100 related articles for article (PubMed ID: 9354782)
1. PEX12 encodes an integral membrane protein of peroxisomes.
Okumoto K; Fujiki Y
Nat Genet; 1997 Nov; 17(3):265-6. PubMed ID: 9354782
[No Abstract] [Full Text] [Related]
2. 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]
3. Restoration of peroxisome biogenesis in a peroxisome-deficient mammalian cell line by expression of either the 35 kDa or the 70 kDa peroxisomal membrane proteins.
Gärtner J; Obie C; Watkins P; Valle D
J Inherit Metab Dis; 1994; 17(3):327-9. PubMed ID: 7528830
[No Abstract] [Full Text] [Related]
4. Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome.
Gärtner J; Moser H; Valle D
Nat Genet; 1992 Apr; 1(1):16-23. PubMed ID: 1301993
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 9837814
[TBL] [Abstract][Full Text] [Related]
6. The 70 kDa peroxisomal membrane protein: an ATP-binding cassette transporter protein involved in peroxisome biogenesis.
Gärtner J; Valle D
Semin Cell Biol; 1993 Feb; 4(1):45-52. PubMed ID: 8453064
[TBL] [Abstract][Full Text] [Related]
7. Absence of mutations raises doubts about the role of the 70-kD peroxisomal membrane protein in Zellweger syndrome.
Paton BC; Heron SE; Nelson PV; Morris CP; Poulos A
Am J Hum Genet; 1997 Jun; 60(6):1535-9. PubMed ID: 9199576
[No Abstract] [Full Text] [Related]
8. [Molecular biology of peroxisome biogenesis].
Fujiki Y
Nihon Rinsho; 1993 Sep; 51(9):2336-42. PubMed ID: 8411711
[TBL] [Abstract][Full Text] [Related]
9. [Biogenesis of peroxisomes and human peroxisomal disorders].
Fujiki Y
Seikagaku; 1995 Mar; 67(3):204-23. PubMed ID: 7602197
[No Abstract] [Full Text] [Related]
10. Restoration of PEX2 peroxisome assembly defects by overexpression of PMP70.
Gärtner J; Brosius U; Obie C; Watkins PA; Valle D
Eur J Cell Biol; 1998 Aug; 76(4):237-45. PubMed ID: 9765053
[TBL] [Abstract][Full Text] [Related]
11. [Clinical and molecular aspects of peroxisome-deficient disorders].
Suzuki Y; Shimozawa N; Orii T
Nihon Rinsho; 1993 Sep; 51(9):2353-8. PubMed ID: 7692118
[TBL] [Abstract][Full Text] [Related]
12. Characterization of the 70-kDa peroxisomal membrane protein, an ATP binding cassette transporter.
Imanaka T; Aihara K; Takano T; Yamashita A; Sato R; Suzuki Y; Yokota S; Osumi T
J Biol Chem; 1999 Apr; 274(17):11968-76. PubMed ID: 10207018
[TBL] [Abstract][Full Text] [Related]
13. Topology of ATP-binding domain of adrenoleukodystrophy gene product in peroxisomes.
Contreras M; Sengupta TK; Sheikh F; Aubourg P; Singh I
Arch Biochem Biophys; 1996 Oct; 334(2):369-79. PubMed ID: 8900413
[TBL] [Abstract][Full Text] [Related]
14. [PMP70, the 70-kDa peroxisomal membrane protein: a member of the ATP-binding cassette transporters].
Kamijo K; Osumi T; Hashimoto T
Nihon Rinsho; 1993 Sep; 51(9):2343-52. PubMed ID: 8411712
[TBL] [Abstract][Full Text] [Related]
15. Peroxisome synthesis in the absence of preexisting peroxisomes.
South ST; Gould SJ
J Cell Biol; 1999 Jan; 144(2):255-66. PubMed ID: 9922452
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. Identification of a common PEX1 mutation in Zellweger syndrome.
Collins CS; Gould SJ
Hum Mutat; 1999; 14(1):45-53. PubMed ID: 10447258
[TBL] [Abstract][Full Text] [Related]
18. Immunocytochemical localization of the 70 kDa peroxisomal membrane protein in connections between peroxisomes in rat liver: support for a reticular organization of peroxisomes maintained by the cytoskeleton.
Häyrinen HM; Svensson LT; Hultenby K; Sormunen RT; Wilcke M; Hiltunen JK; Alexson SE
Eur J Cell Biol; 1997 Jan; 72(1):70-8. PubMed ID: 9013728
[TBL] [Abstract][Full Text] [Related]
19. 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
Science; 1992 Feb; 255(5048):1132-4. PubMed ID: 1546315
[TBL] [Abstract][Full Text] [Related]
20. cDNA cloning and characterization of a constitutively expressed isoform of the human peroxin Pex11p.
Abe I; Fujiki Y
Biochem Biophys Res Commun; 1998 Nov; 252(2):529-33. PubMed ID: 9826565
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
