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Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene.
Sakai T, Ohtani N, McGee TL, Robbins PD, Dryja TP. Sakai T, et al. Among authors: mcgee tl. Nature. 1991 Sep 5;353(6339):83-6. doi: 10.1038/353083a0. Nature. 1991. PMID: 1881452
Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycle.
Hartong DT, Dange M, McGee TL, Berson EL, Dryja TP, Colman RF. Hartong DT, et al. Among authors: mcgee tl. Nat Genet. 2008 Oct;40(10):1230-4. doi: 10.1038/ng.223. Epub 2008 Sep 21. Nat Genet. 2008. PMID: 18806796 Free PMC article.
Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram.
Thiagalingam S, McGee TL, Weleber RG, Sandberg MA, Trzupek KM, Berson EL, Dryja TP. Thiagalingam S, et al. Among authors: mcgee tl. Ophthalmic Genet. 2007 Sep;28(3):135-42. doi: 10.1080/13816810701503681. Ophthalmic Genet. 2007. PMID: 17896311
A homozygous missense mutation in the IRBP gene (RBP3) associated with autosomal recessive retinitis pigmentosa.
den Hollander AI, McGee TL, Ziviello C, Banfi S, Dryja TP, Gonzalez-Fernandez F, Ghosh D, Berson EL. den Hollander AI, et al. Among authors: mcgee tl. Invest Ophthalmol Vis Sci. 2009 Apr;50(4):1864-72. doi: 10.1167/iovs.08-2497. Epub 2008 Dec 13. Invest Ophthalmol Vis Sci. 2009. PMID: 19074801 Free PMC article.
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa.
Sweeney MO, McGee TL, Berson EL, Dryja TP. Sweeney MO, et al. Among authors: mcgee tl. Mol Vis. 2007 Apr 5;13:588-93. Mol Vis. 2007. PMID: 17438524 Free PMC article.
A screen for mutations in the transducin gene GNB1 in patients with autosomal dominant retinitis pigmentosa.
Mylvaganam GH, McGee TL, Berson EL, Dryja TP. Mylvaganam GH, et al. Among authors: mcgee tl. Mol Vis. 2006 Dec 4;12:1496-8. Mol Vis. 2006. PMID: 17167406
Variation in retinitis pigmentosa-11 (PRPF31 or RP11) gene expression between symptomatic and asymptomatic patients with dominant RP11 mutations.
Rivolta C, McGee TL, Rio Frio T, Jensen RV, Berson EL, Dryja TP. Rivolta C, et al. Among authors: mcgee tl. Hum Mutat. 2006 Jul;27(7):644-53. doi: 10.1002/humu.20325. Hum Mutat. 2006. PMID: 16708387
Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and clinical features associated with the most common mutation, Asp226Asn.
Wada Y, Sandberg MA, McGee TL, Stillberger MA, Berson EL, Dryja TP. Wada Y, et al. Among authors: mcgee tl. Invest Ophthalmol Vis Sci. 2005 May;46(5):1735-41. doi: 10.1167/iovs.04-1197. Invest Ophthalmol Vis Sci. 2005. PMID: 15851576
Mutated alleles of the rod and cone Na-Ca+K-exchanger genes in patients with retinal diseases.
Sharon D, Yamamoto H, McGee TL, Rabe V, Szerencsei RT, Winkfein RJ, Prinsen CF, Barnes CS, Andreasson S, Fishman GA, Schnetkamp PP, Berson EL, Dryja TP. Sharon D, et al. Among authors: mcgee tl. Invest Ophthalmol Vis Sci. 2002 Jun;43(6):1971-9. Invest Ophthalmol Vis Sci. 2002. PMID: 12037007
Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa.
McGee TL, Seyedahmadi BJ, Sweeney MO, Dryja TP, Berson EL. McGee TL, et al. J Med Genet. 2010 Jul;47(7):499-506. doi: 10.1136/jmg.2009.075143. Epub 2010 May 27. J Med Genet. 2010. PMID: 20507924 Free PMC article.
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