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Items: 34

1.

A Novel Approach to Identify Photoreceptor Compartment-Specific Tulp1 Binding Partners.

Ebke LA, Pauer GJ, Willard B, Hagstrom SA.

Adv Exp Med Biol. 2016;854:605-11. doi: 10.1007/978-3-319-17121-0_80.

PMID:
26427465
2.

Retinal histopathology in eyes from patients with autosomal dominant retinitis pigmentosa caused by rhodopsin mutations.

Bonilha VL, Rayborn ME, Bell BA, Marino MJ, Beight CD, Pauer GJ, Traboulsi EI, Hollyfield JG, Hagstrom SA.

Graefes Arch Clin Exp Ophthalmol. 2015 Dec;253(12):2161-9. doi: 10.1007/s00417-015-3099-7. Epub 2015 Jul 23.

PMID:
26202387
3.

Histopathological comparison of eyes from patients with autosomal recessive retinitis pigmentosa caused by novel EYS mutations.

Bonilha VL, Rayborn ME, Bell BA, Marino MJ, Pauer GJ, Beight CD, Chiang J, Traboulsi EI, Hollyfield JG, Hagstrom SA.

Graefes Arch Clin Exp Ophthalmol. 2015 Feb;253(2):295-305. doi: 10.1007/s00417-014-2868-z. Epub 2014 Dec 11.

PMID:
25491159
4.

Endothelial PAS domain-containing protein 1 (EPAS1) gene polymorphisms and response to anti-VEGF therapy in the comparison of AMD treatments trials (CATT).

Hagstrom SA, Ying GS, Pauer GJ, Huang J, Maguire MG, Martin DF; CATT Research Group.

Ophthalmology. 2014 Aug;121(8):1663-4.e1. doi: 10.1016/j.ophtha.2014.02.025. Epub 2014 May 9. No abstract available.

5.

Interaction of tubby-like protein-1 (Tulp1) and microtubule-associated protein (MAP) 1A and MAP1B in the mouse retina.

Grossman GH, Beight CD, Ebke LA, Pauer GJ, Hagstrom SA.

Adv Exp Med Biol. 2014;801:511-8. doi: 10.1007/978-1-4614-3209-8_65.

PMID:
24664738
6.

VEGFA and VEGFR2 gene polymorphisms and response to anti-vascular endothelial growth factor therapy: comparison of age-related macular degeneration treatments trials (CATT).

Hagstrom SA, Ying GS, Pauer GJ, Sturgill-Short GM, Huang J, Maguire MG, Martin DF; Comparison of Age-Related Macular Degeneration Treatments Trials (CATT) Research Group.

JAMA Ophthalmol. 2014 May;132(5):521-7.

7.

Predictors of visual acuity and genotype-phenotype correlates in a cohort of patients with Stargardt disease.

Miraldi Utz V, Coussa RG, Marino MJ, Chappelow AV, Pauer GJ, Hagstrom SA, Traboulsi EI.

Br J Ophthalmol. 2014 Apr;98(4):513-8. doi: 10.1136/bjophthalmol-2013-304270. Epub 2014 Jan 23.

PMID:
24457364
8.

Identification of three ABCA4 sequence variations exclusive to African American patients in a cohort of patients with Stargardt disease.

Utz VM, Chappelow AV, Marino MJ, Beight CD, Sturgill-Short GM, Pauer GJ, Crowe S, Hagstrom SA, Traboulsi EI.

Am J Ophthalmol. 2013 Dec;156(6):1220-1227.e2. doi: 10.1016/j.ajo.2013.07.008. Epub 2013 Sep 4.

PMID:
24011517
9.

Retinal deimination and PAD2 levels in retinas from donors with age-related macular degeneration (AMD).

Bonilha VL, Shadrach KG, Rayborn ME, Li Y, Pauer GJ, Hagstrom SA, Bhattacharya SK, Hollyfield JG.

Exp Eye Res. 2013 Jun;111:71-8. doi: 10.1016/j.exer.2013.03.017. Epub 2013 Apr 3.

10.

Seven new loci associated with age-related macular degeneration.

