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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1999 3
2001 1
2004 1
2005 2
2006 1
2007 1
2008 2
2009 1
2010 1
2012 3
2013 2
2014 2
2015 1
2016 6
2017 3
2018 2
2022 10
2023 3
2024 1

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39 results

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Page 1
Regenerating Eye Tissues to Preserve and Restore Vision.
Stern JH, Tian Y, Funderburgh J, Pellegrini G, Zhang K, Goldberg JL, Ali RR, Young M, Xie Y, Temple S. Stern JH, et al. Cell Stem Cell. 2018 Jun 1;22(6):834-849. doi: 10.1016/j.stem.2018.05.013. Cell Stem Cell. 2018. PMID: 29859174 Free PMC article. Review.
Ocular regenerative therapies are on track to revolutionize treatment of numerous blinding disorders, including corneal disease, cataract, glaucoma, retinitis pigmentosa, and age-related macular degeneration. A variety of transplantable products, delivered as cell s …
Ocular regenerative therapies are on track to revolutionize treatment of numerous blinding disorders, including corneal disease, cataract, g …
The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy.
Athanasiou D, Aguila M, Bellingham J, Li W, McCulley C, Reeves PJ, Cheetham ME. Athanasiou D, et al. Prog Retin Eye Res. 2018 Jan;62:1-23. doi: 10.1016/j.preteyeres.2017.10.002. Epub 2017 Oct 16. Prog Retin Eye Res. 2018. PMID: 29042326 Free PMC article. Review.
Inherited mutations in the rod visual pigment, rhodopsin, cause the degenerative blinding condition, retinitis pigmentosa (RP). Over 150 different mutations in rhodopsin have been identified and, collectively, they are the most common cause of autosomal dominant RP …
Inherited mutations in the rod visual pigment, rhodopsin, cause the degenerative blinding condition, retinitis pigmentosa (RP) …
A novel frameshift variant in CEP78 associated with nonsyndromic retinitis pigmentosa, and a review of CEP78-related phenotypes.
Lähteenoja L, Häkli S, Tuupanen S, Kuismin O, Palosaari T, Rahikkala E, Falck A. Lähteenoja L, et al. Ophthalmic Genet. 2022 Apr;43(2):152-158. doi: 10.1080/13816810.2022.2045511. Epub 2022 Mar 3. Ophthalmic Genet. 2022. PMID: 35240912 Review.
BACKGROUND: Pathogenic variants in the CEP78 gene can present as atypical Usher syndrome or as retinitis pigmentosa. Here, we present a review of all reported cases of CEP78 variants in the literature to date and present a novel variant of CEP78, c.1261_1262delinsA, …
BACKGROUND: Pathogenic variants in the CEP78 gene can present as atypical Usher syndrome or as retinitis pigmentosa. Here, we …
Prevalence of RPGR-mutated X-linked retinitis pigmentosa among males.
Vinikoor-Imler LC, Simpson C, Narayanan D, Abbasi S, Lally C. Vinikoor-Imler LC, et al. Ophthalmic Genet. 2022 Oct;43(5):581-588. doi: 10.1080/13816810.2022.2109686. Epub 2022 Aug 25. Ophthalmic Genet. 2022. PMID: 36004681 Review.
BACKGROUND: X-linked retinitis pigmentosa (XLRP) is a rare inherited retinal disease predominantly affecting males. MATERIALS AND METHODS: A comprehensive literature review was conducted to determine the prevalence of retinitis pigmentosa GTPase regula …
BACKGROUND: X-linked retinitis pigmentosa (XLRP) is a rare inherited retinal disease predominantly affecting males. MATERIALS …
Review of Genotype-Phenotype Correlations in Usher Syndrome.
Nisenbaum E, Thielhelm TP, Nourbakhsh A, Yan D, Blanton SH, Shu Y, Koehler KR, El-Amraoui A, Chen Z, Lam BL, Liu X. Nisenbaum E, et al. Ear Hear. 2022 Jan/Feb;43(1):1-8. doi: 10.1097/AUD.0000000000001066. Ear Hear. 2022. PMID: 34039936 Free PMC article. Review.
Mechanism of Cone Degeneration in Retinitis Pigmentosa.
Song DJ, Bao XL, Fan B, Li GY. Song DJ, et al. Cell Mol Neurobiol. 2023 Apr;43(3):1037-1048. doi: 10.1007/s10571-022-01243-2. Epub 2022 Jul 6. Cell Mol Neurobiol. 2023. PMID: 35792991 Review.
Retinitis pigmentosa (RP) is a group of genetic disorders resulting in inherited blindness due to the degeneration of rod and cone photoreceptors. ...
Retinitis pigmentosa (RP) is a group of genetic disorders resulting in inherited blindness due to the degeneration of rod and …
The Argus(®) II Retinal Prosthesis System.
Luo YH, da Cruz L. Luo YH, et al. Prog Retin Eye Res. 2016 Jan;50:89-107. doi: 10.1016/j.preteyeres.2015.09.003. Epub 2015 Sep 25. Prog Retin Eye Res. 2016. PMID: 26404104 Review.
As such it has entered the commercial market as a treatment for patients with profound vision loss from end-stage outer retinal disease, predominantly retinitis pigmentosa. To date, over 100 devices have been implanted worldwide, representing the largest group of pa …
As such it has entered the commercial market as a treatment for patients with profound vision loss from end-stage outer retinal disease, pre …
Hsp90 as a Potential Therapeutic Target in Retinal Disease.
Aguilà M, Cheetham ME. Aguilà M, et al. Adv Exp Med Biol. 2016;854:161-7. doi: 10.1007/978-3-319-17121-0_22. Adv Exp Med Biol. 2016. PMID: 26427407 Free PMC article. Review.
Hsp90 has multiple roles in the retina and the use of different Hsp90 inhibitors has been shown to prevent retinal degeneration in models of retinitis pigmentosa and age-related macular degeneration. Hsp90 is also a potential target in uveal melanoma. ...
Hsp90 has multiple roles in the retina and the use of different Hsp90 inhibitors has been shown to prevent retinal degeneration in models of …
Progression Rate of Visual Function and Affecting Factors at Different Stages of Retinitis Pigmentosa.
Ito N, Miura G, Shiko Y, Kawasaki Y, Baba T, Yamamoto S. Ito N, et al. Biomed Res Int. 2022 Jul 14;2022:7204954. doi: 10.1155/2022/7204954. eCollection 2022. Biomed Res Int. 2022. PMID: 35872870 Free PMC article. Review.
We reviewed medical records of 121 patients/235 eyes of typical retinitis pigmentosa (RP) patients who could be followed up for at least 5 years with the aim of investigating the long-term course of visual function progression at each RP stage and appropriate assess …
We reviewed medical records of 121 patients/235 eyes of typical retinitis pigmentosa (RP) patients who could be followed up fo …
IMPDH1-associated autosomal dominant retinitis pigmentosa: natural history of novel variant Lys314Gln and a comprehensive literature search.
Sakti DH, Cornish EE, Nash BM, Jamieson RV, Grigg JR. Sakti DH, et al. Ophthalmic Genet. 2023 Oct;44(5):437-455. doi: 10.1080/13816810.2023.2215310. Epub 2023 May 31. Ophthalmic Genet. 2023. PMID: 37259572 Review.
Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) are causative for RP10 autosomal dominant retinitis pigmentosa (adRP). This study reports a novel variant in a family with IMPDH1-associated retinopathy. ...The literature review identified a furth …
Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) are causative for RP10 autosomal dominant retinitis pigmentos …
39 results