Werner syndrome with refractory cystoid macular edema and immunohistochemical analysis of WRN proteins in human retinas-Reference-Cited by-同舟云学术

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Werner syndrome with refractory cystoid macular edema and immunohistochemical analysis of WRN proteins in human retinas

Published:2014-03-12 Issue:1 Volume:14 Page:
ISSN:1471-2415
Container-title:BMC Ophthalmology
language:en
Short-container-title:BMC Ophthalmol

Author:

Oshitari Toshiyuki,Kitahashi Masayasu,Mizuno Satoshi,Baba Takayuki,Kubota-Taniai Mariko,Takemoto Minoru,Yokote Koutaro,Yamamoto Shuichi,Roy Sayon

Publisher

Springer Science and Business Media LLC

Subject

Ophthalmology,General Medicine

Link

http://link.springer.com/content/pdf/10.1186/1471-2415-14-31.pdf

Reference25 articles.

1. Rossi ML, Ghosh AK, Bohr VA: Roles of Werner syndrome protein in protection of genome integrity. DNA Repair (Amst). 2010, 9: 331-344. 10.1016/j.dnarep.2009.12.011.

2. Friedrich K, Lee L, Leistritz DF, Nürnberg G, Saha B, Hisama FM, Eyman DK, Lessel D, Nürnberg P, Li C, Garcia-F-Villalta MJ, Kets CM, Schmidtke J, Cruz VT, Van den Akker PC, Boak J, Peter D, Compoginis G, Cefle K, Ozturk S, López N, Wessel T, Poot M, Ippel PF, Groff-Kellermann B, Hoehn H, Martin GM, Kubisch C, Oshima J: WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations. Hum Genet. 2010, 128: 103-111. 10.1007/s00439-010-0832-5.

3. Huang S, Lee L, Hanson NB, Lenaerts C, Hoehn H, Poot M, Rubin CD, Chen DF, Yang CC, Juch H, Dorn T, Spiegel R, Oral EA, Abid M, Battisti C, Lucci-Cordisco E, Neri G, Steed EH, Kidd A, Isley W, Showalter D, Vittone JL, Konstantinow A, Ring J, Meyer P, Wenger SL, von Herbay A, Wollina U, Schuelke M, Huizenga CR, Leistritz DF, Martin GM, Mian IS, Oshima J: The spectrum of WRN mutations in Werner syndrome patients. Hum Mutat. 2006, 27: 558-567. 10.1002/humu.20337.

4. Gee J, Ding Q, Keller JN: Analysis of Werner’s expression within the brain and primary neuronal culture. Brain Res. 2002, 940: 44-48. 10.1016/S0006-8993(02)02588-X.

5. Goto M: Syndrome-causing mutations in Werner syndrome. Biosci Trends. 2008, 2: 147-150.

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. OCT and ERG Techniques in High-Throughput Phenotyping of Mouse Vision;Genes;2023-01-22

2. Optical coherence tomography findings in three patients with Werner syndrome;BMC Ophthalmology;2022-11-19

3. The ophthalmic diagnosis and management of four siblings with Werner syndrome;International Ophthalmology;2018-04-28

4. Primary Bullous Keratopathy in a Patient With Werner Syndrome Treated With Corneal Transplant;Experimental and Clinical Transplantation;2018-03-09

5. A novel splice-site mutation of WRN (c.IVS28+2T>C) identified in a consanguineous family with Werner Syndrome;Molecular Medicine Reports;2017-04-12

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