-
1
-
-
33745275629
-
The chromosomal passenger complex: Guiding Aurora-B through mitosis
-
Vader, G.; Medema, R. H.; Lens, S. M. The chromosomal passenger complex: guiding Aurora-B through mitosis J. Cell Biol. 2006, 173, 833-837
-
(2006)
J. Cell Biol.
, vol.173
, pp. 833-837
-
-
Vader, G.1
Medema, R.H.2
Lens, S.M.3
-
2
-
-
34648825331
-
Chromosomal passengers: Conducting cell division
-
DOI 10.1038/nrm2257, PII NRM2257
-
Ruchaud, S.; Carmena, M.; Earnshaw, W. C. Chromosomal passengers: conducting cell division Nat. Rev. Mol. Cell Biol. 2007, 8, 798-812 (Pubitemid 47462135)
-
(2007)
Nature Reviews Molecular Cell Biology
, vol.8
, Issue.10
, pp. 798-812
-
-
Ruchaud, S.1
Carmena, M.2
Earnshaw, W.C.3
-
3
-
-
51649095569
-
The Aurora kinase family in cell division and cancer
-
Vader, G.; Lens, S. M. The Aurora kinase family in cell division and cancer Biochim. Biophys. Acta 2008, 1786, 60-72
-
(2008)
Biochim. Biophys. Acta
, vol.1786
, pp. 60-72
-
-
Vader, G.1
Lens, S.M.2
-
4
-
-
34648825331
-
Chromosomal passengers: Conducting cell division
-
DOI 10.1038/nrm2257, PII NRM2257
-
Ruchaud, S.; Carmena, M.; Earnshaw, W. C. Chromosomal passengers: conducting cell division Nat. Rev. Mol. Cell Biol. 2007, 8, 798-812 (Pubitemid 47462135)
-
(2007)
Nature Reviews Molecular Cell Biology
, vol.8
, Issue.10
, pp. 798-812
-
-
Ruchaud, S.1
Carmena, M.2
Earnshaw, W.C.3
-
5
-
-
0037044846
-
Crystal structure of Aurora-2, an oncogenic serine/threonine kinase
-
DOI 10.1074/jbc.C200426200
-
Cheetham, G. M. T.; Knegtel, R. M. A.; Coll, J. T.; Renwick, S. B.; Swenson, L.; Weber, P.; Lippke, J. A.; Austen, D. A. Crystal Structure of Aurora-2, an Oncogenic Serine/Threonine Kinase J. Biol. Chem. 2002, 277, 42419-42422 (Pubitemid 35285606)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.45
, pp. 42419-42422
-
-
Cheetham, G.M.T.1
Knegtel, R.M.A.2
Coll, J.T.3
Renwick, S.B.4
Swenson, L.5
Weber, P.6
Lippke, J.A.7
Austen, D.A.8
-
6
-
-
1842848073
-
Structures of the cancer-related Aurora-A, FAK, and EphA2 protein kinases from nanovolume crystallography
-
DOI 10.1016/S0969-2126(02)00907-3, PII S0969212602009073
-
Nowakowski, J.; Cronin, C. N.; McRee, D. E.; Knuth, M. W.; Nelson, C. G.; Pavletich, N. P.; Rogers, J.; Sang, B.-C.; Schelbe, D. N.; Swanson, R. V.; Thompson, D. A. Structures of the Cancer-Related Aurora-A, FAK, and EphA2 Protein Kinases from Nanovolume Crystallography Structure 2002, 10, 1659-1667 (Pubitemid 35452573)
-
(2002)
Structure
, vol.10
, Issue.12
, pp. 1659-1667
-
-
Nowakowski, J.1
Cronin, C.N.2
McRee, D.E.3
