Results 11 to 20 of about 636,170 (221)

The Development of BTK Inhibitors: A Five-Year Update

open access: yesMolecules, 2021
Bruton’s tyrosine kinase (BTK) represented, in the past ten years, an important target for the development of new therapeutic agents that could be useful for cancer and autoimmune disorders.
Bruno Tasso   +3 more
doaj   +2 more sources

Comparison of inhibitory effects of irreversible and reversible Btk inhibitors on platelet function

open access: yeseJHaem, 2021
All irreversible Bruton tyrosine kinase (Btk) inhibitors including ibrutinib and acalabrutinib induce platelet dysfunction and increased bleeding risk. New reversible Btk inhibitors were developed, like MK‐1026.
Bibian M.E. Tullemans   +13 more
doaj   +2 more sources

Evolution of BTK inhibitors [PDF]

open access: yesLynchburg Journal of Medical Science
The purpose of this clinical review evaluates the evolution of bruton’s tyrosine kinase (BTK) inhibitors in becoming the standard of care in treating chronic lymphocytic leukemia (CLL). The first-generation BTK inhibitor ibrutinib has demonstrated superior efficacy over traditional chemotherapy in several randomized clinical trials in terms of ...
Mathew, Dena
openaire   +2 more sources

Targeting Solid Tumors With BTK Inhibitors [PDF]

open access: yesFrontiers in Cell and Developmental Biology, 2021
The repurposing of FDA-approved Bruton’s tyrosine kinase (BTK) inhibitors as therapeutic agents for solid tumors may offer renewed hope for chemotherapy-resistant cancer patients.
Fatih M. Uckun, Taracad Venkatachalam
doaj   +3 more sources

BTK Inhibitors for the Treatment of Mantle Cell Lymphoma-Current Status and Perspectives. [PDF]

open access: yesCancers (Basel)
The introduction of Bruton’s tyrosine kinase inhibitors (BTKis) has significantly improved prognosis in the treatment of MCL. BTK inhibitors have demonstrated strong activity in the treatment of relapsed/refractory patients with mantle cell lymphoma (MCL)
Robak T, Wolska-Washer A, Robak P.
europepmc   +2 more sources

Bruton tyrosine kinase inhibitors as potential therapeutic agents for COVID-19: A review

open access: yesMetabolism Open, 2021
Coronavirus disease 2019 (COVID-19) is first detected in December 2019 in Wuhan, China which is a new pandemic caused by SARS-COV-2 that has greatly affected the whole world.
Zemene Demelash Kifle
doaj   +1 more source

BTK Inhibitors Impair Platelet-Mediated Antifungal Activity [PDF]

open access: yes, 2022
In recent years, the introduction of new drugs targeting Bruton’s tyrosine kinase (BTK) has allowed dramatic improvement in the prognosis of patients with chronic lymphocytic leukemia (CLL) and other B-cell neoplasms. Although these small molecules
Roberto Marasca   +19 more
core   +2 more sources

How We Manage Patients with Indolent B-Cell Malignancies on Bruton’s Tyrosine Kinase Inhibitors: Practical Considerations for Nurses and Pharmacists

open access: yesCurrent Oncology, 2023
The most common forms of B-cell malignancy, non-Hodgkin lymphoma (NHL) and chronic lymphocytic leukemia (CLL), have seen a drastic shift in the treatment landscape over the last two decades with the introduction of targeted agents.
Shannon Nixon   +3 more
doaj   +1 more source

Phylogeny of Tec Family Kinases: Identification of a Pre-Metazoan Origin of Btk, Bmx, Itk, Tec, Txk and the Btk Regulator SH3BP5 [PDF]

open access: yes, 2008
It is generally considered mammals and birds have five Tec family kinases (TFKs): Btk, Bmx (also known as Etk), Itk, Tec, and Txk (also known as Rlk). Here, we discuss the domains and their functions and regulation in TFKs.
Ortutay, Csaba   +3 more
core   +2 more sources

Differential impact of BTK active site inhibitors on the conformational state of full-length BTK

open access: yeseLife, 2020
Bruton’s tyrosine kinase (BTK) is targeted in the treatment of B-cell disorders including leukemias and lymphomas. Currently approved BTK inhibitors, including Ibrutinib, a first-in-class covalent inhibitor of BTK, bind directly to the kinase active site.
Raji E Joseph   +5 more
doaj   +1 more source

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