431 related articles for article (PubMed ID: 15489218)
41. Molecular characterization of X-linked adrenoleukodystrophy in a Tunisian family: identification of a novel missense mutation in the ABCD1 gene.
Kallabi F; Hadj Salem I; Ben Salah G; Ben Turkia H; Ben Chehida A; Tebib N; Fakhfakh F; Kamoun H
Neurodegener Dis; 2013; 12(4):207-11. PubMed ID: 23651979
[TBL] [Abstract][Full Text] [Related]
42. 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; 361(6414):726-30. PubMed ID: 8441467
[TBL] [Abstract][Full Text] [Related]
43. Beneficial Effects of the Direct AMP-Kinase Activator PXL770 in In Vitro and In Vivo Models of X-Linked Adrenoleukodystrophy.
Monternier PA; Parasar P; Theurey P; Gluais Dagorn P; Kaur N; Nagaraja TN; Fouqueray P; Bolze S; Moller DE; Singh J; Hallakou-Bozec S
J Pharmacol Exp Ther; 2022 Aug; 382(2):208-222. PubMed ID: 35764327
[TBL] [Abstract][Full Text] [Related]
44. Induced pluripotent stem cell models from X-linked adrenoleukodystrophy patients.
Jang J; Kang HC; Kim HS; Kim JY; Huh YJ; Kim DS; Yoo JE; Lee JA; Lim B; Lee J; Yoon TM; Park IH; Hwang DY; Daley GQ; Kim DW
Ann Neurol; 2011 Sep; 70(3):402-9. PubMed ID: 21721033
[TBL] [Abstract][Full Text] [Related]
45. Dehydroepiandrosterone up-regulates the Adrenoleukodystrophy-related gene (ABCD2) independently of PPARalpha in rodents.
Gueugnon F; Gondcaille C; Leclercq S; Bellenger J; Bellenger S; Narce M; Pineau T; Bonnetain F; Savary S
Biochimie; 2007 Nov; 89(11):1312-21. PubMed ID: 17686565
[TBL] [Abstract][Full Text] [Related]
46. X-linked adrenoleukodystrophy: clinical, metabolic, genetic and pathophysiological aspects.
Kemp S; Berger J; Aubourg P
Biochim Biophys Acta; 2012 Sep; 1822(9):1465-74. PubMed ID: 22483867
[TBL] [Abstract][Full Text] [Related]
47. ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations.
Kemp S; Pujol A; Waterham HR; van Geel BM; Boehm CD; Raymond GV; Cutting GR; Wanders RJ; Moser HW
Hum Mutat; 2001 Dec; 18(6):499-515. PubMed ID: 11748843
[TBL] [Abstract][Full Text] [Related]
48. Silencing of Abcd1 and Abcd2 genes sensitizes astrocytes for inflammation: implication for X-adrenoleukodystrophy.
Singh J; Khan M; Singh I
J Lipid Res; 2009 Jan; 50(1):135-47. PubMed ID: 18723473
[TBL] [Abstract][Full Text] [Related]
49. C26:0-Carnitine Is a New Biomarker for X-Linked Adrenoleukodystrophy in Mice and Man.
van de Beek MC; Dijkstra IM; van Lenthe H; Ofman R; Goldhaber-Pasillas D; Schauer N; Schackmann M; Engelen-Lee JY; Vaz FM; Kulik W; Wanders RJ; Engelen M; Kemp S
PLoS One; 2016; 11(4):e0154597. PubMed ID: 27124591
[TBL] [Abstract][Full Text] [Related]
50. Induction of the adrenoleukodystrophy-related gene (ABCD2) by thyromimetics.
Genin EC; Gondcaille C; Trompier D; Savary S
J Steroid Biochem Mol Biol; 2009 Aug; 116(1-2):37-43. PubMed ID: 19406244
[TBL] [Abstract][Full Text] [Related]
51. A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression pattern.
Lombard-Platet G; Savary S; Sarde CO; Mandel JL; Chimini G
Proc Natl Acad Sci U S A; 1996 Feb; 93(3):1265-9. PubMed ID: 8577752
[TBL] [Abstract][Full Text] [Related]
52. CRISPR/Cas9-mediated knockout of Abcd1 and Abcd2 genes in BV-2 cells: novel microglial models for X-linked Adrenoleukodystrophy.
Raas Q; Gondcaille C; Hamon Y; Leoni V; Caccia C; Ménétrier F; Lizard G; Trompier D; Savary S
Biochim Biophys Acta Mol Cell Biol Lipids; 2019 May; 1864(5):704-714. PubMed ID: 30769094
[TBL] [Abstract][Full Text] [Related]
53. Accumulation of very long-chain fatty acids does not affect mitochondrial function in adrenoleukodystrophy protein deficiency.
Oezen I; Rossmanith W; Forss-Petter S; Kemp S; Voigtländer T; Moser-Thier K; Wanders RJ; Bittner RE; Berger J
Hum Mol Genet; 2005 May; 14(9):1127-37. PubMed ID: 15772093
[TBL] [Abstract][Full Text] [Related]
54. Exon organisation of the mouse gene encoding the Adrenoleukodystrophy related protein (ALDRP).
Broccardo C; Troffer-Charlier N; Savary S; Mandel JL; Chimini G
Eur J Hum Genet; 1998; 6(6):638-41. PubMed ID: 9887385
[TBL] [Abstract][Full Text] [Related]
55. Evaluation of the therapeutic potential of PPARalpha agonists for X-linked adrenoleukodystrophy.
Rampler H; Weinhofer I; Netik A; Forss-Petter S; Brown PJ; Oplinger JA; Bugaut M; Berger J
Mol Genet Metab; 2003 Dec; 80(4):398-407. PubMed ID: 14654352
[TBL] [Abstract][Full Text] [Related]
56. cDNA cloning and mRNA expression of the human adrenoleukodystrophy related protein (ALDRP), a peroxisomal ABC transporter.
Holzinger A; Kammerer S; Berger J; Roscher AA
Biochem Biophys Res Commun; 1997 Oct; 239(1):261-4. PubMed ID: 9345306
[TBL] [Abstract][Full Text] [Related]
57. The peroxisomal fatty acid transporter ABCD1/PMP-4 is required in the C. elegans hypodermis for axonal maintenance: A worm model for adrenoleukodystrophy.
Coppa A; Guha S; Fourcade S; Parameswaran J; Ruiz M; Moser AB; Schlüter A; Murphy MP; Lizcano JM; Miranda-Vizuete A; Dalfó E; Pujol A
Free Radic Biol Med; 2020 May; 152():797-809. PubMed ID: 32017990
[TBL] [Abstract][Full Text] [Related]
58. Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in patients with X-linked adrenoleukodystrophy (ALD) based on comprehensive resequencing and association studies with ALD phenotypes.
Matsukawa T; Asheuer M; Takahashi Y; Goto J; Suzuki Y; Shimozawa N; Takano H; Onodera O; Nishizawa M; Aubourg P; Tsuji S
Neurogenetics; 2011 Feb; 12(1):41-50. PubMed ID: 20661612
[TBL] [Abstract][Full Text] [Related]
59. Novel
Cho YK; Lee SY; Kim SW
Endocrinol Metab (Seoul); 2020 Mar; 35(1):188-191. PubMed ID: 32207279
[TBL] [Abstract][Full Text] [Related]
60. Cerebral inflammation in X-linked adrenoleukodystrophy.
McGuinness MC; Smith KD
Arch Immunol Ther Exp (Warsz); 1999; 47(5):281-7. PubMed ID: 10604233
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
