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Journal Abstract Search

776 related items for PubMed ID: 9207792

  • 21. Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron gene.
    Gambardella A, Mazzei R, Toscano A, Annesi G, Pasqua A, Annesi F, Quattrone F, Oliveri RL, Valentino P, Bono F, Aguglia U, Zappia M, Vita G, Quattrone A.
    Ann Neurol; 1998 Nov; 44(5):836-9. PubMed ID: 9818944
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  • 22. Clinical application of the molecular diagnosis of spinal muscular atrophy: deletions of neuronal apoptosis inhibitor protein and survival motor neuron genes.
    Somerville MJ, Hunter AG, Aubry HL, Korneluk RG, MacKenzie AE, Surh LC.
    Am J Med Genet; 1997 Mar 17; 69(2):159-65. PubMed ID: 9056553
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  • 23. Analysis of the survival motor neuron and neuronal apoptosis inhibitory protein genes in Malay patients with Spinal Muscular Atrophy.
    Zilfalil BA, Zabidi-Hussin AM, Watihayati MS, Rozainah MY, Naing L, Sutomo R, Nishio H, Narazah MY, Matsuo M.
    Med J Malaysia; 2004 Oct 17; 59(4):512-4. PubMed ID: 15779584
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  • 26. Activation of RNA metabolism-related genes in mouse but not human tissues deficient in SMN.
    Olaso R, Joshi V, Fernandez J, Roblot N, Courageot S, Bonnefont JP, Melki J.
    Physiol Genomics; 2006 Jan 12; 24(2):97-104. PubMed ID: 16118268
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  • 27. Application of DNA-based tests for diagnosis of spinal muscular atrophy in Saudi Arabia.
    al-Rajeh S, Majumdar R, Awada A, al-Jumah M.
    East Mediterr Health J; 1999 Nov 12; 5(6):1225-9. PubMed ID: 11924116
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  • 29. Cell-specific survival motor neuron gene expression during human development of the central nervous system: implications for the pathogenesis of spinal muscular atrophy.
    Tizzano EF, Cabot C, Baiget M.
    Am J Pathol; 1998 Aug 12; 153(2):355-61. PubMed ID: 9708795
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  • 30. Structure and organization of the human survival motor neurone (SMN) gene.
    Bürglen L, Lefebvre S, Clermont O, Burlet P, Viollet L, Cruaud C, Munnich A, Melki J.
    Genomics; 1996 Mar 15; 32(3):479-82. PubMed ID: 8838816
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  • 33. The survival motor neuron protein in spinal muscular atrophy.
    Coovert DD, Le TT, McAndrew PE, Strasswimmer J, Crawford TO, Mendell JR, Coulson SE, Androphy EJ, Prior TW, Burghes AH.
    Hum Mol Genet; 1997 Aug 15; 6(8):1205-14. PubMed ID: 9259265
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  • 34. Prenatal prediction of spinal muscular atrophy. Experience with linkage studies and consequences of present SMN deletion analysis.
    Cobben JM, Scheffer H, De Visser M, Van der Steege G, Verhey JB, Osinga J, Burton M, Mensink RG, Grootscholten PM, Ten Kate LP, Buys CH.
    Eur J Hum Genet; 1996 Aug 15; 4(4):231-6. PubMed ID: 8875190
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  • 38. Smn deficiency causes neuritogenesis and neurogenesis defects in the retinal neurons of a mouse model of spinal muscular atrophy.
    Liu H, Beauvais A, Baker AN, Tsilfidis C, Kothary R.
    Dev Neurobiol; 2011 Feb 15; 71(2):153-69. PubMed ID: 20862739
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  • 39. Specific interaction of Smn, the spinal muscular atrophy determining gene product, with hnRNP-R and gry-rbp/hnRNP-Q: a role for Smn in RNA processing in motor axons?
    Rossoll W, Kröning AK, Ohndorf UM, Steegborn C, Jablonka S, Sendtner M.
    Hum Mol Genet; 2002 Jan 01; 11(1):93-105. PubMed ID: 11773003
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  • 40. The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophy.
    Burlet P, Huber C, Bertrandy S, Ludosky MA, Zwaenepoel I, Clermont O, Roume J, Delezoide AL, Cartaud J, Munnich A, Lefebvre S.
    Hum Mol Genet; 1998 Nov 01; 7(12):1927-33. PubMed ID: 9811937
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