364 related articles for article (PubMed ID: 8900413)
1. 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]
2. Intraperoxisomal localization of very-long-chain fatty acyl-CoA synthetase: implication in X-adrenoleukodystrophy.
Smith BT; Sengupta TK; Singh I
Exp Cell Res; 2000 Feb; 254(2):309-20. PubMed ID: 10640429
[TBL] [Abstract][Full Text] [Related]
3. Peroxisomal very long chain fatty acid beta-oxidation activity is determined by the level of adrenodeukodystrophy protein (ALDP) expression.
Braiterman LT; Watkins PA; Moser AB; Smith KD
Mol Genet Metab; 1999 Feb; 66(2):91-9. PubMed ID: 10068511
[TBL] [Abstract][Full Text] [Related]
4. Adrenoleukodystrophy-related protein can compensate functionally for adrenoleukodystrophy protein deficiency (X-ALD): implications for therapy.
Netik A; Forss-Petter S; Holzinger A; Molzer B; Unterrainer G; Berger J
Hum Mol Genet; 1999 May; 8(5):907-13. PubMed ID: 10196381
[TBL] [Abstract][Full Text] [Related]
5. ATP binding/hydrolysis by and phosphorylation of peroxisomal ATP-binding cassette proteins PMP70 (ABCD3) and adrenoleukodystrophy protein (ABCD1).
Tanaka AR; Tanabe K; Morita M; Kurisu M; Kasiwayama Y; Matsuo M; Kioka N; Amachi T; Imanaka T; Ueda K
J Biol Chem; 2002 Oct; 277(42):40142-7. PubMed ID: 12176987
[TBL] [Abstract][Full Text] [Related]
6. Co-expression of mutated and normal adrenoleukodystrophy protein reduces protein function: implications for gene therapy of X-linked adrenoleukodystrophy.
Unterrainer G; Molzer B; Forss-Petter S; Berger J
Hum Mol Genet; 2000 Nov; 9(18):2609-16. PubMed ID: 11063720
[TBL] [Abstract][Full Text] [Related]
7. Homo- and heterodimerization of peroxisomal ATP-binding cassette half-transporters.
Liu LX; Janvier K; Berteaux-Lecellier V; Cartier N; Benarous R; Aubourg P
J Biol Chem; 1999 Nov; 274(46):32738-43. PubMed ID: 10551832
[TBL] [Abstract][Full Text] [Related]
8. Transport of fatty acids into human and rat peroxisomes. Differential transport of palmitic and lignoceric acids and its implication to X-adrenoleukodystrophy.
Singh I; Lazo O; Dhaunsi GS; Contreras M
J Biol Chem; 1992 Jul; 267(19):13306-13. PubMed ID: 1618832
[TBL] [Abstract][Full Text] [Related]
9. Human adrenoleukodystrophy protein and related peroxisomal ABC transporters interact with the peroxisomal assembly protein PEX19p.
Gloeckner CJ; Mayerhofer PU; Landgraf P; Muntau AC; Holzinger A; Gerber JK; Kammerer S; Adamski J; Roscher AA
Biochem Biophys Res Commun; 2000 Apr; 271(1):144-50. PubMed ID: 10777694
[TBL] [Abstract][Full Text] [Related]
10. Impaired very long-chain acyl-CoA β-oxidation in human X-linked adrenoleukodystrophy fibroblasts is a direct consequence of ABCD1 transporter dysfunction.
Wiesinger C; Kunze M; Regelsberger G; Forss-Petter S; Berger J
J Biol Chem; 2013 Jun; 288(26):19269-79. PubMed ID: 23671276
[TBL] [Abstract][Full Text] [Related]
11. Functional characterization of the adrenoleukodystrophy protein (ALDP) and disease pathogenesis.
Gärtner J; Dehmel T; Klusmann A; Roerig P
Endocr Res; 2002 Nov; 28(4):741-8. PubMed ID: 12530690
[TBL] [Abstract][Full Text] [Related]
12. Characterization and functional analysis of the nucleotide binding fold in human peroxisomal ATP binding cassette transporters.
Roerig P; Mayerhofer P; Holzinger A; Gärtner J
FEBS Lett; 2001 Mar; 492(1-2):66-72. PubMed ID: 11248239
[TBL] [Abstract][Full Text] [Related]
13. [Adrenoleukodystrophy: structure and function of ALDP, and intracellular behavior of mutant ALDP with naturally occurring missense mutations].
Takahashi N; Morita M; Imanaka T
Yakugaku Zasshi; 2007 Jan; 127(1):163-72. PubMed ID: 17202797
[TBL] [Abstract][Full Text] [Related]
14. Suppression of peroxisomal membrane protein defects by peroxisomal ATP binding cassette (ABC) proteins.
Braiterman LT; Zheng S; Watkins PA; Geraghty MT; Johnson G; McGuinness MC; Moser AB; Smith KD
Hum Mol Genet; 1998 Feb; 7(2):239-47. PubMed ID: 9425230
[TBL] [Abstract][Full Text] [Related]
15. Altered expression of ALDP in X-linked adrenoleukodystrophy.
Watkins PA; Gould SJ; Smith MA; Braiterman LT; Wei HM; Kok F; Moser AB; Moser HW; Smith KD
Am J Hum Genet; 1995 Aug; 57(2):292-301. PubMed ID: 7668254
[TBL] [Abstract][Full Text] [Related]
16. Adrenoleukodystrophy: the restoration of peroxisomal beta-oxidation by transfection of normal cDNA.
Shinnoh N; Yamada T; Yoshimura T; Furuya H; Yoshida Y; Suzuki Y; Shimozawa N; Orii T; Kobayashi T
Biochem Biophys Res Commun; 1995 May; 210(3):830-6. PubMed ID: 7763255
[TBL] [Abstract][Full Text] [Related]
17. ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophy.
Kemp S; Mooyer PA; Bolhuis PA; van Geel BM; Mandel JL; Barth PG; Aubourg P; Wanders RJ
J Inherit Metab Dis; 1996; 19(5):667-74. PubMed ID: 8892025
[TBL] [Abstract][Full Text] [Related]
18. Adrenoleukodystrophy: subcellular localization and degradation of adrenoleukodystrophy protein (ALDP/ABCD1) with naturally occurring missense mutations.
Takahashi N; Morita M; Maeda T; Harayama Y; Shimozawa N; Suzuki Y; Furuya H; Sato R; Kashiwayama Y; Imanaka T
J Neurochem; 2007 Jun; 101(6):1632-43. PubMed ID: 17542813
[TBL] [Abstract][Full Text] [Related]
19. Adrenoleukodystrophy protein enhances association of very long-chain acyl-coenzyme A synthetase with the peroxisome.
Yamada T; Taniwaki T; Shinnoh N; Uchiyama A; Shimozawa N; Ohyagi Y; Asahara H; Kira J
Neurology; 1999 Feb; 52(3):614-6. PubMed ID: 10025797
[TBL] [Abstract][Full Text] [Related]
20. PXA1, a possible Saccharomyces cerevisiae ortholog of the human adrenoleukodystrophy gene.
Shani N; Watkins PA; Valle D
Proc Natl Acad Sci U S A; 1995 Jun; 92(13):6012-6. PubMed ID: 7597071
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
