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150 related items for PubMed ID: 9389483

  • 1. Synergistic anti-apoptotic activity between Bcl-2 and SMN implicated in spinal muscular atrophy.
    Iwahashi H, Eguchi Y, Yasuhara N, Hanafusa T, Matsuzawa Y, Tsujimoto Y.
    Nature; 1997 Nov 27; 390(6658):413-7. PubMed ID: 9389483
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  • 2. Regions essential for the interaction between Bcl-2 and SMN, the spinal muscular atrophy disease gene product.
    Sato K, Eguchi Y, Kodama TS, Tsujimoto Y.
    Cell Death Differ; 2000 Apr 27; 7(4):374-83. PubMed ID: 10773822
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  • 3. SMN oligomerization defect correlates with spinal muscular atrophy severity.
    Lorson CL, Strasswimmer J, Yao JM, Baleja JD, Hahnen E, Wirth B, Le T, Burghes AH, Androphy EJ.
    Nat Genet; 1998 May 27; 19(1):63-6. PubMed ID: 9590291
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  • 5. Molecular analysis of the spinal muscular atrophy and neuronal apoptosis inhibitory protein genes in Saudi patients with spinal muscular atrophy.
    Al-Jumah M, Majumdar R, Al-Rajeh S, Awada A, Chaves-Carbello E, Salih M, Al-Shahwan S, Al-Subiey K, Al-Uthaim S.
    Saudi Med J; 2003 Oct 27; 24(10):1052-4. PubMed ID: 14578966
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  • 6. High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patients.
    Bouhouche A, Benomar A, Birouk N, Bouslam N, Ouazzani R, Yahyaoui M, Chkili T.
    J Neurol; 2003 Oct 27; 250(10):1209-13. PubMed ID: 14586604
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  • 7. An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA).
    Wirth B.
    Hum Mutat; 2000 Oct 27; 15(3):228-37. PubMed ID: 10679938
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  • 13. Genetic study of SMA patients without homozygous SMN1 deletions: identification of compound heterozygotes and characterisation of novel intragenic SMN1 mutations.
    Martín Y, Valero A, del Castillo E, Pascual SI, Hernández-Chico C.
    Hum Genet; 2002 Mar 27; 110(3):257-63. PubMed ID: 11935338
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  • 14. Molecular genetics of spinal muscular atrophy: contribution of the NAIP gene to clinical severity.
    Akutsu T, Nishio H, Sumino K, Takeshima Y, Tsuneishi S, Wada H, Takada S, Matsuo M, Nakamura H.
    Kobe J Med Sci; 2002 Apr 27; 48(1-2):25-31. PubMed ID: 11912351
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  • 16. NAIP-deletion analysis in Malaysian patients with spinal muscular atrophy.
    Watihayati MS, Zabidi AM, Tang TH, Nishio H, Zilfalil BA.
    Kobe J Med Sci; 2007 Apr 27; 53(4):171-5. PubMed ID: 17932457
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  • 18. SMA type 2 unrelated to chromosome 5q13.
    Nevo Y, Kramer U, Legum C, Shomrat R, Fatal A, Soffer D, Harel S, Shapira Y.
    Am J Med Genet; 1998 Jan 13; 75(2):193-5. PubMed ID: 9450884
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  • 19. Deletion analysis of Bulgarian SMA families.
    Jordanova A, Stoyanova V, Uzunova M, Litvinenko I, Kremensky I.
    Hum Mutat; 1998 Jan 13; 12(1):33-8. PubMed ID: 9633817
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  • 20. Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomics.
    Scharf JM, Endrizzi MG, Wetter A, Huang S, Thompson TG, Zerres K, Dietrich WF, Wirth B, Kunkel LM.
    Nat Genet; 1998 Sep 13; 20(1):83-6. PubMed ID: 9731538
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