198 related articles for article (PubMed ID: 2689450)
1. Chinese hamster ovary cell mutants defective in peroxisome biogenesis. Comparison to Zellweger syndrome.
Zoeller RA; Allen LA; Santos MJ; Lazarow PB; Hashimoto T; Tartakoff AM; Raetz CR
J Biol Chem; 1989 Dec; 264(36):21872-8. PubMed ID: 2689450
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes.
Tsukamoto T; Yokota S; Fujiki Y
J Cell Biol; 1990 Mar; 110(3):651-60. PubMed ID: 1689731
[TBL] [Abstract][Full Text] [Related]
4. 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
J Biol Chem; 1998 Sep; 273(37):24122-30. PubMed ID: 9727033
[TBL] [Abstract][Full Text] [Related]
5. Isolation of animal cell mutants deficient in plasmalogen biosynthesis and peroxisome assembly.
Zoeller RA; Raetz CR
Proc Natl Acad Sci U S A; 1986 Jul; 83(14):5170-4. PubMed ID: 3460088
[TBL] [Abstract][Full Text] [Related]
6. Partial phenotypic suppression of a peroxisome-deficient animal cell mutant treated with aminoglycoside G418.
Allen LA; Raetz CR
J Biol Chem; 1992 Jul; 267(19):13191-9. PubMed ID: 1618823
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes.
Tager JM; Brul S; Wiemer EA; Strijland A; Van Driel R; Schutgens RB; Van den Bosch H; Wanders RJ; Westerveld A
Prog Clin Biol Res; 1990; 321():545-58. PubMed ID: 2183242
[TBL] [Abstract][Full Text] [Related]
9. Defective lipid remodeling of GPI anchors in peroxisomal disorders, Zellweger syndrome, and rhizomelic chondrodysplasia punctata.
Kanzawa N; Shimozawa N; Wanders RJ; Ikeda K; Murakami Y; Waterham HR; Mukai S; Fujita M; Maeda Y; Taguchi R; Fujiki Y; Kinoshita T
J Lipid Res; 2012 Apr; 53(4):653-63. PubMed ID: 22253471
[TBL] [Abstract][Full Text] [Related]
10. [Human peroxisome-deficient disorders and pathogenic gene].
Fujiki Y
Rinsho Shinkeigaku; 1994 Dec; 34(12):1219-21. PubMed ID: 7539728
[TBL] [Abstract][Full Text] [Related]
11. Mutants in a macrophage-like cell line are defective in plasmalogen biosynthesis, but contain functional peroxisomes.
Zoeller RA; Rangaswamy S; Herscovitz H; Rizzo WB; Hajra AK; Das AK; Moser HW; Moser A; Lazarow PB; Santos MJ
J Biol Chem; 1992 Apr; 267(12):8299-306. PubMed ID: 1569085
[TBL] [Abstract][Full Text] [Related]
12. 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; 1841(4):610-9. PubMed ID: 24418004
[TBL] [Abstract][Full Text] [Related]
13. Presence of peroxisomal membrane proteins in liver and fibroblasts from patients with the Zellweger syndrome and related disorders: evidence for the existence of peroxisomal ghosts.
Wiemer EA; Brul S; Just WW; Van Driel R; Brouwer-Kelder E; Van Den Berg M; Weijers PJ; Schutgens RB; Van Den Bosch H; Schram A
Eur J Cell Biol; 1989 Dec; 50(2):407-17. PubMed ID: 2697558
[TBL] [Abstract][Full Text] [Related]
14. Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G.
Muntau AC; Mayerhofer PU; Paton BC; Kammerer S; Roscher AA
Am J Hum Genet; 2000 Oct; 67(4):967-75. PubMed ID: 10958759
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts.
Shimozawa N; Suzuki Y; Zhang Z; Imamura A; Kondo N; Kinoshita N; Fujiki Y; Tsukamoto T; Osumi T; Imanaka T; Orii T; Beemer F; Mooijer P; Dekker C; Wanders RJ
Am J Hum Genet; 1998 Dec; 63(6):1898-903. PubMed ID: 9837841
[No Abstract] [Full Text] [Related]
17. 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]
18. Analysis of peroxisomes in lymphoblasts: Zellweger syndrome and a patient with a deletion in chromosome 7.
Santos MJ; Moser AB; Drwinga H; Moser HW; Lazarow PB
Pediatr Res; 1993 May; 33(5):441-4. PubMed ID: 8511016
[TBL] [Abstract][Full Text] [Related]
19. Complementation in Zellweger syndrome: biochemical analysis of newly generated peroxisomes.
Stanczak H; Kremser K; Singh AK; Ashcraft J; Stanley W; Singh I
Hum Hered; 1992; 42(3):172-8. PubMed ID: 1511996
[TBL] [Abstract][Full Text] [Related]
20. Class F Thy-1-negative murine lymphoma cells are deficient in ether lipid biosynthesis.
Stevens VL; Raetz CR
J Biol Chem; 1990 Sep; 265(26):15653-8. PubMed ID: 1975590
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
