BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

201 related articles for article (PubMed ID: 9556303)

  • 21. Role of ALDP (ABCD1) and mitochondria in X-linked adrenoleukodystrophy.
    McGuinness MC; Lu JF; Zhang HP; Dong GX; Heinzer AK; Watkins PA; Powers J; Smith KD
    Mol Cell Biol; 2003 Jan; 23(2):744-53. PubMed ID: 12509471
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. X-linked adrenomyeloneuropathy associated with 14 novel ALD-gene mutations: no correlation between type of mutation and age of onset.
    Wichers M; Köhler W; Brennemann W; Boese V; Sokolowski P; Bidlingmaier F; Ludwig M
    Hum Genet; 1999; 105(1-2):116-9. PubMed ID: 10480364
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Adrenoleukodystrophy: the restoration of peroxisomal beta-oxidation by transfection of normal cDNA.
    Shinnoh N; Yamada T; Yoshimura T; Furuya H; Yoshida Y; Suzuki Y; Shimozawa N; Orii T; Kobayashi T
    Biochem Biophys Res Commun; 1995 May; 210(3):830-6. PubMed ID: 7763255
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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; 14(10):1293-303. PubMed ID: 15800013
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Eight novel mutations in the ABCD1 gene and clinical characteristics of 25 Chinese patients with X-linked adrenoleukodystrophy.
    Chu SS; Ye J; Zhang HW; Han LS; Qiu WJ; Gao XL; Gu XF
    World J Pediatr; 2015 Nov; 11(4):366-73. PubMed ID: 26454440
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [X-linked adrenoleukodystrophy].
    Aubourg P
    Ann Endocrinol (Paris); 2007 Dec; 68(6):403-11. PubMed ID: 17532287
    [TBL] [Abstract][Full Text] [Related]  

  • 28. X-linked adrenoleukodystrophy: genes, mutations, and phenotypes.
    Smith KD; Kemp S; Braiterman LT; Lu JF; Wei HM; Geraghty M; Stetten G; Bergin JS; Pevsner J; Watkins PA
    Neurochem Res; 1999 Apr; 24(4):521-35. PubMed ID: 10227685
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. [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]  

  • 31. Adrenoleukodystrophy.
    Cappa M; Bizzarri C; Vollono C; Petroni A; Banni S
    Endocr Dev; 2011; 20():149-160. PubMed ID: 21164268
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Probing substrate-induced conformational alterations in adrenoleukodystrophy protein by proteolysis.
    Guimarães CP; Sá-Miranda C; Azevedo JE
    J Hum Genet; 2005; 50(2):99-105. PubMed ID: 15682271
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Substrate specificity overlap and interaction between adrenoleukodystrophy protein (ALDP/ABCD1) and adrenoleukodystrophy-related protein (ALDRP/ABCD2).
    Genin EC; Geillon F; Gondcaille C; Athias A; Gambert P; Trompier D; Savary S
    J Biol Chem; 2011 Mar; 286(10):8075-8084. PubMed ID: 21209459
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. 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]  

  • 36. Adrenoleukodystrophy protein enhances association of very long-chain acyl-coenzyme A synthetase with the peroxisome.
    Yamada T; Taniwaki T; Shinnoh N; Uchiyama A; Shimozawa N; Ohyagi Y; Asahara H; Kira J
    Neurology; 1999 Feb; 52(3):614-6. PubMed ID: 10025797
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 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]  

  • 39. 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]  

  • 40. Bezafibrate lowers very long-chain fatty acids in X-linked adrenoleukodystrophy fibroblasts by inhibiting fatty acid elongation.
    Engelen M; Schackmann MJ; Ofman R; Sanders RJ; Dijkstra IM; Houten SM; Fourcade S; Pujol A; Poll-The BT; Wanders RJ; Kemp S
    J Inherit Metab Dis; 2012 Nov; 35(6):1137-45. PubMed ID: 22447153
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.