Fujiki Y; Orii T; Wanders RJ; Barth PG; Moser HW; Paton BC; Besley GT; Kondo N Hum Mutat; 1999; 13(6):487-96. PubMed ID: 10408779 [TBL] [Abstract][Full Text] [Related]
11. The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6. Matsumoto N; Tamura S; Moser A; Moser HW; Braverman N; Suzuki Y; Shimozawa N; Kondo N; Fujiki Y J Hum Genet; 2001; 46(5):273-7. PubMed ID: 11355018 [TBL] [Abstract][Full Text] [Related]
12. 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 Proc Natl Acad Sci U S A; 1998 Apr; 95(8):4350-5. PubMed ID: 9539740 [TBL] [Abstract][Full Text] [Related]
13. 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 Mol Cell Biol; 1998 Jul; 18(7):4324-36. PubMed ID: 9632816 [TBL] [Abstract][Full Text] [Related]
14. Molecular cloning and functional expression of a human peroxisomal acyl-coenzyme A oxidase. Aoyama T; Tsushima K; Souri M; Kamijo T; Suzuki Y; Shimozawa N; Orii T; Hashimoto T Biochem Biophys Res Commun; 1994 Feb; 198(3):1113-8. PubMed ID: 8117268 [TBL] [Abstract][Full Text] [Related]
15. Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome. Shimozawa N; Tsukamoto T; Suzuki Y; Orii T; Fujiki Y J Clin Invest; 1992 Nov; 90(5):1864-70. PubMed ID: 1430210 [TBL] [Abstract][Full Text] [Related]
16. A temperature-sensitive CHO pex1 mutant with a novel mutation in the AAA Walker A1 motif. Fan W; Fujiki Y Biochem Biophys Res Commun; 2006 Jul; 345(4):1434-9. PubMed ID: 16723118 [TBL] [Abstract][Full Text] [Related]
17. Isolation and characterization of novel phenotype CHO cell mutants defective in peroxisome assembly, using ICR191 as a potent mutagenic agent. Ghaedi K; Fujiki Y Cell Biochem Funct; 2008 Aug; 26(6):684-91. PubMed ID: 18543353 [TBL] [Abstract][Full Text] [Related]
18. Restoration by a 35K membrane protein of peroxisome assembly in a peroxisome-deficient mammalian cell mutant. Tsukamoto T; Miura S; Fujiki Y Nature; 1991 Mar; 350(6313):77-81. PubMed ID: 1750930 [TBL] [Abstract][Full Text] [Related]
20. Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders. Chang CC; Lee WH; Moser H; Valle D; Gould SJ Nat Genet; 1997 Apr; 15(4):385-8. PubMed ID: 9090384 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]