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PUBMED FOR HANDHELDS

Journal Abstract Search


132 related items for PubMed ID: 15591271

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  • 7. PITX2 deficiency and associated human disease: insights from the zebrafish model.
    Hendee KE, Sorokina EA, Muheisen SS, Reis LM, Tyler RC, Markovic V, Cuturilo G, Link BA, Semina EV.
    Hum Mol Genet; 2018 May 15; 27(10):1675-1695. PubMed ID: 29506241
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  • 13. PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome.
    Zhao CM, Peng LY, Li L, Liu XY, Wang J, Zhang XL, Yuan F, Li RG, Qiu XB, Yang YQ.
    PLoS One; 2015 May 15; 10(4):e0124409. PubMed ID: 25893250
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  • 15. PITX2 gain-of-function in Rieger syndrome eye model.
    Holmberg J, Liu CY, Hjalt TA.
    Am J Pathol; 2004 Nov 15; 165(5):1633-41. PubMed ID: 15509533
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