Knuth, M.W.4
Nelson, C.G.5
Pavletich, N.P.6
Rogers, J.7
Sang, B.-C.8
Scheibe, D.N.9
Swanson, R.V.10
Thompson, D.A.11
-
7
-
-
0242330123
-
Structural basis of Aurora-A activation by TPX2 at the mitotic spindle
-
DOI 10.1016/S1097-2765(03)00392-7
-
Bayliss, R.; Sardon, T.; Vernos, I.; Conti, E. Structural Basis of Aurora-A Activation by TPX2 at the Mitotic Spindle Mol. Cell 2003, 12, 851-862 (Pubitemid 37352779)
-
(2003)
Molecular Cell
, vol.12
, Issue.4
, pp. 851-862
-
-
Bayliss, R.1
Sardon, T.2
Vernos, I.3
Conti, E.4
-
8
-
-
20844436307
-
Mechanism of Aurora B activation by INCENP and inhibition by hesperadin
-
DOI 10.1016/j.molcel.2005.03.031, PII S1097276505012244
-
Sessa, F.; Mapelli, M.; Ciferri, C.; Tarricone, C.; Areces, L. B.; Schneider, T. R.; Stukenberg, P. T.; Musacchio, A. Mechanism of Aurora B Activation by INCENP and Inhibition by Hesperadin Mol. Cell 2005, 18, 379-391 (Pubitemid 41350542)
-
(2005)
Molecular Cell
, vol.18
, Issue.3
, pp. 379-391
-
-
Sessa, F.1
Mapelli, M.2
Ciferri, C.3
Tarricone, C.4
Areces, L.B.5
Schneider, T.R.6
Stukenberg, P.T.7
Musacchio, A.8
-
9
-
-
44949157910
-
Molecular Basis of Drug Resistance in Aurora Kinases
-
DOI 10.1016/j.chembiol.2008.04.013, PII S1074552108001671
-
Girdler, F.; Sessa, F.; Patercoli, S.; Villa, F.; Musacchio, A.; Taylor, S. Molecular basis of drug resistance in aurora kinases Chem. Biol. 2008, 15, 552-562 (Pubitemid 351815053)
-
(2008)
Chemistry and Biology
, vol.15
, Issue.6
, pp. 552-562
-
-
Girdler, F.1
Sessa, F.2
Patercoli, S.3
Villa, F.4
Musacchio, A.5
Taylor, S.6
-
10
-
-
84862946285
-
Selective aurora kinase inhibitors identified using a taxol-induced checkpoint sensitivity screen
-
Kwiatkowski, N.; Deng, X.; Wang, J.; Tan, L.; Villa, F.; Santaguida, S.; Huang, H. C.; Mitchison, T.; Musacchio, A.; Gray, N. Selective aurora kinase inhibitors identified using a taxol-induced checkpoint sensitivity screen ACS Chem. Biol. 2012, 7, 185-196
-
(2012)
ACS Chem. Biol.
, vol.7
, pp. 185-196
-
-
Kwiatkowski, N.1
Deng, X.2
Wang, J.3
Tan, L.4
Villa, F.5
Santaguida, S.6
Huang, H.C.7
Mitchison, T.8
Musacchio, A.9
Gray, N.10
-
11
-
-
49849100633
-
Reversine, a novel Aurora kinases inhibitor, inhibits colony formation of human acute myeloid leukemia cells
-
D'Alise, A. M.; Amabile, G.; Iovino, M.; Di Giorgio, F. P.; Bartiromo, M.; Sessa, F.; Villa, F.; Musacchio, A.; Cortese, R. Reversine, a novel Aurora kinases inhibitor, inhibits colony formation of human acute myeloid leukemia cells Mol. Cancer Ther. 2008, 7, 1140-1149
-
(2008)
Mol. Cancer Ther.
