152 related articles for article (PubMed ID: 16223892)
1. Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage.
Ferrer I; Kapfhammer JP; Hindelang C; Kemp S; Troffer-Charlier N; Broccoli V; Callyzot N; Mooyer P; Selhorst J; Vreken P; Wanders RJ; Mandel JL; Pujol A
Hum Mol Genet; 2005 Dec; 14(23):3565-77. PubMed ID: 16223892
[TBL] [Abstract][Full Text] [Related]
2. Functional overlap between ABCD1 (ALD) and ABCD2 (ALDR) transporters: a therapeutic target for X-adrenoleukodystrophy.
Pujol A; Ferrer I; Camps C; Metzger E; Hindelang C; Callizot N; Ruiz M; Pàmpols T; Giròs M; Mandel JL
Hum Mol Genet; 2004 Dec; 13(23):2997-3006. PubMed ID: 15489218
[TBL] [Abstract][Full Text] [Related]
3. Metformin-induced mitochondrial function and ABCD2 up-regulation in X-linked adrenoleukodystrophy involves AMP-activated protein kinase.
Singh J; Olle B; Suhail H; Felicella MM; Giri S
J Neurochem; 2016 Jul; 138(1):86-100. PubMed ID: 26849413
[TBL] [Abstract][Full Text] [Related]
4. Impaired mitochondrial oxidative phosphorylation in the peroxisomal disease X-linked adrenoleukodystrophy.
López-Erauskin J; Galino J; Ruiz M; Cuezva JM; Fabregat I; Cacabelos D; Boada J; Martínez J; Ferrer I; Pamplona R; Villarroya F; Portero-Otín M; Fourcade S; Pujol A
Hum Mol Genet; 2013 Aug; 22(16):3296-305. PubMed ID: 23604518
[TBL] [Abstract][Full Text] [Related]
5. Abcd2 is a strong modifier of the metabolic impairments in peritoneal macrophages of ABCD1-deficient mice.
Muneer Z; Wiesinger C; Voigtländer T; Werner HB; Berger J; Forss-Petter S
PLoS One; 2014; 9(9):e108655. PubMed ID: 25255441
[TBL] [Abstract][Full Text] [Related]
6. ABCD1 deletion-induced mitochondrial dysfunction is corrected by SAHA: implication for adrenoleukodystrophy.
Baarine M; Beeson C; Singh A; Singh I
J Neurochem; 2015 May; 133(3):380-96. PubMed ID: 25393703
[TBL] [Abstract][Full Text] [Related]
7. Late onset neurological phenotype of the X-ALD gene inactivation in mice: a mouse model for adrenomyeloneuropathy.
Pujol A; Hindelang C; Callizot N; Bartsch U; Schachner M; Mandel JL
Hum Mol Genet; 2002 Mar; 11(5):499-505. PubMed ID: 11875044
[TBL] [Abstract][Full Text] [Related]
8. Targeted Brain Delivery of Dendrimer-4-Phenylbutyrate Ameliorates Neurological Deficits in a Long-Term ABCD1-Deficient Mouse Model of X-Linked Adrenoleukodystrophy.
Nemeth CL; Gӧk Ö; Tomlinson SN; Sharma A; Moser AB; Kannan S; Kannan RM; Fatemi A
Neurotherapeutics; 2023 Jan; 20(1):272-283. PubMed ID: 36207570
[TBL] [Abstract][Full Text] [Related]
9. A key role for the peroxisomal ABCD2 transporter in fatty acid homeostasis.
Fourcade S; Ruiz M; Camps C; Schlüter A; Houten SM; Mooyer PA; Pàmpols T; Dacremont G; Wanders RJ; Giròs M; Pujol A
Am J Physiol Endocrinol Metab; 2009 Jan; 296(1):E211-21. PubMed ID: 18854420
[TBL] [Abstract][Full Text] [Related]
10. Caffeic acid phenethyl ester induces adrenoleukodystrophy (Abcd2) gene in human X-ALD fibroblasts and inhibits the proinflammatory response in Abcd1/2 silenced mouse primary astrocytes.
