-
1
-
-
84871806385
-
Bruton tyrosine kinase inhibitor ibrutinib (PCI-32765) has significant activity in patients with relapsed/refractory B-cell malignancies
-
Advani, R.H., Buggy, J.J., Sharman, J.P., Smith, S.M., Boyd, T.E., Grant, B.,.. Smith, M., Bruton tyrosine kinase inhibitor ibrutinib (PCI-32765) has significant activity in patients with relapsed/refractory B-cell malignancies. Journal of Clinical Oncology, 30, 2012, 10.1200/JCO.2012.42.7906.
-
(2012)
Journal of Clinical Oncology
, vol.30
-
-
Advani, R.H.1
Buggy, J.J.2
Sharman, J.P.3
Smith, S.M.4
Boyd, T.E.5
Grant, B.6
Smith, M.7
-
2
-
-
78649992238
-
Dihydrofolate reductase gene variations in susceptibility to disease and treatment outcomes
-
Askari, B.S., Krajinovic, M., Dihydrofolate reductase gene variations in susceptibility to disease and treatment outcomes. Current Genomics 11:8 (2010), 578–583, 10.2174/138920210793360925.
-
(2010)
Current Genomics
, vol.11
, Issue.8
, pp. 578-583
-
-
Askari, B.S.1
Krajinovic, M.2
-
3
-
-
16844385435
-
Characterization of the FKBP-rapamycin-FRB ternary complex
-
Banaszynski, L.A., Liu, C.W., Wandless, T.J., Characterization of the FKBP-rapamycin-FRB ternary complex. Journal of the American Chemical Society 127:13 (2005), 4715–4721.
-
(2005)
Journal of the American Chemical Society
, vol.127
, Issue.13
, pp. 4715-4721
-
-
Banaszynski, L.A.1
Liu, C.W.2
Wandless, T.J.3
-
4
-
-
84954099191
-
RNA interference (RNAi)-based therapeutics: Delivering on the promise?
-
Bobbin, M.L., Rossi, J.J., RNA interference (RNAi)-based therapeutics: Delivering on the promise?. Annual Review of Pharmacology and Toxicology 56 (2016), 103–122, 10.1146/annurev-pharmtox-010715-103633.
-
(2016)
Annual Review of Pharmacology and Toxicology
, vol.56
, pp. 103-122
-
-
Bobbin, M.L.1
Rossi, J.J.2
-
5
-
-
84937514576
-
Catalytic in vivo protein knockdown by small-molecule PROTACs
-
Bondeson, D.P., Mares, A., Smith, I.E.D., Ko, E., Campos, S., Miah, A.H.,.. Crews, C.M., Catalytic in vivo protein knockdown by small-molecule PROTACs. Nature Chemical Biology 11:8 (2015), 611–617, 10.1038/nchembio.1858.
-
(2015)
Nature Chemical Biology
, vol.11
, Issue.8
, pp. 611-617
-
-
Bondeson, D.P.1
Mares, A.2
Smith, I.E.D.3
Ko, E.4
Campos, S.5
Miah, A.H.6
Crews, C.M.7
-
6
-
-
77949848854
-
Prion-like transmission of protein aggregates in neurodegenerative diseases
-
Brundin, P., Melki, R., Kopito, R., Prion-like transmission of protein aggregates in neurodegenerative diseases. Nature Reviews. Molecular Cell Biology 11:4 (2010), 301–307, 10.1038/nrm2873.
-
(2010)
Nature Reviews. Molecular Cell Biology
, vol.11
, Issue.4
, pp. 301-307
-
-
Brundin, P.1
Melki, R.2
Kopito, R.3
-
7
-
-
84868522211
-
Small-molecule inhibitors of the interaction between the E3 ligase VHL and HIF1α
-
Buckley, D.L., Gustafson, J.L., Van Molle, I., Roth, A.G., Tae, H.S., Gareiss, P.C.,.. Crews, C.M., Small-molecule inhibitors of the interaction between the E3 ligase VHL and HIF1α. Angewandte Chemie (International Ed. in English) 51:46 (2012), 11463–11467, 10.1002/anie.201206231.
