scholarly article | Q13442814 |
P819 | ADS bibcode | 2006PNAS..10316870H |
P356 | DOI | 10.1073/PNAS.0606509103 |
P932 | PMC publication ID | 1629087 |
P698 | PubMed publication ID | 17077147 |
P5875 | ResearchGate publication ID | 6719703 |
P50 | author | Yiguo Hu | Q59549068 |
P2093 | author name string | Francis Y Lee | |
Shaoguang Li | |||
Sarah Swerdlow | |||
Roberto Weinmann | |||
Theodore M Duffy | |||
P2860 | cites work | Dasatinib in imatinib-resistant Philadelphia chromosome-positive leukemias | Q28246193 |
Tyrosine phosphorylation of Grb2 by Bcr/Abl and epidermal growth factor receptor: a novel regulatory mechanism for tyrosine kinase signaling | Q28365521 | ||
Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia | Q29547900 | ||
Granulocyte-macrophage progenitors as candidate leukemic stem cells in blast-crisis CML | Q29614278 | ||
Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification | Q29618788 | ||
Isolation and functional properties of murine hematopoietic stem cells that are replicating in vivo | Q29619355 | ||
Overriding imatinib resistance with a novel ABL kinase inhibitor | Q30014844 | ||
Activity of a specific inhibitor of the BCR-ABL tyrosine kinase in the blast crisis of chronic myeloid leukemia and acute lymphoblastic leukemia with the Philadelphia chromosome | Q33336718 | ||
Clinical resistance to the kinase inhibitor STI-571 in chronic myeloid leukemia by mutation of Tyr-253 in the Abl kinase domain P-loop | Q34075619 | ||
Inhibition of wild-type and mutant Bcr-Abl by AP23464, a potent ATP-based oncogenic protein kinase inhibitor: implications for CML. | Q34333693 | ||
Arf gene loss enhances oncogenicity and limits imatinib response in mouse models of Bcr-Abl-induced acute lymphoblastic leukemia | Q34546468 | ||
Inhibition of KIT tyrosine kinase activity: a novel molecular approach to the treatment of KIT-positive malignancies | Q34564857 | ||
Punish the parent not the progeny. | Q35940421 | ||
The P190, P210, and P230 forms of the BCR/ABL oncogene induce a similar chronic myeloid leukemia-like syndrome in mice but have different lymphoid leukemogenic activity | Q36368162 | ||
p53 in chronic myelogenous leukemia in acute phase | Q37550931 | ||
Characterization of AMN107, a selective inhibitor of native and mutant Bcr-Abl. | Q40458599 | ||
The src homology 2 domain of Bcr/Abl is required for efficient induction of chronic myeloid leukemia-like disease in mice but not for lymphoid leukemogenesis or activation of phosphatidylinositol 3-kinase | Q40835186 | ||
Establishment of a murine model for therapy-treated chronic myelogenous leukemia using the tyrosine kinase inhibitor STI571. | Q43775891 | ||
Primitive, quiescent, Philadelphia-positive stem cells from patients with chronic myeloid leukemia are insensitive to STI571 in vitro | Q43833442 | ||
Imatinib mesylate (STI571) inhibits growth of primitive malignant progenitors in chronic myelogenous leukemia through reversal of abnormally increased proliferation | Q43977712 | ||
Dual-specific Src and Abl kinase inhibitors, PP1 and CGP76030, inhibit growth and survival of cells expressing imatinib mesylate-resistant Bcr-Abl kinases | Q44189751 | ||
Selective pyrrolo-pyrimidine inhibitors reveal a necessary role for Src family kinases in Bcr-Abl signal transduction and oncogenesis. | Q44224219 | ||
BCR-ABL independence and LYN kinase overexpression in chronic myelogenous leukemia cells selected for resistance to STI571. | Q44267685 | ||
Requirement of Src kinases Lyn, Hck and Fgr for BCR-ABL1-induced B-lymphoblastic leukemia but not chronic myeloid leukemia | Q44851706 | ||
A tail of two src's: mutatis mutandis | Q45248634 | ||
Absence of the human retinoblastoma gene product in the megakaryoblastic crisis of chronic myelogenous leukemia | Q46466215 | ||
Homozygous deletions of the p16 tumor-suppressor gene are associated with lymphoid transformation of chronic myeloid leukemia. | Q53464437 | ||
The tyrosine kinase inhibitor STI571, like interferon-alpha, preferentially reduces the capacity for amplification of granulocyte-macrophage progenitors from patients with chronic myeloid leukemia | Q73795156 | ||
Efficient and rapid induction of a chronic myelogenous leukemia-like myeloproliferative disease in mice receiving P210 bcr/abl-transduced bone marrow | Q77531813 | ||
P433 | issue | 45 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | leukemia | Q29496 |
P304 | page(s) | 16870-16875 | |
