Year |
Citation |
Score |
2023 |
Luo W, Demidov V, Shen Q, Girão H, Chakraborty M, Maiorov A, Ataullakhanov FI, Lin C, Maiato H, Grishchuk EL. CLASP2 recognizes tubulins exposed at the microtubule plus-end in a nucleotide state-sensitive manner. Science Advances. 9: eabq5404. PMID 36598991 DOI: 10.1126/sciadv.abq5404 |
0.726 |
|
2022 |
Tripathy SK, Demidov VM, Gonchar IV, Wu S, Ataullakhanov FI, Grishchuk EL. Ultrafast Force-Clamp Spectroscopy of Microtubule-Binding Proteins. Methods in Molecular Biology (Clifton, N.J.). 2478: 609-650. PMID 36063336 DOI: 10.1007/978-1-0716-2229-2_22 |
0.44 |
|
2021 |
Tarasovetc EV, Allu PK, Wimbish RT, DeLuca JG, Cheeseman IM, Black BE, Grishchuk EL. Permitted and restricted steps of human kinetochore assembly in mitotic cell extracts. Molecular Biology of the Cell. mbcE20070461. PMID 33956511 DOI: 10.1091/mbc.E20-07-0461 |
0.497 |
|
2021 |
Zaytsev AV, Ataullakhanov FI, Grishchuk EL. Highly Transient Molecular Interactions Underlie the Stability of Kinetochore-Microtubule Attachment During Cell Division. Cellular and Molecular Bioengineering. 6. PMID 24376473 DOI: 10.1007/s12195-013-0309-4 |
0.61 |
|
2019 |
Chakraborty M, Tarasovetc EV, Zaytsev AV, Godzi M, Figueiredo AC, Ataullakhanov FI, Grishchuk EL. Microtubule end conversion mediated by motors and diffusing proteins with no intrinsic microtubule end-binding activity. Nature Communications. 10: 1673. PMID 30975984 DOI: 10.1038/s41467-019-09411-7 |
0.753 |
|
2019 |
Trivedi P, Zaytsev AV, Godzi M, Ataullakhanov FI, Grishchuk EL, Stukenberg PT. The binding of Borealin to microtubules underlies a tension independent kinetochore-microtubule error correction pathway. Nature Communications. 10: 682. PMID 30737408 DOI: 10.1038/s41467-019-08418-4 |
0.569 |
|
2018 |
Gudimchuk N, Tarasovetc EV, Mustyatsa V, Drobyshev AL, Vitre B, Cleveland DW, Ataullakhanov FI, Grishchuk EL. Probing Mitotic CENP-E Kinesin with the Tethered Cargo Motion Assay and Laser Tweezers. Biophysical Journal. 114: 2640-2652. PMID 29874614 DOI: 10.1016/j.bpj.2018.04.017 |
0.454 |
|
2018 |
Chakraborty M, Tarasovetc EV, Grishchuk EL. In vitro reconstitution of lateral to end-on conversion of kinetochore-microtubule attachments. Methods in Cell Biology. 144: 307-327. PMID 29804674 DOI: 10.1016/bs.mcb.2018.03.018 |
0.753 |
|
2017 |
Monda JK, Whitney IP, Tarasovetc EV, Wilson-Kubalek E, Milligan RA, Grishchuk EL, Cheeseman IM. Microtubule Tip Tracking by the Spindle and Kinetochore Protein Ska1 Requires Diverse Tubulin-Interacting Surfaces. Current Biology : Cb. PMID 29153323 DOI: 10.1016/J.Cub.2017.10.018 |
0.644 |
|
2017 |
Lampson MA, Grishchuk EL. Mechanisms to Avoid and Correct Erroneous Kinetochore-Microtubule Attachments. Biology. 6. PMID 28067761 DOI: 10.3390/Biology6010001 |
0.527 |
|
2015 |
Barisic M, Silva e Sousa R, Tripathy SK, Magiera MM, Zaytsev AV, Pereira AL, Janke C, Grishchuk EL, Maiato H. Mitosis. Microtubule detyrosination guides chromosomes during mitosis. Science (New York, N.Y.). 348: 799-803. PMID 25908662 DOI: 10.1126/Science.Aaa5175 |
0.515 |
|
2015 |
