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Journal Abstract Search

143 related items for PubMed ID: 11823444

  • 21. Loss of ATRX leads to chromosome cohesion and congression defects.
    Ritchie K, Seah C, Moulin J, Isaac C, Dick F, Bérubé NG.
    J Cell Biol; 2008 Jan 28; 180(2):315-24. PubMed ID: 18227278
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  • 22. Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53.
    Seah C, Levy MA, Jiang Y, Mokhtarzada S, Higgs DR, Gibbons RJ, Bérubé NG.
    J Neurosci; 2008 Nov 19; 28(47):12570-80. PubMed ID: 19020049
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  • 23. Heterochromatin and ND10 are cell-cycle regulated and phosphorylation-dependent alternate nuclear sites of the transcription repressor Daxx and SWI/SNF protein ATRX.
    Ishov AM, Vladimirova OV, Maul GG.
    J Cell Sci; 2004 Aug 01; 117(Pt 17):3807-20. PubMed ID: 15252119
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  • 24. The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies.
    Xue Y, Gibbons R, Yan Z, Yang D, McDowell TL, Sechi S, Qin J, Zhou S, Higgs D, Wang W.
    Proc Natl Acad Sci U S A; 2003 Sep 16; 100(19):10635-40. PubMed ID: 12953102
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  • 25. Alpha-thalassemia/mental retardation syndrome, X-Linked (ATR-X, MIM #301040, ATR-X/XNP/XH2 gene MIM #300032).
    Villard L, Fontes M.
    Eur J Hum Genet; 2002 Apr 16; 10(4):223-5. PubMed ID: 12032728
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  • 31. ATRX, a member of the SNF2 family of helicase/ATPases, is required for chromosome alignment and meiotic spindle organization in metaphase II stage mouse oocytes.
    De La Fuente R, Viveiros MM, Wigglesworth K, Eppig JJ.
    Dev Biol; 2004 Aug 01; 272(1):1-14. PubMed ID: 15242786
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  • 34. ATRX and sex differentiation.
    Tang P, Park DJ, Marshall Graves JA, Harley VR.
    Trends Endocrinol Metab; 2004 Sep 01; 15(7):339-44. PubMed ID: 15350606
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  • 35. Mutational analysis of the ATRX gene by DGGE: a powerful diagnostic approach for the ATRX syndrome.
    Borgione E, Sturnio M, Spalletta A, Angela Lo Giudice M, Castiglia L, Galesi O, Ragusa A, Fichera M.
    Hum Mutat; 2003 May 01; 21(5):529-34. PubMed ID: 12673795
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  • 36. Decreased expression of GRAF1/OPHN-1-L in the X-linked alpha thalassemia mental retardation syndrome.
    Barresi V, Ragusa A, Fichera M, Musso N, Castiglia L, Rappazzo G, Travali S, Mattina T, Romano C, Cocchi G, Condorelli DF.
    BMC Med Genomics; 2010 Jul 06; 3():28. PubMed ID: 20602808
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  • 38. Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients.
    Al-Nafie AN, Borgio JF, AbdulAzeez S, Al-Suliman AM, Qaw FS, Naserullah ZA, Al-Jarrash S, Al-Madan MS, Al-Ali RA, AlKhalifah MA, Al-Muhanna F, Steinberg MH, Al-Ali AK.
    Blood Cells Mol Dis; 2015 Jun 06; 55(1):27-9. PubMed ID: 25976463
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