Showing results (1151-1160 of 1,250) with videos related to

Sort By:
Pageof 125
BMJ Open|March 20, 2023
Can artificial intelligence accelerate the diagnosis of inherited retinal diseases? Protocol for a data-only retrospective cohort study (Eye2Gene)Quang Nguyen, William Woof, Nathaniel Kabiri, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 18, 2010
Loss of lysophosphatidylcholine acyltransferase 1 leads to photoreceptor degeneration in rd11 miceJames S Friedman, Bo Chang, Daniel S Krauth, et al.
Scientific Reports|October 19, 2021
Comparison of in silico strategies to prioritize rare genomic variants impacting RNA splicing for the diagnosis of genomic disordersCharlie Rowlands, Huw B Thomas, Jenny Lord, et al.
Eclinicalmedicine|April 30, 2024
Health equity assessment of machine learning performance (HEAL): a framework and dermatology AI model case studyMike Schaekermann, Terry Spitz, Malcolm Pyles, et al.
Cancer Discovery|June 6, 2020
Changes in Aged Fibroblast Lipid Metabolism Induce Age-Dependent Melanoma Cell Resistance to Targeted Therapy via the Fatty Acid Transporter FATP2Gretchen M Alicea, Vito W Rebecca, Aaron R Goldman, et al.
Molecular Cancer Therapeutics|October 10, 2020
Targeting Oncogene mRNA Translation in B-Cell Malignancies with eFT226, a Potent and Selective Inhibitor of eIF4APeggy A Thompson, Boreth Eam, Nathan P Young, et al.
Human Mutation|January 1, 1996
Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and JapanB Zbar, T Kishida, F Chen, et al.
Bioorganic & Medicinal Chemistry Letters|May 26, 2023
Synthesis, modeling, and biological evaluation of anti-tubulin indole-substituted furanonesBrianna Hurysz, Blake A Evans, Reuben N Laryea, et al.
NPJ Genomic Medicine|June 30, 2021
Broadening INPP5E phenotypic spectrum: detection of rare variants in syndromic and non-syndromic IRDRiccardo Sangermano, Iris Deitch, Virginie G Peter, et al.
Genome Medicine|January 6, 2024
Combining a prioritization strategy and functional studies nominates 5'UTR variants underlying inherited retinal diseaseAlfredo Dueñas Rey, Marta Del Pozo Valero, Manon Bouckaert, et al.
Pageof 125