Zaytsev AV, Mick JE, Maslennikov E, Nikashin B, DeLuca JG, Grishchuk EL. Multisite phosphorylation of the NDC80 complex gradually tunes its microtubule-binding affinity. Molecular Biology of the Cell. 26: 1829-44. PMID 25808492 DOI: 10.1091/Mbc.E14-11-1539 |
0.458 |
|
2014 |
Kononova O, Kholodov Y, Theisen KE, Marx KA, Dima RI, Ataullakhanov FI, Grishchuk EL, Barsegov V. Tubulin bond energies and microtubule biomechanics determined from nanoindentation in silico. Journal of the American Chemical Society. 136: 17036-45. PMID 25389565 DOI: 10.1021/Ja506385P |
0.498 |
|
2014 |
Zaytsev AV, Sundin LJ, DeLuca KF, Grishchuk EL, DeLuca JG. Accurate phosphoregulation of kinetochore-microtubule affinity requires unconstrained molecular interactions. The Journal of Cell Biology. 206: 45-59. PMID 24982430 DOI: 10.1083/Jcb.201312107 |
0.512 |
|
2014 |
Vitre B, Gudimchuk N, Borda R, Kim Y, Heuser JE, Cleveland DW, Grishchuk EL. Kinetochore-microtubule attachment throughout mitosis potentiated by the elongated stalk of the kinetochore kinesin CENP-E. Molecular Biology of the Cell. 25: 2272-81. PMID 24920822 DOI: 10.1091/Mbc.E14-01-0698 |
0.479 |
|
2014 |
Volkov VA, Zaytsev AV, Grishchuk EL. Preparation of segmented microtubules to study motions driven by the disassembling microtubule ends. Journal of Visualized Experiments : Jove. PMID 24686554 DOI: 10.3791/51150 |
0.543 |
|
2013 |
Gudimchuk N, Vitre B, Kim Y, Kiyatkin A, Cleveland DW, Ataullakhanov FI, Grishchuk EL. Kinetochore kinesin CENP-E is a processive bi-directional tracker of dynamic microtubule tips. Nature Cell Biology. 15: 1079-88. PMID 23955301 DOI: 10.1038/Ncb2831 |
0.581 |
|
2013 |
Volkov VA, Zaytsev AV, Gudimchuk N, Grissom PM, Gintsburg AL, Ataullakhanov FI, McIntosh JR, Grishchuk EL. Long tethers provide high-force coupling of the Dam1 ring to shortening microtubules. Proceedings of the National Academy of Sciences of the United States of America. 110: 7708-13. PMID 23610433 DOI: 10.1073/Pnas.1305821110 |
0.688 |
|
2013 |
McIntosh JR, O'Toole E, Zhudenkov K, Morphew M, Schwartz C, Ataullakhanov FI, Grishchuk EL. Conserved and divergent features of kinetochores and spindle microtubule ends from five species. The Journal of Cell Biology. 200: 459-74. PMID 23420873 DOI: 10.1083/Jcb.201209154 |
0.675 |
|
2012 |
Schmidt JC, Arthanari H, Boeszoermenyi A, Dashkevich NM, Wilson-Kubalek EM, Monnier N, Markus M, Oberer M, Milligan RA, Bathe M, Wagner G, Grishchuk EL, Cheeseman IM. The kinetochore-bound Ska1 complex tracks depolymerizing microtubules and binds to curved protofilaments. Developmental Cell. 23: 968-80. PMID 23085020 DOI: 10.1016/J.Devcel.2012.09.012 |
0.589 |
|
2010 |
McIntosh JR, Volkov V, Ataullakhanov FI, Grishchuk EL. Tubulin depolymerization may be an ancient biological motor. Journal of Cell Science. 123: 3425-34. PMID 20930138 DOI: 10.1242/Jcs.067611 |
0.721 |
|
2010 |
Grishchuk EL, Ataullakhanov FI. In vitro assays to study the tracking of shortening microtubule ends and to measure associated forces. Methods in Cell Biology. 95: 657-76. PMID 20466158 DOI: 10.1016/S0091-679X(10)95033-4 |
0.55 |
|
2009 |
Fedyanina OS, Book AJ, Grishchuk EL. Tubulin heterodimers remain functional for one cell cycle after the inactivation of tubulin-folding cofactor D in fission yeast cells. Yeast (Chichester, England). 26: 235-47. PMID 19330768 DOI: 10.1002/yea.1663 |