-
(2012)
Angewandte Chemie (International Ed. in English)
, vol.51
, Issue.46
, pp. 11463-11467
-
-
Buckley, D.L.1
Gustafson, J.L.2
Van Molle, I.3
Roth, A.G.4
Tae, H.S.5
Gareiss, P.C.6
Crews, C.M.7
-
8
-
-
84939794726
-
HaloPROTACS: Use of small molecule PROTACs to induce degradation of HaloTag fusion proteins
-
Buckley, D.L., Raina, K., Darricarrere, N., Hines, J., Gustafson, J.L., Smith, I.E.,.. Crews, C.M., HaloPROTACS: Use of small molecule PROTACs to induce degradation of HaloTag fusion proteins. ACS Chemical Biology 10:8 (2015), 1831–1837, 10.1021/acschembio.5b00442.
-
(2015)
ACS Chemical Biology
, vol.10
, Issue.8
, pp. 1831-1837
-
-
Buckley, D.L.1
Raina, K.2
Darricarrere, N.3
Hines, J.4
Gustafson, J.L.5
Smith, I.E.6
Crews, C.M.7
-
9
-
-
84858201095
-
Targeting the von Hippel-Lindau E3 ubiquitin ligase using small molecules to disrupt the VHL/HIF-1α interaction
-
Buckley, D.L., Van Molle, I., Gareiss, P.C., Tae, H.S., Michel, J., Noblin, D.J.,.. Crews, C.M., Targeting the von Hippel-Lindau E3 ubiquitin ligase using small molecules to disrupt the VHL/HIF-1α interaction. Journal of the American Chemical Society 134:10 (2012), 4465–4468, 10.1021/ja209924v.
-
(2012)
Journal of the American Chemical Society
, vol.134
, Issue.10
, pp. 4465-4468
-
-
Buckley, D.L.1
Van Molle, I.2
Gareiss, P.C.3
Tae, H.S.4
Michel, J.5
Noblin, D.J.6
Crews, C.M.7
-
10
-
-
80054761058
-
Androgen receptor gene expression in prostate cancer is directly suppressed by the androgen receptor through recruitment of lysine-specific demethylase 1
-
Cai, C., He, H.H., Chen, S., Coleman, I., Wang, H., Fang, Z.,.. Balk, S.P., Androgen receptor gene expression in prostate cancer is directly suppressed by the androgen receptor through recruitment of lysine-specific demethylase 1. Cancer Cell 20 (2011), 457–471, 10.1016/j.ccr.2011.09.001.
-
(2011)
Cancer Cell
, vol.20
, pp. 457-471
-
-
Cai, C.1
He, H.H.2
Chen, S.3
Coleman, I.4
Wang, H.5
Fang, Z.6
Balk, S.P.7
-
11
-
-
84923269246
-
Novel selection methods for DNA-encoded chemical libraries
-
Chan, A.I., McGregor, L.M., Liu, D.R., Novel selection methods for DNA-encoded chemical libraries. Current Opinion in Chemical Biology 26 (2015), 55–61, 10.1016/j.cbpa.2015.02.010.
-
(2015)
Current Opinion in Chemical Biology
, vol.26
, pp. 55-61
-
-
Chan, A.I.1
McGregor, L.M.2
Liu, D.R.3
-
12
-
-
77953699074
-
Targeting the undruggable proteome: The small molecules of my dreams
-
Crews, C.M., Targeting the undruggable proteome: The small molecules of my dreams. Chemistry & Biology 17:6 (2010), 551–555, 10.1016/j.chembiol.2010.05.011.
-
(2010)
Chemistry & Biology
, vol.17
, Issue.6
, pp. 551-555
-
-
Crews, C.M.1
-
13
-
-
0032883932
-
Switch from antagonist to agonist of the androgen receptor bicalutamide is associated with prostate tumour progression in a new model system
-
Culig, Z., Hoffmann, J., Erdel, M., Eder, I.E., Hobisch, A., Hittmair, A.,.. Klocker, H., Switch from antagonist to agonist of the androgen receptor bicalutamide is associated with prostate tumour progression in a new model system. British Journal of Cancer 81:2 (1999), 242–251, 10.1038/sj.bjc.6690684.
-
(1999)
British Journal of Cancer
, vol.81
, Issue.2
, pp. 242-251
-
-
Culig, Z.1
Hoffmann, J.2
Erdel, M.3
Eder, I.E.4
Hobisch, A.5
Hittmair, A.6
Klocker, H.7
-
14
-
-
84873728334
-
Modelling vemurafenib resistance in melanoma reveals a strategy to forestall drug resistance
-
Das Thakur, M., Salangsang, F., Landman, A.S., Sellers, W.R., Pryer, N.K., Levesque, M.P.,.. Stuart, D.D., Modelling vemurafenib resistance in melanoma reveals a strategy to forestall drug resistance. Nature 494:7436 (2013), 251–255, 10.1038/nature11814.
