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Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module.
Koss M, Bolze A, Brendolan A, Saggese M, Capellini TD, Bojilova E, Boisson B, Prall OW, Elliott DA, Solloway M, Lenti E, Hidaka C, Chang CP, Mahlaoui N, Harvey RP, Casanova JL, Selleri L. Koss M, et al. Among authors: elliott da. Dev Cell. 2012 May 15;22(5):913-26. doi: 10.1016/j.devcel.2012.02.009. Epub 2012 May 3. Dev Cell. 2012. PMID: 22560297 Free PMC article.
Homeobox genes and heart development.
Biben C, Palmer S, Elliott DA, Harvey RP. Biben C, et al. Among authors: elliott da. Cold Spring Harb Symp Quant Biol. 1997;62:395-403. Cold Spring Harb Symp Quant Biol. 1997. PMID: 9598374 No abstract available.
Time to mend a broken heart.
Elliott DA, Harvey RP. Elliott DA, et al. Stem Cell Res. 2007 Oct;1(1):4-6. doi: 10.1016/j.scr.2007.09.001. Epub 2007 Sep 17. Stem Cell Res. 2007. PMID: 19383381 Free article. No abstract available.
NKX2-5(eGFP/w) hESCs for isolation of human cardiac progenitors and cardiomyocytes.
Elliott DA, Braam SR, Koutsis K, Ng ES, Jenny R, Lagerqvist EL, Biben C, Hatzistavrou T, Hirst CE, Yu QC, Skelton RJ, Ward-van Oostwaard D, Lim SM, Khammy O, Li X, Hawes SM, Davis RP, Goulburn AL, Passier R, Prall OW, Haynes JM, Pouton CW, Kaye DM, Mummery CL, Elefanty AG, Stanley EG. Elliott DA, et al. Nat Methods. 2011 Oct 23;8(12):1037-40. doi: 10.1038/nmeth.1740. Nat Methods. 2011. PMID: 22020065
171 results