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Nature|October 18, 2013
Slowly fading super-luminous supernovae that are not pair-instability explosionsM Nicholl, S J Smartt, A Jerkstrand, et al.Biodata Mining|August 4, 2017
Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individualsEmily R Holzinger, Shefali S Verma, Carrie B Moore, et al.Nature Communications|February 14, 2026
Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxiaBenita Menden, Rana D Incebacak Eltemur, German Demidov, et al.Cancer Discovery|April 17, 2023
Comutations and KRASG12C Inhibitor Efficacy in Advanced NSCLCMarcelo V Negrao, Haniel A Araujo, Giuseppe Lamberti, et al.Blood|June 25, 2015
Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWFJennifer E Huffman, Paul S de Vries, Alanna C Morrison, et al.Plos Pathogens|December 23, 2024
Systematic assessment of COVID-19 host genetics using whole genome sequencing dataAxel Schmidt, Nicolas Casadei, Fabian Brand, et al.Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|March 29, 2026
Next generation sequencing approaches for the detection and characterization of enteroviruses in clinical, public health, and research settings: Expert view of the European non-polio enterovirus network (ENPEN)Kimberley S M Benschop, Florian Zwagemaker, Lili Andersson-Li, et al.Science (New York, N.Y.)|October 31, 2024
Brain malformations and seizures by impaired chaperonin function of TRiCFlorian Kraft, Piere Rodriguez-Aliaga, Weimin Yuan, et al.Nature Communications|February 1, 2020
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathyHolger Hengel, Célia Bosso-Lefèvre, George Grady, et al.Nature Medicine|January 17, 2025
Genomic reanalysis of a pan-European rare-disease resource yields new diagnosesSteven Laurie, Wouter Steyaert, Elke de Boer, et al.Pageof 149