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Cancer Discovery|October 10, 2013
Hypoxia induces phenotypic plasticity and therapy resistance in melanoma via the tyrosine kinase receptors ROR1 and ROR2Michael P O'Connell, Katie Marchbank, Marie R Webster, et al.American Journal of Human Genetics|December 3, 2013
Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinismJames A Poulter, Musallam Al-Araimi, Ivan Conte, et al.American Journal of Human Genetics|November 28, 2016
Mutations in REEP6 Cause Autosomal-Recessive Retinitis PigmentosaGavin Arno, Smriti A Agrawal, Aiden Eblimit, et al.NPJ Digital Medicine|July 16, 2019
Deep learning versus human graders for classifying diabetic retinopathy severity in a nationwide screening programPaisan Raumviboonsuk, Jonathan Krause, Peranut Chotcomwongse, et al.NPJ Digital Medicine|July 26, 2019
Erratum: Author Correction: Deep learning versus human graders for classifying diabetic retinopathy severity in a nationwide screening programPaisan Ruamviboonsuk, Jonathan Krause, Peranut Chotcomwongse, et al.The New England Journal of Medicine|July 29, 2011
Origins of the E. coli strain causing an outbreak of hemolytic-uremic syndrome in GermanyDavid A Rasko, Dale R Webster, Jason W Sahl, et al.Human Mutation|November 30, 2020
New variants and in silico analyses in GRK1 associated Oguchi diseaseJames A Poulter, Molly S C Gravett, Rachel L Taylor, et al.Science (New York, N.Y.)|February 13, 2001
The detection of large HNO3-containing particles in the winter Arctic stratosphereD W Fahey, R S Gao, K S Carslaw, et al.Journal of Medicinal Chemistry|March 13, 2018
Structure-based Design of Pyridone-Aminal eFT508 Targeting Dysregulated Translation by Selective Mitogen-activated Protein Kinase Interacting Kinases 1 and 2 (MNK1/2) InhibitionSiegfried H Reich, Paul A Sprengeler, Gary G Chiang, et al.Nature Genetics|July 31, 2012
NMNAT1 mutations cause Leber congenital amaurosisMarni J Falk, Qi Zhang, Eiko Nakamaru-Ogiso, et al.Pageof 125