-
(2013)
Nature
, vol.494
, Issue.7436
, pp. 251-255
-
-
Das Thakur, M.1
Salangsang, F.2
Landman, A.S.3
Sellers, W.R.4
Pryer, N.K.5
Levesque, M.P.6
Stuart, D.D.7
-
15
-
-
84939552495
-
Protein degradation: Prime time for PROTACs
-
Deshaies, R.J., Protein degradation: Prime time for PROTACs. Nature Chemical Biology 11:9 (2015), 634–635, 10.1038/nchembio.1887.
-
(2015)
Nature Chemical Biology
, vol.11
, Issue.9
, pp. 634-635
-
-
Deshaies, R.J.1
-
16
-
-
84880447005
-
Inhibition of Btk with CC-292 provides early pharmacodynamic assessment of activity in mice and humans
-
Evans, E.K., Tester, R., Aslanian, S., Karp, R., Sheets, M., Labenski, M.T.,.. Westlin, W.F., Inhibition of Btk with CC-292 provides early pharmacodynamic assessment of activity in mice and humans. The Journal of Pharmacology and Experimental Therapeutics 346:2 (2013), 219–228, 10.1124/jpet.113.203489.
-
(2013)
The Journal of Pharmacology and Experimental Therapeutics
, vol.346
, Issue.2
, pp. 219-228
-
-
Evans, E.K.1
Tester, R.2
Aslanian, S.3
Karp, R.4
Sheets, M.5
Labenski, M.T.6
Westlin, W.F.7
-
17
-
-
79955759159
-
Smac mimetics activate the E3 ligase activity of cIAP1 protein by promoting RING domain dimerization
-
Feltham, R., Bettjeman, B., Budhidarmo, R., Mace, P.D., Shirley, S., Condon, S.M.,.. Day, C.L., Smac mimetics activate the E3 ligase activity of cIAP1 protein by promoting RING domain dimerization. The Journal of Biological Chemistry 286:19 (2011), 17015–17028, 10.1074/jbc.M111.222919.
-
(2011)
The Journal of Biological Chemistry
, vol.286
, Issue.19
, pp. 17015-17028
-
-
Feltham, R.1
Bettjeman, B.2
Budhidarmo, R.3
Mace, P.D.4
Shirley, S.5
Condon, S.M.6
Day, C.L.7
-
18
-
-
84926034005
-
Investigation of incidence and risk factors of subcutaneous granulomas induced by injection of leuprorelin acetate
-
(Retrieved from)
-
Fukui, S., Nakai, Y., Matsumoto, Y., Kagebayashi, Y., Samma, S., Investigation of incidence and risk factors of subcutaneous granulomas induced by injection of leuprorelin acetate. Hinyokika Kiyo. Acta Urologica Japonica 61:2 (2015), 55–59 (Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/25812594).
-
(2015)
Hinyokika Kiyo. Acta Urologica Japonica
, vol.61
, Issue.2
, pp. 55-59
-
-
Fukui, S.1
Nakai, Y.2
Matsumoto, Y.3
Kagebayashi, Y.4
Samma, S.5
-
19
-
-
84938415968
-
Small-molecule-mediated degradation of the androgen receptor through hydrophobic tagging
-
Gustafson, J.L., Neklesa, T.K., Cox, C.S., Roth, A.G., Buckley, D.L., Tae, H.S.,.. Crews, C.M., Small-molecule-mediated degradation of the androgen receptor through hydrophobic tagging. Angewandte Chemie International Edition, 54(33), 2015, 10.1002/anie.201503720.
-
(2015)
Angewandte Chemie International Edition
, vol.54
, Issue.33
-
-
Gustafson, J.L.1
Neklesa, T.K.2
Cox, C.S.3
Roth, A.G.4
Buckley, D.L.5
Tae, H.S.6
Crews, C.M.7
-
20
-
-
84908133543
-
Protein tyrosine phosphatases as potential therapeutic targets
-
He, R., Yu, Z., Zhang, R., Zhang, Z., Protein tyrosine phosphatases as potential therapeutic targets. Acta Pharmacologica Sinica 35:10 (2014), 1227–1246, 10.1038/aps.2014.80.
