Results 21 to 30 of about 399,504 (355)

The Janus kinase 1/2 inhibitor ruxolitinib in COVID-19 [PDF]

open access: bronzeLeukemia, 2020
La Rosee F, Bremer HC, Gehrke I, Kehr A, Hochhaus A, Birndt S, et al. The Janus kinase 1/2 inhibitor ruxolitinib in COVID-19 with severe systemic hyperinflammation. Leukemia. 2020;34:1805–15. https://doi.org/10.1038/s41375-020-0891-0. CAS Article PubMed Google Scholar Download references Division of Hematology, University of Siena, Siena, Italy ...
Alessandro Gozzetti   +2 more
openalex   +5 more sources

Janus kinase-2 inhibitor fedratinib in patients with myelofibrosis previously treated with ruxolitinib (JAKARTA-2): a single-arm, open-label, non-randomised, phase 2, multicentre study [PDF]

open access: bronzeThe Lancet Haematology, 2017
Claire Harrison   +15 more
openalex   +2 more sources

Janus kinase-1 and Janus kinase-2 inhibitors for treating myelofibrosis.

open access: yesCochrane Database of Systematic Reviews, 2015
Myelofibrosis is a bone marrow disorder characterized by excessive production of reticulin and collagen fiber deposition caused by hematological and non-hematological disorders. The prognosis of myelofibrosis is poor and treatment is mainly palliative.
A. Martí-Carvajal   +2 more
semanticscholar   +5 more sources

Janus kinase inhibitors - their current applications and future prospects [PDF]

open access: yesFarmacja Polska, 2022
Janus kinase inhibitors are a group of drugs that provide an alternative to conventional therapy for numerous diseases. The most studied drug of this group is tofacitinib.
Natalia Wierzbowska   +4 more
doaj   +1 more source

Covalent Modification of the JH2 Domain of Janus Kinase 2. [PDF]

open access: yesACS Med Chem Lett, 2022
Probe molecules that covalently modify the JAK2 pseudokinase domain (JH2) are reported. Selective targeting of JH2 domains over the kinase (JH1) domains is a necessary feature for ligands intended to evaluate JH2 domains as therapeutic targets. The JH2 domains of three Janus kinases (JAK1, JAK2, and TYK2) possess a cysteine residue in the catalytic ...
Henry SP   +6 more
europepmc   +3 more sources

Selectivity Profile of the Tyrosine Kinase 2 Inhibitor Deucravacitinib Compared with Janus Kinase 1/2/3 Inhibitors

open access: yesDermatologic Therapy, 2021
Deucravacitinib, a novel, oral, selective inhibitor of tyrosine kinase 2 (TYK2) signaling, acts via an allosteric mechanism by binding to the enzyme’s regulatory domain instead of the catalytic domain.
A. Chimalakonda   +10 more
semanticscholar   +1 more source

Itch and Janus Kinase Inhibitors

open access: yesActa Dermato-Venereologica, 2023
Itch is a common skin symptom, with complex aetiology and pathogenesis. It is mediated by 2 pathways, the histaminergic and non-histaminergic pathways.
Yujin Han   +4 more
doaj   +1 more source

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