Can we trust docking results? Evaluation of seven commonly used programs on PDBbind database D Plewczynski, M Łaźniewski, R Augustyniak, K Ginalski Journal of computational chemistry 32 (4), 742-755, 2011 | 325 | 2011 |
Detailed mechanism of squalene epoxidase inhibition by terbinafine M Nowosielski, M Hoffmann, LS Wyrwicz, P Stepniak, DM Plewczynski, ... Journal of chemical information and modeling 51 (2), 455-462, 2011 | 83 | 2011 |
VoteDock: consensus docking method for prediction of protein–ligand interactions D Plewczynski, M Łażniewski, MV Grotthuss, L Rychlewski, K Ginalski Journal of computational chemistry 32 (4), 568-581, 2011 | 80 | 2011 |
C16orf57, a gene mutated in poikiloderma with neutropenia, encodes a putative phosphodiesterase responsible for the U6 snRNA 3′ end modification S Mroczek, J Krwawicz, J Kutner, M Lazniewski, I Kuciński, K Ginalski, ... Genes & development 26 (17), 1911-1925, 2012 | 70 | 2012 |
Unfolding the mechanism of the AAA+ unfoldase VAT by a combined cryo-EM, solution NMR study R Huang, ZA Ripstein, R Augustyniak, M Lazniewski, K Ginalski, LE Kay, ... Proceedings of the National Academy of Sciences 113 (29), E4190-E4199, 2016 | 45 | 2016 |
Novel neuro-audiological findings and further evidence for TWNK involvement in Perrault syndrome M Ołdak, D Oziębło, A Pollak, I Stępniak, M Lazniewski, U Lechowicz, ... Journal of Translational Medicine 15 (1), 1-13, 2017 | 24 | 2017 |
The structural variability of the influenza A hemagglutinin receptor-binding site M Lazniewski, WK Dawson, T Szczepińska, D Plewczynski Briefings in functional genomics 17 (6), 415-427, 2018 | 23 | 2018 |
Novel transmembrane lipases of alpha/beta hydrolase fold M Lazniewski, K Steczkiewicz, L Knizewski, I Wawer, K Ginalski FEBS letters 585 (6), 870-874, 2011 | 15 | 2011 |
A heterozygous mutation in GOT1 is associated with familial macro-aspartate aminotransferase M Kulecka, A Wierzbicka, A Paziewska, M Mikula, A Habior, W Janczyk, ... Journal of hepatology 67 (5), 1026-1030, 2017 | 12 | 2017 |
RNA structure interactions and ribonucleoprotein processes of the influenza A virus WK Dawson, M Lazniewski, D Plewczynski Briefings in functional genomics 17 (6), 402-414, 2018 | 11 | 2018 |
Clinical and molecular characteristics of newly reported mitochondrial disease entity caused by biallelic PARS2 mutations E Ciara, D Rokicki, M Lazniewski, H Mierzewska, E Jurkiewicz, ... Journal of human genetics 63 (4), 473-485, 2018 | 11 | 2018 |
Binding Activity Prediction of Cyclin-Dependent Inhibitors I Saha, B Rak, SS Bhowmick, U Maulik, D Bhattacharjee, U Koch, ... Journal of chemical information and modeling 55 (7), 1469-1482, 2015 | 9 | 2015 |
Upregulation of MLK4 promotes migratory and invasive potential of breast cancer cells AA Marusiak, MK Prelowska, D Mehlich, M Lazniewski, K Kaminska, ... Oncogene 38 (15), 2860-2875, 2019 | 6 | 2019 |
One protein to rule them all: The role of CCCTC-binding factor in shaping human genome in health and disease M Lazniewski, WK Dawson, AM Rusek, D Plewczynski Seminars in cell & developmental biology 90, 114-127, 2019 | 4 | 2019 |
Inhibition of protein disulfide isomerase induces differentiation of acute myeloid leukemia cells J Chlebowska-Tuz, O Sokolowska, P Gaj, M Lazniewski, M Firczuk, ... Haematologica 103 (11), 1843-1852, 2018 | 4 | 2018 |
3DFlu: database of sequence and structural variability of the influenza hemagglutinin at population scale G Mazzocco, M Lazniewski, P Migdał, T Szczepińska, JP Radomski, ... Database 2016, 2016 | 4 | 2016 |
Novel COL12A1 variant as a cause of mild familial extracellular matrix-related myopathy A Jezela-Stanek, A Walczak, M Łaźniewski, J Kosińska, P Stawiński, ... Clinical genetics 95 (6), 736-738, 2019 | 1 | 2019 |
Free energy-based model of CTCF-mediated chromatin looping in the human genome WK Dawson, M Lazniewski, D Plewczynski Methods 181, 35-51, 2020 | | 2020 |
Chromatin: A Semi-Structured Polymer WK Dawson, M Lazniewski, D Plewczynski Academic Press, 2019 | | 2019 |
Novel neuro-audiological findings and further evidence for TWNK involvement in Perrault syndrome M Oldak, D Ozieblo, A Pollak, I Stepniak, M Lazniewski, U Lechowicz, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 189-189, 2018 | | 2018 |