-
1
-
-
27844445642
-
Perturbations of the AKT signaling pathway in human cancer
-
D. A. Altomare, J. R. Testa, Perturbations of the AKT signaling pathway in human cancer. Oncogene 24, 7455-7464 (2005).
-
(2005)
Oncogene
, vol.24
, pp. 7455-7464
-
-
Altomare, D.A.1
Testa, J.R.2
-
2
-
-
33747889727
-
Functional distinctions of protein kinase B/Akt isoforms defined by their influence on cell migration
-
V. Stambolic, J. R. Woodgett, Functional distinctions of protein kinase B/Akt isoforms defined by their influence on cell migration. Trends Cell Biol. 16, 461-466 (2006).
-
(2006)
Trends Cell Biol.
, vol.16
, pp. 461-466
-
-
Stambolic, V.1
Woodgett, J.R.2
-
4
-
-
0032189381
-
Protein kinase B (c-Akt): A multifunctional mediator of phosphatidylinositol 3-kinase activation
-
P. J. Coffer, J. Jin, J. R. Woodgett, Protein kinase B (c-Akt): A multifunctional mediator of phosphatidylinositol 3-kinase activation. Biochem. J. 335 (Pt. 1), 1-13 (1998).
-
(1998)
Biochem. J.
, vol.335
, Issue.PART 1
, pp. 1-13
-
-
Coffer, P.J.1
Jin, J.2
Woodgett, J.R.3
-
5
-
-
0031913246
-
Mechanism of activation and function of protein kinase B
-
D. R. Alessi, P. Cohen, Mechanism of activation and function of protein kinase B. Curr. Opin. Genet. Dev. 8, 55-62 (1998).
-
(1998)
Curr. Opin. Genet. Dev.
, vol.8
, pp. 55-62
-
-
Alessi, D.R.1
Cohen, P.2
-
6
-
-
18744373865
-
Crystal structure of an activated Akt/protein kinase B ternary complex with GSK3-peptide and AMP-PNP
-
J. Yang, P. Cron, V. M. Good, V. Thompson, B. A. Hemmings, D. Barford, Crystal structure of an activated Akt/protein kinase B ternary complex with GSK3-peptide and AMP-PNP. Nat. Struct. Biol. 9, 940-944 (2002).
-
(2002)
Nat. Struct. Biol.
, vol.9
, pp. 940-944
-
-
Yang, J.1
Cron, P.2
Good, V.M.3
Thompson, V.4
Hemmings, B.A.5
Barford, D.6
-
7
-
-
0036295728
-
Molecular mechanism for the regulation of protein kinase B/Akt by hydrophobic motif phosphorylation
-
J. Yang, P. Cron, V. Thompson, V. M. Good, D. Hess, B. A. Hemmings, D. Barford, Molecular mechanism for the regulation of protein kinase B/Akt by hydrophobic motif phosphorylation. Mol. Cell 9, 1227-1240 (2002).
-
(2002)
Mol. Cell
, vol.9
, pp. 1227-1240
-
-
Yang, J.1
Cron, P.2
Thompson, V.3
Good, V.M.4
Hess, D.5
Hemmings, B.A.6
Barford, D.7
-
8
-
-
34247391898
-
Intramolecular and intermolecular interactions of protein kinase B define its activation in vivo
-
V. Calleja, D. Alcor, M. Laguerre, J. Park, B. Vojnovic, B. A. Hemmings, J. Downward, P. J. Parker, B. Larijani, Intramolecular and intermolecular interactions of protein kinase B define its activation in vivo. PLoS Biol. 5, e95 (2007).
-
(2007)
PLoS Biol.
, vol.5
-
-
Calleja, V.1
Alcor, D.2
Laguerre, M.3
Park, J.4
Vojnovic, B.5
Hemmings, B.A.6
Downward, J.7
Parker, P.J.8
Larijani, B.9
-
9
-
-
77958576132
-
Crystal structure of human AKT1 with an allosteric inhibitor reveals a new mode of kinase inhibition
-
W. I. Wu, W. C. Voegtli, H. L. Sturgis, F. P. Dizon, G. P. Vigers, B. J. Brandhuber, Crystal structure of human AKT1 with an allosteric inhibitor reveals a new mode of kinase inhibition. PLoS One 5, e12913 (2010).