Fritsche LG, Chen W, Schu M, Yaspan BL, Yu Y, Thorleifsson G, Zack DJ, Arakawa S, Cipriani V, Ripke S, Igo RP Jr, Buitendijk GH, Sim X, Weeks DE, Guymer RH, Merriam JE, Francis PJ, Hannum G, Agarwal A, Armbrecht AM, Audo I, Aung T, Barile GR, Benchaboune M, Bird AC, Bishop PN, Branham KE, Brooks M, Brucker AJ, Cade WH, Cain MS, Campochiaro PA, Chan CC, Cheng CY, Chew EY, Chin KA, Chowers I, Clayton DG, Cojocaru R, Conley YP, Cornes BK, Daly MJ, Dhillon B, Edwards AO, Evangelou E, Fagerness J, Ferreyra HA, Friedman JS, Geirsdottir A, George RJ, Gieger C, Gupta N, Hagstrom SA, Harding SP, Haritoglou C, Heckenlively JR, Holz FG, Hughes G, Ioannidis JP, Ishibashi T, Joseph P, Jun G, Kamatani Y, Katsanis N, N Keilhauer C, Khan JC, Kim IK, Kiyohara Y, Klein BE, Klein R, Kovach JL, Kozak I, Lee CJ, Lee KE, Lichtner P, Lotery AJ, Meitinger T, Mitchell P, Mohand-Saïd S, Moore AT, Morgan DJ, Morrison MA, Myers CE, Naj AC, Nakamura Y, Okada Y, Orlin A, Ortube MC, Othman MI, Pappas C, Park KH, Pauer GJ, Peachey NS, Poch O, Priya RR, Reynolds R, Richardson AJ, Ripp R, Rudolph G, Ryu E, Sahel JA, Schaumberg DA, Scholl HP, Schwartz SG, Scott WK, Shahid H, Sigurdsson H, Silvestri G, Sivakumaran TA, Smith RT, Sobrin L, Souied EH, Stambolian DE, Stefansson H, Sturgill-Short GM, Takahashi A, Tosakulwong N, Truitt BJ, Tsironi EE, Uitterlinden AG, van Duijn CM, Vijaya L, Vingerling JR, Vithana EN, Webster AR, Wichmann HE, Winkler TW, Wong TY, Wright AF, Zelenika D, Zhang M, Zhao L, Zhang K, Klein ML, Hageman GS, Lathrop GM, Stefansson K, Allikmets R, Baird PN, Gorin MB, Wang JJ, Klaver CC, Seddon JM, Pericak-Vance MA, Iyengar SK, Yates JR, Swaroop A, Weber BH, Kubo M, Deangelis MM, Léveillard T, Thorsteinsdottir U, Haines JL, Farrer LA, Heid IM, Abecasis GR; AMD Gene Consortium.

Nat Genet. 2013 Apr;45(4):433-9, 439e1-2. doi: 10.1038/ng.2578. Epub 2013 Mar 3.

11.

Pharmacogenetics for genes associated with age-related macular degeneration in the Comparison of AMD Treatments Trials (CATT).

Hagstrom SA, Ying GS, Pauer GJT, Sturgill-Short GM, Huang J, Callanan DG, Kim IK, Klein ML, Maguire MG, Martin DF; Comparison of AMD Treatments Trials Research Group.

Ophthalmology. 2013 Mar;120(3):593-599. doi: 10.1016/j.ophtha.2012.11.037. Epub 2013 Jan 18.

12.

Tulp1 is involved in specific photoreceptor protein transport pathways.

Hagstrom SA, Watson RF, Pauer GJ, Grossman GH.

Adv Exp Med Biol. 2012;723:783-9. doi: 10.1007/978-1-4614-0631-0_100. No abstract available.

PMID:
22183407
13.

Isolating photoreceptor compartment-specific protein complexes for subsequent proteomic analysis.

Grossman GH, Pauer GJ, Hoppe G, Hagstrom SA.

Adv Exp Med Biol. 2012;723:701-7. doi: 10.1007/978-1-4614-0631-0_89. No abstract available.

PMID:
22183396
14.

Immunocytochemical evidence of Tulp1-dependent outer segment protein transport pathways in photoreceptor cells.

Grossman GH, Watson RF, Pauer GJ, Bollinger K, Hagstrom SA.

Exp Eye Res. 2011 Nov;93(5):658-68. doi: 10.1016/j.exer.2011.08.005. Epub 2011 Aug 16.

15.

Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration.

Kopplin LJ, Igo RP Jr, Wang Y, Sivakumaran TA, Hagstrom SA, Peachey NS, Francis PJ, Klein ML, SanGiovanni JP, Chew EY, Pauer GJ, Sturgill GM, Joshi T, Tian L, Xi Q, Henning AK, Lee KE, Klein R, Klein BE, Iyengar SK.

Genes Immun. 2010 Dec;11(8):609-21. doi: 10.1038/gene.2010.39. Epub 2010 Sep 23.

16.

Proteomic and genomic biomarkers for age-related macular degeneration.

Gu J, Pauer GJ, Yue X, Narendra U, Sturgill GM, Bena J, Gu X, Peachey NS, Salomon RG, Hagstrom SA, Crabb JW; Clinical Genomic and Proteomic AMD Study Group.

Adv Exp Med Biol. 2010;664:411-7. doi: 10.1007/978-1-4419-1399-9_47.

