» Articles » PMID: 12843338

Study of the Involvement of the RGR, CRPB1, and CRB1 Genes in the Pathogenesis of Autosomal Recessive Retinitis Pigmentosa

Overview
Journal J Med Genet
Specialty Genetics
Date 2003 Jul 5
PMID 12843338
Citations 19
Authors
Affiliations
Soon will be listed here.
Citing Articles

Human CRB1 and CRB2 form homo- and heteromeric protein complexes in the retina.

Stehle I, Imventarza J, Woerz F, Hoffmann F, Boldt K, Beyer T Life Sci Alliance. 2024; 7(6).

PMID: 38570189 PMC: 10992996. DOI: 10.26508/lsa.202302440.


-Related Retinal Dystrophies in a Cohort of 50 Patients: A Reappraisal in the Light of Specific Müller Cell and Photoreceptor Isoforms.

Mairot K, Smirnov V, Bocquet B, Labesse G, Arndt C, Defoort-Dhellemmes S Int J Mol Sci. 2021; 22(23).

PMID: 34884448 PMC: 8657784. DOI: 10.3390/ijms222312642.


Defining inclusion criteria and endpoints for clinical trials: a prospective cross-sectional study in CRB1-associated retinal dystrophies.

Talib M, van Schooneveld M, Wijnholds J, van Genderen M, Schalij-Delfos N, Talsma H Acta Ophthalmol. 2021; 99(3):e402-e414.

PMID: 33528094 PMC: 8248330. DOI: 10.1111/aos.14597.


Retinal Dystrophies and the Road to Treatment: Clinical Requirements and Considerations.

Talib M, Boon C Asia Pac J Ophthalmol (Phila). 2020; 9(3):159-179.

PMID: 32511120 PMC: 7299224. DOI: 10.1097/APO.0000000000000290.


Expression Profiling Analysis Reveals Key MicroRNA-mRNA Interactions in Early Retinal Degeneration in Retinitis Pigmentosa.

Anasagasti A, Ezquerra-Inchausti M, Barandika O, Munoz-Culla M, Caffarel M, Otaegui D Invest Ophthalmol Vis Sci. 2018; 59(6):2381-2392.

PMID: 29847644 PMC: 5939684. DOI: 10.1167/iovs.18-24091.