Wen R - Search Results

1

Aberrant dolichol chain lengths as biomarkers for retinitis pigmentosa caused by impaired dolichol biosynthesis.

Wen R, Lam BL, Guan Z. Wen R, et al. J Lipid Res. 2013 Dec;54(12):3516-22. doi: 10.1194/jlr.M043232. Epub 2013 Sep 27. J Lipid Res. 2013. PMID: 24078709 Free PMC article.

2

Knock-down DHDDS expression induces photoreceptor degeneration in zebrafish.

Wen R, Dallman JE, Li Y, Züchner SL, Vance JM, Peričak-Vance MA, Lam BL. Wen R, et al. Adv Exp Med Biol. 2014;801:543-50. doi: 10.1007/978-1-4614-3209-8_69. Adv Exp Med Biol. 2014. PMID: 24664742

3

Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa.

Züchner S, Dallman J, Wen R, Beecham G, Naj A, Farooq A, Kohli MA, Whitehead PL, Hulme W, Konidari I, Edwards YJ, Cai G, Peter I, Seo D, Buxbaum JD, Haines JL, Blanton S, Young J, Alfonso E, Vance JM, Lam BL, Peričak-Vance MA. Züchner S, et al. Among authors: wen r. Am J Hum Genet. 2011 Feb 11;88(2):201-6. doi: 10.1016/j.ajhg.2011.01.001. Epub 2011 Feb 3. Am J Hum Genet. 2011. PMID: 21295283 Free PMC article.

4

Mutation K42E in dehydrodolichol diphosphate synthase (DHDDS) causes recessive retinitis pigmentosa.

Lam BL, Züchner SL, Dallman J, Wen R, Alfonso EC, Vance JM, Peričak-Vance MA. Lam BL, et al. Among authors: wen r. Adv Exp Med Biol. 2014;801:165-70. doi: 10.1007/978-1-4614-3209-8_21. Adv Exp Med Biol. 2014. PMID: 24664694

5

Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical Aspects.

Kimchi A, Khateb S, Wen R, Guan Z, Obolensky A, Beryozkin A, Kurtzman S, Blumenfeld A, Pras E, Jacobson SG, Ben-Yosef T, Newman H, Sharon D, Banin E. Kimchi A, et al. Among authors: wen r. Ophthalmology. 2018 May;125(5):725-734. doi: 10.1016/j.ophtha.2017.11.014. Epub 2017 Dec 22. Ophthalmology. 2018. PMID: 29276052

6

In vivo imaging rhodopsin distribution in the photoreceptors with nano-second pulsed scanning laser ophthalmoscopy.

Liu T, Liu X, Wen R, Lam BL, Jiao S. Liu T, et al. Among authors: wen r. Quant Imaging Med Surg. 2015 Feb;5(1):63-8. doi: 10.3978/j.issn.2223-4292.2014.11.06. Quant Imaging Med Surg. 2015. PMID: 25694955 Free PMC article.

7

Mutation of Nogo-B receptor, a subunit of cis-prenyltransferase, causes a congenital disorder of glycosylation.

Park EJ, Grabińska KA, Guan Z, Stránecký V, Hartmannová H, Hodaňová K, Barešová V, Sovová J, Jozsef L, Ondrušková N, Hansíková H, Honzík T, Zeman J, Hůlková H, Wen R, Kmoch S, Sessa WC. Park EJ, et al. Among authors: wen r. Cell Metab. 2014 Sep 2;20(3):448-57. doi: 10.1016/j.cmet.2014.06.016. Epub 2014 Jul 24. Cell Metab. 2014. PMID: 25066056 Free PMC article.

8

Depth-resolved rhodopsin molecular contrast imaging for functional assessment of photoreceptors.

Liu T, Wen R, Lam BL, Puliafito CA, Jiao S. Liu T, et al. Among authors: wen r. Sci Rep. 2015 Sep 11;5:13992. doi: 10.1038/srep13992. Sci Rep. 2015. PMID: 26358529 Free PMC article.

9

Photoreceptor Protection by Mesencephalic Astrocyte-Derived Neurotrophic Factor (MANF).

Lu J, Luo L, Huang D, Liu X, Xia X, Wang Z, Lam BL, Yi J, Wen R, Li Y. Lu J, et al. Among authors: wen r. eNeuro. 2018 Apr 20;5(2):ENEURO.0109-18.2018. doi: 10.1523/ENEURO.0109-18.2018. eCollection 2018 Mar-Apr. eNeuro. 2018. PMID: 29687079 Free PMC article.

10

A2E Distribution in RPE Granules in Human Eyes.

Guan Z, Li Y, Jiao S, Yeasmin N, Rosenfeld PJ, Dubovy SR, Lam BL, Wen R. Guan Z, et al. Among authors: wen r. Molecules. 2020 Mar 20;25(6):1413. doi: 10.3390/molecules25061413. Molecules. 2020. PMID: 32244898 Free PMC article.

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