0.318 |
|
2009 |
Welburn JP, Grishchuk EL, Backer CB, Wilson-Kubalek EM, Yates JR, Cheeseman IM. The human kinetochore Ska1 complex facilitates microtubule depolymerization-coupled motility. Developmental Cell. 16: 374-85. PMID 19289083 DOI: 10.1016/J.Devcel.2009.01.011 |
0.591 |
|
2009 |
Grissom PM, Fiedler T, Grishchuk EL, Nicastro D, West RR, McIntosh JR. Kinesin-8 from fission yeast: a heterodimeric, plus-end-directed motor that can couple microtubule depolymerization to cargo movement. Molecular Biology of the Cell. 20: 963-72. PMID 19037096 DOI: 10.1091/Mbc.E08-09-0979 |
0.757 |
|
2008 |
McIntosh JR, Grishchuk EL, Morphew MK, Efremov AK, Zhudenkov K, Volkov VA, Cheeseman IM, Desai A, Mastronarde DN, Ataullakhanov FI. Fibrils connect microtubule tips with kinetochores: a mechanism to couple tubulin dynamics to chromosome motion. Cell. 135: 322-33. PMID 18957206 DOI: 10.1016/J.Cell.2008.08.038 |
0.687 |
|
2008 |
Grishchuk EL, Efremov AK, Volkov VA, Spiridonov IS, Gudimchuk N, Westermann S, Drubin D, Barnes G, McIntosh JR, Ataullakhanov FI. The Dam1 ring binds microtubules strongly enough to be a processive as well as energy-efficient coupler for chromosome motion. Proceedings of the National Academy of Sciences of the United States of America. 105: 15423-8. PMID 18824692 DOI: 10.1073/Pnas.0807859105 |
0.627 |
|
2007 |
Efremov A, Grishchuk EL, McIntosh JR, Ataullakhanov FI. In search of an optimal ring to couple microtubule depolymerization to processive chromosome motions. Proceedings of the National Academy of Sciences of the United States of America. 104: 19017-22. PMID 18029449 DOI: 10.1073/Pnas.0709524104 |
0.643 |
|
2007 |
Grishchuk EL, Spiridonov IS, McIntosh JR. Mitotic chromosome biorientation in fission yeast is enhanced by dynein and a minus-end-directed, kinesin-like protein. Molecular Biology of the Cell. 18: 2216-25. PMID 17409356 DOI: 10.1091/Mbc.E06-11-0987 |
0.669 |
|
2006 |
Grishchuk EL, McIntosh JR. Microtubule depolymerization can drive poleward chromosome motion in fission yeast. The Embo Journal. 25: 4888-96. PMID 17036054 DOI: 10.1038/Sj.Emboj.7601353 |
0.647 |
|
2006 |
Fedyanina OS, Mardanov PV, Tokareva EM, McIntosh JR, Grishchuk EL. Chromosome segregation in fission yeast with mutations in the tubulin folding cofactor D. Current Genetics. 50: 281-94. PMID 17004072 DOI: 10.1007/S00294-006-0095-9 |
0.594 |
|
2005 |
Grishchuk EL, Molodtsov MI, Ataullakhanov FI, McIntosh JR. Force production by disassembling microtubules. Nature. 438: 384-8. PMID 16292315 DOI: 10.1038/Nature04132 |
0.65 |
|
2005 |
Molodtsov MI, Ermakova EA, Shnol EE, Grishchuk EL, McIntosh JR, Ataullakhanov FI. A molecular-mechanical model of the microtubule. Biophysical Journal. 88: 3167-79. PMID 15722432 DOI: 10.1529/Biophysj.104.051789 |
0.628 |
|
2002 |
McIntosh JR, Grishchuk EL, West RR. Chromosome-microtubule interactions during mitosis. Annual Review of Cell and Developmental Biology. 18: 193-219. PMID 12142285 DOI: 10.1146/Annurev.Cellbio.18.032002.132412 |
0.693 |
|
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