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Journal Abstract Search

341 related items for PubMed ID: 30012555

  • 21.
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  • 23. A mouse p53 mutant lacking the proline-rich domain rescues Mdm4 deficiency and provides insight into the Mdm2-Mdm4-p53 regulatory network.
    Toledo F, Krummel KA, Lee CJ, Liu CW, Rodewald LW, Tang M, Wahl GM.
    Cancer Cell; 2006 Apr; 9(4):273-85. PubMed ID: 16616333
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  • 24. Cellular bases of the RNA metabolism dysfunction in motor neurons of a murine model of spinal muscular atrophy: Role of Cajal bodies and the nucleolus.
    Tapia O, Narcís JO, Riancho J, Tarabal O, Piedrafita L, Calderó J, Berciano MT, Lafarga M.
    Neurobiol Dis; 2017 Dec; 108():83-99. PubMed ID: 28823932
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  • 25. Spinal muscular atrophy: a deficiency in a ubiquitous protein; a motor neuron-specific disease.
    Monani UR.
    Neuron; 2005 Dec 22; 48(6):885-96. PubMed ID: 16364894
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  • 26. MDM2 but not MDM4 promotes retinoblastoma cell proliferation through p53-independent regulation of MYCN translation.
    Qi DL, Cobrinik D.
    Oncogene; 2017 Mar 30; 36(13):1760-1769. PubMed ID: 27748758
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  • 27. A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing.
    Pellizzoni L, Kataoka N, Charroux B, Dreyfuss G.
    Cell; 1998 Nov 25; 95(5):615-24. PubMed ID: 9845364
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  • 28. Oxidative Stress Triggers Body-Wide Skipping of Multiple Exons of the Spinal Muscular Atrophy Gene.
    Seo J, Singh NN, Ottesen EW, Sivanesan S, Shishimorova M, Singh RN.
    PLoS One; 2016 Nov 25; 11(4):e0154390. PubMed ID: 27111068
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  • 29. Dysregulation of Aldh1a2 underlies motor neuron degeneration in spinal muscular atrophy.
    Kataoka M, Sahashi K, Tsujikawa K, Takeda JI, Hirunagi T, Iida M, Katsuno M.
    Neurosci Res; 2023 Sep 25; 194():58-65. PubMed ID: 37146794
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  • 30. Combination of SMN trans-splicing and a neurotrophic factor increases the life span and body mass in a severe model of spinal muscular atrophy.
    Shababi M, Glascock J, Lorson CL.
    Hum Gene Ther; 2011 Feb 25; 22(2):135-44. PubMed ID: 20804424
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  • 31. Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy.
    Sun Y, Grimmler M, Schwarzer V, Schoenen F, Fischer U, Wirth B.
    Hum Mutat; 2005 Jan 25; 25(1):64-71. PubMed ID: 15580564
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  • 32. Mouse models of Mdm2 and Mdm4 and their clinical implications.
    Xiong S.
    Chin J Cancer; 2013 Jul 25; 32(7):371-5. PubMed ID: 23327795
    [Abstract] [Full Text] [Related]

  • 33. Is good housekeeping the key to motor neuron survival?
    Talbot K, Davies KE.
    Cell; 2008 May 16; 133(4):572-4. PubMed ID: 18485864
    [Abstract] [Full Text] [Related]

  • 34. Rescue of embryonic lethality in Mdm4-null mice by loss of Trp53 suggests a nonoverlapping pathway with MDM2 to regulate p53.
    Parant J, Chavez-Reyes A, Little NA, Yan W, Reinke V, Jochemsen AG, Lozano G.
    Nat Genet; 2001 Sep 16; 29(1):92-5. PubMed ID: 11528400
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  • 37. Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients.
    Gennarelli M, Lucarelli M, Capon F, Pizzuti A, Merlini L, Angelini C, Novelli G, Dallapiccola B.
    Biochem Biophys Res Commun; 1995 Aug 04; 213(1):342-8. PubMed ID: 7639755
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  • 39. SMN Is Physiologically Downregulated at Wild-Type Motor Nerve Terminals but Aggregates Together with Neurofilaments in SMA Mouse Models.
    Franco-Espin J, Gatius A, Armengol JÁ, Arumugam S, Moradi M, Sendtner M, Calderó J, Tabares L.
    Biomolecules; 2022 Oct 20; 12(10):. PubMed ID: 36291733
    [Abstract] [Full Text] [Related]

  • 40. Small nuclear RNAs and mRNAs: linking RNA processing and transport to spinal muscular atrophy.
    Sleeman J.
    Biochem Soc Trans; 2013 Aug 20; 41(4):871-5. PubMed ID: 23863147
    [Abstract] [Full Text] [Related]

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