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Science (New York, N.Y.)|August 30, 2008
The structure of an open form of an E. coli mechanosensitive channel at 3.45 A resolutionWenjian Wang, Susan S Black, Michelle D Edwards, et al.Proceedings of the National Academy of Sciences of the United States of America|September 27, 2012
Conformational state of the MscS mechanosensitive channel in solution revealed by pulsed electron-electron double resonance (PELDOR) spectroscopyChristos Pliotas, Richard Ward, Emma Branigan, et al.Immunology and Cell Biology|January 25, 2018
GPR65 inhibits experimental autoimmune encephalomyelitis through CD4+ T cell independent mechanisms that include effects on iNKT cellsRushika C Wirasinha, Dipti Vijayan, Nicola J Smith, et al.Genes and Immunity|October 12, 2007
Haplotypes of the interleukin 7 receptor alpha gene are correlated with altered expression in whole blood cells in multiple sclerosisF C McKay, L I Swain, S D Schibeci, et al.Journal of Autoimmunity|April 15, 2008
CD127 immunophenotyping suggests altered CD4+ T cell regulation in primary progressive multiple sclerosisFiona C McKay, Louisa I Swain, Stephen D Schibeci, et al.Biophysical Journal|February 25, 2014
Probing the structure of the mechanosensitive channel of small conductance in lipid bilayers with pulsed electron-electron double resonanceRichard Ward, Christos Pliotas, Emma Branigan, et al.Mutation Research|December 6, 2001
Cellular determinants of the mutational specificity of 1-nitroso-6-nitropyrene and 1-nitroso-8-nitropyrene in the lacI gene of Escherichia coliI B Lambert, C Carroll, N Laycock, et al.European Journal of Human Genetics : EJHG|December 4, 2002
The significance of paired MEFV mutations in individuals without symptoms of familial Mediterranean feverMehmet Tunca, Servet Akar, Philip N Hawkins, et al.Journal of Structural Biology|October 18, 2008
JADAS: a customizable automated data acquisition system and its application to ice-embedded single particlesJunjie Zhang, Natsuko Nakamura, Yuko Shimizu, et al.The Quarterly Journal of Medicine|March 1, 1994
Familial nephropathic systemic amyloidosis caused by apolipoprotein AI variant Arg26D M Vigushin, J Gough, D Allan, et al.Pageof 64