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Journal of Human Genetics|July 10, 2021
Novel PRMT7 mutation in a rare case of dysmorphism and intellectual disabilityJessie Poquérusse, Whitney Whitford, Juliet Taylor, et al.
Scientific Reports|May 20, 2022
Proof of concept for multiplex amplicon sequencing for mutation identification using the MinION nanopore sequencerWhitney Whitford, Victoria Hawkins, Kriebashne S Moodley, et al.
Genetics, Selection, Evolution : GSE|April 11, 2025
Comparison of genomic prediction accuracies in dairy cattle lactation traits using five classes of functional variants versus generic SNPSetegn Worku Alemu, Thomas J Lopdell, Alexander J Trevarton, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 3, 2020
Natural cryptic variation in epigenetic modulation of an embryonic gene regulatory networkChee Kiang Ewe, Yamila N Torres Cleuren, Sagen E Flowers, et al.
Journal of Huntington'S Disease|October 8, 2016
Comparison of Huntington's disease CAG Repeat Length Stability in Human Motor Cortex and Cingulate GyrusFiona C A Geraerts, Russell G Snell, Richard L M Faull, et al.
Disease Models & Mechanisms|September 30, 2018
Modelling brain dopamine-serotonin vesicular transport disease in Caenorhabditis elegansAlexander T Young, Kien N Ly, Callum Wilson, et al.
Advances in Neurobiology|July 5, 2017
The Complexity of Clinical Huntington's Disease: Developments in Molecular Genetics, Neuropathology and Neuroimaging BiomarkersLynette J Tippett, Henry J Waldvogel, Russell G Snell, et al.
RNA (New York, N.Y.)|December 12, 2018
Widespread cis-regulation of RNA editing in a large mammalThomas J Lopdell, Victoria Hawkins, Christine Couldrey, et al.
Brain Research. Molecular Brain Research|January 18, 2003
Insoluble TATA-binding protein accumulation in Huntington's disease cortexWilleke M C van Roon-Mom, Suzanne J Reid, A Lesley Jones, et al.
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