scholarly article | Q13442814 |
P356 | DOI | 10.1002/AJH.24282 |
P8608 | Fatcat ID | release_qoocxhk3b5berj4mmeewjxunwu |
P698 | PubMed publication ID | 26690614 |
P50 | author | Preetesh Jain | Q41349775 |
P2093 | author name string | Kanti R Rai | |
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Chronic lymphocytic leukemias utilizing the VH3-21 gene display highly restricted Vlambda2-14 gene use and homologous CDR3s: implicating recognition of a common antigen epitope. | Q54789536 | ||
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Sequential ofatumumab and lenalidomide for the treatment of relapsed and refractory chronic lymphocytic leukemia and small lymphocytic lymphoma | Q33417117 | ||
Ibrutinib for previously untreated and relapsed or refractory chronic lymphocytic leukaemia with TP53 aberrations: a phase 2, single-arm trial | Q33419580 | ||
Incidence and description of autoimmune cytopenias during treatment with ibrutinib for chronic lymphocytic leukemia | Q33426511 | ||
Selinexor suppresses downstream effectors of B-cell activation, proliferation and migration in chronic lymphocytic leukemia cells. | Q33578875 | ||
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Chronic lymphocytic leukemia cells in a lymph node microenvironment depict molecular signature associated with an aggressive disease | Q33934606 | ||
Discovery of selective irreversible inhibitors for Bruton's tyrosine kinase | Q34001339 | ||
The Bruton tyrosine kinase inhibitor PCI-32765 thwarts chronic lymphocytic leukemia cell survival and tissue homing in vitro and in vivo | Q34029869 | ||
Egress of CD19(+)CD5(+) cells into peripheral blood following treatment with the Bruton tyrosine kinase inhibitor ibrutinib in mantle cell lymphoma patients | Q34037828 | ||
Familial predisposition and genetic risk factors for lymphoma | Q34044984 | ||
Ibrutinib versus ofatumumab in previously treated chronic lymphoid leukemia | Q34052075 | ||
SF3B1 and other novel cancer genes in chronic lymphocytic leukemia | Q34093678 | ||
Addition of rituximab to fludarabine and cyclophosphamide in patients with chronic lymphocytic leukaemia: a randomised, open-label, phase 3 trial | Q34141305 | ||
Phosphatidylinositol 3-kinase-δ inhibitor CAL-101 shows promising preclinical activity in chronic lymphocytic leukemia by antagonizing intrinsic and extrinsic cellular survival signals | Q34184717 | ||
Safety and activity of ibrutinib plus rituximab for patients with high-risk chronic lymphocytic leukaemia: a single-arm, phase 2 study | Q34240404 | ||
The clinically active BTK inhibitor PCI-32765 targets B-cell receptor- and chemokine-controlled adhesion and migration in chronic lymphocytic leukemia | Q34249777 | ||
Early results of a chemoimmunotherapy regimen of fludarabine, cyclophosphamide, and rituximab as initial therapy for chronic lymphocytic leukemia | Q34402999 | ||
Serum beta(2)-microglobulin and serum thymidine kinase are independent predictors of progression-free survival in chronic lymphocytic leukemia and immunocytoma | Q34403901 | ||
Development of a comprehensive prognostic index for patients with chronic lymphocytic leukemia | Q34418874 | ||
Long-term results of first salvage treatment in CLL patients treated initially with FCR (fludarabine, cyclophosphamide, rituximab) | Q34508322 | ||
The lymph node microenvironment promotes B-cell receptor signaling, NF-κB activation, and tumor proliferation in chronic lymphocytic leukemia | Q34542102 | ||
Chemoimmunotherapy with fludarabine and rituximab produces extended overall survival and progression-free survival in chronic lymphocytic leukemia: long-term follow-up of CALGB study 9712 | Q34879367 | ||
Not all IGHV3-21 chronic lymphocytic leukemias are equal: prognostic considerations | Q35029461 | ||
The PI3-kinase delta inhibitor idelalisib (GS-1101) targets integrin-mediated adhesion of chronic lymphocytic leukemia (CLL) cell to endothelial and marrow stromal cells | Q35078248 | ||
Three-year follow-up of treatment-naïve and previously treated patients with CLL and SLL receiving single-agent ibrutinib | Q35450520 | ||
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The Bruton tyrosine kinase inhibitor ibrutinib with chemoimmunotherapy in patients with chronic lymphocytic leukemia. | Q35583403 | ||
