Mistrafficking of prenylated proteins causes retinitis pigmentosa 2-Reference-Cited by-同舟云学术

Mistrafficking of prenylated proteins causes retinitis pigmentosa 2

Published:2014-11-24 Issue:3 Volume:29 Page:932-942
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

Zhang Houbin¹²,Hanke‐Gogokhia Christin²³,Jiang Li⁴,Li Xiaobo¹,Wang Pu¹,Gerstner Cecilia D.⁴,Frederick Jeanne M.⁴,Yang Zhenglin¹²,Baehr Wolfgang¹⁴⁵⁶

Affiliation:

1. The Sichuan Provincial Key Laboratory for Human Disease Gene StudyThe Institute of Laboratory MedicineHospital of University of Electronic Science and Technology of China and Sichuan Provincial People's HospitalChengduSichuanChina

2. School of MedicineUniversity of Electronic Science and Technology of ChinaChengduSichuanChina

3. Department of Biochemistry and BiologyUniversity of PotsdamPotsdam‐GolmGermany

4. Department of Ophthalmology and Visual SciencesJohn A. Moran Eye CenterUniversity of Utah School of MedicineSalt Lake CityUtahUSA

5. Department of Neurobiology and AnatomyUniversity of Utah School of MedicineSalt Lake CityUtahUSA

6. Department of BiologyUniversity of UtahSalt Lake CityUtahUSA

Funder

National Institutes of Health

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.14-257915

Reference54 articles.

1. Retinitis pigmentosa

2. Retinitis pigmentosa

3. Phenotypes in Three Swedish Families With X-linked Retinitis Pigmentosa Caused by Different Mutations in the RPGR Gene

4. X-linked Retinitis Pigmentosa Profile of Clinical Findings

5. Positional cloning of the gene for X-linked retinitis pigmentosa 2

Cited by 57 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. Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes;Progress in Retinal and Eye Research;2024-05

2. RP2-associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History in a Large Cohort of Female Carriers;American Journal of Ophthalmology;2023-11

3. RP2-Associated X-linked Retinopathy;Ophthalmology;2023-04

4. Control of protein and lipid composition of photoreceptor outer segments—Implications for retinal disease;Current Topics in Developmental Biology;2023

5. A Natural History Study of RP2-Related Retinopathy;Journal of Clinical Medicine;2022-11-22