Daiger SP - Search Results

1

Progressive photoreceptor degeneration, outer segment dysplasia, and rhodopsin mislocalization in mice with targeted disruption of the retinitis pigmentosa-1 (Rp1) gene.

Gao J, Cheon K, Nusinowitz S, Liu Q, Bei D, Atkins K, Azimi A, Daiger SP, Farber DB, Heckenlively JR, Pierce EA, Sullivan LS, Zuo J. Gao J, et al. Among authors: daiger sp. Proc Natl Acad Sci U S A. 2002 Apr 16;99(8):5698-703. doi: 10.1073/pnas.042122399. Proc Natl Acad Sci U S A. 2002. PMID: 11960024 Free PMC article.

2

Essential and synergistic roles of RP1 and RP1L1 in rod photoreceptor axoneme and retinitis pigmentosa.

Yamashita T, Liu J, Gao J, LeNoue S, Wang C, Kaminoh J, Bowne SJ, Sullivan LS, Daiger SP, Zhang K, Fitzgerald ME, Kefalov VJ, Zuo J. Yamashita T, et al. Among authors: daiger sp. J Neurosci. 2009 Aug 5;29(31):9748-60. doi: 10.1523/JNEUROSCI.5854-08.2009. J Neurosci. 2009. PMID: 19657028 Free PMC article.

3

Identification and subcellular localization of the RP1 protein in human and mouse photoreceptors.

Liu Q, Zhou J, Daiger SP, Farber DB, Heckenlively JR, Smith JE, Sullivan LS, Zuo J, Milam AH, Pierce EA. Liu Q, et al. Among authors: daiger sp. Invest Ophthalmol Vis Sci. 2002 Jan;43(1):22-32. Invest Ophthalmol Vis Sci. 2002. PMID: 11773008 Free PMC article.

4

Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene.

Bowne SJ, Daiger SP, Malone KA, Heckenlively JR, Kennan A, Humphries P, Hughbanks-Wheaton D, Birch DG, Liu Q, Pierce EA, Zuo J, Huang Q, Donovan DD, Sullivan LS. Bowne SJ, et al. Among authors: daiger sp. Mol Vis. 2003 Apr 24;9:129-37. Mol Vis. 2003. PMID: 12724644 Free PMC article.

5

Why do mutations in the ubiquitously expressed housekeeping gene IMPDH1 cause retina-specific photoreceptor degeneration?

Bowne SJ, Liu Q, Sullivan LS, Zhu J, Spellicy CJ, Rickman CB, Pierce EA, Daiger SP. Bowne SJ, et al. Among authors: daiger sp. Invest Ophthalmol Vis Sci. 2006 Sep;47(9):3754-65. doi: 10.1167/iovs.06-0207. Invest Ophthalmol Vis Sci. 2006. PMID: 16936083 Free PMC article.

6

Targeted high-throughput DNA sequencing for gene discovery in retinitis pigmentosa.

Daiger SP, Sullivan LS, Bowne SJ, Birch DG, Heckenlively JR, Pierce EA, Weinstock GM. Daiger SP, et al. Adv Exp Med Biol. 2010;664:325-31. doi: 10.1007/978-1-4419-1399-9_37. Adv Exp Med Biol. 2010. PMID: 20238032 Free PMC article.

7

Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin.

Heckenlively JR, Rodriguez JA, Daiger SP. Heckenlively JR, et al. Among authors: daiger sp. Arch Ophthalmol. 1991 Jan;109(1):84-91. doi: 10.1001/archopht.1991.01080010086038. Arch Ophthalmol. 1991. PMID: 1987955

8

Inherited retinal degeneration: exceptional genetic and clinical heterogeneity.

Sullivan LS, Daiger SP. Sullivan LS, et al. Among authors: daiger sp. Mol Med Today. 1996 Sep;2(9):380-6. doi: 10.1016/s1357-4310(96)10037-x. Mol Med Today. 1996. PMID: 8885257 Review.

9

Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa.

Sullivan LS, Heckenlively JR, Bowne SJ, Zuo J, Hide WA, Gal A, Denton M, Inglehearn CF, Blanton SH, Daiger SP. Sullivan LS, et al. Among authors: daiger sp. Nat Genet. 1999 Jul;22(3):255-9. doi: 10.1038/10314. Nat Genet. 1999. PMID: 10391212 Free PMC article.

10

Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa.

Bowne SJ, Daiger SP, Hims MM, Sohocki MM, Malone KA, McKie AB, Heckenlively JR, Birch DG, Inglehearn CF, Bhattacharya SS, Bird A, Sullivan LS. Bowne SJ, et al. Among authors: daiger sp. Hum Mol Genet. 1999 Oct;8(11):2121-8. doi: 10.1093/hmg/8.11.2121. Hum Mol Genet. 1999. PMID: 10484783 Free PMC article.

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