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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

224 related items for PubMed ID: 15333588

  • 41. Lmo7 is an emerin-binding protein that regulates the transcription of emerin and many other muscle-relevant genes.
    Holaska JM, Rais-Bahrami S, Wilson KL.
    Hum Mol Genet; 2006 Dec 01; 15(23):3459-72. PubMed ID: 17067998
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  • 43. Repressor domain and nuclear localization signal of the murine Hoxa-11 protein are located in the homeodomain: no evidence for role of poly alanine stretches in transcriptional repression.
    Roth JJ, Breitenbach M, Wagner GP.
    J Exp Zool B Mol Dev Evol; 2005 Sep 15; 304(5):468-75. PubMed ID: 16032701
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  • 44. A splice donor site mutation in HOXD13 underlies synpolydactyly with cortical bone thinning.
    Shi X, Ji C, Cao L, Wu Y, Shang Y, Wang W, Luo Y.
    Gene; 2013 Dec 15; 532(2):297-301. PubMed ID: 24055421
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  • 50. Biochemical consequences of sedlin mutations that cause spondyloepiphyseal dysplasia tarda.
    Choi MY, Chan CC, Chan D, Luk KD, Cheah KS, Tanner JA.
    Biochem J; 2009 Sep 25; 423(2):233-42. PubMed ID: 19650763
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  • 51. Hsp105beta upregulates hsp70 gene expression through signal transducer and activator of transcription-3.
    Yamagishi N, Fujii H, Saito Y, Hatayama T.
    FEBS J; 2009 Oct 25; 276(20):5870-80. PubMed ID: 19754877
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  • 52. Activation of the heat shock response in familial amyloidotic polyneuropathy.
    Santos SD, Magalhães J, Saraiva MJ.
    J Neuropathol Exp Neurol; 2008 May 25; 67(5):449-55. PubMed ID: 18431252
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  • 53. [Dynamics of chaperone complex Hdj1-Hsp70-Bag1 as a response of erythroleukemia K562 cells to heat stress].
    Novoselov SS, Novoselova TV, Moskaleva OS, Margulis BA, Guzhova IV.
    Tsitologiia; 2004 May 25; 46(7):620-7. PubMed ID: 15473372
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  • 54. Interaction of Hsp70 with p49/STRAP, a serum response factor binding protein.
    Lin JL, Liu FH, Wang C.
    Biochem Biophys Res Commun; 2009 Nov 27; 389(4):607-11. PubMed ID: 19751705
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  • 59. Molecular consequences of PHOX2B missense, frameshift and alanine expansion mutations leading to autonomic dysfunction.
    Trochet D, Hong SJ, Lim JK, Brunet JF, Munnich A, Kim KS, Lyonnet S, Goridis C, Amiel J.
    Hum Mol Genet; 2005 Dec 01; 14(23):3697-708. PubMed ID: 16249188
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