Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
6 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Gene augmentation therapy to rescue degenerative photoreceptors in a Cwc27 mutant mouse model.
Exp Eye Res. 2023 Sep;234:109596. doi: 10.1016/j.exer.2023.109596. Epub 2023 Jul 20.
Exp Eye Res. 2023.
PMID: 37479075
Gene Therapy Rescues Retinal Degeneration in Receptor Expression-Enhancing Protein 6 Mutant Mice.
Zaneveld SA, Eblimit A, Liang Q, Bertrand R, Wu N, Liu H, Nguyen Q, Zaneveld J, Wang K, Li Y, Chen R.
Zaneveld SA, et al.
Hum Gene Ther. 2019 Mar;30(3):302-315. doi: 10.1089/hum.2018.078. Epub 2018 Oct 16.
Hum Gene Ther. 2019.
PMID: 30101608
Free PMC article.
Item in Clipboard
Cwc27, associated with retinal degeneration, functions as a splicing factor in vivo.
Bertrand RE, Wang J, Li Y, Cheng X, Wang K, Stoilov P, Chen R.
Bertrand RE, et al.
Hum Mol Genet. 2022 Apr 22;31(8):1278-1292. doi: 10.1093/hmg/ddab319.
Hum Mol Genet. 2022.
PMID: 34726245
Free PMC article.
Item in Clipboard
Transcript isoforms of Reep6 have distinct functions in the retina.
Liang Q, Wu N, Zaneveld S, Liu H, Fu S, Wang K, Bertrand R, Wang J, Li Y, Chen R.
Liang Q, et al.
Hum Mol Genet. 2021 Oct 13;30(21):1907-1918. doi: 10.1093/hmg/ddab157.
Hum Mol Genet. 2021.
PMID: 34104971
Free PMC article.
Item in Clipboard
Ceramide synthase TLCD3B is a novel gene associated with human recessive retinal dystrophy.
Bertrand RE, Wang J, Xiong KH, Thangavel C, Qian X, Ba-Abbad R, Liang Q, Simões RT, Sampaio SAM, Carss KJ, Lucy Raymond F, Robson AG, Webster AR, Arno G, Porto FBO, Chen R.
Bertrand RE, et al.
Genet Med. 2021 Mar;23(3):488-497. doi: 10.1038/s41436-020-01003-x. Epub 2020 Oct 20.
Genet Med. 2021.
PMID: 33077892
Free PMC article.
Item in Clipboard
A novel statistical method for interpreting the pathogenicity of rare variants.
Wang J, Liu H, Bertrand RE, Sarrion-Perdigones A, Gonzalez Y, Venken KJT, Chen R.
Wang J, et al. Among authors: bertrand re.
Genet Med. 2021 Jan;23(1):59-68. doi: 10.1038/s41436-020-00948-3. Epub 2020 Sep 4.
Genet Med. 2021.
PMID: 32884132
Free PMC article.
Item in Clipboard
Cite
Cite