-
(2014)
Acta Pharmacologica Sinica
, vol.35
, Issue.10
, pp. 1227-1246
-
-
He, R.1
Yu, Z.2
Zhang, R.3
Zhang, Z.4
-
21
-
-
0035917313
-
2 sensing
-
2 sensing. Science (New York, N.Y.) 292:5516 (2001), 464–468, 10.1126/science.1059817.
-
(2001)
Science (New York, N.Y.)
, vol.292
, Issue.5516
, pp. 464-468
-
-
Ivan, M.1
Kondo, K.2
Yang, H.3
Kim, W.4
Valiando, J.5
Ohh, M.6
Kaelin, W.G.7
-
22
-
-
0035917808
-
2-regulated prolyl hydroxylation
-
2-regulated prolyl hydroxylation. Science (New York, N.Y.) 292:5516 (2001), 468–472, 10.1126/science.1059796.
-
(2001)
Science (New York, N.Y.)
, vol.292
, Issue.5516
, pp. 468-472
-
-
Jaakkola, P.1
Mole, D.R.2
Tian, Y.M.3
Wilson, M.I.4
Gielbert, J.5
Gaskell, S.J.6
Ratcliffe, P.J.7
-
23
-
-
84898717745
-
Emergence of constitutively active estrogen receptor-α mutations in pretreated advanced estrogen receptor-positive breast cancer
-
Jeselsohn, R., Yelensky, R., Buchwalter, G., Frampton, G., Meric-Bernstam, F., Gonzalez-Angulo, A.M.,.. Miller, V.A., Emergence of constitutively active estrogen receptor-α mutations in pretreated advanced estrogen receptor-positive breast cancer. Clinical Cancer Research: An Official Journal of the American Association for Cancer Research 20:7 (2014), 1757–1767, 10.1158/1078-0432.CCR-13-2332.
-
(2014)
Clinical Cancer Research: An Official Journal of the American Association for Cancer Research
, vol.20
, Issue.7
, pp. 1757-1767
-
-
Jeselsohn, R.1
Yelensky, R.2
Buchwalter, G.3
Frampton, G.4
Meric-Bernstam, F.5
Gonzalez-Angulo, A.M.6
Miller, V.A.7
-
24
-
-
84885210324
-
A clinically relevant androgen receptor mutation confers resistance to second-generation antiandrogens enzalutamide and ARN-509
-
Joseph, J.D., Lu, N., Qian, J., Sensintaffar, J., Shao, G., Brigham, D.,.. Hager, J.H., A clinically relevant androgen receptor mutation confers resistance to second-generation antiandrogens enzalutamide and ARN-509. Cancer Discovery 3:9 (2013), 1020–1029, 10.1158/2159-8290.CD-13-0226.
-
(2013)
Cancer Discovery
, vol.3
, Issue.9
, pp. 1020-1029
-
-
Joseph, J.D.1
Lu, N.2
Qian, J.3
Sensintaffar, J.4
Shao, G.5
Brigham, D.6
Hager, J.H.7
-
25
-
-
79956318797
-
Therapeutic strategies to overcome crizotinib resistance in non-small cell lung cancers harboring the fusion oncogene EML4-ALK
-
Katayama, R., Khan, T.M., Benes, C., Lifshits, E., Ebi, H., Rivera, V.M.,.. Shaw, A.T., Therapeutic strategies to overcome crizotinib resistance in non-small cell lung cancers harboring the fusion oncogene EML4-ALK. Proceedings of the National Academy of Sciences of the United States of America 108:18 (2011), 7535–7540, 10.1073/pnas.1019559108.
-
(2011)
Proceedings of the National Academy of Sciences of the United States of America
, vol.108
, Issue.18
, pp. 7535-7540
-
-
Katayama, R.1
Khan, T.M.2
Benes, C.3
Lifshits, E.4
Ebi, H.5
Rivera, V.M.6
Shaw, A.T.7
-
26
-
-
84875396927
-
Heterogeneity of genetic changes associated with acquired crizotinib resistance in ALK-rearranged lung cancer
-
Kim, S., Kim, T.M., Kim, D.-W., Go, H., Keam, B., Lee, S.-H.,.. Doebele, R., Heterogeneity of genetic changes associated with acquired crizotinib resistance in ALK-rearranged lung cancer. Journal of Thoracic Oncology 8:4 (2013), 415–422, 10.1097/JTO.0b013e318283dcc0.
