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TG02
National Institutes of Health
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Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Centimeter-Level Orbit Determination for TG02 Spacelab Using Onboard GNSS Data
Kai Li
,
Xuhua Zhou
,
+4 authors
Kexin Xu
Italian National Conference on Sensors
2018
Corpus ID: 52009082
Tiangong-2, the second Chinese manned spacecraft, was launched into low Earth orbit on 15 September 2016. The dual-frequency…
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2017
2017
EXTH-67. TG02, A BRAIN-PENETRANT MULTI-CDK INHIBITOR, POTENTLY SUPPRESSES MYC-DRIVEN GLIOBLASTOMA
J. Tsang
,
Sarah Sung
,
Laura Gosa
,
K. Meetze
,
T. Cloughesy
,
D. Nathanson
2017
Corpus ID: 57827758
2016
2016
Complementary dynamic BH3 profiles predict co-operativity between the multi-kinase inhibitor TG02 and the BH3 mimetic ABT-199 in acute myeloid leukaemia cells
M. Pallis
,
F. Burrows
,
+6 authors
N. Russell
OncoTarget
2016
Corpus ID: 13385327
Direct co-operation between sensitiser molecules BAD and NOXA in mediating apoptosis suggests that therapeutic agents which…
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2014
2014
Abstract 4536: ABT-737 and ABT-199 complement the multikinase inhibitor TG02 to induce apoptosis in acute myeloid leukemia cells
A. Abdul-Aziz
,
F. Burrows
,
N. Yu
,
N. Russell
,
C. Seedhouse
,
M. Pallis
2014
Corpus ID: 70499042
Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA TG02 is a novel multikinase inhibitor currently in Phase 1…
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2013
2013
Dual inhibition of Mcl-1 by the combination of carfilzomib and TG02 in multiple myeloma
Katelyn G. Ponder
,
Shannon M Matulis
,
+7 authors
L. Boise
Cancer Biology & Therapy
2013
Corpus ID: 205878803
ABSTRACT Carfilzomib (Kyprolis®), a second generation proteasome inhibitor, is FDA approved for single-agent use among relapsed…
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2012
2012
The multi‐kinase inhibitor TG02 overcomes signalling activation by survival factors to deplete MCL1 and XIAP and induce cell death in primary acute myeloid leukaemia cells
M. Pallis
,
A. Abdul-Aziz
,
F. Burrows
,
C. Seedhouse
,
Martin Grundy
,
N. Russell
British Journal of Haematology
2012
Corpus ID: 24893181
The novel multi‐kinase inhibitor TG02 has selectivity against cell cycle and transcriptional cyclin dependent kinases (CDKs) as…
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2012
2012
Preclinical metabolism and pharmacokinetics of SB1317 (TG02), a potent CDK/JAK2/FLT3 inhibitor.
M. K. Pasha
,
R. Jayaraman
,
+5 authors
E. Kantharaj
Drug Metabolism Letters
2012
Corpus ID: 39113450
SB1317 (TG02) is a novel small molecule potent CDK/JAK2/FLT3 inhibitor. To evaluate full potential of this development candidate…
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2012
2012
Abstract 2830: Multikinase inhibition by TG02 is therapeutically effective in two forms of breast cancer
M. Ortiz-Ruiz
,
F. Burrows
,
M. F. Re-Louhau
,
A. Ocaña
,
A. Pandiella
,
A. Esparís-Ogando
2012
Corpus ID: 75610370
Breast cancer (BC) is a heterogeneous disease in which several distinct genetic and histopathological types have been defined…
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2010
2010
Antimyeloma Action of the Multikinase Inhibitor TG02
Stela Álvarez-Fernández
,
Susana Hernández-García
,
+7 authors
A. Pandiella
2010
Corpus ID: 88823695
Abstract 4062 Multiple myeloma (MM) is the second most common hematologic malignancy and remains incurable, despite recent…
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2010
2010
Abstract 2542: TG02, a novel multi-kinase inhibitor with potent anti-leukemic activity
K. Goh
,
V. Novotny‐Diermayr
,
+12 authors
F. Burrows
2010
Corpus ID: 72379381
Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC Kinase inhibitors have found applications in…
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