, vol.7
, pp. 1140-1149
-
-
D'Alise, A.M.1
Amabile, G.2
Iovino, M.3
Di Giorgio, F.P.4
Bartiromo, M.5
Sessa, F.6
Villa, F.7
Musacchio, A.8
Cortese, R.9
-
12
-
-
42449137119
-
Discovery of selective aminothiazole aurora kinase inhibitors
-
Andersen, C. B.; Wan, Y.; Chang, J. W.; Riggs, B.; Lee, C.; Liu, Y.; Sessa, F.; Villa, F.; Kwiatkowski, N.; Suzuki, M.; Nallan, L.; Heald, R.; Musacchio, A.; Gray, N. S. Discovery of selective aminothiazole aurora kinase inhibitors ACS Chem. Biol. 2008, 3, 180-192
-
(2008)
ACS Chem. Biol.
, vol.3
, pp. 180-192
-
-
Andersen, C.B.1
Wan, Y.2
Chang, J.W.3
Riggs, B.4
Lee, C.5
Liu, Y.6
Sessa, F.7
Villa, F.8
Kwiatkowski, N.9
Suzuki, M.10
Nallan, L.11
Heald, R.12
Musacchio, A.13
Gray, N.S.14
-
13
-
-
52949141884
-
Modulation of kinase-inhibitor interactions by auxiliary protein binding: Crystallography studies on Aurora A interactions with VX-680 and with TPX2
-
Zhao, B.; Smallwood, A.; Yang, J.; Koretke, K.; Nurse, K.; Calamari, A.; Kirkpatrick, R. B.; Lai, Z. Modulation of kinase-inhibitor interactions by auxiliary protein binding: Crystallography studies on Aurora A interactions with VX-680 and with TPX2 Protein Sci. 2008, 17, 1791-1797
-
(2008)
Protein Sci.
, vol.17
, pp. 1791-1797
-
-
Zhao, B.1
Smallwood, A.2
Yang, J.3
Koretke, K.4
Nurse, K.5
Calamari, A.6
Kirkpatrick, R.B.7
Lai, Z.8
-
14
-
-
34247615972
-
Structural basis for potent inhibition of the Aurora kinases and a T315I multi-drug resistant mutant form of Abl kinase by VX-680
-
DOI 10.1016/j.canlet.2006.12.004, PII S0304383506006707
-
Cheetham, G. M.; Charlton, P. A.; Golec, J. M.; Pollard, J. R. Structural basis for potent inhibition of the Aurora kinases and a T315I multi-drug resistant mutant form of Abl kinase by VX-680 Cancer Lett. 2007, 251, 323-329 (Pubitemid 46669805)
-
(2007)
Cancer Letters
, vol.251
, Issue.2
, pp. 323-329
-
-
Cheetham, G.M.T.1
Charlton, P.A.2
Golec, J.M.C.3
Pollard, J.R.4
-
15
-
-
0041968963
-
Exploring the functional interactions between Aurora B, INCENP, and survivin in mitosis
-
DOI 10.1091/mbc.E02-11-0769
-
Honda, R.; Körner, R.; Nigg, E. Exploring the Functional Interactions between Aurora B, INCENP, and Survivin in Mitosis Mol. Biol. Cell 2003, 14, 3325-3341 (Pubitemid 37013130)
-
(2003)
Molecular Biology of the Cell
, vol.14
, Issue.8
, pp. 3325-3341
-
-
Honda, R.1
Korner, R.2
Nigg, E.A.3
-
16
-
-
84855724543
-
Phosphorylation at serine 331 is required for Aurora B activation
-
Petsalaki, E.; Akoumianaki, T.; Black, E. J.; Gillespie, D. A. F.; Zachos, G. Phosphorylation at serine 331 is required for Aurora B activation J. Cell Biol. 2011, 195, 449-466
-
(2011)
