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Results: 1 to 20 of 378

1.

Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice.

Forss-Petter S, Werner H, Berger J, Lassmann H, Molzer B, Schwab MH, Bernheimer H, Zimmermann F, Nave KA.

J Neurosci Res. 1997 Dec 1;50(5):829-43.

PMID:
9418970
[PubMed - indexed for MEDLINE]
2.

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.

PMID:
11330052
[PubMed - indexed for MEDLINE]
3.

Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters.

Mosser J, Douar AM, Sarde CO, Kioschis P, Feil R, Moser H, Poustka AM, Mandel JL, Aubourg P.

Nature. 1993 Feb 25;361(6414):726-30.

PMID:
8441467
[PubMed - indexed for MEDLINE]
4.

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.

PMID:
8651290
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Evaluation of pharmacological induction of fatty acid beta-oxidation in X-linked adrenoleukodystrophy.

McGuinness MC, Zhang HP, Smith KD.

Mol Genet Metab. 2001 Sep-Oct;74(1-2):256-63.

PMID:
11592822
[PubMed - indexed for MEDLINE]
6.

[X-linked adrenoleukodystrophy].

Aubourg P.

Ann Endocrinol (Paris). 2007 Dec;68(6):403-11. Epub 2007 May 29. Review. French.

PMID:
17532287
[PubMed - indexed for MEDLINE]
7.

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 1;9(18):2609-16.

PMID:
11063720
[PubMed - indexed for MEDLINE]
Free Article
8.

[Adrenoleukodystrophy: molecular pathogenesis and development of therapeutic agents].

Morita M.

Yakugaku Zasshi. 2007 Jul;127(7):1059-64. Review. Japanese.

PMID:
17603264
[PubMed - indexed for MEDLINE]
Free Article
9.

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.

PMID:
10196381
[PubMed - indexed for MEDLINE]
Free Article
10.

Adrenoleukodystrophy protein-deficient mice represent abnormality of very long chain fatty acid metabolism.

Kobayashi T, Shinnoh N, Kondo A, Yamada T.

Biochem Biophys Res Commun. 1997 Mar 27;232(3):631-6.

PMID:
9126326
[PubMed - indexed for MEDLINE]
11.

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.

PMID:
9425230
[PubMed - indexed for MEDLINE]
Free Article
12.

Decreased expression of ABCD4 and BG1 genes early in the pathogenesis of X-linked adrenoleukodystrophy.

Asheuer M, Bieche I, Laurendeau I, Moser A, Hainque B, Vidaud M, Aubourg P.

Hum Mol Genet. 2005 May 15;14(10):1293-303. Epub 2005 Mar 30.

PMID:
15800013
[PubMed - indexed for MEDLINE]
Free Article
13.

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. Epub 2002 Apr 29.

PMID:
11992258
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

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.

PMID:
10068511
[PubMed - indexed for MEDLINE]
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. Review. Japanese.

PMID:
17202797
[PubMed - indexed for MEDLINE]
Free Article
16.

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.

PMID:
7668254
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Full length cDNA cloning, promoter sequence, and genomic organization of the human adrenoleukodystrophy related (ALDR) gene functionally redundant to the gene responsible for X-linked adrenoleukodystrophy.

Holzinger A, Mayerhofer P, Berger J, Lichtner P, Kammerer S, Roscher AA.

Biochem Biophys Res Commun. 1999 May 10;258(2):436-42.

PMID:
10329405
[PubMed - indexed for MEDLINE]
18.

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 13;76(5):424-7.

PMID:
9556303
[PubMed - indexed for MEDLINE]
19.

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.

PMID:
12530690
[PubMed - indexed for MEDLINE]
20.

Biochemical aspects of X-linked adrenoleukodystrophy.

Kemp S, Wanders R.

Brain Pathol. 2010 Jul;20(4):831-7. doi: 10.1111/j.1750-3639.2010.00391.x. Review.

PMID:
20626744
[PubMed - indexed for MEDLINE]

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