Targeting BTK for the treatment of FLT3-ITD mutated acute myeloid leukemia [PDF]
Approximately 20% of patients with acute myeloid leukaemia (AML) have a mutation in FMS-like-tyrosine-kinase-3 (FLT3). FLT3 is a trans-membrane receptor with a tyrosine kinase domain which, when activated, initiates a cascade of phosphorylated proteins ...
A Puissant +49 more
core +2 more sources
Bruton’s Tyrosine Kinase and Its Isoforms in Cancer
Bruton’s tyrosine kinase (BTK) is a soluble tyrosine kinase with central roles in the development, maturation, and signaling of B cells. BTK has been found to regulate cell proliferation, survival, and migration in various B-cell malignancies.
Xianhui Wang +3 more
doaj +1 more source
Btk inhibitors in atherosclerosis [PDF]
In this issue of Blood, Busygina et al provide provocative evidence that there is a potential role for Bruton tyrosine kinase (Btk) inhibitors in inhibiting platelet aggregation specifically at the site of unstable atherosclerotic plaques ...
openaire +2 more sources
Tumor suppressor function of Bruton tyrosine kinase is independent of its catalytic activity [PDF]
During B-cell development in the mouse, Bruton tyrosine kinase (Btk) and the adaptor protein SLP-65 (Src homology 2 [SH2] domain-containing leukocyte protein of 65 kDa) limit the expansion and promote the differentiation of pre-B cells.
Dingjan, G.M. (Gemma) +5 more
core +3 more sources
BTK Inhibitors in Chronic Lymphocytic Leukemia: Biological Activity and Immune Effects
Bruton´s tyrosine kinase (BTK) inhibitor (BTKi)s block the B-cell receptor (BCR) signaling cascade by binding to the BTK enzyme preventing the proliferation and survival of malignant and normal B cells.
M. Palma, T. Mulder, A. Österborg
semanticscholar +1 more source
Bruton Tyrosine Kinase Inhibition and Its Role as an Emerging Treatment in Pemphigus
Bruton Tyrosine Kinase (BTK) has a key role in multiple pathways involved in inflammation and autoimmunity. Therefore, BTK has become a new therapeutic target for a group of hematologic and autoimmune disorders.
Aikaterini Patsatsi, Dedee F. Murrell
doaj +1 more source
Kinase-impaired BTK mutations are susceptible to clinical-stage BTK and IKZF1/3 degrader NX-2127
Increasing use of covalent and noncovalent inhibitors of Bruton’s tyrosine kinase (BTK) has elucidated a series of acquired drug-resistant BTK mutations in patients with B cell malignancies.
S. Montoya +52 more
semanticscholar +1 more source
Coexistence of two order parameters and a pseudogaplike feature in the iron-based superconductor LaFeAsO_(1-x)F_x [PDF]
The nature and value of the order parameters (OPs) in the superconducting Fe-based oxypnictides REFeAsO_(1-x)F_x (RE = rare earth) are a matter of intense debate, also connected to the pairing mechanism which is probably unconventional.
Daghero, D. +6 more
core +1 more source
Managing Waldenström’s macroglobulinemia with BTK inhibitors
Bruton’s tyrosine kinase (BTK) inhibition is one of the treatment standards for patients with relapsed/refractory Waldenström’s macroglobulinemia (WM) and for patients with WM who are unsuitable for immunochemotherapy (ICT).
C. Buske +3 more
semanticscholar +1 more source
BTK inhibitors in CLL: second-generation drugs and beyond
BTK inhibitors (BTKis) are established standards of care in multiple B-cell malignancies including chronic lymphocytic leukemia, mantle cell lymphoma, and Waldenstrom macroglobulinemia.
Constantine S. Tam, Philip A Thompson
semanticscholar +1 more source