J. Cell Biol.
, vol.195
, pp. 449-466
-
-
Petsalaki, E.1
Akoumianaki, T.2
Black, E.J.3
Gillespie, D.A.F.4
Zachos, G.5
-
17
-
-
10344236486
-
Aurora-kinase inhibitors as anticancer agents
-
DOI 10.1038/nrc1502
-
Keen, N.; Taylor, S. Aurora-Kinase Inhibitors As Anticancer Agents Nat. Rev. Cancer 2002, 4, 927-936 (Pubitemid 39626216)
-
(2004)
Nature Reviews Cancer
, vol.4
, Issue.12
, pp. 927-936
-
-
Keen, N.1
Taylor, S.2
-
18
-
-
66549124940
-
Biochemical characterization of GSK1070916, a potent and selective inhibitor of Aurora B and Aurora C kinases with an extremely long residence time1
-
Anderson, K.; Lai, Z.; McDonald, O. B.; Stuart, J. D.; Nartey, E. N.; Hardwicke, M. A.; Newlander, K.; Dhanak, D.; Adams, J.; Patrick, D.; Copeland, R. A.; Tummino, P. J.; Yang, J. Biochemical characterization of GSK1070916, a potent and selective inhibitor of Aurora B and Aurora C kinases with an extremely long residence time1 Biochem. J. 2009, 420, 259-265
-
(2009)
Biochem. J.
, vol.420
, pp. 259-265
-
-
Anderson, K.1
Lai, Z.2
McDonald, O.B.3
Stuart, J.D.4
Nartey, E.N.5
Hardwicke, M.A.6
Newlander, K.7
Dhanak, D.8
Adams, J.9
Patrick, D.10
Copeland, R.A.11
Tummino, P.J.12
Yang, J.13
-
19
-
-
77952684936
-
Discovery of GSK1070916, a potent and selective inhibitor of Aurora B/C kinase
-
Adams, N. D.; Adams, J. L.; Burgess, J. L.; Chaudhari, A. M.; Copeland, R. A.; Donatelli, C. A.; Drewry, D. H.; Fisher, K. E.; Hamajima, T.; Hardwicke, M. A.; Huffman, W. F.; Koretke-Brown, K. K.; Lai, Z. V.; McDonald, O. B.; Nakamura, H.; Newlander, K. A.; Oleykowski, C. A.; Parrish, C. A.; Patrick, D. R.; Plant, R.; Sarpong, M. A.; Sasaki, K.; Schmidt, S. J.; Silva, D. J.; Sutton, D.; Tang, J.; Thompson, C. S.; Tummino, P. J.; Wang, J. C.; Xiang, H.; Yang, J.; Dhanak, D. Discovery of GSK1070916, a potent and selective inhibitor of Aurora B/C kinase J. Med. Chem. 2010, 53, 3973-4001
-
(2010)
J. Med. Chem.
, vol.53
, pp. 3973-4001
-
-
Adams, N.D.1
Adams, J.L.2
Burgess, J.L.3
Chaudhari, A.M.4
Copeland, R.A.5
Donatelli, C.A.6
Drewry, D.H.7
Fisher, K.E.8
Hamajima, T.9
Hardwicke, M.A.10
Huffman, W.F.11
Koretke-Brown, K.K.12
Lai, Z.V.13
McDonald, O.B.14
Nakamura, H.15
Newlander, K.A.16
Oleykowski, C.A.17
Parrish, C.A.18
Patrick, D.R.19
Plant, R.20
Sarpong, M.A.21
Sasaki, K.22
Schmidt, S.J.23
Silva, D.J.24
Sutton, D.25
Tang, J.26
Thompson, C.S.27
Tummino, P.J.28
Wang, J.C.29
Xiang, H.30
Yang, J.31
Dhanak, D.32
more..
-
20
-
-
73949087301
-
MK-5108, a Highly Selective Aurora-A Kinase Inhibitor, Shows Antitumor Activity Alone and in Combination with Docetaxel
-
Shimomura, T.; Hasako, S.; Nakatsuru, Y.; Mita, T.; Ichikawa, K.; Kodera, T.; Sakai, T.; Nambu, T.; Miyamoto, M.; Takahashi, I.; Miki, S.; Kawanishi, N.; Ohkubo, M.; Kotani, H.; Iwasawa, Y. MK-5108, a Highly Selective Aurora-A Kinase Inhibitor, Shows Antitumor Activity Alone and in Combination with Docetaxel Mol. Cancer Ther. 2010, 9, 157-166
-
(2010)
Mol. Cancer Ther.
