Showing results (1741-1750 of 2,138) with videos related to

Sort By:
Pageof 214
Biorxiv : the Preprint Server for Biology|April 10, 2026
Single-Cell Gene Expression and eQTL Analyses in the Human Retina, RPE, and Choroid in Macular DegenerationAndrew P Voigt, Nathaniel K Mullin, Kelly Mulfaul, et al.
Nature Nanotechnology|September 14, 2023
Wireless electrical-molecular quantum signalling for cancer cell apoptosisAkhil Jain, Jonathan Gosling, Shaochuang Liu, et al.
Human Molecular Genetics|February 19, 2022
Choroidal endothelial and macrophage gene expression in atrophic and neovascular macular degenerationAndrew P Voigt, Nathaniel K Mullin, Kelly Mulfaul, et al.
Frontiers in Medicine|July 3, 2023
Long-term functional and structural outcomes in X-linked retinoschisis: implications for clinical trialsBeau J Fenner, Jonathan F Russell, Arlene V Drack, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 20, 2006
Regulation of gene expression in the mammalian eye and its relevance to eye diseaseTodd E Scheetz, Kwang-Youn A Kim, Ruth E Swiderski, et al.
The CRISPR Journal|April 26, 2019
CRISPR-Cas9-Mediated Correction of the 1.02 kb Common Deletion in <i>CLN3</i> in Induced Pluripotent Stem Cells from Patients with Batten DiseaseErin R Burnight, Laura R Bohrer, Joseph C Giacalone, et al.
Human Molecular Genetics|January 12, 2001
Non-secretion of mutant proteins of the glaucoma gene myocilin in cultured trabecular meshwork cells and in aqueous humorN Jacobson, M Andrews, A R Shepard, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 20, 2001
Mutations in the CRB1 gene cause Leber congenital amaurosisA J Lotery, S G Jacobson, G A Fishman, et al.
Investigative Ophthalmology & Visual Science|October 27, 2006
Retinal disease expression in Bardet-Biedl syndrome-1 (BBS1) is a spectrum from maculopathy to retina-wide degenerationAmir A Azari, Tomas S Aleman, Artur V Cideciyan, et al.
Cancer Research|October 28, 2016
Mutational Landscape and Gene Expression Patterns in Adult Acute Myeloid Leukemias with Monosomy 7 as a Sole AbnormalityAnn-Kathrin Eisfeld, Jessica Kohlschmidt, Krzysztof Mrózek, et al.
Pageof 214