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Clinical Genetics|May 8, 2024
FGF12 copy number variant associated with epileptic encephalopathyAnna Abraham, Keri Ramsey, Newell Belnap, et al.
Neurology. Genetics|March 26, 2026
The Genetics of TDP-43 Type C Neurodegeneration: A Whole-Genome Sequencing Study and Literature ReviewMalik Nassan, Ivan Ayala, Jennifer Sloan, et al.
Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
The genetics of TDP43-Type-C neurodegeneration: a whole genome sequencing studyMalik Nassan, Ivan Alejandro Ayala, Jennifer Sloan, et al.
International Journal of Molecular Sciences|November 27, 2024
Duchenne Muscular Dystrophy in Two Half-Brothers Due to Inherited 306 Kb Inverted Insertion of 10p15.1 into Intron 44 of the Dp427m Transcript of the DMD GeneWayne M Jepsen, Andrew Fazenbaker, Keri Ramsey, et al.
Journal of the American Veterinary Medical Association|August 2, 2025
Intravenous allogeneic mesenchymal stromal cell therapy in 13 Pugs with presumptive early necrotizing meningoencephalitisRebecca C Windsor, Samuel Stewart, Jennifer M Cassano, et al.
Rare (Amsterdam, Netherlands)|May 21, 2024
Snyder-Robinson syndrome presenting with learning disability, epilepsy, and osteoporosis: a novel SMS gene variantMegumi Leung, Meredith Sanchez-Castillo, Newell Belnap, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Transcriptomic and protein analysis of human cortex reveals genes and pathways linked to NPTX2 disruption in Alzheimer's diseaseYuelin Lao, Mei-Fang Xiao, Shiyu Ji, et al.
Physiological Genomics|October 24, 2022
Muscle transcriptomic circuits linked to periarticular physiology in end-stage osteoarthritisDevin J Drummer, Kaleen M Lavin, Zachary A Graham, et al.
Physiological Genomics|February 27, 2025
Divergent multiomic acute exercise responses reveal the impact of sex as a biological variableKaleen M Lavin, Samia M O'Bryan, Khyatiben V Pathak, et al.
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