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Journal Abstract Search

173 related items for PubMed ID: 14729260

  • 21.
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  • 23. BRG1 contains a conserved domain of the SWI2/SNF2 family necessary for normal mitotic growth and transcription.
    Khavari PA, Peterson CL, Tamkun JW, Mendel DB, Crabtree GR.
    Nature; 1993 Nov 11; 366(6451):170-4. PubMed ID: 8232556
    [Abstract] [Full Text] [Related]

  • 24. Molecular genetic study of japanese patients with X-linked alpha-thalassemia/mental retardation syndrome (ATR-X).
    Wada T, Kubota T, Fukushima Y, Saitoh S.
    Am J Med Genet; 2000 Sep 18; 94(3):242-8. PubMed ID: 10995512
    [Abstract] [Full Text] [Related]

  • 25. Determination of the genomic structure of the XNP/ATRX gene encoding a potential zinc finger helicase.
    Villard L, Lossi AM, Cardoso C, Proud V, Chiaroni P, Colleaux L, Schwartz C, Fontés M.
    Genomics; 1997 Jul 15; 43(2):149-55. PubMed ID: 9244431
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  • 27. Characterization of the isoforms of MOVO zinc finger protein, a mouse homologue of Drosophila Ovo, as transcription factors.
    Unezaki S, Nishizawa M, Okuda-Ashitaka E, Masu Y, Mukai M, Kobayashi S, Sawamoto K, Okano H, Ito S.
    Gene; 2004 Jul 07; 336(1):47-58. PubMed ID: 15225875
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  • 29. Colocalization and heteromerization between the two human oncogene POZ/zinc finger proteins, LAZ3 (BCL6) and PLZF.
    Dhordain P, Albagli O, Honore N, Guidez F, Lantoine D, Schmid M, The HD, Zelent A, Koken MH.
    Oncogene; 2000 Dec 14; 19(54):6240-50. PubMed ID: 11175338
    [Abstract] [Full Text] [Related]

  • 30. Functional significance of mutations in the Snf2 domain of ATRX.
    Mitson M, Kelley LA, Sternberg MJ, Higgs DR, Gibbons RJ.
    Hum Mol Genet; 2011 Jul 01; 20(13):2603-10. PubMed ID: 21505078
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  • 31.
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  • 33. Neurodevelopmental defects resulting from ATRX overexpression in transgenic mice.
    Bérubé NG, Jagla M, Smeenk C, De Repentigny Y, Kothary R, Picketts DJ.
    Hum Mol Genet; 2002 Feb 01; 11(3):253-61. PubMed ID: 11823444
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  • 34. Cell cycle behavior of human HP1 subtypes: distinct molecular domains of HP1 are required for their centromeric localization during interphase and metaphase.
    Hayakawa T, Haraguchi T, Masumoto H, Hiraoka Y.
    J Cell Sci; 2003 Aug 15; 116(Pt 16):3327-38. PubMed ID: 12840071
    [Abstract] [Full Text] [Related]

  • 35. PIC 1, a novel ubiquitin-like protein which interacts with the PML component of a multiprotein complex that is disrupted in acute promyelocytic leukaemia.
    Boddy MN, Howe K, Etkin LD, Solomon E, Freemont PS.
    Oncogene; 1996 Sep 05; 13(5):971-82. PubMed ID: 8806687
    [Abstract] [Full Text] [Related]

  • 36. A novel 5' ATRX mutation with splicing consequences in acquired alpha thalassemia-myelodysplastic syndrome.
    Nelson ME, Thurmes PJ, Hoyer JD, Steensma DP.
    Haematologica; 2005 Nov 05; 90(11):1463-70. PubMed ID: 16266892
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  • 37. Cooperation between C/EBPalpha TBP/TFIIB and SWI/SNF recruiting domains is required for adipocyte differentiation.
    Pedersen TA, Kowenz-Leutz E, Leutz A, Nerlov C.
    Genes Dev; 2001 Dec 01; 15(23):3208-16. PubMed ID: 11731483
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  • 38. Architectural DNA binding by a high-mobility-group/kinesin-like subunit in mammalian SWI/SNF-related complexes.
    Wang W, Chi T, Xue Y, Zhou S, Kuo A, Crabtree GR.
    Proc Natl Acad Sci U S A; 1998 Jan 20; 95(2):492-8. PubMed ID: 9435219
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  • 39. hZimp7, a novel PIAS-like protein, enhances androgen receptor-mediated transcription and interacts with SWI/SNF-like BAF complexes.
    Huang CY, Beliakoff J, Li X, Lee J, Li X, Sharma M, Lim B, Sun Z.
    Mol Endocrinol; 2005 Dec 20; 19(12):2915-29. PubMed ID: 16051670
    [Abstract] [Full Text] [Related]

  • 40. [X-linked alpha-thalassemia/mental retardation syndrome].
    Wada T.
    Rinsho Byori; 2009 Apr 20; 57(4):382-90. PubMed ID: 19489441
    [Abstract] [Full Text] [Related]

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