P577 | publication date | 2006-10-31 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | Targeting multiple kinase pathways in leukemic progenitors and stem cells is essential for improved treatment of Ph+ leukemia in mice | |
P478 | volume | 103 |
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Q28540033 | ATRA-induced cellular differentiation and CD38 expression inhibits acquisition of BCR-ABL mutations for CML acquired resistance |
Q36835733 | Ablation of PI3K blocks BCR-ABL leukemogenesis in mice, and a dual PI3K/mTOR inhibitor prevents expansion of human BCR-ABL+ leukemia cells |
Q47113874 | Activation of TRKA receptor elicits mastocytosis in mice and is involved in the development of resistance to KIT-targeted therapy |
Q34547402 | Activation of the Hedgehog pathway in chronic myelogeneous leukemia patients |
Q39663467 | Activity of the potent dual Abl/Src tyrosine kinase inhibitor FB2 against Bcr–Abl positive cell lines in vitro and in vivo |
Q61449792 | Advances in biology of acute lymphoblastic leukemia (ALL) and therapeutic implications |
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Q35931271 | Alternative approaches to eradicating the malignant clone in chronic myeloid leukemia: tyrosine-kinase inhibitor combinations and beyond |
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Q54655112 | Are SRC family kinases responsible for imatinib- and dasatinib-resistant chronic myeloid leukemias? |
Q33988398 | Association between imatinib-resistant BCR-ABL mutation-negative leukemia and persistent activation of LYN kinase |
Q35441406 | BCL6-mediated repression of p53 is critical for leukemia stem cell survival in chronic myeloid leukemia |
Q33806036 | BCR-ABL enhances differentiation of long-term repopulating hematopoietic stem cells |
Q36970694 | BCR-ABL-transformed GMP as myeloid leukemic stem cells |
Q39974408 | BCR-ABL1-induced expression of HSPA8 promotes cell survival in chronic myeloid leukaemia |
Q37531026 | BCR/ABL can promote CD19+ cell growth but not render them long-term stemness |
Q33947776 | Bcl2 is not required for the development and maintenance of leukemia stem cells in mice. |
Q46774789 | Bcr-Abl induces autocrine IGF-1 signaling |
Q33442587 | Bosutinib as a fourth-line therapy for a patient with T315I-positive lymphoid blastic phase chronic myeloid leukemia: A case report |
Q37810115 | Bosutinib: a dual SRC/ABL kinase inhibitor for the treatment of chronic myeloid leukemia |
Q36463738 | CD150(-) Side Population Defines Leukemia Stem Cells in a BALB/c Mouse Model of CML and Is Depleted by Genetic Loss of SIRT1 |
Q34251497 | CD44 targets Wnt/β-catenin pathway to mediate the proliferation of K562 cells |
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Q38133575 | Changes in molecular biology of chronic myeloid leukemia in tyrosine kinase inhibitor era. |
Q24622397 | Chemotherapeutic agents circumvent emergence of dasatinib-resistant BCR-ABL kinase mutations in a precise mouse model of Philadelphia chromosome-positive acute lymphoblastic leukemia |
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Q27025242 | Current concepts in pediatric Philadelphia chromosome-positive acute lymphoblastic leukemia |
Q37650203 | Current treatment options for adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia |
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Q58921972 | DNA Microarray Assay Helps to Identify Functional Genes Specific for Leukemia Stem Cells |
Q33384766 | Dasatinib in the treatment of chronic myeloid leukemia in accelerated phase after imatinib failure: the START a trial |
Q34335004 | Dasatinib inhibits the growth of molecularly heterogeneous myeloid leukemias |
Q43178572 | Deletion of the RNA-editing enzyme ADAR1 causes regression of established chronic myelogenous leukemia in mice |
Q42017483 | Development of resistance to dasatinib in Bcr/Abl-positive acute lymphoblastic leukemia |
Q37308308 | Differential regulation of myeloid leukemias by the bone marrow microenvironment |
Q38782370 | Disarming an Electrophilic Warhead: Retaining Potency in Tyrosine Kinase Inhibitor (TKI)-Resistant CML Lines While Circumventing Pharmacokinetic Liabilities |
Q36780139 | Distinct GAB2 signaling pathways are essential for myeloid and lymphoid transformation and leukemogenesis by BCR-ABL1. |
Q35651730 | Distinct graft-versus-leukemic stem cell effects of early or delayed donor leukocyte infusions in a mouse chronic myeloid leukemia model |
Q36445910 | Effective and selective inhibition of chronic myeloid leukemia primitive hematopoietic progenitors by the dual Src/Abl kinase inhibitor SKI-606. |
Q33597663 | Effective and selective targeting of leukemia cells using a TORC1/2 kinase inhibitor |
