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F1000Research|December 7, 2021
A signaling pathway-driven bioinformatics pipeline for predicting therapeutics against emerging infectious diseasesTiana M Scott, Sam Jensen, Brett E PickettCurrent Protocols|August 26, 2022
Genetic Modification of Primary Human Myeloid Cells to Study Cell Migration, Activation, and Organelle DynamicsDaniel Greiner, Tiana M Scott, Gregory S Olson, et al.Frontiers in Cellular and Infection Microbiology|October 7, 2022
Comparison of Intracellular Transcriptional Response of NHBE Cells to Infection with SARS-CoV-2 Washington and New York StrainsTiana M Scott, Antonio Solis-Leal, J Brandon Lopez, et al.Human Molecular Genetics|March 27, 2021
RERE deficiency contributes to the development of orofacial clefts in humans and miceBum Jun Kim, Hitisha P Zaveri, Peter N Kundert, et al.Journal of Medical Genetics|January 19, 2021
Clinical exome sequencing data reveal high diagnostic yields for congenital diaphragmatic hernia plus (CDH+) and new phenotypic expansions involving CDHTiana M Scott, Ian M Campbell, Andres Hernandez-Garcia, et al.Plos Pathogens|January 28, 2025
Cell-free assays reveal that the HIV-1 capsid protects reverse transcripts from cGAS immune sensingTiana M Scott, Lydia M Arnold, Jordan A Powers, et al.Biorxiv : the Preprint Server for Biology|May 7, 2024
Cell-free assays reveal that the HIV-1 capsid protects reverse transcripts from cGASTiana M Scott, Lydia M Arnold, Jordan A Powers, et al.Human Mutation|January 31, 2020
BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorderTiana M Scott, Hui Guo, Evan E Eichler, et al.Human Mutation|January 30, 2022
Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiencyYoel Gofin, Tianyun Wang, Madelyn A Gillentine, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Retrospective analysis of a clinical exome sequencing cohort reveals the mutational spectrum and identifies candidate disease-associated loci for BAFopathiesChun-An Chen, John Lattier, Wenmiao Zhu, et al.Pageof 2