-
(2010)
PLoS One
, vol.5
-
-
Wu, W.I.1
Voegtli, W.C.2
Sturgis, H.L.3
Dizon, F.P.4
Vigers, G.P.5
Brandhuber, B.J.6
-
10
-
-
33745298429
-
Rational design of inhibitors that bind to inactive kinase conformations
-
Y. Liu, N. S. Gray, Rational design of inhibitors that bind to inactive kinase conformations. Nat. Chem. Biol. 2, 358-364 (2006).
-
(2006)
Nat. Chem. Biol.
, vol.2
, pp. 358-364
-
-
Liu, Y.1
Gray, N.S.2
-
11
-
-
77958509195
-
Akt inhibitors in clinical development for the treatment of cancer
-
S. K. Pal, K. Reckamp, H. Yu, R. A. Figlin, Akt inhibitors in clinical development for the treatment of cancer. Expert Opin. Investig. Drugs 19, 1355-1366 (2010).
-
(2010)
Expert Opin. Investig. Drugs
, vol.19
, pp. 1355-1366
-
-
Pal, S.K.1
Reckamp, K.2
Yu, H.3
Figlin, R.A.4
-
12
-
-
77953721226
-
An allosteric Akt inhibitor effectively blocks Akt signaling and tumor growth with only transient effects on glucose and insulin levels in vivo
-
C. Cherrin, K. Haskell, B. Howell, R. Jones, K. Leander, R. Robinson, A. Watkins, M. Bilodeau, J. Hoffman, P. Sanderson, G. Hartman, E. Mahan, T. Prueksaritanont, G. Jiang, Q. B. She, N. Rosen, L. Sepp-Lorenzino, D. Defeo-Jones, H. E. Huber, An allosteric Akt inhibitor effectively blocks Akt signaling and tumor growth with only transient effects on glucose and insulin levels in vivo. Cancer Biol. Ther. 9, 493-503 (2010).
-
(2010)
Cancer Biol. Ther.
, vol.9
, pp. 493-503
-
-
Cherrin, C.1
Haskell, K.2
Howell, B.3
Jones, R.4
Leander, K.5
Robinson, R.6
Watkins, A.7
Bilodeau, M.8
Hoffman, J.9
Sanderson, P.10
Hartman, G.11
Mahan, E.12
Prueksaritanont, T.13
Jiang, G.14
She, Q.B.15
Rosen, N.16
Sepp-Lorenzino, L.17
Defeo-Jones, D.18
Huber, H.E.19
-
13
-
-
34547933680
-
Akt inhibitor A-443654 induces rapid Akt Ser-473 phosphorylation independent of mTORC1 inhibition
-
E. K. Han, J. D. Leverson, T. McGonigal, O. J. Shah, K.W.Woods, T. Hunter, V. L. Giranda, Y. Luo, Akt inhibitor A-443654 induces rapid Akt Ser-473 phosphorylation independent of mTORC1 inhibition. Oncogene 26, 5655-5661 (2007).
-
(2007)
Oncogene
, vol.26
, pp. 5655-5661
-
-
Han, E.K.1
Leverson, J.D.2
McGonigal, T.3
Shah, O.J.4
Woods, K.W.5
Hunter, T.6
Giranda, V.L.7
Luo, Y.8
-
14
-
-
42049115641
-
Characterization of an Akt kinase inhibitor with potent pharmacodynamic and antitumor activity
-
N. Rhodes, D. A. Heerding, D. R. Duckett, D. J. Eberwein, V. B. Knick, T. J. Lansing, R. T. McConnell, T. M. Gilmer, S. Y. Zhang, K. Robell, J. A. Kahana, R. S. Geske, E. V. Kleymenova, A. E. Choudhry, Z. Lai, J. D. Leber, E. A. Minthorn, S. L. Strum, E. R. Wood, P. S. Huang, R. A. Copeland, R. Kumar, Characterization of an Akt kinase inhibitor with potent pharmacodynamic and antitumor activity. Cancer Res. 68, 2366-2374 (2008).
-
(2008)
Cancer Res.
, vol.68
, pp. 2366-2374
-
-
Rhodes, N.1
Heerding, D.A.2
Duckett, D.R.3
Eberwein, D.J.4
Knick, V.B.5
Lansing, T.J.6
McConnell, R.T.7
Gilmer, T.M.8
Zhang, S.Y.9
Robell, K.10
Kahana, J.A.11
Geske, R.S.12
Kleymenova, E.V.13
Choudhry, A.E.14
Lai, Z.15
Leber, J.D.16
Minthorn, E.A.17
Strum, S.L.18
Wood, E.R.19
Huang, P.S.20
Copeland, R.A.21
Kumar, R.22
more..