-
(2013)
Journal of Thoracic Oncology
, vol.8
, Issue.4
, pp. 415-422
-
-
Kim, S.1
Kim, T.M.2
Kim, D.-W.3
Go, H.4
Keam, B.5
Lee, S.-H.6
Doebele, R.7
-
27
-
-
84879754813
-
Dabrafenib; preclinical characterization, increased efficacy when combined with trametinib, while BRAF/MEK tool combination reduced skin lesions
-
King, A.J., Arnone, M.R., Bleam, M.R., Moss, K.G., Yang, J., Fedorowicz, K.E.,.. Laquerre, S.G., Dabrafenib; preclinical characterization, increased efficacy when combined with trametinib, while BRAF/MEK tool combination reduced skin lesions. PloS One, 8(7), 2013, e67583, 10.1371/journal.pone.0067583.
-
(2013)
PloS One
, vol.8
, Issue.7
-
-
King, A.J.1
Arnone, M.R.2
Bleam, M.R.3
Moss, K.G.4
Yang, J.5
Fedorowicz, K.E.6
Laquerre, S.G.7
-
28
-
-
84865735256
-
Heterodimeric JAK-STAT activation as a mechanism of persistence to JAK2 inhibitor therapy
-
Koppikar, P., Bhagwat, N., Kilpivaara, O., Manshouri, T., Adli, M., Hricik, T.,.. Levine, R.L., Heterodimeric JAK-STAT activation as a mechanism of persistence to JAK2 inhibitor therapy. Nature 489:7414 (2012), 155–159, 10.1038/nature11303.
-
(2012)
Nature
, vol.489
, Issue.7414
, pp. 155-159
-
-
Koppikar, P.1
Bhagwat, N.2
Kilpivaara, O.3
Manshouri, T.4
Adli, M.5
Hricik, T.6
Levine, R.L.7
-
29
-
-
84958748153
-
Modular PROTAC design for the degradation of oncogenic BCR-ABL
-
Lai, A.C., Toure, M., Hellerschmied, D., Salami, J., Jaime-Figueroa, S., Ko, E.,.. Crews, C.M., Modular PROTAC design for the degradation of oncogenic BCR-ABL. Angewandte Chemie (International Ed. in English) 55:2 (2016), 807–810, 10.1002/anie.201507634.
-
(2016)
Angewandte Chemie (International Ed. in English)
, vol.55
, Issue.2
, pp. 807-810
-
-
Lai, A.C.1
Toure, M.2
Hellerschmied, D.3
Salami, J.4
Jaime-Figueroa, S.5
Ko, E.6
Crews, C.M.7
-
30
-
-
84924697369
-
Potent and selective small-molecule MCL-1 inhibitors demonstrate on-target cancer cell killing activity as single agents and in combination with ABT-263 (navitoclax)
-
Leverson, J.D., Zhang, H., Chen, J., Tahir, S.K., Phillips, D.C., Xue, J.,.. Souers, A.J., Potent and selective small-molecule MCL-1 inhibitors demonstrate on-target cancer cell killing activity as single agents and in combination with ABT-263 (navitoclax). Cell Death and Disease, 6(1), 2015, e1590, 10.1038/cddis.2014.561.
-
(2015)
Cell Death and Disease
, vol.6
, Issue.1
-
-
Leverson, J.D.1
Zhang, H.2
Chen, J.3
Tahir, S.K.4
Phillips, D.C.5
Xue, J.6
Souers, A.J.7
-
31
-
-
0035328474
-
Amplification and overexpression of androgen receptor gene in hormone-refractory prostate cancer
-
(Retrieved from)
-
Linja, M.J., Savinainen, K.J., Saramäki, O.R., Tammela, T.L., Vessella, R.L., Visakorpi, T., Amplification and overexpression of androgen receptor gene in hormone-refractory prostate cancer. Cancer Research 61:9 (2001), 3550–3555 (Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/11325816).
