Chapple JP - Search Results

1

An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 gene.

Dandekar SS, Ebenezer ND, Grayson C, Chapple JP, Egan CA, Holder GE, Jenkins SA, Fitzke FW, Cheetham ME, Webster AR, Hardcastle AJ. Dandekar SS, et al. Among authors: chapple jp. Br J Ophthalmol. 2004 Apr;88(4):528-32. doi: 10.1136/bjo.2003.027979. Br J Ophthalmol. 2004. PMID: 15031171 Free PMC article.

2

Delineation of the plasma membrane targeting domain of the X-linked retinitis pigmentosa protein RP2.

Chapple JP, Hardcastle AJ, Grayson C, Willison KR, Cheetham ME. Chapple JP, et al. Invest Ophthalmol Vis Sci. 2002 Jun;43(6):2015-20. Invest Ophthalmol Vis Sci. 2002. PMID: 12037013

3

Assay and functional analysis of the ARL3 effector RP2 involved in X-linked retinitis pigmentosa.

Evans RJ, Chapple JP, Grayson C, Hardcastle AJ, Cheetham ME. Evans RJ, et al. Among authors: chapple jp. Methods Enzymol. 2005;404:468-80. doi: 10.1016/S0076-6879(05)04041-3. Methods Enzymol. 2005. PMID: 16413292

4

Mutations in the N-terminus of the X-linked retinitis pigmentosa protein RP2 interfere with the normal targeting of the protein to the plasma membrane.

Chapple JP, Hardcastle AJ, Grayson C, Spackman LA, Willison KR, Cheetham ME. Chapple JP, et al. Hum Mol Genet. 2000 Aug 12;9(13):1919-26. doi: 10.1093/hmg/9.13.1919. Hum Mol Genet. 2000. PMID: 10942419

5

Localization in the human retina of the X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the RP2 interacting protein Arl3.

Grayson C, Bartolini F, Chapple JP, Willison KR, Bhamidipati A, Lewis SA, Luthert PJ, Hardcastle AJ, Cowan NJ, Cheetham ME. Grayson C, et al. Among authors: chapple jp. Hum Mol Genet. 2002 Nov 15;11(24):3065-74. doi: 10.1093/hmg/11.24.3065. Hum Mol Genet. 2002. PMID: 12417528

6

Organization on the plasma membrane of the retinitis pigmentosa protein RP2: investigation of association with detergent-resistant membranes and polarized sorting.

Chapple JP, Grayson C, Hardcastle AJ, Bailey TA, Matter K, Adamson P, Graham CH, Willison KR, Cheetham ME. Chapple JP, et al. Biochem J. 2003 Jun 1;372(Pt 2):427-33. doi: 10.1042/BJ20021475. Biochem J. 2003. PMID: 12648035 Free PMC article.

7

Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy.

Mendes HF, van der Spuy J, Chapple JP, Cheetham ME. Mendes HF, et al. Among authors: chapple jp. Trends Mol Med. 2005 Apr;11(4):177-85. doi: 10.1016/j.molmed.2005.02.007. Trends Mol Med. 2005. PMID: 15823756 Review.

8

Arl3 and RP2 regulate the trafficking of ciliary tip kinesins.

Schwarz N, Lane A, Jovanovic K, Parfitt DA, Aguila M, Thompson CL, da Cruz L, Coffey PJ, Chapple JP, Hardcastle AJ, Cheetham ME. Schwarz N, et al. Among authors: chapple jp. Hum Mol Genet. 2017 Jul 1;26(13):2480-2492. doi: 10.1093/hmg/ddx143. Hum Mol Genet. 2017. PMID: 28444310 Free PMC article.

9

Unfolding retinal dystrophies: a role for molecular chaperones?

Chapple JP, Grayson C, Hardcastle AJ, Saliba RS, van der Spuy J, Cheetham ME. Chapple JP, et al. Trends Mol Med. 2001 Sep;7(9):414-21. doi: 10.1016/s1471-4914(01)02103-7. Trends Mol Med. 2001. PMID: 11530337 Review.

10

In vitro analysis of aminoglycoside therapy for the Arg120stop nonsense mutation in RP2 patients.

Grayson C, Chapple JP, Willison KR, Webster AR, Hardcastle AJ, Cheetham ME. Grayson C, et al. Among authors: chapple jp. J Med Genet. 2002 Jan;39(1):62-7. doi: 10.1136/jmg.39.1.62. J Med Genet. 2002. PMID: 11826029 Free PMC article. No abstract available.

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