, vol.9
, pp. 157-166
-
-
Shimomura, T.1
Hasako, S.2
Nakatsuru, Y.3
Mita, T.4
Ichikawa, K.5
Kodera, T.6
Sakai, T.7
Nambu, T.8
Miyamoto, M.9
Takahashi, I.10
Miki, S.11
Kawanishi, N.12
Ohkubo, M.13
Kotani, H.14
Iwasawa, Y.15
-
21
-
-
34247259822
-
Antitumor activity of MLN8054, an orally active small-molecule inhibitor of Aurora a kinase
-
DOI 10.1073/pnas.0608798104
-
Manfredi, M. G.; Ecsedy, J. A.; Meetze, K. A.; Balani, S. K.; Burenkova, O.; Chen, W.; Galvin, K. M.; Hoar, K. M.; Huck, J. J.; LeRoy, P. J.; Ray, E. T.; Sells, T. B.; Stringer, B.; Stroud, S. G.; Vos, T. J.; Weatherhead, G. S.; Wysong, D. R.; Zhang, M.; Bolen, J. B.; Claiborne, C. F. Antitumor activity of MLN8054, an orally active small-molecule inhibitor of Aurora A kinase Proc. Natl. Acad. Sci. U.S.A. 2007, 104, 4106-4111 (Pubitemid 47181586)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.10
, pp. 4106-4111
-
-
Manfredi, M.G.1
Ecsedy, J.A.2
Meetze, K.A.3
Balani, S.K.4
Burenkova, O.5
Chen, W.6
Galvin, K.M.7
Hoar, K.M.8
Huck, J.J.9
LeRoy, P.J.10
Ray, E.T.11
Sells, T.B.12
Stringer, B.13
Stroud, S.G.14
Vos, T.J.15
Weatherhead, G.S.16
Wysong, D.R.17
Zhang, M.18
Bolen, J.B.19
Claiborne, C.F.20
more..
-
22
-
-
34247603906
-
Discovery, synthesis, and in vivo activity of a new class of pyrazoloquinazolines as selective inhibitors of aurora B kinase
-
DOI 10.1021/jm061335f
-
Mortlock, A. A.; Foote, K. M.; Heron, N. M.; Jung, F. H.; Pasquet, G.; Lohmann, J.-J. M.; Warin, N.; Renaud, F.; De Savi, C.; Roberts, N. J.; Johnson, T.; Dousson, C. B.; Hill, G. B.; Perkins, D.; Hatter, G.; Wilkinson, R. W.; Wedge, S. R.; Heaton, S. P.; Odedra, R.; Keen, N. J.; Crafter, C.; Brown, E.; Thompson, K.; Brightwell, S.; Khatri, L.; Brady, M. C.; Kearney, S.; McKillop, D.; Rhead, S.; Parry, T.; Green, S. Discovery, Synthesis, and in Vivo Activity of a New Class of Pyrazoloquinazolines as Selective Inhibitors of Aurora B Kinase J. Med. Chem. 2007, 50, 2213-2224 (Pubitemid 46683074)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.9
, pp. 2213-2224
-
-
Mortlock, A.A.1
Foote, K.M.2
Heron, N.M.3
Jung, F.H.4
Pasquet, G.5
Lohmann, J.-J.M.6
Warin, N.7
Renaud, F.8
De Savi, C.9
Roberts, N.J.10
Johnson, T.11
Dousson, C.B.12
Hill, G.B.13
Perkins, D.14
Hatter, G.15
Wilkinson, R.W.16
Wedge, S.R.17
Heaton, S.P.18
Odedra, R.19
Keen, N.J.20
Crafter, C.21
Brown, E.22
Thompson, K.23
Brightwell, S.24
Khatri, L.25
Brady, M.C.26
Kearney, S.27
McKillop, D.28
Rhead, S.29
Parry, T.30
Green, S.31
more..