-
(2001)
Cancer Research
, vol.61
, Issue.9
, pp. 3550-3555
-
-
Linja, M.J.1
Savinainen, K.J.2
Saramäki, O.R.3
Tammela, T.L.4
Vessella, R.L.5
Visakorpi, T.6
-
32
-
-
84896295869
-
Discovery of ledipasvir (GS-5885): A potent, once-daily oral NS5A inhibitor for the treatment of hepatitis C virus infection
-
Link, J.O., Taylor, J.G., Xu, L., Mitchell, M., Guo, H., Liu, H.,.. Desai, M.C., Discovery of ledipasvir (GS-5885): A potent, once-daily oral NS5A inhibitor for the treatment of hepatitis C virus infection. Journal of Medicinal Chemistry 57:5 (2014), 2033–2046, 10.1021/jm401499g.
-
(2014)
Journal of Medicinal Chemistry
, vol.57
, Issue.5
, pp. 2033-2046
-
-
Link, J.O.1
Taylor, J.G.2
Xu, L.3
Mitchell, M.4
Guo, H.5
Liu, H.6
Desai, M.C.7
-
33
-
-
4444368187
-
Argonaute2 is the catalytic engine of mammalian RNAi
-
Liu, J., Carmell, M.A., Rivas, F.V., Marsden, C.G., Thomson, J.M., Song, J.-J.,.. Hannon, G.J., Argonaute2 is the catalytic engine of mammalian RNAi. Science (New York, N.Y.) 305:5689 (2004), 1437–1441, 10.1126/science.1102513.
-
(2004)
Science (New York, N.Y.)
, vol.305
, Issue.5689
, pp. 1437-1441
-
-
Liu, J.1
Carmell, M.A.2
Rivas, F.V.3
Marsden, C.G.4
Thomson, J.M.5
Song, J.-J.6
Hannon, G.J.7
-
34
-
-
84931560527
-
Hijacking the E3 ubiquitin ligase cereblon to efficiently target BRD4
-
Lu, J., Qian, Y., Altieri, M., Dong, H., Wang, J., Raina, K.,.. Crews, C.M., Hijacking the E3 ubiquitin ligase cereblon to efficiently target BRD4. Chemistry & Biology 22:6 (2015), 755–763, 10.1016/j.chembiol.2015.05.009.
-
(2015)
Chemistry & Biology
, vol.22
, Issue.6
, pp. 755-763
-
-
Lu, J.1
Qian, Y.2
Altieri, M.3
Dong, H.4
Wang, J.5
Raina, K.6
Crews, C.M.7
-
35
-
-
84954095264
-
The cellular thermal shift assay: A novel biophysical assay for in situ drug target engagement and mechanistic biomarker studies
-
Martinez Molina, D., Nordlund, P., The cellular thermal shift assay: A novel biophysical assay for in situ drug target engagement and mechanistic biomarker studies. Annual Review of Pharmacology and Toxicology 56 (2016), 141–161, 10.1146/annurev-pharmtox-010715-103715.
-
(2016)
Annual Review of Pharmacology and Toxicology
, vol.56
, pp. 141-161
-
-
Martinez Molina, D.1
Nordlund, P.2
-
36
-
-
79955461011
-
Subcutaneous versus intravenous administration of bortezomib in patients with relapsed multiple myeloma: A randomised, phase 3, non-inferiority study
-
Moreau, P., Pylypenko, H., Grosicki, S., Karamanesht, I., Leleu, X., Grishunina, M.,.. Harousseau, J.-L., Subcutaneous versus intravenous administration of bortezomib in patients with relapsed multiple myeloma: A randomised, phase 3, non-inferiority study. The Lancet. Oncology 12:5 (2011), 431–440, 10.1016/S1470-2045(11)70081-X.
-
(2011)
The Lancet. Oncology
, vol.12
, Issue.5
, pp. 431-440
-
-
Moreau, P.1
Pylypenko, H.2
Grosicki, S.3
Karamanesht, I.4
Leleu, X.5
Grishunina, M.6
Harousseau, J.-L.7
-
37
-
-
2342624080
-
EGFR mutations in lung cancer: Correlation with clinical response to gefitinib therapy
-
Paez, J.G., Jänne, P.A., Lee, J.C., Tracy, S., Greulich, H., Gabriel, S.,.. Meyerson, M., EGFR mutations in lung cancer: Correlation with clinical response to gefitinib therapy. Science (New York, N.Y.) 304:5676 (2004), 1497–1500, 10.1126/science.1099314.
-
(2004)
Science (New York, N.Y.)
