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The Journal of Chemical Physics|September 11, 2012
High resolution NMR study of T1 magnetic relaxation dispersion. III. Influence of spin 1/2 hetero-nuclei on spin relaxation and polarization transfer among strongly coupled protonsSergey E Korchak, Konstantin L Ivanov, Andrey N Pravdivtsev, et al.Journal of Molecular Biology|September 23, 2008
Solution structure and characterization of the DNA-binding activity of the B3BP-Smr domainTammo Diercks, Eiso AB, Mark A Daniels, et al.Proteins|October 4, 2007
The HhH domain of the human DNA repair protein XPF forms stable homodimersDevashish Das, Konstantinos Tripsianes, Nicolaas G J Jaspers, et al.Science (New York, N.Y.)|July 17, 2004
Structure and flexibility adaptation in nonspecific and specific protein-DNA complexesCharalampos G Kalodimos, Nikolaos Biris, Alexandre M J J Bonvin, et al.Journal of Molecular Biology|May 20, 2009
Specificity and affinity of Lac repressor for the auxiliary operators O2 and O3 are explained by the structures of their protein-DNA complexesJulija Romanuka, Gert E Folkers, Nikolaos Biris, et al.Journal of Magnetic Resonance (San Diego, Calif. : 1997)|November 4, 2015
Spin polarization transfer mechanisms of SABRE: A magnetic field dependent studyAndrey N Pravdivtsev, Konstantin L Ivanov, Alexandra V Yurkovskaya, et al.Biochemistry|June 12, 2002
Mapping the targeted membrane pore formation mechanism by solution NMR: the nisin Z and lipid II interaction in SDS micellesShang-Te Hsu, Eefjan Breukink, Ben de Kruijff, et al.Structure (London, England : 1993)|April 10, 2012
The structure of the XPF-ssDNA complex underscores the distinct roles of the XPF and ERCC1 helix- hairpin-helix domains in ss/ds DNA recognitionDevashish Das, Gert E Folkers, Marc van Dijk, et al.Chembiochem : a European Journal of Chemical Biology|December 3, 2005
The solution structure of the AppA BLUF domain: insight into the mechanism of light-induced signalingJeffrey S Grinstead, Shang-Te D Hsu, Wouter Laan, et al.The Journal of Biological Chemistry|June 19, 2015
The Cerebro-oculo-facio-skeletal Syndrome Point Mutation F231L in the ERCC1 DNA Repair Protein Causes Dissociation of the ERCC1-XPF ComplexMaryam Faridounnia, Hans Wienk, Lidija Kovačič, et al.Pageof 6