Zobrazeno 1 - 8
of 8
pro vyhledávání: '"J. Kyle Bruner"'
Autor:
Donald Small, Christine A. Pratilas, Keith W. Pratz, Mark J. Levis, Richard J. Jones, Michelle A. Rudek, Alice Can Ran Qin, Li Li, Hayley S. Ma, J. Kyle Bruner
Table S1: AML Patient Characteristics Table S2: Plasma sample characteristics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23681dc443118c6a306f8231da28ee2f
https://doi.org/10.1158/0008-5472.22414568.v1
https://doi.org/10.1158/0008-5472.22414568.v1
Autor:
Donald Small, Christine A. Pratilas, Keith W. Pratz, Mark J. Levis, Richard J. Jones, Michelle A. Rudek, Alice Can Ran Qin, Li Li, Hayley S. Ma, J. Kyle Bruner
Figure S1: Sorafenib treatment induces phospho-ERK rebound in 32D/ITD cells. Figure S2: Further characterization of FLT3 inhibitor-mediated signaling adaptation. Figure S3: FLT3 signaling is maintained in low serum conditions. Figure S4: MEK inhibito
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fab0992900dd1d02e43c4ebf8f2c310
https://doi.org/10.1158/0008-5472.22414571
https://doi.org/10.1158/0008-5472.22414571
Autor:
Donald Small, Christine A. Pratilas, Keith W. Pratz, Mark J. Levis, Richard J. Jones, Michelle A. Rudek, Alice Can Ran Qin, Li Li, Hayley S. Ma, J. Kyle Bruner
FMS-like tyrosine kinase-3 (FLT3) tyrosine kinase inhibitors (TKI) have been tested extensively to limited benefit in acute myeloid leukemia (AML). We hypothesized that FLT3/internal tandem duplication (ITD) leukemia cells exhibit mechanisms of intri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::498ec01b8b7cb5fbbc354902e39bf311
https://doi.org/10.1158/0008-5472.c.6509027.v1
https://doi.org/10.1158/0008-5472.c.6509027.v1
Autor:
Courtney M. Shirley, Peter D. Aplan, Li Li, Bao Nguyen, Sarah Greenblatt, Richard J. Jones, J. Kyle Bruner, Hayley S Ma, Amy S. Duffield, Donald Small, Eric Jung, Gabriel Ghiaur
Publikováno v:
Blood. 127:2867-2878
FMS-like tyrosine kinase 3 (FLT3)-mutant acute myeloid leukemia (AML) portends a poor prognosis, and ineffective targeting of the leukemic stem cell (LSC) population remains one of several obstacles in treating this disease. All-trans retinoic acid (
Publikováno v:
European Journal of Pharmacology. 740:603-610
Two-pore domain potassium (K2P) channels are responsible for background potassium (K+) current, which is crucial for the maintenance of resting membrane potential. K2P18.1, also called TWIK-related spinal cord K+ channel (TRESK) or KCNK18, is thought
Autor:
Keith W. Pratz, Hayley S Ma, Michelle A. Rudek, Donald Small, Li Li, Richard J. Jones, Alice Can Ran Qin, J. Kyle Bruner, Mark J. Levis, Christine A. Pratilas
Publikováno v:
Cancer research. 77(20)
FMS-like tyrosine kinase-3 (FLT3) tyrosine kinase inhibitors (TKI) have been tested extensively to limited benefit in acute myeloid leukemia (AML). We hypothesized that FLT3/internal tandem duplication (ITD) leukemia cells exhibit mechanisms of intri
Publikováno v:
Cancer Research. 76:4785-4785
The use of FLT3 tyrosine kinase inhibitors (TKIs) for the treatment of FLT3 mutant acute myeloid leukemia (AML) has been explored as a promising strategy for over a decade. However, FLT3 TKIs have thus far shown limited clinical benefit in patients w
Autor:
Richard J. Jones, Donald Small, J. Kyle Bruner, Sarah Greenblatt, Peter D. Aplan, Megan E McCray, Bao Nguyen, Gabriel Ghiaur, Eric Jung, Li Li, Courtney M. Shirley, Amy S. Duffield, Hayley S Ma
Publikováno v:
Blood. 126:790-790
While novel FLT3 tyrosine kinase inhibitors (TKIs) are increasingly efficient, when used as monotherapy they achieve only limited clinical responses in patients with FLT3/ITD acute myeloid leukemia (AML). Leukemia stem cells (LSCs) that share charact