-
23
-
-
2342639645
-
VX-680, a potent and selective small-molecule inhibitor of the Aurora kinases, suppresses tumor growth in vivo
-
DOI 10.1038/nm1003
-
Harrington, E. A.; Bebbington, D.; Moore, J.; Rasmussen, R. K.; Ajose-Adeogun, A. O.; Nakayama, T.; Graham, J. A.; Demur, C.; Hercend, T.; Diu-Hercend, A.; Su, M.; Golec, J. M.; Miller, K. M. VX-680, a potent and selective small-molecule inhibitor of the Aurora kinases, suppresses tumor growth in vivo Nat. Med. 2004, 10, 262-267 (Pubitemid 38667616)
-
(2004)
Nature Medicine
, vol.10
, Issue.3
, pp. 262-267
-
-
Harrington, E.A.1
Bebbington, D.2
Moore, J.3
Rasmussen, R.K.4
Ajose-Adeogun, A.O.5
Nakayama, T.6
Graham, J.A.7
Demur, C.8
Hercend, T.9
Diu-Hercend, A.10
Su, M.11
Golec, J.M.C.12
Miller, K.M.13
-
24
-
-
31644438945
-
Structure of the kinase domain of an imatinib-resistant Abl mutant in complex with the aurora kinase inhibitor VX-680
-
DOI 10.1158/0008-5472.CAN-05-2788
-
Young, M. A.; Shah, N. P.; Chao, L. H.; Seeliger, M.; Milanov, Z. V.; Biggs, W. H., 3rd; Treiber, D. K.; Patel, H. K.; Zarrinkar, P. P.; Lockhart, D. J.; Sawyers, C. L.; Kuriyan, J. Structure of the Kinase Domain of an Imatinib-Resistant Abl Mutant in Complex with the Aurora Kinase Inhibitor VX-680 Cancer Res. 2006, 66, 1007-1014 (Pubitemid 43168337)
-
(2006)
Cancer Research
, vol.66
, Issue.2
, pp. 1007-1014
-
-
Young, M.A.1
Shah, N.P.2
Chao, L.H.3
Seeliger, M.4
Milanov, Z.V.5
Biggs III, W.H.6
Treiber, D.K.7
Patel, H.K.8
Zarrinkar, P.P.9
Lockhart, D.J.10
Sawyers, C.L.11
Kuriyan, J.12
-
25
-
-
79953774130
-
Crystal structures of ABL-related gene (ABL2) in complex with imatinib, tozasertib (VX-680), and a type i inhibitor of the triazole carbothioamide class
-
Salah, E.; Ugochukwu, E.; Barr, A. J.; von Delft, F.; Knapp, S.; Elkins, J. M. Crystal structures of ABL-related gene (ABL2) in complex with imatinib, tozasertib (VX-680), and a type I inhibitor of the triazole carbothioamide class J. Med. Chem. 2011, 54, 2359-2367
-
(2011)
