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Journal Abstract Search

224 related items for PubMed ID: 15333588

  • 21. The chimeric oncoproteins E2A-PBX1 and E2A-HLF are concentrated within spherical nuclear domains.
    LeBrun DP, Matthews BP, Feldman BJ, Cleary ML.
    Oncogene; 1997 Oct 23; 15(17):2059-67. PubMed ID: 9366523
    [Abstract] [Full Text] [Related]

  • 22. Fork stalling and template switching as a mechanism for polyalanine tract expansion affecting the DYC mutant of HOXD13, a new murine model of synpolydactyly.
    Cocquempot O, Brault V, Babinet C, Herault Y.
    Genetics; 2009 Sep 23; 183(1):23-30. PubMed ID: 19546318
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  • 23. Functional characterization of the human SOX3 promoter: identification of transcription factors implicated in basal promoter activity.
    Kovacevic Grujicic N, Mojsin M, Krstic A, Stevanovic M.
    Gene; 2005 Jan 03; 344():287-97. PubMed ID: 15656994
    [Abstract] [Full Text] [Related]

  • 24. Molecular characterization of HOXA13 polyalanine expansion proteins in hand-foot-genital syndrome.
    Utsch B, McCabe CD, Galbraith K, Gonzalez R, Born M, Dötsch J, Ludwig M, Reutter H, Innis JW.
    Am J Med Genet A; 2007 Dec 15; 143A(24):3161-8. PubMed ID: 17935235
    [Abstract] [Full Text] [Related]

  • 25. Molecular pathology of expanded polyalanine tract mutations in the Aristaless-related homeobox gene.
    Shoubridge C, Cloosterman D, Parkinson-Lawerence E, Brooks D, Gécz J.
    Genomics; 2007 Jul 15; 90(1):59-71. PubMed ID: 17490853
    [Abstract] [Full Text] [Related]

  • 26. A stress regulatory network for co-ordinated activation of proteasome expression mediated by yeast heat shock transcription factor.
    Hahn JS, Neef DW, Thiele DJ.
    Mol Microbiol; 2006 Apr 15; 60(1):240-51. PubMed ID: 16556235
    [Abstract] [Full Text] [Related]

  • 27. A Novel mouse model of enhanced proteostasis: Full-length human heat shock factor 1 transgenic mice.
    Pierce A, Wei R, Halade D, Yoo SE, Ran Q, Richardson A.
    Biochem Biophys Res Commun; 2010 Nov 05; 402(1):59-65. PubMed ID: 20920476
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  • 28. Synpolydactyly in mice with a targeted deficiency in the HoxD complex.
    Zákány J, Duboule D.
    Nature; 1996 Nov 07; 384(6604):69-71. PubMed ID: 8900279
    [Abstract] [Full Text] [Related]

  • 29. Misfolded proteins inhibit proliferation and promote stress-induced death in SV40-transformed mammalian cells.
    Arslan MA, Chikina M, Csermely P, Soti C.
    FASEB J; 2012 Feb 07; 26(2):766-77. PubMed ID: 22049061
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  • 30. Heat shock transcription factor 1 down-regulates spermatocyte-specific 70 kDa heat shock protein expression prior to the induction of apoptosis in mouse testes.
    Widlak W, Vydra N, Malusecka E, Dudaladava V, Winiarski B, Scieglińska D, Widlak P.
    Genes Cells; 2007 Apr 07; 12(4):487-99. PubMed ID: 17397396
    [Abstract] [Full Text] [Related]

  • 31. Chaperonin TRiC promotes the assembly of polyQ expansion proteins into nontoxic oligomers.
    Behrends C, Langer CA, Boteva R, Böttcher UM, Stemp MJ, Schaffar G, Rao BV, Giese A, Kretzschmar H, Siegers K, Hartl FU.
    Mol Cell; 2006 Sep 15; 23(6):887-97. PubMed ID: 16973440
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  • 32. Deficit of heat shock transcription factor 1-heat shock 70 kDa protein 1A axis determines the cell death vulnerability in a model of spinocerebellar ataxia type 6.
    Li L, Saegusa H, Tanabe T.
    Genes Cells; 2009 Nov 15; 14(11):1253-69. PubMed ID: 19817876
    [Abstract] [Full Text] [Related]

  • 33. Unblending of Transcriptional Condensates in Human Repeat Expansion Disease.
    Basu S, Mackowiak SD, Niskanen H, Knezevic D, Asimi V, Grosswendt S, Geertsema H, Ali S, Jerković I, Ewers H, Mundlos S, Meissner A, Ibrahim DM, Hnisz D.
    Cell; 2020 May 28; 181(5):1062-1079.e30. PubMed ID: 32386547
    [Abstract] [Full Text] [Related]

  • 34. Limb skeletal malformations - what the HOX is going on?
    Brison N, Tylzanowski P, Debeer P.
    Eur J Med Genet; 2012 Jan 28; 55(1):1-7. PubMed ID: 21782042
    [Abstract] [Full Text] [Related]

  • 35. Limb malformations and the human HOX genes.
    Goodman FR.
    Am J Med Genet; 2002 Oct 15; 112(3):256-65. PubMed ID: 12357469
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  • 36. The synpolydactyly homolog (spdh) mutation in the mouse -- a defect in patterning and growth of limb cartilage elements.
    Albrecht AN, Schwabe GC, Stricker S, Böddrich A, Wanker EE, Mundlos S.
    Mech Dev; 2002 Mar 15; 112(1-2):53-67. PubMed ID: 11850178
    [Abstract] [Full Text] [Related]

  • 37. Mutation analysis of HOXD13 gene in a Chinese pedigree with synpolydactyly.
    Dai L, Heng ZC, Zhu J, Cai R, Mao M, Wang H, Lin MJ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun 15; 22(3):277-80. PubMed ID: 15952114
    [Abstract] [Full Text] [Related]

  • 38. Hsp105 reduces the protein aggregation and cytotoxicity by expanded-polyglutamine proteins through the induction of Hsp70.
    Yamagishi N, Goto K, Nakagawa S, Saito Y, Hatayama T.
    Exp Cell Res; 2010 Sep 10; 316(15):2424-33. PubMed ID: 20542028
    [Abstract] [Full Text] [Related]

  • 39. Misexpression of Sox9 in mouse limb bud mesenchyme induces polydactyly and rescues hypodactyly mice.
    Akiyama H, Stadler HS, Martin JF, Ishii TM, Beachy PA, Nakamura T, de Crombrugghe B.
    Matrix Biol; 2007 May 10; 26(4):224-33. PubMed ID: 17222543
    [Abstract] [Full Text] [Related]

  • 40. In vitro analysis of partial loss-of-function ZIC2 mutations in holoprosencephaly: alanine tract expansion modulates DNA binding and transactivation.
    Brown L, Paraso M, Arkell R, Brown S.
    Hum Mol Genet; 2005 Feb 01; 14(3):411-20. PubMed ID: 15590697
    [Abstract] [Full Text] [Related]

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