Hagstrom SA - Search Results

1

Tulp1 is involved in specific photoreceptor protein transport pathways.

Hagstrom SA, Watson RF, Pauer GJ, Grossman GH. Hagstrom SA, et al. Adv Exp Med Biol. 2012;723:783-9. doi: 10.1007/978-1-4614-0631-0_100. Adv Exp Med Biol. 2012. PMID: 22183407 No abstract available.

2

Chemical Characterization of Polysaccharide from the Slime Layer of the Cyanobacterium Microcystis flos-aquae C3-40.

Plude JL, Parker DL, Schommer OJ, Timmerman RJ, Hagstrom SA, Joers JM, Hnasko R. Plude JL, et al. Among authors: hagstrom sa. Appl Environ Microbiol. 1991 Jun;57(6):1696-1700. doi: 10.1128/aem.57.6.1696-1700.1991. Appl Environ Microbiol. 1991. PMID: 16348506 Free PMC article.

3

Thirty-year follow-up of a patient with leber congenital amaurosis and novel RPE65 mutations.

Al-Khayer K, Hagstrom S, Pauer G, Zegarra H, Sears J, Traboulsi EI. Al-Khayer K, et al. Am J Ophthalmol. 2004 Feb;137(2):375-7. doi: 10.1016/S0002-9394(03)00913-9. Am J Ophthalmol. 2004. PMID: 14962443

4

Retinal degeneration caused by mutations in TULP1.

Xi Q, Pauer GJ, West KA, Crabb JW, Hagstrom SA. Xi Q, et al. Among authors: hagstrom sa. Adv Exp Med Biol. 2003;533:303-8. doi: 10.1007/978-1-4615-0067-4_37. Adv Exp Med Biol. 2003. PMID: 15180277 No abstract available.

5

An Arg311Gln NR2E3 mutation in a family with classic Goldmann-Favre syndrome.

Chavala SH, Sari A, Lewis H, Pauer GJ, Simpson E, Hagstrom SA, Traboulsi EI. Chavala SH, et al. Among authors: hagstrom sa. Br J Ophthalmol. 2005 Aug;89(8):1065-6. doi: 10.1136/bjo.2005.068130. Br J Ophthalmol. 2005. PMID: 16024868 Free PMC article. No abstract available.

6

SOX2 mutation causes anophthalmia, hearing loss, and brain anomalies.

Hagstrom SA, Pauer GJ, Reid J, Simpson E, Crowe S, Maumenee IH, Traboulsi EI. Hagstrom SA, et al. Am J Med Genet A. 2005 Oct 1;138A(2):95-8. doi: 10.1002/ajmg.a.30803. Am J Med Genet A. 2005. PMID: 16145681

7

Tubby-like protein 1 (TULP1) interacts with F-actin in photoreceptor cells.

Xi Q, Pauer GJ, Marmorstein AD, Crabb JW, Hagstrom SA. Xi Q, et al. Among authors: hagstrom sa. Invest Ophthalmol Vis Sci. 2005 Dec;46(12):4754-61. doi: 10.1167/iovs.05-0693. Invest Ophthalmol Vis Sci. 2005. PMID: 16303976 Free PMC article.

8

Mutation screen of the membrane-type frizzled-related protein (MFRP) gene in patients with inherited retinal degenerations.

Pauer GJ, Xi Q, Zhang K, Traboulsi EI, Hagstrom SA. Pauer GJ, et al. Among authors: hagstrom sa. Ophthalmic Genet. 2005 Dec;26(4):157-61. doi: 10.1080/13816810500374425. Ophthalmic Genet. 2005. PMID: 16352475

9

Mutation screen of the TUB gene in patients with retinitis pigmentosa and Leber congenital amaurosis.

Xi Q, Pauer GJ, Traboulsi EI, Hagstrom SA. Xi Q, et al. Among authors: hagstrom sa. Exp Eye Res. 2006 Sep;83(3):569-73. doi: 10.1016/j.exer.2006.02.003. Epub 2006 Apr 27. Exp Eye Res. 2006. PMID: 16643894 Free PMC article.

10

Mutation screen of the cone-specific gene, CLUL1, in 376 patients with age-related macular degeneration.

Sturgill GM, Pauer GJ, Bala E, Simpson E, Yaniglos SS, Crabb JW, Hollyfield JG, Lewis H, Peachey NS, Hagstrom SA. Sturgill GM, et al. Among authors: hagstrom sa. Ophthalmic Genet. 2006 Dec;27(4):151-5. doi: 10.1080/13816810600976871. Ophthalmic Genet. 2006. PMID: 17148042 Free PMC article.

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