Q37450433 | Effects of dasatinib on SRC kinase activity and downstream intracellular signaling in primitive chronic myelogenous leukemia hematopoietic cells |
Q34596305 | Efficacy and safety of dasatinib in imatinib-resistant or -intolerant patients with chronic myeloid leukemia in blast phase. |
Q46755224 | Enhanced BCR-ABL kinase inhibition does not result in increased inhibition of downstream signaling pathways or increased growth suppression in CML progenitors |
Q35987068 | Essential role for telomerase in chronic myeloid leukemia induced by BCR-ABL in mice |
Q42223517 | Evi1 defines leukemia-initiating capacity and tyrosine kinase inhibitor resistance in chronic myeloid leukemia |
Q35571035 | Final report of a phase II study of imatinib mesylate with hyper-CVAD for the front-line treatment of adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia |
Q34972855 | From Hen House to Bedside: Tracing Hanafusa's Legacy from Avian Leukemia Viruses to SRC to ABL and Beyond |
Q34062313 | Functional ramifications for the loss of P-selectin expression on hematopoietic and leukemic stem cells |
Q53197147 | Fyn is not essential for Bcr-Abl-induced leukemogenesis in mouse bone marrow transplantation models. |
Q36598249 | GABP transcription factor is required for development of chronic myelogenous leukemia via its control of PRKD2 |
Q47210315 | GZD824 suppresses the growth of human B cell precursor acute lymphoblastic leukemia cells by inhibiting the SRC kinase and PI3K/AKT pathways |
Q33753325 | Global phosphoproteomics reveals crosstalk between Bcr-Abl and negative feedback mechanisms controlling Src signaling |
Q35849333 | HIF1α is required for survival maintenance of chronic myeloid leukemia stem cells |
Q35176353 | HS-543 induces apoptosis of Imatinib-resistant chronic myelogenous leukemia with T315I mutation |
Q42110946 | HSP90 inhibitor AUY922 induces cell death by disruption of the Bcr-Abl, Jak2 and HSP90 signaling network complex in leukemia cells |
Q38166527 | Heat shock protein 90 and role of its chemical inhibitors in treatment of hematologic malignancies |
Q34157874 | Hedgehog signalling is essential for maintenance of cancer stem cells in myeloid leukaemia |
Q28393898 | Hypoxia-inducing factors as master regulators of stemness properties and altered metabolism of cancer- and metastasis-initiating cells |
Q37697852 | IKK-dependent activation of NF-κB contributes to myeloid and lymphoid leukemogenesis by BCR-ABL1. |
Q39255906 | IL-6 controls leukemic multipotent progenitor cell fate and contributes to chronic myelogenous leukemia development |
Q36948612 | IRF-4 functions as a tumor suppressor in early B-cell development |
Q36240238 | Inhibition of IGF-IR tyrosine kinase induces apoptosis and cell cycle arrest in imatinib-resistant chronic myeloid leukaemia cells |
Q35900937 | Inhibition of heat shock protein 90 prolongs survival of mice with BCR-ABL-T315I-induced leukemia and suppresses leukemic stem cells. |
Q42178606 | Inhibitor mediated protein degradation. |
Q37303829 | Inhibitory effects of omacetaxine on leukemic stem cells and BCR-ABL-induced chronic myeloid leukemia and acute lymphoblastic leukemia in mice |
Q90702236 | Integrin α6 mediates drug resistance of acute lymphoblastic B-cell leukemia |
Q36799469 | Is phosphoproteomics ready for clinical research? |
Q35126258 | Janus kinase inhibition by ruxolitinib extends dasatinib- and dexamethasone-induced remissions in a mouse model of Ph+ ALL. |
Q26849792 | Kinase-independent mechanisms of resistance of leukemia stem cells to tyrosine kinase inhibitors |
Q28484079 | LSK derived LSK- cells have a high apoptotic rate related to survival regulation of hematopoietic and leukemic stem cells |
Q36007673 | Leukemia stem cells in a genetically defined murine model of blast-crisis CML. |
Q53293069 | Leukemia stem cells. |
Q36488720 | Loss of beta-catenin impairs the renewal of normal and CML stem cells in vivo |
Q33921399 | Loss of the Alox5 gene impairs leukemia stem cells and prevents chronic myeloid leukemia |
Q36508969 | Lyn regulates BCR-ABL and Gab2 tyrosine phosphorylation and c-Cbl protein stability in imatinib-resistant chronic myelogenous leukemia cells |
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Q37283128 | Molecular biology of bcr-abl1-positive chronic myeloid leukemia |
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Q36758024 | Oncogenic signaling: new insights and controversies from chronic myeloid leukemia |
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