Singh J; Khan M; Singh I
Biochim Biophys Acta; 2013 Apr; 1831(4):747-58. PubMed ID: 23318275
[TBL] [Abstract][Full Text] [Related]
11. Spinocerebellar variant of adrenoleukodystrophy with a novel ABCD1 gene mutation.
Li JY; Hsu CC; Tsai CR
J Neurol Sci; 2010 Mar; 290(1-2):163-5. PubMed ID: 20042197
[TBL] [Abstract][Full Text] [Related]
12. Peroxisomal ABC transporters: structure, function and role in disease.
Morita M; Imanaka T
Biochim Biophys Acta; 2012 Sep; 1822(9):1387-96. PubMed ID: 22366764
[TBL] [Abstract][Full Text] [Related]
13. Astrocytes and mitochondria from adrenoleukodystrophy protein (ABCD1)-deficient mice reveal that the adrenoleukodystrophy-associated very long-chain fatty acids target several cellular energy-dependent functions.
Kruska N; Schönfeld P; Pujol A; Reiser G
Biochim Biophys Acta; 2015 May; 1852(5):925-36. PubMed ID: 25583114
[TBL] [Abstract][Full Text] [Related]
14. ABC Transporter Subfamily D: Distinct Differences in Behavior between ABCD1-3 and ABCD4 in Subcellular Localization, Function, and Human Disease.
Kawaguchi K; Morita M
Biomed Res Int; 2016; 2016():6786245. PubMed ID: 27766264
[TBL] [Abstract][Full Text] [Related]
15. The role of peroxisomal ABC transporters in the mouse adrenal gland: the loss of Abcd2 (ALDR), Not Abcd1 (ALD), causes oxidative damage.
Lu JF; Barron-Casella E; Deering R; Heinzer AK; Moser AB; deMesy Bentley KL; Wand GS; C McGuinness M; Pei Z; Watkins PA; Pujol A; Smith KD; Powers JM
Lab Invest; 2007 Mar; 87(3):261-72. PubMed ID: 17260006
[TBL] [Abstract][Full Text] [Related]
16. Valproic acid induces antioxidant effects in X-linked adrenoleukodystrophy.
Fourcade S; Ruiz M; Guilera C; Hahnen E; Brichta L; Naudi A; Portero-Otín M; Dacremont G; Cartier N; Wanders R; Kemp S; Mandel JL; Wirth B; Pamplona R; Aubourg P; Pujol A
Hum Mol Genet; 2010 May; 19(10):2005-14. PubMed ID: 20179078
[TBL] [Abstract][Full Text] [Related]
17. Effect of dietary polyunsaturated fatty acids on the expression of peroxisomal ABC transporters.
Leclercq S; Skrzypski J; Courvoisier A; Gondcaille C; Bonnetain F; André A; Chardigny JM; Bellenger S; Bellenger J; Narce M; Savary S
Biochimie; 2008 Oct; 90(10):1602-7. PubMed ID: 18585430
[TBL] [Abstract][Full Text] [Related]
18. X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism, ABC half-transporters and the complicated route to treatment.
Kemp S; Wanders RJ
Mol Genet Metab; 2007 Mar; 90(3):268-76. PubMed ID: 17092750
[TBL] [Abstract][Full Text] [Related]
19. Fibrate induction of the adrenoleukodystrophy-related gene (ABCD2): promoter analysis and role of the peroxisome proliferator-activated receptor PPARalpha.
Fourcade S; Savary S; Albet S; Gauthé D; Gondcaille C; Pineau T; Bellenger J; Bentejac M; Holzinger A; Berger J; Bugaut M
Eur J Biochem; 2001 Jun; 268(12):3490-500. PubMed ID: 11422379
[TBL] [Abstract][Full Text] [Related]
20. Predictive Structure and Topology of Peroxisomal ATP-Binding Cassette (ABC) Transporters.
Andreoletti P; Raas Q; Gondcaille C; Cherkaoui-Malki M; Trompier D; Savary S
Int J Mol Sci; 2017 Jul; 18(7):. PubMed ID: 28737695
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