Selinexor is effective in acquired resistance to ibrutinib and synergizes with ibrutinib in chronic lymphocytic leukemia | Q35607285 | ||
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Functional loss of IκBε leads to NF-κB deregulation in aggressive chronic lymphocytic leukemia | Q35671227 | ||
Excessive antigen reactivity may underlie the clinical aggressiveness of chronic lymphocytic leukemia stereotyped subset #8. | Q35692395 | ||
Single-Cell Analysis and Next-Generation Immuno-Sequencing Show That Multiple Clones Persist in Patients with Chronic Lymphocytic Leukemia | Q35768156 | ||
Hypermorphic mutation of phospholipase C, γ2 acquired in ibrutinib-resistant CLL confers BTK independency upon B-cell receptor activation | Q35820367 | ||
Clinical staging and prognostic markers in chronic lymphocytic leukemia | Q35869482 | ||
Etiology of Ibrutinib Therapy Discontinuation and Outcomes in Patients With Chronic Lymphocytic Leukemia | Q35903984 | ||
High fluorescence in situ hybridization percentage of deletion 11q in patients with chronic lymphocytic leukemia is an independent predictor of adverse outcome | Q35906329 | ||
Safety and activity of BTK inhibitor ibrutinib combined with ofatumumab in chronic lymphocytic leukemia: a phase 1b/2 study | Q35953518 | ||
Novel targeted agents and the need to refine clinical end points in chronic lymphocytic leukemia | Q36135185 | ||
Partial reconstitution of humoral immunity and fewer infections in patients with chronic lymphocytic leukemia treated with ibrutinib | Q36253983 | ||
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Ibrutinib as Initial Therapy for Patients with Chronic Lymphocytic Leukemia | Q36490049 | ||
A phase 2 study of idelalisib plus rituximab in treatment-naïve older patients with chronic lymphocytic leukemia | Q36519986 | ||
Evolution and impact of subclonal mutations in chronic lymphocytic leukemia | Q36619124 | ||
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Phase II study of lenalidomide and rituximab as salvage therapy for patients with relapsed or refractory chronic lymphocytic leukemia | Q36929831 | ||
De novo deletion 17p13.1 chronic lymphocytic leukemia shows significant clinical heterogeneity: the M. D. Anderson and Mayo Clinic experience | Q37028638 | ||
Sequential therapy with fludarabine, high-dose cyclophosphamide, and rituximab in previously untreated patients with chronic lymphocytic leukemia produces high-quality responses: molecular remissions predict for durable complete responses | Q37104775 | ||
Prolonged lymphocytosis during ibrutinib therapy is associated with distinct molecular characteristics and does not indicate a suboptimal response to therapy | Q37655012 | ||
Genetic lesions associated with chronic lymphocytic leukemia chemo-refractoriness | Q37697850 | ||
Targeting Bruton's tyrosine kinase in B cell malignancies | Q38198490 | ||
How does lenalidomide target the chronic lymphocytic leukemia microenvironment? | Q38243771 | ||
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What is the status of novel anti-CD20 antibodies for chronic lymphocytic leukemia and are they set to leave rituximab in the shadows? | Q38586543 | ||
The CLL12 trial protocol: a placebo-controlled double-blind Phase III study of ibrutinib in the treatment of early-stage chronic lymphocytic leukemia patients with risk of early disease progression | Q38986156 | ||
CAL-101, a p110delta selective phosphatidylinositol-3-kinase inhibitor for the treatment of B-cell malignancies, inhibits PI3K signaling and cellular viability | Q39642145 | ||
Mutations driving CLL and their evolution in progression and relapse | Q39714436 | ||
The phosphoinositide 3'-kinase delta inhibitor, CAL-101, inhibits B-cell receptor signaling and chemokine networks in chronic lymphocytic leukemia | Q39722770 | ||
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P433 | issue | 3 | |
P921 | main subject | lymphocyte | Q715347 |
chronic lymphocytic leukemia | Q1088156 | ||
P304 | page(s) | 330-340 | |
P577 | publication date | 2016-03-01 | |
P1433 | published in | American Journal of Hematology | Q4744246 |
P1476 | title | Chronic lymphocytic leukemia (CLL)-Then and now | |
P478 | volume | 91 |
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