Molday RS - Search Results

1

Identification of photoreceptor genes affected by PRPF31 mutations associated with autosomal dominant retinitis pigmentosa.

Mordes D, Yuan L, Xu L, Kawada M, Molday RS, Wu JY. Mordes D, et al. Among authors: molday rs. Neurobiol Dis. 2007 May;26(2):291-300. doi: 10.1016/j.nbd.2006.08.026. Epub 2007 Mar 9. Neurobiol Dis. 2007. PMID: 17350276 Free PMC article.

2

Role of subunit assembly in autosomal dominant retinitis pigmentosa linked to mutations in peripherin 2.

Molday RS, Molday LL, Loewen CJ. Molday RS, et al. Among authors: molday ll. Novartis Found Symp. 2004;255:95-112; discussion 113-6, 177-8. Novartis Found Symp. 2004. PMID: 14750599 Review.

3

Cysteine residues of photoreceptor peripherin/rds: role in subunit assembly and autosomal dominant retinitis pigmentosa.

Goldberg AF, Loewen CJ, Molday RS. Goldberg AF, et al. Among authors: molday rs. Biochemistry. 1998 Jan 13;37(2):680-5. doi: 10.1021/bi972036i. Biochemistry. 1998. PMID: 9425091

4

The role of subunit assembly in peripherin-2 targeting to rod photoreceptor disk membranes and retinitis pigmentosa.

Loewen CJ, Moritz OL, Tam BM, Papermaster DS, Molday RS. Loewen CJ, et al. Among authors: molday rs. Mol Biol Cell. 2003 Aug;14(8):3400-13. doi: 10.1091/mbc.e03-02-0077. Epub 2003 May 3. Mol Biol Cell. 2003. PMID: 12925772 Free PMC article.

5

Molecular characterization of peripherin-2 and rom-1 mutants responsible for digenic retinitis pigmentosa.

Loewen CJ, Moritz OL, Molday RS. Loewen CJ, et al. Among authors: molday rs. J Biol Chem. 2001 Jun 22;276(25):22388-96. doi: 10.1074/jbc.M011710200. Epub 2001 Apr 10. J Biol Chem. 2001. PMID: 11297544 Free article.

6

Defective subunit assembly underlies a digenic form of retinitis pigmentosa linked to mutations in peripherin/rds and rom-1.

Goldberg AF, Molday RS. Goldberg AF, et al. Among authors: molday rs. Proc Natl Acad Sci U S A. 1996 Nov 26;93(24):13726-30. doi: 10.1073/pnas.93.24.13726. Proc Natl Acad Sci U S A. 1996. PMID: 8943002 Free PMC article.

7

Interaction and localization of the retinitis pigmentosa protein RP2 and NSF in retinal photoreceptor cells.

Holopainen JM, Cheng CL, Molday LL, Johal G, Coleman J, Dyka F, Hii T, Ahn J, Molday RS. Holopainen JM, et al. Among authors: molday rs, molday ll. Biochemistry. 2010 Sep 7;49(35):7439-47. doi: 10.1021/bi1005249. Biochemistry. 2010. PMID: 20669900 Free PMC article.

8

Temporal and tissue specific regulation of RP-associated splicing factor genes PRPF3, PRPF31 and PRPC8--implications in the pathogenesis of RP.

Cao H, Wu J, Lam S, Duan R, Newnham C, Molday RS, Graziotto JJ, Pierce EA, Hu J. Cao H, et al. Among authors: molday rs. PLoS One. 2011 Jan 19;6(1):e15860. doi: 10.1371/journal.pone.0015860. PLoS One. 2011. PMID: 21283520 Free PMC article.

9

Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa.

Olsson JE, Gordon JW, Pawlyk BS, Roof D, Hayes A, Molday RS, Mukai S, Cowley GS, Berson EL, Dryja TP. Olsson JE, et al. Among authors: molday rs. Neuron. 1992 Nov;9(5):815-30. doi: 10.1016/0896-6273(92)90236-7. Neuron. 1992. PMID: 1418997

10

Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis.

Clarke G, Goldberg AF, Vidgen D, Collins L, Ploder L, Schwarz L, Molday LL, Rossant J, Szél A, Molday RS, Birch DG, McInnes RR. Clarke G, et al. Among authors: molday rs, molday ll. Nat Genet. 2000 May;25(1):67-73. doi: 10.1038/75621. Nat Genet. 2000. PMID: 10802659

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