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Spectrum of heart disease associated with murine and human GATA4 mutation.
Rajagopal SK, Ma Q, Obler D, Shen J, Manichaikul A, Tomita-Mitchell A, Boardman K, Briggs C, Garg V, Srivastava D, Goldmuntz E, Broman KW, Benson DW, Smoot LB, Pu WT. Rajagopal SK, et al. Among authors: garg v. J Mol Cell Cardiol. 2007 Dec;43(6):677-85. doi: 10.1016/j.yjmcc.2007.06.004. Epub 2007 Jun 21. J Mol Cell Cardiol. 2007. PMID: 17643447 Free PMC article.
Mutations in NOTCH1 cause aortic valve disease.
Garg V, Muth AN, Ransom JF, Schluterman MK, Barnes R, King IN, Grossfeld PD, Srivastava D. Garg V, et al. Nature. 2005 Sep 8;437(7056):270-4. doi: 10.1038/nature03940. Epub 2005 Jul 17. Nature. 2005. PMID: 16025100
GATA4 sequence variants in patients with congenital heart disease.
Tomita-Mitchell A, Maslen CL, Morris CD, Garg V, Goldmuntz E. Tomita-Mitchell A, et al. Among authors: garg v. J Med Genet. 2007 Dec;44(12):779-83. doi: 10.1136/jmg.2007.052183. J Med Genet. 2007. PMID: 18055909 Free PMC article.
A rare human sequence variant reveals myocardin autoinhibition.
Ransom JF, King IN, Garg V, Srivastava D. Ransom JF, et al. Among authors: garg v. J Biol Chem. 2008 Dec 19;283(51):35845-52. doi: 10.1074/jbc.M805909200. Epub 2008 Oct 13. J Biol Chem. 2008. PMID: 18852265 Free PMC article.
1,076 results