EY-13203/EY/NEI NIH HHS/United States[Grant Number] - Search Results

Year	Number of Results
2001	1
2002	4
2003	3
2004	2
2024	0

1

Macular pigment and lutein supplementation in choroideremia.

Duncan JL, Aleman TS, Gardner LM, De Castro E, Marks DA, Emmons JM, Bieber ML, Steinberg JD, Bennett J, Stone EM, MacDonald IM, Cideciyan AV, Maguire MG, Jacobson SG. Duncan JL, et al. Exp Eye Res. 2002 Mar;74(3):371-81. doi: 10.1006/exer.2001.1126. Exp Eye Res. 2002. PMID: 12014918 Clinical Trial.

2

Spinocerebellar ataxia type 7 (SCA7) shows a cone-rod dystrophy phenotype.

Aleman TS, Cideciyan AV, Volpe NJ, Stevanin G, Brice A, Jacobson SG. Aleman TS, et al. Exp Eye Res. 2002 Jun;74(6):737-45. doi: 10.1006/exer.2002.1169. Exp Eye Res. 2002. PMID: 12126946

3

De novo mutation in the RP1 gene (Arg677ter) associated with retinitis pigmentosa.

Schwartz SB, Aleman TS, Cideciyan AV, Swaroop A, Jacobson SG, Stone EM. Schwartz SB, et al. Invest Ophthalmol Vis Sci. 2003 Aug;44(8):3593-7. doi: 10.1167/iovs.03-0155. Invest Ophthalmol Vis Sci. 2003. PMID: 12882812

4

In vivo micropathology of Best macular dystrophy with optical coherence tomography.

Pianta MJ, Aleman TS, Cideciyan AV, Sunness JS, Li Y, Campochiaro BA, Campochiaro PA, Zack DJ, Stone EM, Jacobson SG. Pianta MJ, et al. Exp Eye Res. 2003 Feb;76(2):203-11. doi: 10.1016/s0014-4835(02)00280-4. Exp Eye Res. 2003. PMID: 12565808

5

Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome.

Wright AF, Reddick AC, Schwartz SB, Ferguson JS, Aleman TS, Kellner U, Jurklies B, Schuster A, Zrenner E, Wissinger B, Lennon A, Shu X, Cideciyan AV, Stone EM, Jacobson SG, Swaroop A. Wright AF, et al. Hum Mutat. 2004 Nov;24(5):439. doi: 10.1002/humu.9285. Hum Mutat. 2004. PMID: 15459973

6

The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration.

Milam AH, Rose L, Cideciyan AV, Barakat MR, Tang WX, Gupta N, Aleman TS, Wright AF, Stone EM, Sheffield VC, Jacobson SG. Milam AH, et al. Proc Natl Acad Sci U S A. 2002 Jan 8;99(1):473-8. doi: 10.1073/pnas.022533099. Epub 2002 Jan 2. Proc Natl Acad Sci U S A. 2002. PMID: 11773633 Free PMC article.

7

Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequence.

Cideciyan AV, Aleman TS, Swider M, Schwartz SB, Steinberg JD, Brucker AJ, Maguire AM, Bennett J, Stone EM, Jacobson SG. Cideciyan AV, et al. Hum Mol Genet. 2004 Mar 1;13(5):525-34. doi: 10.1093/hmg/ddh048. Epub 2004 Jan 6. Hum Mol Genet. 2004. PMID: 14709597

8

Clinicopathologic effects of mutant GUCY2D in Leber congenital amaurosis.

Milam AH, Barakat MR, Gupta N, Rose L, Aleman TS, Pianta MJ, Cideciyan AV, Sheffield VC, Stone EM, Jacobson SG. Milam AH, et al. Ophthalmology. 2003 Mar;110(3):549-58. doi: 10.1016/S0161-6420(02)01757-8. Ophthalmology. 2003. PMID: 12623820

9

Augmented rod bipolar cell function in partial receptor loss: an ERG study in P23H rhodopsin transgenic and aging normal rats.

Aleman TS, LaVail MM, Montemayor R, Ying G, Maguire MM, Laties AM, Jacobson SG, Cideciyan AV. Aleman TS, et al. Vision Res. 2001 Sep;41(21):2779-97. doi: 10.1016/s0042-6989(01)00157-2. Vision Res. 2001. PMID: 11587727 Free article.

10

Early age-related maculopathy and self-reported visual difficulty in daily life.

Scilley K, Jackson GR, Cideciyan AV, Maguire MG, Jacobson SG, Owsley C. Scilley K, et al. Ophthalmology. 2002 Jul;109(7):1235-42. doi: 10.1016/s0161-6420(02)01060-6. Ophthalmology. 2002. PMID: 12093644

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