J. Med. Chem.
, vol.54
, pp. 2359-2367
-
-
Salah, E.1
Ugochukwu, E.2
Barr, A.J.3
Von Delft, F.4
Knapp, S.5
Elkins, J.M.6
-
26
-
-
33746318035
-
Trans-activation of the DNA-damage signalling protein kinase Chk2 by T-loop exchange
-
DOI 10.1038/sj.emboj.7601209, PII 7601209
-
Oliver, A. W.; Paul, A.; Boxall, K. J.; Barrie, S. E.; Aherne, G. W.; Garrett, M. D.; Mittnacht, S.; Pearl, L. H. Trans-activation of the DNA-damage signalling protein kinase Chk2 by T-loop exchange EMBO J. 2006, 25, 3179-3190 (Pubitemid 44106768)
-
(2006)
EMBO Journal
, vol.25
, Issue.13
, pp. 3179-3190
-
-
Oliver, A.W.1
Paul, A.2
Boxall, K.J.3
Barrie, S.E.4
Aherne, G.W.5
Garrett, M.D.6
Mittnacht, S.7
Pearl, L.H.8
-
27
-
-
39449119544
-
Activation segment dimerization: A mechanism for kinase autophosphorylation of non-consensus sites
-
DOI 10.1038/emboj.2008.8, PII EMBOJ20088
-
Pike, A. C.; Rellos, P.; Niesen, F. H.; Turnbull, A.; Oliver, A. W.; Parker, S. A.; Turk, B. E.; Pearl, L. H.; Knapp, S. Activation segment dimerization: a mechanism of kinase autophosphorylation of non-consensus sites EMBO J. 2008, 27, 704-714 (Pubitemid 351273130)
-
(2008)
EMBO Journal
, vol.27
, Issue.4
, pp. 704-714
-
-
Pike, A.C.W.1
Rellos, P.2
Niesen, F.H.3
Turnbull, A.4
Oliver, A.W.5
Parker, S.A.6
Turk, B.E.7
Pearl, L.H.8
Knapp, S.9
-
28
-
-
34547154729
-
Activation segment exchange: A common mechanism of kinase autophosphorylation?
-
DOI 10.1016/j.tibs.2007.06.004, PII S0968000407001478
-
Oliver, A. W.; Knapp, S.; Pearl, L. H. Activation segment exchange: A common mechanism of kinase autophosphorylation? Trends Biochem. Sci. 2007, 32, 351-356 (Pubitemid 47126856)
-
(2007)
Trends in Biochemical Sciences
, vol.32
, Issue.8
, pp. 351-356
-
-
Oliver, A.W.1
Knapp, S.2
Pearl, L.H.3
-
29
-
-
33744809773
-
Macromolecular size-and-shape distributions by sedimentation velocity analytical ultracentrifugation
-
DOI 10.1529/biophysj.106.081372
-
Brown, P. H.; Schuck, P. Macromolecular Size-and-Shape Distributions by Sedimentation Velocity Analytical Ultracentrifugation Biophys. J. 2006, 90, 4651-4661 (Pubitemid 43830909)
-
(2006)
Biophysical Journal
, vol.90
, Issue.12
, pp. 4651-4661
-
-
Brown, P.H.1
Schuck, P.2
-
30
-
-
77954698217
-
Dissecting the role of MPS1 in chromosome biorientation and the spindle checkpoint through the small molecule inhibitor reversine
-
Santaguida, S.; Tighe, A.; D'Alise, A. M.; Taylor, S. S.; Musacchio, A. Dissecting the role of MPS1 in chromosome biorientation and the spindle checkpoint through the small molecule inhibitor reversine. J. Cell Biol. 2010, 190, 73-87
-
(2010)
J. Cell Biol.
, vol.190
, pp. 73-87
-
-
Santaguida, S.1
Tighe, A.2
D'Alise, A.M.3
Taylor, S.S.4
Musacchio, A.5
-
31
-
-
35148883144
-
Binding of TPX2 to Aurora A alters substrate and inhibitor interactions
-
DOI 10.1021/bi7011355
-
Anderson, K.; Yang, J.; Koretke, K.; Nurse, K.; Calamari, A.; Kirkpatrick, R. B.; Patrick, D.; Silva, D.; Tummino, P. J.; Copeland, R. A.; Lai, Z. Binding of TPX2 to Aurora A alters substrate and inhibitor interactions Biochemistry 2007, 46, 10287-10295 (Pubitemid 350067622)
-
(2007)
Biochemistry
, vol.46
, Issue.36
, pp. 10287-10295
-
-
Anderson, K.1
Yang, J.2
Koretke, K.3
Nurse, K.4
Calamari, A.5
Kirkpatrick, R.B.6
Patrick, D.7
Silva, D.8
Tummino, P.J.9
Copeland, R.A.10
Lai, Z.11
-
32
-
-
77956181585
-
High-throughput production of human proteins for crystallization: The SGC experience
-
Savitsky, P.; Bray, J.; Cooper, C. D. O.; Marsden, B. D.; Mahajan, P.; Burgess-Brown, N. A.; Gileadi, O. High-throughput production of human proteins for crystallization: The SGC experience J. Struct. Biol. 2010, 172, 3-13
-
(2010)