-
15
-
-
67650337799
-
Inhibitor hijacking of Akt activation
-
T. Okuzumi, D. Fiedler, C. Zhang, D. C. Gray, B. Aizenstein, R. Hoffman, K. M. Shokat, Inhibitor hijacking of Akt activation. Nat. Chem. Biol. 5, 484-493 (2009).
-
(2009)
Nat. Chem. Biol.
, vol.5
, pp. 484-493
-
-
Okuzumi, T.1
Fiedler, D.2
Zhang, C.3
Gray, D.C.4
Aizenstein, B.5
Hoffman, R.6
Shokat, K.M.7
-
16
-
-
84871711021
-
GDC-0068: A novel, selective, ATP-competitive inhibitor of Akt
-
Abstract DDT02-01
-
K. Lin, GDC-0068: A novel, selective, ATP-competitive inhibitor of Akt, in Proceedings of the 102nd Annual Meeting of the American Association for Cancer Research, Orlando, FL, 2 to 6 April 2011. Abstract DDT02-01.
-
Proceedings of the 102nd Annual Meeting of the American Association for Cancer Research, Orlando, FL, 2 to 6 April 2011
-
-
Lin, K.1
-
17
-
-
8444224619
-
Balancing Akt with S6K: Implications for both metabolic diseases and tumorigenesis
-
B. D. Manning, Balancing Akt with S6K: Implications for both metabolic diseases and tumorigenesis. J. Cell Biol. 167, 399-403 (2004).
-
(2004)
J. Cell Biol.
, vol.167
, pp. 399-403
-
-
Manning, B.D.1
-
18
-
-
17044393948
-
Regulation of Akt/PKB Ser473 phosphorylation
-
J. R. Bayascas, D. R. Alessi, Regulation of Akt/PKB Ser473 phosphorylation. Mol. Cell 18, 143-145 (2005).
-
(2005)
Mol. Cell
, vol.18
, pp. 143-145
-
-
Bayascas, J.R.1
Alessi, D.R.2
-
19
-
-
78149285243
-
Discovery of dihydrothienoand dihydrofuropyrimidines as potent pan Akt inhibitors
-
J. R. Bencsik, D. Xiao, J. F. Blake, N. C. Kallan, I. S. Mitchell, K. L. Spencer, R. Xu, S. L. Gloor, M. Martinson, T. Risom, R. D. Woessner, F. Dizon, W. I. Wu, G. P. Vigers, B. J. Brandhuber, N. J. Skelton, W. W. Prior, L. J. Murray, Discovery of dihydrothienoand dihydrofuropyrimidines as potent pan Akt inhibitors. Bioorg. Med. Chem. Lett. 20, 7037-7041 (2010).
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 7037-7041
-
-
Bencsik, J.R.1
Xiao, D.2
Blake, J.F.3
Kallan, N.C.4
Mitchell, I.S.5
Spencer, K.L.6
Xu, R.7
Gloor, S.L.8
Martinson, M.9
Risom, T.10
Woessner, R.D.11
Dizon, F.12
Wu, W.I.13
Vigers, G.P.14
Brandhuber, B.J.15
Skelton, N.J.16
Prior, W.W.17
Murray, L.J.18
-
20
-
-
77957596001
-
Discovery of pyrrolopyrimidine inhibitors of Akt
-
J. F. Blake, N. C. Kallan, D. Xiao, R. Xu, J. R. Bencsik, N. J. Skelton, K. L. Spencer, I. S. Mitchell, R. D.Woessner, S. L. Gloor,T. Risom, S. D. Gross, M. Martinson, T. H. Morales, G. P. Vigers, B. J. Brandhuber, Discovery of pyrrolopyrimidine inhibitors of Akt. Bioorg. Med. Chem. Lett. 20, 5607-5612 (2010).
