Mardon G - Search Results

1

NMNAT1 E257K variant, associated with Leber Congenital Amaurosis (LCA9), causes a mild retinal degeneration phenotype.

Eblimit A, Zaneveld SA, Liu W, Thomas K, Wang K, Li Y, Mardon G, Chen R. Eblimit A, et al. Among authors: mardon g. Exp Eye Res. 2018 Aug;173:32-43. doi: 10.1016/j.exer.2018.04.010. Epub 2018 Apr 17. Exp Eye Res. 2018. PMID: 29674119 Free PMC article.

2

Dachshund and eyes absent proteins form a complex and function synergistically to induce ectopic eye development in Drosophila.

Chen R, Amoui M, Zhang Z, Mardon G. Chen R, et al. Among authors: mardon g. Cell. 1997 Dec 26;91(7):893-903. doi: 10.1016/s0092-8674(00)80481-x. Cell. 1997. PMID: 9428513 Free article.

3

Signaling by the TGF-beta homolog decapentaplegic functions reiteratively within the network of genes controlling retinal cell fate determination in Drosophila.

Chen R, Halder G, Zhang Z, Mardon G. Chen R, et al. Among authors: mardon g. Development. 1999 Feb;126(5):935-43. doi: 10.1242/dev.126.5.935. Development. 1999. PMID: 9927595

4

Mechanism of hedgehog signaling during Drosophila eye development.

Pappu KS, Chen R, Middlebrooks BW, Woo C, Heberlein U, Mardon G. Pappu KS, et al. Among authors: mardon g. Development. 2003 Jul;130(13):3053-62. doi: 10.1242/dev.00534. Development. 2003. PMID: 12756186

5

Keeping an eye on the fly genome.

Chen R, Mardon G. Chen R, et al. Among authors: mardon g. Dev Biol. 2005 Jun 15;282(2):285-93. doi: 10.1016/j.ydbio.2005.04.015. Dev Biol. 2005. PMID: 15893305 Free article. Review.

6

Dual regulation and redundant function of two eye-specific enhancers of the Drosophila retinal determination gene dachshund.

Pappu KS, Ostrin EJ, Middlebrooks BW, Sili BT, Chen R, Atkins MR, Gibbs R, Mardon G. Pappu KS, et al. Among authors: mardon g. Development. 2005 Jun;132(12):2895-905. doi: 10.1242/dev.01869. Development. 2005. PMID: 15930118 Free article.

7

Genome-wide identification of direct targets of the Drosophila retinal determination protein Eyeless.

Ostrin EJ, Li Y, Hoffman K, Liu J, Wang K, Zhang L, Mardon G, Chen R. Ostrin EJ, et al. Among authors: mardon g. Genome Res. 2006 Apr;16(4):466-76. doi: 10.1101/gr.4673006. Epub 2006 Mar 13. Genome Res. 2006. PMID: 16533912 Free PMC article.

8

Mutation survey of known LCA genes and loci in the Saudi Arabian population.

Li Y, Wang H, Peng J, Gibbs RA, Lewis RA, Lupski JR, Mardon G, Chen R. Li Y, et al. Among authors: mardon g. Invest Ophthalmol Vis Sci. 2009 Mar;50(3):1336-43. doi: 10.1167/iovs.08-2589. Epub 2008 Oct 20. Invest Ophthalmol Vis Sci. 2009. PMID: 18936139 Free PMC article.

9

Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa.

Wang H, den Hollander AI, Moayedi Y, Abulimiti A, Li Y, Collin RW, Hoyng CB, Lopez I, Abboud EB, Al-Rajhi AA, Bray M, Lewis RA, Lupski JR, Mardon G, Koenekoop RK, Chen R. Wang H, et al. Among authors: mardon g. Am J Hum Genet. 2009 Mar;84(3):380-7. doi: 10.1016/j.ajhg.2009.02.005. Epub 2009 Mar 5. Am J Hum Genet. 2009. PMID: 19268277 Free PMC article.

10

Potential involvement of more than one locus in trait manifestation for individuals with Leber congenital amaurosis.

Wiszniewski W, Lewis RA, Stockton DW, Peng J, Mardon G, Chen R, Lupski JR. Wiszniewski W, et al. Among authors: mardon g. Hum Genet. 2011 Mar;129(3):319-27. doi: 10.1007/s00439-010-0928-y. Epub 2010 Dec 14. Hum Genet. 2011. PMID: 21153841 Free PMC article.

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