, vol.304
, Issue.5676
, pp. 1497-1500
-
-
Paez, J.G.1
Jänne, P.A.2
Lee, J.C.3
Tracy, S.4
Greulich, H.5
Gabriel, S.6
Meyerson, M.7
-
38
-
-
0036080310
-
Ligand-specific regulation of proteasome-mediated proteolysis of estrogen receptor-alpha
-
Preisler-Mashek, M.T., Solodin, N., Stark, B.L., Tyriver, M.K., Alarid, E.T., Ligand-specific regulation of proteasome-mediated proteolysis of estrogen receptor-alpha. American Journal of Physiology. Endocrinology and Metabolism 282:4 (2002), E891–E898, 10.1152/ajpendo.00353.2001.
-
(2002)
American Journal of Physiology. Endocrinology and Metabolism
, vol.282
, Issue.4
, pp. E891-E898
-
-
Preisler-Mashek, M.T.1
Solodin, N.2
Stark, B.L.3
Tyriver, M.K.4
Alarid, E.T.5
-
39
-
-
84976614642
-
PROTAC-induced BET protein degradation as a therapy for castration-resistant prostate cancer
-
Raina, K., Lu, J., Qian, Y., Altieri, M., Gordon, D., Rossi, A.M.K.,.. Coleman, K.G., PROTAC-induced BET protein degradation as a therapy for castration-resistant prostate cancer. Proceedings of the National Academy of Sciences, 2016, 201521738, 10.1073/pnas.1521738113.
-
(2016)
Proceedings of the National Academy of Sciences
, pp. 201521738
-
-
Raina, K.1
Lu, J.2
Qian, Y.3
Altieri, M.4
Gordon, D.5
Rossi, A.M.K.6
Coleman, K.G.7
-
40
-
-
79961007572
-
Trends in the exploitation of novel drug targets
-
Rask-Andersen, M., Almén, M.S., Schiöth, H.B., Trends in the exploitation of novel drug targets. Nature Reviews Drug Discovery 10:8 (2011), 579–590, 10.1038/nrd3478.
-
(2011)
Nature Reviews Drug Discovery
, vol.10
, Issue.8
, pp. 579-590
-
-
Rask-Andersen, M.1
Almén, M.S.2
Schiöth, H.B.3
-
41
-
-
0035902475
-
Protacs: Chimeric molecules that target proteins to the Skp1-Cullin-F box complex for ubiquitination and degradation
-
Sakamoto, K.M., Kim, K.B., Kumagai, A., Mercurio, F., Crews, C.M., Deshaies, R.J., Protacs: Chimeric molecules that target proteins to the Skp1-Cullin-F box complex for ubiquitination and degradation. Proceedings of the National Academy of Sciences of the United States of America 98:15 (2001), 8554–8559, 10.1073/pnas.141230798.
-
(2001)
Proceedings of the National Academy of Sciences of the United States of America
, vol.98
, Issue.15
, pp. 8554-8559
-
-
Sakamoto, K.M.1
Kim, K.B.2
Kumagai, A.3
Mercurio, F.4
Crews, C.M.5
Deshaies, R.J.6
-
42
-
-
79952108510
-
Oncogenic mutations of PIK3CA in human cancers
-
Samuels, Y., Waldman, T., Oncogenic mutations of PIK3CA in human cancers. Current Topics in Microbiology and Immunology 347 (2010), 21–41, 10.1007/82_2010_68.
-
(2010)
Current Topics in Microbiology and Immunology
, vol.347
, pp. 21-41
-
-
Samuels, Y.1
Waldman, T.2
-
43
-
-
60149109196
-
Lapatinib, a HER2 tyrosine kinase inhibitor, induces stabilization and accumulation of HER2 and potentiates trastuzumab-dependent cell cytotoxicity
-
Scaltriti, M., Verma, C., Guzman, M., Jimenez, J., Parra, J.L., Pedersen, K.,.. Baselga, J., Lapatinib, a HER2 tyrosine kinase inhibitor, induces stabilization and accumulation of HER2 and potentiates trastuzumab-dependent cell cytotoxicity. Oncogene 28:6 (2009), 803–814, 10.1038/onc.2008.432.
