100 related articles for article (PubMed ID: 26503938)
1. Cerebral adrenoleukodystrophy: a demyelinating disease that leaves the door wide open.
Aubourg P
Brain; 2015 Nov; 138(Pt 11):3133-6. PubMed ID: 26503938
[No Abstract] [Full Text] [Related]
2. Brain endothelial dysfunction in cerebral adrenoleukodystrophy.
Musolino PL; Gong Y; Snyder JM; Jimenez S; Lok J; Lo EH; Moser AB; Grabowski EF; Frosch MP; Eichler FS
Brain; 2015 Nov; 138(Pt 11):3206-20. PubMed ID: 26377633
[TBL] [Abstract][Full Text] [Related]
3. ABC transporters, cytochromes P450 and their main transcription factors: expression at the human blood-brain barrier.
Dauchy S; Dutheil F; Weaver RJ; Chassoux F; Daumas-Duport C; Couraud PO; Scherrmann JM; De Waziers I; Declèves X
J Neurochem; 2008 Dec; 107(6):1518-28. PubMed ID: 19094056
[TBL] [Abstract][Full Text] [Related]
4. X-linked adrenomyeloneuropathy due to a novel missense mutation in the ABCD1 start codon presenting as demyelinating neuropathy.
Engelen M; van der Kooi AJ; Kemp S; Wanders RJ; Sistermans EA; Waterham HR; Koelman JT; van Geel BM; de Visser M
J Peripher Nerv Syst; 2011 Dec; 16(4):353-5. PubMed ID: 22176151
[No Abstract] [Full Text] [Related]
5. 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]
6. Altered glycaemia differentially modulates efflux transporter expression and activity in hCMEC/D3 cell line.
Sajja RK; Cucullo L
Neurosci Lett; 2015 Jun; 598():59-65. PubMed ID: 25982326
[TBL] [Abstract][Full Text] [Related]
7. Modeling and rescue of defective blood-brain barrier function of induced brain microvascular endothelial cells from childhood cerebral adrenoleukodystrophy patients.
Lee CAA; Seo HS; Armien AG; Bates FS; Tolar J; Azarin SM
Fluids Barriers CNS; 2018 Apr; 15(1):9. PubMed ID: 29615068
[TBL] [Abstract][Full Text] [Related]
8. Modulation of transendothelial permeability and expression of ATP-binding cassette transporters in cultured brain capillary endothelial cells by astrocytic factors and cell-culture conditions.
Török M; Huwyler J; Gutmann H; Fricker G; Drewe J
Exp Brain Res; 2003 Dec; 153(3):356-65. PubMed ID: 14610630
[TBL] [Abstract][Full Text] [Related]
9. Lack of adrenoleukodystrophy protein enhances oligodendrocyte disturbance and microglia activation in mice with combined Abcd1/Mag deficiency.
Dumser M; Bauer J; Lassmann H; Berger J; Forss-Petter S
Acta Neuropathol; 2007 Dec; 114(6):573-86. PubMed ID: 17828604
[TBL] [Abstract][Full Text] [Related]
10. Expression and splicing of ABC and SLC transporters in the human blood-brain barrier measured with RNAseq.
Suhy AM; Webb A; Papp AC; Geier EG; Sadee W
Eur J Pharm Sci; 2017 May; 103():47-51. PubMed ID: 28188910
[TBL] [Abstract][Full Text] [Related]
11. Gene symbol: ABCD1. Disease: Adrenoleukodystrophy.
Shukla P
Hum Genet; 2008 Oct; 124(3):312. PubMed ID: 18846654
[No Abstract] [Full Text] [Related]
12. Regulation of breast cancer resistant protein by peroxisome proliferator-activated receptor α in human brain microvessel endothelial cells.
Hoque MT; Robillard KR; Bendayan R
Mol Pharmacol; 2012 Apr; 81(4):598-609. PubMed ID: 22266374
[TBL] [Abstract][Full Text] [Related]
13. Comparative gene expression profiles of ABC transporters in brain microvessel endothelial cells and brain in five species including human.
Warren MS; Zerangue N; Woodford K; Roberts LM; Tate EH; Feng B; Li C; Feuerstein TJ; Gibbs J; Smith B; de Morais SM; Dower WJ; Koller KJ
Pharmacol Res; 2009 Jun; 59(6):404-13. PubMed ID: 19429473
[TBL] [Abstract][Full Text] [Related]
14. De novo ABCD1 gene mutation in an Indian patient with adrenoleukodystrophy.
Kumar N; Shukla P; Taneja KK; Kalra V; Bansal SK
Pediatr Neurol; 2008 Oct; 39(4):289-92. PubMed ID: 18805372
[TBL] [Abstract][Full Text] [Related]
15. Novel human pathological mutations. Gene symbol: ABCD1. Disease: X-linked adrenoleukodystrophy.
Amorosi CA; Treslova H; Dodelson de Kremer R; Coll MJ; Dvoráková L; Oller Ramírez AM
Hum Genet; 2010 Apr; 127(4):486. PubMed ID: 21488262
[No Abstract] [Full Text] [Related]
16. Gene symbol: ABCD1. Disease: Adrenoleukodystrophy.
Shukla P
Hum Genet; 2008 Oct; 124(3):312. PubMed ID: 18846655
[No Abstract] [Full Text] [Related]
17. Gene symbol: ABCD1. Disease: Adrenoleukodystrophy.
Shukla P
Hum Genet; 2008 Oct; 124(3):311. PubMed ID: 18846653
[No Abstract] [Full Text] [Related]
18. Novel human pathological mutations. Gene symbol: ABCD1. Disease: X-linked adrenoleukodystrophy.
Amorosi CA; Treslova H; Dodelson de Kremer R; Coll MJ; Dvoráková L; Oller Ramírez AM
Hum Genet; 2010 Apr; 127(4):486. PubMed ID: 21488311
[No Abstract] [Full Text] [Related]
19. Novel exon nucleotide deletion causes adrenoleukodystrophy in a Brazilian family.
Valadares ER; Trindade AL; Oliveira LR; Arantes RR; Daker MV; Viana BM; Haase VG; Jardim LB; Lopes GC; Godard AL
Genet Mol Res; 2011 Jan; 10(1):65-74. PubMed ID: 21264817
[TBL] [Abstract][Full Text] [Related]
20. Linking mutated primary structure of adrenoleukodystrophy protein with X-linked adrenoleukodystrophy.
Yan S; Wu G
Comput Methods Biomech Biomed Engin; 2010 Jun; 13(3):403-11. PubMed ID: 20077240
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
