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Journal Abstract Search

147 related items for PubMed ID: 8975718

  • 1. The mouse region syntenic for human spinal muscular atrophy lies within the Lgn1 critical interval and contains multiple copies of Naip exon 5.
    Scharf JM, Damron D, Frisella A, Bruno S, Beggs AH, Kunkel LM, Dietrich WF.
    Genomics; 1996 Dec 15; 38(3):405-17. PubMed ID: 8975718
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  • 2. Comparative sequence analysis of the mouse and human Lgn1/SMA interval.
    Endrizzi M, Huang S, Scharf JM, Kelter AR, Wirth B, Kunkel LM, Miller W, Dietrich WF.
    Genomics; 1999 Sep 01; 60(2):137-51. PubMed ID: 10486205
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  • 4. Evolutionary divergence of the mouse and human Lgn1/SMA repeat structures.
    Growney JD, Scharf JM, Kunkel LM, Dietrich WF.
    Genomics; 2000 Feb 15; 64(1):62-81. PubMed ID: 10708519
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  • 7. 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 15; 24(10):1052-4. PubMed ID: 14578966
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  • 9. Identification of two distinct transcripts for the neuronal apoptosis inhibitory protein gene.
    Yamamoto K, Sakai H, Hadano S, Gondo Y, Ikeda JE.
    Biochem Biophys Res Commun; 1999 Nov 02; 264(3):998-1006. PubMed ID: 10544044
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  • 10. A YAC contig of the region containing the spinal muscular atrophy gene (SMA): identification of an unstable region.
    Carpten JD, DiDonato CJ, Ingraham SE, Wagner-McPherson C, Nieuwenhuijsen BW, Wasmuth JJ, Burghes AH.
    Genomics; 1994 Nov 15; 24(2):351-6. PubMed ID: 7698758
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  • 11. Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy.
    Watihayati MS, Fatemeh H, Marini M, Atif AB, Zahiruddin WM, Sasongko TH, Tang TH, Zabidi-Hussin ZA, Nishio H, Zilfalil BA.
    Brain Dev; 2009 Jan 15; 31(1):42-5. PubMed ID: 18842367
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  • 12. Deletion analysis of Bulgarian SMA families.
    Jordanova A, Stoyanova V, Uzunova M, Litvinenko I, Kremensky I.
    Hum Mutat; 1998 Jan 15; 12(1):33-8. PubMed ID: 9633817
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  • 17. Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals.
    Hahnen E, Forkert R, Marke C, Rudnik-Schöneborn S, Schönling J, Zerres K, Wirth B.
    Hum Mol Genet; 1995 Oct 15; 4(10):1927-33. PubMed ID: 8595417
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  • 18. 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 15; 20(1):83-6. PubMed ID: 9731538
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