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Journal Abstract Search

175 related items for PubMed ID: 12649809

  • 1. Conditional JAG1 mutation shows the developing heart is more sensitive than developing liver to JAG1 dosage.
    Lu F, Morrissette JJ, Spinner NB.
    Am J Hum Genet; 2003 Apr; 72(4):1065-70. PubMed ID: 12649809
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  • 2. Clinical and molecular genetics of Alagille syndrome.
    Krantz ID, Piccoli DA, Spinner NB.
    Curr Opin Pediatr; 1999 Dec; 11(6):558-64. PubMed ID: 10590916
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  • 5. Defective intracellular transport and processing of JAG1 missense mutations in Alagille syndrome.
    Morrissette JD, Colliton RP, Spinner NB.
    Hum Mol Genet; 2001 Feb 15; 10(4):405-13. PubMed ID: 11157803
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  • 7. [From gene to disease: arteriohepatic dysplasia or Alagille syndrome].
    Brooks AS, Dooijes D.
    Ned Tijdschr Geneeskd; 2003 Jun 21; 147(25):1213-5. PubMed ID: 12848056
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  • 8. Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patients.
    Colliton RP, Bason L, Lu FM, Piccoli DA, Krantz ID, Spinner NB.
    Hum Mutat; 2001 Feb 21; 17(2):151-2. PubMed ID: 11180599
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  • 9. Human Jagged 1 mutants cause liver defect in Alagille syndrome by overexpression of hepatocyte growth factor.
    Yuan ZR, Kobayashi N, Kohsaka T.
    J Mol Biol; 2006 Feb 24; 356(3):559-68. PubMed ID: 16403414
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  • 11. Jagged1 (JAG1) mutations in patients with tetralogy of Fallot or pulmonic stenosis.
    Bauer RC, Laney AO, Smith R, Gerfen J, Morrissette JJ, Woyciechowski S, Garbarini J, Loomes KM, Krantz ID, Urban Z, Gelb BD, Goldmuntz E, Spinner NB.
    Hum Mutat; 2010 May 24; 31(5):594-601. PubMed ID: 20437614
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  • 12. Bile duct proliferation in liver-specific Jag1 conditional knockout mice: effects of gene dosage.
    Loomes KM, Russo P, Ryan M, Nelson A, Underkoffler L, Glover C, Fu H, Gridley T, Kaestner KH, Oakey RJ.
    Hepatology; 2007 Feb 24; 45(2):323-30. PubMed ID: 17366661
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  • 17. DHPLC mutation analysis of Jagged1 (JAG1) reveals six novel mutations in Australian alagille syndrome patients.
    Heritage ML, MacMillan JC, Anderson GJ.
    Hum Mutat; 2002 Dec 24; 20(6):481. PubMed ID: 12442286
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  • 18. Familial Tetralogy of Fallot caused by mutation in the jagged1 gene.
    Eldadah ZA, Hamosh A, Biery NJ, Montgomery RA, Duke M, Elkins R, Dietz HC.
    Hum Mol Genet; 2001 Jan 15; 10(2):163-9. PubMed ID: 11152664
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