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Generation of Cre transgenic mice with postnatal RPE-specific ocular expression.
Iacovelli J, Zhao C, Wolkow N, Veldman P, Gollomp K, Ojha P, Lukinova N, King A, Feiner L, Esumi N, Zack DJ, Pierce EA, Vollrath D, Dunaief JL. Iacovelli J, et al. Among authors: vollrath d. Invest Ophthalmol Vis Sci. 2011 Mar 14;52(3):1378-83. doi: 10.1167/iovs.10-6347. Print 2011 Mar. Invest Ophthalmol Vis Sci. 2011. PMID: 21212186 Free PMC article.
mTOR pathway activation in age-related retinal disease.
Zhao C, Vollrath D. Zhao C, et al. Among authors: vollrath d. Aging (Albany NY). 2011 Apr;3(4):346-7. doi: 10.18632/aging.100303. Aging (Albany NY). 2011. PMID: 21483039 Free PMC article. No abstract available.
Targeted sequencing of 179 genes associated with hereditary retinal dystrophies and 10 candidate genes identifies novel and known mutations in patients with various retinal diseases.
Chen X, Zhao K, Sheng X, Li Y, Gao X, Zhang X, Kang X, Pan X, Liu Y, Jiang C, Shi H, Chen X, Rong W, Chen LJ, Lai TY, Liu Y, Wang X, Yuan S, Liu Q, Vollrath D, Pang CP, Zhao C. Chen X, et al. Among authors: vollrath d. Invest Ophthalmol Vis Sci. 2013 Mar 1;54(3):2186-97. doi: 10.1167/iovs.12-10967. Invest Ophthalmol Vis Sci. 2013. PMID: 23462753
PRPF4 mutations cause autosomal dominant retinitis pigmentosa.
Chen X, Liu Y, Sheng X, Tam PO, Zhao K, Chen X, Rong W, Liu Y, Liu X, Pan X, Chen LJ, Zhao Q, Vollrath D, Pang CP, Zhao C. Chen X, et al. Among authors: vollrath d. Hum Mol Genet. 2014 Jun 1;23(11):2926-39. doi: 10.1093/hmg/ddu005. Epub 2014 Jan 12. Hum Mol Genet. 2014. PMID: 24419317
Vascular tone pathway polymorphisms in relation to primary open-angle glaucoma.
Kang JH, Loomis SJ, Yaspan BL, Bailey JC, Weinreb RN, Lee RK, Lichter PR, Budenz DL, Liu Y, Realini T, Gaasterland D, Gaasterland T, Friedman DS, McCarty CA, Moroi SE, Olson L, Schuman JS, Singh K, Vollrath D, Wollstein G, Zack DJ, Brilliant M, Sit AJ, Christen WG, Fingert J, Forman JP, Buys ES, Kraft P, Zhang K, Allingham RR, Pericak-Vance MA, Richards JE, Hauser MA, Haines JL, Wiggs JL, Pasquale LR. Kang JH, et al. Among authors: vollrath d. Eye (Lond). 2014 Jun;28(6):662-71. doi: 10.1038/eye.2014.42. Epub 2014 Mar 7. Eye (Lond). 2014. PMID: 24603425 Free PMC article.
SPP2 Mutations Cause Autosomal Dominant Retinitis Pigmentosa.
Liu Y, Chen X, Xu Q, Gao X, Tam PO, Zhao K, Zhang X, Chen LJ, Jia W, Zhao Q, Vollrath D, Pang CP, Zhao C. Liu Y, et al. Among authors: vollrath d. Sci Rep. 2015 Oct 13;5:14867. doi: 10.1038/srep14867. Sci Rep. 2015. PMID: 26459573 Free PMC article.
Abnormal mTORC1 signaling leads to retinal pigment epithelium degeneration.
Huang J, Gu S, Chen M, Zhang SJ, Jiang Z, Chen X, Jiang C, Liu G, Radu RA, Sun X, Vollrath D, Du J, Yan B, Zhao C. Huang J, et al. Among authors: vollrath d. Theranostics. 2019 Jan 30;9(4):1170-1180. doi: 10.7150/thno.26281. eCollection 2019. Theranostics. 2019. PMID: 30867823 Free PMC article.
107 results