-
(2009)
Oncogene
, vol.28
, Issue.6
, pp. 803-814
-
-
Scaltriti, M.1
Verma, C.2
Guzman, M.3
Jimenez, J.4
Parra, J.L.5
Pedersen, K.6
Baselga, J.7
-
44
-
-
1642343326
-
Chemical genetic control of protein levels: Selective in vivo targeted degradation
-
Schneekloth, J.S., Fonseca, F.N., Koldobskiy, M., Mandal, A., Deshaies, R., Sakamoto, K., Crews, C.M., Chemical genetic control of protein levels: Selective in vivo targeted degradation. Journal of the American Chemical Society 126:12 (2004), 3748–3754, 10.1021/ja039025z.
-
(2004)
Journal of the American Chemical Society
, vol.126
, Issue.12
, pp. 3748-3754
-
-
Schneekloth, J.S.1
Fonseca, F.N.2
Koldobskiy, M.3
Mandal, A.4
Deshaies, R.5
Sakamoto, K.6
Crews, C.M.7
-
45
-
-
55549137044
-
Targeted intracellular protein degradation induced by a small molecule: En route to chemical proteomics
-
Schneekloth, A.R., Pucheault, M., Tae, H.S., Crews, C.M., Targeted intracellular protein degradation induced by a small molecule: En route to chemical proteomics. Bioorganic & Medicinal Chemistry Letters 18:22 (2008), 5904–5908, 10.1016/j.bmcl.2008.07.114.
-
(2008)
Bioorganic & Medicinal Chemistry Letters
, vol.18
, Issue.22
, pp. 5904-5908
-
-
Schneekloth, A.R.1
Pucheault, M.2
Tae, H.S.3
Crews, C.M.4
-
46
-
-
37849030901
-
Polyglutamine diseases: Emerging concepts in pathogenesis and therapy
-
Shao, J., Diamond, M.I., Polyglutamine diseases: Emerging concepts in pathogenesis and therapy. Human Molecular Genetics, 2007, R115–R123, 10.1093/hmg/ddm213.
-
(2007)
Human Molecular Genetics
, pp. R115-R123
-
-
Shao, J.1
Diamond, M.I.2
-
47
-
-
84940759062
-
Efficacy and safety of patisiran for familial amyloidotic polyneuropathy: A phase II multi-dose study
-
Suhr, O.B., Coelho, T., Buades, J., Pouget, J., Conceicao, I., Berk, J.,.. Melton, B., Efficacy and safety of patisiran for familial amyloidotic polyneuropathy: A phase II multi-dose study. Orphanet Journal of Rare Diseases, 10(1), 2015, 109, 10.1186/s13023-015-0326-6.
-
(2015)
Orphanet Journal of Rare Diseases
, vol.10
, Issue.1
, pp. 109
-
-
Suhr, O.B.1
Coelho, T.2
Buades, J.3
Pouget, J.4
Conceicao, I.5
Berk, J.6
Melton, B.7
-
48
-
-
84961285814
-
Small-molecule PROTACS: New approaches to protein degradation
-
Toure, M., Crews, C.M., Small-molecule PROTACS: New approaches to protein degradation. Angewandte Chemie (International Ed. in English) 55:6 (2016), 1966–1973, 10.1002/anie.201507978.
-
(2016)
Angewandte Chemie (International Ed. in English)
, vol.55
, Issue.6
, pp. 1966-1973
-
-
Toure, M.1
Crews, C.M.2
-
49
-
-
84932634729
-
Phthalimide conjugation as a strategy for in vivo target protein degradation
-
Winter, G.E., Buckley, D.L., Paulk, J., Roberts, J.M., Souza, A., Dhe-Paganon, S., Bradner, J.E., Phthalimide conjugation as a strategy for in vivo target protein degradation. Science, 348(6241), 2015.
-
(2015)
Science
, vol.348
, Issue.6241
-
-
Winter, G.E.1
Buckley, D.L.2
Paulk, J.3
Roberts, J.M.4
Souza, A.5
Dhe-Paganon, S.6
Bradner, J.E.7
-
50
-
-
84939788143
-
Selective small molecule induced degradation of the BET bromodomain protein BRD4
-
Zengerle, M., Chan, K.-H., Ciulli, A., Selective small molecule induced degradation of the BET bromodomain protein BRD4. ACS Chemical Biology 10:8 (2015), 1770–1777, 10.1021/acschembio.5b00216.
-
(2015)
ACS Chemical Biology
, vol.10
, Issue.8
, pp. 1770-1777
-
-
Zengerle, M.1
Chan, K.-H.2
Ciulli, A.3
|