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JAMA Neurology|December 17, 2019
Nilotinib Effects on Safety, Tolerability, and Potential Biomarkers in Parkinson Disease: A Phase 2 Randomized Clinical TrialFernando L Pagan, Michaeline L Hebron, Barbara Wilmarth, et al.Blood|July 9, 2020
Phosphoproteomic quantitation and causal analysis reveal pathways in GPVI/ITAM-mediated platelet activation programsÖzgün Babur, Alexander R Melrose, Jennifer M Cunliffe, et al.Scientific Reports|October 9, 2023
The amniotic fluid proteome changes across gestation in humans and rhesus macaquesLyndsey E Shorey-Kendrick, B Adam Crosland, Eliot R Spindel, et al.Research and Practice in Thrombosis and Haemostasis|March 12, 2025
Characterization of the procoagulant phenotype of amniotic fluid across gestation in rhesus macaques and humansChih Jen Yang, Lyndsey E Shorey-Kendrick, Cristina Puy, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 16, 2024
Clinical signatures of genetic epilepsies precede diagnosis in electronic medical records of 32,000 individualsPeter D Galer, Shridhar Parthasarathy, Julie Xian, et al.American Journal of Human Genetics|November 22, 2022
A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanismShridhar Parthasarathy, Sarah McKeown Ruggiero, Antoinette Gelot, et al.Journal of Proteomics|January 15, 2018
MHC class I loaded ligands from breast cancer cell lines: A potential HLA-I-typed antigen collectionDmitri V Rozanov, Nikita D Rozanov, Kami E Chiotti, et al.Medrxiv : the Preprint Server for Health Sciences|March 13, 2026
Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant ClassificationTobias Brünger, Ilona Krey, Suyeon Kim, et al.Pageof 14