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 5607-5612
-
-
Blake, J.F.1
Kallan, N.C.2
Xiao, D.3
Xu, R.4
Bencsik, J.R.5
Skelton, N.J.6
Spencer, K.L.7
Mitchell, I.S.8
Woessner, R.D.9
Gloor, S.L.10
Risom, T.11
Gross, S.D.12
Martinson, M.13
Morales, T.H.14
Vigers, G.P.15
Brandhuber, B.J.16
-
21
-
-
15944406764
-
PHLPP: A phosphatase that directly dephosphorylates Akt, promotes apoptosis, and suppresses tumor growth
-
T. Gao, F. Furnari, A. C. Newton, PHLPP: A phosphatase that directly dephosphorylates Akt, promotes apoptosis, and suppresses tumor growth. Mol. Cell 18, 13-24 (2005).
-
(2005)
Mol. Cell
, vol.18
, pp. 13-24
-
-
Gao, T.1
Furnari, F.2
Newton, A.C.3
-
22
-
-
44149104593
-
Allosteric inhibitors of Akt1 and Akt2: A naphthyridinone with efficacy in an A2780 tumor xenograft model
-
M. T. Bilodeau, A. E. Balitza, J. M. Hoffman, P. J. Manley, S. F. Barnett, D. Defeo-Jones, K. Haskell, R. E. Jones, K. Leander, R. G. Robinson, A. M. Smith, H. E. Huber, G. D. Hartman, Allosteric inhibitors of Akt1 and Akt2: A naphthyridinone with efficacy in an A2780 tumor xenograft model. Bioorg. Med. Chem. Lett. 18, 3178-3182 (2008).
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 3178-3182
-
-
Bilodeau, M.T.1
Balitza, A.E.2
Hoffman, J.M.3
Manley, P.J.4
Barnett, S.F.5
Defeo-Jones, D.6
Haskell, K.7
Jones, R.E.8
Leander, K.9
Robinson, R.G.10
Smith, A.M.11
Huber, H.E.12
Hartman, G.D.13
-
23
-
-
13844312400
-
Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex
-
D. D. Sarbassov, D. A. Guertin, S. M. Ali, D. M. Sabatini, Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex. Science 307, 1098-1101 (2005).
-
(2005)
Science
, vol.307
, pp. 1098-1101
-
-
Sarbassov, D.D.1
Guertin, D.A.2
Ali, S.M.3
Sabatini, D.M.4
-
24
-
-
77249137785
-
Discovery of (thienopyrimidin-2- Yl)aminopyrimidines as potent, selective, and orally available pan-PI3-kinase and dual pan-PI3-kinase/mTOR inhibitors for the treatment of cancer
-
D. P. Sutherlin, D. Sampath, M. Berry, G. Castanedo, Z. Chang, I. Chuckowree, J. Dotson, A. Folkes, L. Friedman,R. Goldsmith, T. Heffron, L. Lee, J. Lesnick, C. Lewis, S. Mathieu, J. Nonomiya, A. Olivero, J. Pang, W. W. Prior, L. Salphati, S. Sideris, Q. Tian, V. Tsui, N. C. Wan, S.Wang, C.Wiesmann, S. Wong, B. Y. Zhu, Discovery of (thienopyrimidin-2- yl)aminopyrimidines as potent, selective, and orally available pan-PI3-kinase and dual pan-PI3-kinase/mTOR inhibitors for the treatment of cancer. J. Med. Chem. 53, 1086-1097 (2010).
-
(2010)
J. Med. Chem.
, vol.53
, pp. 1086-1097
-
-
Sutherlin, D.P.1
Sampath, D.2
Berry, M.3
Castanedo, G.4
Chang, Z.5
Chuckowree, I.6
Dotson, J.7
Folkes, A.8
Friedman, L.9
Goldsmith, R.10
Heffron, T.11
Lee, L.12
Lesnick, J.13
Lewis, C.14
Mathieu, S.15
Nonomiya, J.16
Olivero, A.17
Pang, J.18
Prior, W.W.19
Salphati, L.20
Sideris, S.21
Tian, Q.22
Tsui, V.23
Wan, N.C.24
Wang, S.25
Wiesmann, C.26
Wong, S.27
Zhu, B.Y.28
more..
-
25
-
-
21244435590
-
Novel small molecule inhibitors of 3-phosphoinositide-dependent kinase-1
-
R. I. Feldman, J. M. Wu, M. A. Polokoff, M. J. Kochanny, H. Dinter, D. Zhu, S. L. Biroc, B. Alicke, J. Bryant, S. Yuan, B. O. Buckman, D. Lentz, M. Ferrer, M. Whitlow, M. Adler, S. Finster, Z. Chang, D. O. Arnaiz, Novel small molecule inhibitors of 3-phosphoinositide-dependent kinase-1. J. Biol. Chem. 280, 19867-19874 (2005).
