We believe that basic research and the cultivation of scientific knowledge is critical for us to stay connected with our customers and to drive scientific breakthroughs. At NEB, over 30 labs participate in research projects, which are aided by post-doctoral fellows and students in Masters and Ph.D. programs. NEB researchers have authored or co-authored over 1,200 publications (as of 1/19) many of which are in peer-reviewed journals. Further, NEB products have been used successfully in numerous publications by scientists throughout the world.
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Your search returned 2114 results.
|2010||Visualizing the structural changes of bacteriophage epsilon 15 and its Salmonella host during infection||J. Mol. Biol.||Chang, J.T., Schmid, M.F., Haase-Pettingell, C., Weigele, P.R., King, J.A., and Chiu, W.|
|1988||Cloning and sequencing the HinfI restriction and modification genes.||Gene||Chandrasegaran, S., Lunnen, K.D., Smith, H.O., and Wilson, G.G.|
|2015||Tissue-specific epigenetics in gene neighborhoods: myogenic transcription factor genes||Hum Mol Genet||Chandra, S., Terragni, J., Zhang, G., Pradhan, S., Haushka, S., Johnston, D., Baribault, C., Lacey, M. and Ehrlich, M.|
|2014||Myogenic differential methylation: diverse associations with chromatin structure||Biology (Basel)||Chandra S, Baribault C, Lacey M, Ehrlich M||Epigenetics|
|2004||Cloning of CviPII nicking and modification system from chlorella virus NYs-1 and application of Nt.CviPII in random DNA amplification.||Nucl.Acids Res.||Chan, S.H., Zhu, Z., Van Etten, J.L.and Xu, S.Y.|
|2006||Cloning of Nt.CviQII nicking endonuclease and its cognate methyltransferase: M.CviQII methylates AG sequences.||Protein Expr.Purif.||Chan, S.H., Zhu, Z., Van Etten, J.L.and Xu, S.Y.|
|2011||Natural and engineered nicking endonucleases--from cleavage mechanism to engineering of strand-specificity.||Nucl.Acids.Res.||Chan, S.H., Stoddard, B.L.and Xu, S.Y.|
|2010||Cofactor requirement of HpyAV restriction endonuclease.||PLoS ONE||Chan, S.H., Opitz, L., Higgins, L., O'loane, D.and Xu, S.Y.|
|2007||Catalytic domain of restriction endonuclease BmrI as a cleavage module for engineering endonucleases with novel substrate specificities.||Nucl.Acids.Res.||Chan, S-H, Boa, Y., Ciszak, E., Laget, S.and Xu, S-Y.|
|2015||Accurate DNA Assembly and Genome Engineering with Optimied Uracil Excision Cloning||ACS Synthetic Biology||Cavaleiro, A.M., Kim, S.H., Seppälä, S., Nielsen, M.T., Nørholm, M.H.H.|