PMID:
20238042
17.

Tubby-like protein 1 (Tulp1) is required for normal photoreceptor synaptic development.

Grossman GH, Pauer GJ, Narendra U, Hagstrom SA.

Adv Exp Med Biol. 2010;664:89-96. doi: 10.1007/978-1-4419-1399-9_11.

PMID:
20238006
18.

Protective effect of paraoxonase 1 gene variant Gln192Arg in age-related macular degeneration.

Pauer GJ, Sturgill GM, Peachey NS, Hagstrom SA; Clinical Genomic And Proteomic AMD Study Group.

Am J Ophthalmol. 2010 Mar;149(3):513-22. doi: 10.1016/j.ajo.2009.09.024. Epub 2009 Dec 30.

19.
20.

Early synaptic defects in tulp1-/- mice.

Grossman GH, Pauer GJ, Narendra U, Peachey NS, Hagstrom SA.

Invest Ophthalmol Vis Sci. 2009 Jul;50(7):3074-83. doi: 10.1167/iovs.08-3190. Epub 2009 Feb 14.

21.

Assessing susceptibility to age-related macular degeneration with proteomic and genomic biomarkers.

Gu J, Pauer GJ, Yue X, Narendra U, Sturgill GM, Bena J, Gu X, Peachey NS, Salomon RG, Hagstrom SA, Crabb JW; Clinical Genomic and Proteomic AMD Study Group.

Mol Cell Proteomics. 2009 Jun;8(6):1338-49. doi: 10.1074/mcp.M800453-MCP200. Epub 2009 Feb 6.

22.

Sequence alterations in RX in patients with microphthalmia, anophthalmia, and coloboma.

London NJ, Kessler P, Williams B, Pauer GJ, Hagstrom SA, Traboulsi EI.

Mol Vis. 2009;15:162-7. Epub 2009 Jan 21.

23.

Interaction between the photoreceptor-specific tubby-like protein 1 and the neuronal-specific GTPase dynamin-1.

Xi Q, Pauer GJ, Ball SL, Rayborn M, Hollyfield JG, Peachey NS, Crabb JW, Hagstrom SA.

Invest Ophthalmol Vis Sci. 2007 Jun;48(6):2837-44.

24.

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.

Ophthalmic Genet. 2006 Dec;27(4):151-5.

25.

Fibrin glue system for adjuvant brachytherapy of brain tumors with 188Re and 186Re-labeled microspheres.

Häfeli UO, Pauer GJ, Unnithan J, Prayson RA.

Eur J Pharm Biopharm. 2007 Mar;65(3):282-8. Epub 2006 Nov 10.

PMID:
17129715
26.

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

Xi Q, Pauer GJ, Traboulsi EI, Hagstrom SA.

Exp Eye Res. 2006 Sep;83(3):569-73. Epub 2006 Apr 27.

27.

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.

Ophthalmic Genet. 2005 Dec;26(4):157-61.

PMID:
16352475
28.

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

Xi Q, Pauer GJ, Marmorstein AD, Crabb JW, Hagstrom SA.

Invest Ophthalmol Vis Sci. 2005 Dec;46(12):4754-61.

29.

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

Hagstrom SA, Pauer GJ, Reid J, Simpson E, Crowe S, Maumenee IH, Traboulsi EI.

Am J Med Genet A. 2005 Oct 1;138A(2):95-8.

PMID:
16145681
30.

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.

Br J Ophthalmol. 2005 Aug;89(8):1065-6. No abstract available.

31.

Retinal degeneration caused by mutations in TULP1.

Xi Q, Pauer GJ, West KA, Crabb JW, Hagstrom SA.

Adv Exp Med Biol. 2003;533:303-8. No abstract available.

PMID:
15180277
32.

Stability of biodegradable radioactive rhenium (Re-186 and Re-188) microspheres after neutron-activation.

Häfeli UO, Roberts WK, Pauer GJ, Kraeft SK, Macklis RM.

Appl Radiat Isot. 2001 Jun;54(6):869-79.

PMID:
11300399
33.

Dosimetry of a W-188/Re-188 beta line source for endovascular brachytherapy.

Häfeli UO, Roberts WK, Meier DS, Ciezki JP, Pauer GJ, Lee EJ, Weinhous MS.

Med Phys. 2000 Apr;27(4):668-75.

PMID:
10798688
34.

Hepatic tumor radioembolization in a rat model using radioactive rhenium (186Re/188Re) glass microspheres.

Häfeli UO, Casillas S, Dietz DW, Pauer GJ, Rybicki LA, Conzone SD, Day DE.

Int J Radiat Oncol Biol Phys. 1999 Apr 1;44(1):189-99.

PMID:
10219814

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