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 19867-19874
-
-
Feldman, R.I.1
Wu, J.M.2
Polokoff, M.A.3
Kochanny, M.J.4
Dinter, H.5
Zhu, D.6
Biroc, S.L.7
Alicke, B.8
Bryant, J.9
Yuan, S.10
Buckman, B.O.11
Lentz, D.12
Ferrer, M.13
Whitlow, M.14
Adler, M.15
Finster, S.16
Chang, Z.17
Arnaiz, D.O.18
-
26
-
-
0031444107
-
Participation of ADP dissociation in the rate-determining step in cAMP-dependent protein kinase
-
J. Zhou, J. A. Adams, Participation of ADP dissociation in the rate-determining step in cAMP-dependent protein kinase. Biochemistry 36, 15733-15738 (1997).
-
(1997)
Biochemistry
, vol.36
, pp. 15733-15738
-
-
Zhou, J.1
Adams, J.A.2
-
28
-
-
0032439795
-
Purine nucleotide- and sugar phosphate-induced inhibition of the carboxyl methylation and catalysis of protein phosphatase-2A in insulin-secreting cells: Protection by divalent cations
-
A. Kowluru, S. A. Metz, Purine nucleotide- and sugar phosphate-induced inhibition of the carboxyl methylation and catalysis of protein phosphatase-2A in insulin-secreting cells: Protection by divalent cations. Biosci. Rep. 18, 171-186 (1998).
-
(1998)
Biosci. Rep.
, vol.18
, pp. 171-186
-
-
Kowluru, A.1
Metz, S.A.2
-
29
-
-
19944431003
-
Allosteric Akt (PKB) inhibitors: Discovery and SAR of isozyme selective inhibitors
-
C. W. Lindsley, Z. Zhao, W. H. Leister, R. G. Robinson, S. F. Barnett, D. Defeo-Jones, R. E. Jones, G. D. Hartman, J. R. Huff, H. E. Huber, M. E. Duggan, Allosteric Akt (PKB) inhibitors: Discovery and SAR of isozyme selective inhibitors. Bioorg. Med. Chem. Lett. 15, 761-764 (2005).
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 761-764
-
-
Lindsley, C.W.1
Zhao, Z.2
Leister, W.H.3
Robinson, R.G.4
Barnett, S.F.5
Defeo-Jones, D.6
Jones, R.E.7
Hartman, G.D.8
Huff, J.R.9
Huber, H.E.10
Duggan, M.E.11
-
30
-
-
34547172596
-
A transforming mutation in the pleckstrin homology domain of AKT1 in cancer
-
J. D. Carpten, A. L. Faber, C. Horn, G. P. Donoho, S. L. Briggs, C. M. Robbins, G. Hostetter, S. Boguslawski, T. Y. Moses, S. Savage, M. Uhlik, A. Lin, J. Du, Y. W. Qian, D. J. Zeckner, G. Tucker-Kellogg, J. Touchman, K. Patel, S. Mousses, M. Bittner, R. Schevitz, M. H. Lai, K. L. Blanchard, J. E. Thomas, A transforming mutation in the pleckstrin homology domain of AKT1 in cancer. Nature 448, 439-444 (2007).
-
(2007)
Nature
, vol.448
, pp. 439-444
-
-
Carpten, J.D.1
Faber, A.L.2
Horn, C.3
Donoho, G.P.4
Briggs, S.L.5
Robbins, C.M.6
Hostetter, G.7
Boguslawski, S.8
Moses, T.Y.9
Savage, S.10
Uhlik, M.11
Lin, A.12
Du, J.13
Qian, Y.W.14
Zeckner, D.J.15
Tucker-Kellogg, G.16
Touchman, J.17
Patel, K.18
Mousses, S.19
Bittner, M.20
Schevitz, R.21
Lai, M.H.22
Blanchard, K.L.23
Thomas, J.E.24
more..
-
31
-
-
55549088220
-
Use of Akt inhibitor and a drug-resistant mutant validates a critical role for protein kinase B/Akt in the insulin-dependent regulation of glucose and system A amino acid uptake
-
C. J. Green, O. Goransson, G. S. Kular, N. R. Leslie, A. Gray, D. R. Alessi, K. Sakamoto, H. S. Hundal, Use of Akt inhibitor and a drug-resistant mutant validates a critical role for protein kinase B/Akt in the insulin-dependent regulation of glucose and system A amino acid uptake. J. Biol. Chem. 283, 27653-27667 (2008).
