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Frontiers in Genetics|April 8, 2022
CLCC1 c. 75C>A Mutation in Pakistani Derived Retinitis Pigmentosa Families Likely Originated With a Single Founder Mutation 2,000-5,000 Years AgoYan Ma, Xun Wang, Nadav Shoshany, et al.Human Molecular Genetics|October 4, 2017
A mutation in IFT43 causes non-syndromic recessive retinal degenerationPooja Biswas, Jacque L Duncan, Muhammad Ali, et al.Physical Review Letters|September 16, 2000
Complete stabilization of neoclassical tearing modes with lower hybrid current drive on COMPASS-D. RF teamsC D Warrick, R J Buttery, G Cunningham, et al.Science (New York, N.Y.)|October 19, 2019
Hierarchical interlocked orthogonal faulting in the 2019 Ridgecrest earthquake sequenceZachary E Ross, Benjamín Idini, Zhe Jia, et al.Science (New York, N.Y.)|February 11, 2012
Near-field deformation from the El Mayor-Cucapah earthquake revealed by differential LIDARMichael E Oskin, J Ramon Arrowsmith, Alejandro Hinojosa Corona, et al.The Journal of Cell Biology|March 19, 2025
Structural characterization and inhibition of the interaction between ch-TOG and TACC3James Shelford, Selena G Burgess, Elena Rostkova, et al.Ophthalmology Science|May 27, 2026
Association of Autosomal Dominant Snowflake Vitreoretinal Degeneration with RetinoschisisBikash R Pattnaik, Ken K Nischal, Oleg Alekseev, et al.Human Genetics|January 22, 2005
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient populationXiao Mei Ouyang, Denise Yan, Li Lin Du, et al.Proceedings of the National Academy of Sciences of the United States of America|September 19, 2019
Heme binding to human CLOCK affects interactions with the E-boxSamuel L Freeman, Hanna Kwon, Nicola Portolano, et al.Nature|December 5, 2008
Partial rupture of a locked patch of the Sumatra megathrust during the 2007 earthquake sequenceA Ozgun Konca, Jean-Philippe Avouac, Anthony Sladen, et al.Pageof 42