J. Struct. Biol.
, vol.172
, pp. 3-13
-
-
Savitsky, P.1
Bray, J.2
Cooper, C.D.O.3
Marsden, B.D.4
Mahajan, P.5
Burgess-Brown, N.A.6
Gileadi, O.7
-
34
-
-
0028103275
-
The CCP4 Suite: Programs for Protein Crystallography
-
Collaborative Computational Project Number 4
-
Collaborative Computational Project Number 4. The CCP4 Suite: Programs for Protein Crystallography. Acta Crystallogr. 1994, D50, 760-763.
-
(1994)
Acta Crystallogr.
, vol.50
, pp. 760-763
-
-
-
35
-
-
33644875355
-
Scaling and assessment of data quality
-
Evans, P. Scaling and assessment of data quality Acta Crystallogr. 2006, D62, 72-82
-
(2006)
Acta Crystallogr.
, vol.62
, pp. 72-82
-
-
Evans, P.1
-
36
-
-
34447508216
-
Phaser crystallographic software
-
DOI 10.1107/S0021889807021206, PII S0021889807021206
-
McCoy, A. J.; Grosse-Kunstleve, R. W.; Adams, P. D.; Winn, M. D.; Storoni, L. C.; Read, R. J. Phaser crystallographic software J. Appl. Crystallogr. 2007, 40, 658-674 (Pubitemid 47080256)
-
(2007)
Journal of Applied Crystallography
, vol.40
, Issue.4
, pp. 658-674
-
-
McCoy, A.J.1
Grosse-Kunstleve, R.W.2
Adams, P.D.3
Winn, M.D.4
Storoni, L.C.5
Read, R.J.6
-
37
-
-
0030924992
-
Refinement of macromolecular structures by the maximum-likelihood method
-
DOI 10.1107/S0907444996012255
-
Murshudov, G. N.; Vagin, A. A.; Dodson, E. J. Refinement of Macromolecular Structures by the Maximum-Likelihood Method Acta Crystallogr. 1997, D53, 240-255 (Pubitemid 27235885)
-
(1997)
Acta Crystallographica Section D: Biological Crystallography
, vol.53
, Issue.3
, pp. 240-255
-
-
Murshudov, G.N.1
Vagin, A.A.2
Dodson, E.J.3
-
39
-
-
0034009520
-
Size-distribution analysis of macromolecules by sedimentation velocity ultracentrifugation and Lamm equation modeling
-
Schuck, P. Size-Distribution Analysis of Macromolecules by Sedimenation Velocity Ultracentrifugation and Lamm Equation Modeling Biophys. J. 2000, 78, 1606-1619 (Pubitemid 30141584)
-
(2000)
Biophysical Journal
, vol.78
, Issue.3
, pp. 1606-1619
-
-
Schuck, P.1
-
40
-
-
0036154258
-
Size-distribution analysis of proteins by analytical ultracentrifugation: Strategies and application to model systems
-
Schuck, P.; Perugini, M. A.; Gonzales, N. R.; Howlett, G. J.; Schubert, D. Size-Distribution Analysis of Proteins by Analytical Ultracentrifugation: Strategies and Application to Model Systems Biophys. J. 2002, 82, 1096-1111 (Pubitemid 34111246)
-
(2002)
Biophysical Journal
, vol.82
, Issue.2
, pp. 1096-1111
-
-
Schuck, P.1
Perugini, M.A.2
Gonzales, N.R.3
Hewlett, G.J.4
Schubert, D.5
|