196 related articles for article (PubMed ID: 8892025)
1. 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]
2. Mutational and protein analysis of patients and heterozygous women with X-linked adrenoleukodystrophy.
Feigenbaum V; Lombard-Platet G; Guidoux S; Sarde CO; Mandel JL; Aubourg P
Am J Hum Genet; 1996 Jun; 58(6):1135-44. PubMed ID: 8651290
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. X-linked adrenoleukodystrophy: phenotype distribution and expression of ALDP in Spanish kindreds.
Ruiz M; Coll MJ; Pàmpols T; Girós M
Am J Med Genet; 1998 Apr; 76(5):424-7. PubMed ID: 9556303
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. Characterization of a novel mutation in exon 10 of the adrenoleukodystrophy gene.
Holzinger A; Maier E; Stöckler-Ipsiroglu S; Braun A; Roscher AA
Clin Genet; 1998 Jun; 53(6):482-7. PubMed ID: 9712540
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders.
Corzo D; Gibson W; Johnson K; Mitchell G; LePage G; Cox GF; Casey R; Zeiss C; Tyson H; Cutting GR; Raymond GV; Smith KD; Watkins PA; Moser AB; Moser HW; Steinberg SJ
Am J Hum Genet; 2002 Jun; 70(6):1520-31. PubMed ID: 11992258
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Eight novel ABCD1 gene mutations and three polymorphisms in patients with X-linked adrenoleukodystrophy: The first polymorphism causing an amino acid exchange.
Dvoráková L; Storkánová G; Unterrainer G; Hujová J; Kmoch S; Zeman J; Hrebícek M; Berger J
Hum Mutat; 2001; 18(1):52-60. PubMed ID: 11438993
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. 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]
17. Mutational analysis of patients with X-linked adrenoleukodystrophy.
Kok F; Neumann S; Sarde CO; Zheng S; Wu KH; Wei HM; Bergin J; Watkins PA; Gould S; Sack G
Hum Mutat; 1995; 6(2):104-15. PubMed ID: 7581394
[TBL] [Abstract][Full Text] [Related]
18. Spectrum of mutations in the gene encoding the adrenoleukodystrophy protein.
Ligtenberg MJ; Kemp S; Sarde CO; van Geel BM; Kleijer WJ; Barth PG; Mandel JL; van Oost BA; Bolhuis PA
Am J Hum Genet; 1995 Jan; 56(1):44-50. PubMed ID: 7825602
[TBL] [Abstract][Full Text] [Related]
19. Very-long-chain fatty acid metabolism in adrenoleukodystrophy protein-deficient mice.
Yamada T; Shinnoh N; Kondo A; Uchiyama A; Shimozawa N; Kira J; Kobayashi T
Cell Biochem Biophys; 2000; 32 Spring():239-46. PubMed ID: 11330052
[TBL] [Abstract][Full Text] [Related]
20. Biochemical aspects of X-linked adrenoleukodystrophy.
Kemp S; Wanders R
Brain Pathol; 2010 Jul; 20(4):831-7. PubMed ID: 20626744
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