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 27653-27667
-
-
Green, C.J.1
Goransson, O.2
Kular, G.S.3
Leslie, N.R.4
Gray, A.5
Alessi, D.R.6
Sakamoto, K.7
Hundal, H.S.8
-
32
-
-
84860389181
-
A mosaic activating mutation in AKT1 associated with the Proteus syndrome
-
M. J. Lindhurst, J. C. Sapp, J. K. Teer, J. J. Johnston, E. M. Finn, K. Peters, J. Turner, J. L. Cannons, D. Bick, L. Blakemore, C. Blumhorst, K. Brockmann, P. Calder, N. Cherman, M. A. Deardorff, D. B. Everman, G. Golas, R.M. Greenstein, B.M. Kato, K. M. Keppler-Noreuil, S. A. Kuznetsov, R. T. Miyamoto, K. Newman, D. Ng, K. O'Brien, S. Rothenberg, D. J. Schwartzentruber, V. Singhal, R. Tirabosco, J. Upton, S. Wientroub, E. H. Zackai, K. Hoag, T. Whitewood-Neal, P. G. Robey, P. L. Schwartzberg, T. N. Darling, L. L. Tosi, J. C. Mullikin, L. G. Biesecker, A mosaic activating mutation in AKT1 associated with the Proteus syndrome. N. Engl. J. Med. 365, 611-619 (2011).
-
(2011)
N. Engl. J. Med.
, vol.365
, pp. 611-619
-
-
Lindhurst, M.J.1
Sapp, J.C.2
Teer, J.K.3
Johnston, J.J.4
Finn, E.M.5
Peters, K.6
Turner, J.7
Cannons, J.L.8
Bick, D.9
Blakemore, L.10
Blumhorst, C.11
Brockmann, K.12
Calder, P.13
Cherman, N.14
Deardorff, M.A.15
Everman, D.B.16
Golas, G.17
Greenstein, R.M.18
Kato, B.M.19
Keppler-Noreuil, K.M.20
Kuznetsov, S.A.21
Miyamoto, R.T.22
Newman, K.23
Ng, D.24
O'Brien, K.25
Rothenberg, S.26
Schwartzentruber, D.J.27
Singhal, V.28
Tirabosco, R.29
Upton, J.30
Wientroub, S.31
Zackai, E.H.32
Hoag, K.33
Whitewood-Neal, T.34
Robey, P.G.35
Schwartzberg, P.L.36
Darling, T.N.37
Tosi, L.L.38
Mullikin, J.C.39
Biesecker, L.G.40
more..
-
33
-
-
0028103275
-
Number 4, the CCP4 suite: Programs for protein crystallography
-
Collaborative Computational Project
-
Collaborative Computational Project, Number 4, The CCP4 suite: Programs for protein crystallography. Acta Crystallogr. D Biol. Crystallogr. 50, 760-763 (1994).
-
(1994)
Acta Crystallogr. D Biol. Crystallogr.
, vol.50
, pp. 760-763
-
-
-
35
-
-
79551571726
-
Data transformation practices in biomedical sciences
-
M. Valcu, C. M. Valcu, Data transformation practices in biomedical sciences. Nat. Methods 8, 104-105 (2011).
-
(2011)
Nat. Methods
, vol.8
, pp. 104-105
-
-
Valcu, M.1
Valcu, C.M.2
-
36
-
-
81755163634
-
Resistance of Akt kinases to dephosphorylation through ATP-dependent conformational plasticity
-
T. O. Chan, J. Zhang, U. Rodeck, J. M. Pascal, R. S. Armen, M. Spring, C. D. Dumitru, V. Myers, X. Li, J. Y. Cheung, A. M. Feldman, Resistance of Akt kinases to dephosphorylation through ATP-dependent conformational plasticity. Proc. Natl. Acad. Sci. U.S.A. 108, E1120-E1127 (2011).
-
(2011)
Proc. Natl. Acad. Sci. U.S.A.
, vol.108
-
-
Chan, T.O.1
Zhang, J.2
Rodeck, U.3
Pascal, J.M.4
Armen, R.S.5
Spring, M.6
Dumitru, C.D.7
Myers, V.8
Li, X.9
Cheung, J.Y.10
Feldman, A.M.11
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