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Journal Abstract Search

229 related items for PubMed ID: 15772854

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  • 3. 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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  • 4. Jagged-1 mutation analysis in Italian Alagille syndrome patients.
    Pilia G, Uda M, Macis D, Frau F, Crisponi L, Balli F, Barbera C, Colombo C, Frediani T, Gatti R, Iorio R, Marazzi MG, Marcellini M, Musumeci S, Nebbia G, Vajro P, Ruffa G, Zancan L, Cao A, DeVirgilis S.
    Hum Mutat; 1999 Feb 24; 14(5):394-400. PubMed ID: 10533065
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  • 5. Spectrum and frequency of jagged1 (JAG1) mutations in Alagille syndrome patients and their families.
    Krantz ID, Colliton RP, Genin A, Rand EB, Li L, Piccoli DA, Spinner NB.
    Am J Hum Genet; 1998 Jun 24; 62(6):1361-9. PubMed ID: 9585603
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  • 7. Identification of 36 novel Jagged1 (JAG1) mutations in patients with Alagille syndrome.
    Röpke A, Kujat A, Gräber M, Giannakudis J, Hansmann I.
    Hum Mutat; 2003 Jan 24; 21(1):100. PubMed ID: 12497640
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  • 8. 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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  • 16. Functional analysis of the Notch ligand Jagged1 missense mutant proteins underlying Alagille syndrome.
    Tada M, Itoh S, Ishii-Watabe A, Suzuki T, Kawasaki N.
    FEBS J; 2012 Jun 15; 279(12):2096-107. PubMed ID: 22487239
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  • 17. Jagged1 gene mutation for abdominal coarctation of the aorta in Alagille syndrome.
    Raas-Rothschild A, Shteyer E, Lerer I, Nir A, Granot E, Rein AJ.
    Am J Med Genet; 2002 Sep 15; 112(1):75-8. PubMed ID: 12239725
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  • 19. Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1.
    Li L, Krantz ID, Deng Y, Genin A, Banta AB, Collins CC, Qi M, Trask BJ, Kuo WL, Cochran J, Costa T, Pierpont ME, Rand EB, Piccoli DA, Hood L, Spinner NB.
    Nat Genet; 1997 Jul 15; 16(3):243-51. PubMed ID: 9207788
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