Selective inhibition of BTK prevents murine lupus and antibody-mediated glomerulonephritis
Rankin, Andrew L, Seth, Nilufer, Keegan, Sean, Andreyeva, Tatyana, Cook, Tim A, Edmonds, Jason, Mathialagan, Nagappan, Benson, Micah J +14 more·2013·The Journal of Immunology
Cited by (125)
Items 101–125 of 125
- Lupus and Lupus Overlap Diseases: Emerging TherapiesVasileios C. Kyttaris · 2016 · Elsevier eBooks
- Management of Autoimmune and Inflammatory Disorders in the Setting of Infection or ImmunodeficiencyWinn W Chatham · 2018 · Springer eBooks
- New treatments of systemic lupus erythematosusVasileios C. Kyttaris · 2020 · Elsevier eBooks
- Therapeutic Effects of Bruton’s Tyrosine Kinase Inhibitor HM71224 as Monotherapy and in Combination with Methotrexate on Collagen-Induced Arthritis in RatsInHwan Bae, Yu-Yon Kim, Sunyoung Jang, Joo‐Yun Byun, Taehun Song, Kyung-Jin Choi, Yongwei Piao, Kwee Hyun Suh, YoungGil Ahn, Young‐Hoon Kim et al. · 2020
- Faculty Opinions recommendation of Delineating the role of cooperativity in the design of potent PROTACs for BTK.Robert A. Copeland · 2018 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
- Clinical advances in immunotherapy for immune-mediated glomerular diseasesBihui Tang, Xiao Yang · 2023 · Clinical and Experimental Medicine
- Synthesis of a Potent Bruton's Tyrosine Kinase Inhibitor Labelled With Carbon‐14 and DeuteriumBachir Latli, Magnus Eriksson · 2025 · Journal of Labelled Compounds and Radiopharmaceuticals
- Additional file 1 of Bruton’s tyrosine kinase-bearing B cells and microglia in neuromyelitis optica spectrum disorderYe Liu, Huang, Zhenning, Zhang, Tian-Xiang, Han, Bin, Guili Yang, Jia, Dongmei, Yang, Li, Liu, Qiang, Lau, Alexander Y. L., Paul, Friedemann et al. · 2024 · Figshare
- Traitement de l’hémophilie A à l’aide d’ARNm codant le facteur VIII et prévention de la réponse immunitaire dirigée contre le facteur VIII thérapeutiqueJules Russick · 2018
- First-in-Human Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single and Multiple Ascending Oral Doses of BIIB091, an Oral BTK Inhibitor, in Healthy Adult ParticipantsHui‐Hsin Tsai, Yi Gu, Katherine A. Riester, Sherman Chu, Eris Bame, Million Arefayene, Jeanelle LYL Kam, Alex Coppell, Jerome Hanna, Brian T. Hopkins et al. · 2026 · Drug Design Development and Therapy
- Emerging pharmacotherapies for chronic spontaneous urticaria: spotlight on BTK inhibitorsÖzge Sevil Karstarlı Bakay, Emek Kocatürk · 2026 · Expert Opinion on Pharmacotherapy
- Molecular endotyping in systemic lupus erythematosus: an integrative framework toward precision therapyYuya Terajima, Yoshinori Matsumoto, Shoichi Nawachi, Yosuke Asano, Keigo Hayashi, Yoshia Miyawaki, Haruki Watanabe, Eri Katsuyama, Takayuki Katsuyama, Jun Wada · 2026 · Frontiers in Immunology
- BindingDB Entry 50003078: Identification of Cyanamide-Based Janus Kinase 3 (JAK3) Covalent Inhibitors.BindingDB · 2020 · UC San Diego
- BindingDB Entry 50000272: Discovery of GDC-0853: A Potent, Selective, and Noncovalent Bruton's Tyrosine Kinase Inhibitor in Early Clinical Development.BindingDB · 2019 · UC San Diego
- BindingDB Entry 50001805: The development of Bruton's tyrosine kinase (BTK) inhibitors from 2012 to 2017: A mini-review.BindingDB · 2020 · UC San Diego
- BindingDB Entry 50010916: Stereochemical Differences in Fluorocyclopropyl Amides Enable Tuning of Btk Inhibition and Off-Target Activity.BindingDB · 2021 · UC San Diego
- BindingDB Entry 50011454: Driving Potency with Rotationally Stable Atropisomers: Discovery of Pyridopyrimidinedione-Carbazole Inhibitors of BTK.BindingDB · 2022 · UC San Diego
- BindingDB Entry 50007980: Discovery of LOU064 (Remibrutinib), a Potent and Highly Selective Covalent Inhibitor of Bruton's Tyrosine Kinase.BindingDB · 2021 · UC San Diego
- BindingDB Entry 50047871: Discovery of 6-Fluoro-5-(R)-(3-(S)-(8-fluoro-1-methyl-2,4-dioxo-1,2-dihydroquinazolin-3(4H)-yl)-2-methylphenyl)-2-(S)-(2-hydroxypropan-2-yl)-2,3,4,9-tetrahydro-1H-carbazole-8-carboxamide (BMS-986142): A Reversible Inhibitor of Bruton's Tyrosine Kinase (BTK) Conformationally Constrained by Two LockeBindingDB · 2018 · UC San Diego
- BindingDB Entry 50018849: Discovery of BGB-8035, a Highly Selective Covalent Inhibitor of Bruton's Tyrosine Kinase for B-Cell Malignancies and Autoimmune Diseases.BindingDB · 2024 · UC San Diego
- BindingDB Entry 50018682: 4-Aminopyrazolopyrimidine scaffold and its deformation in the design of tyrosine and serine/threonine kinase inhibitors in medicinal chemistry.BindingDB · 2024 · UC San Diego
- BindingDB Entry 50008690: Aminopyrazole Carboxamide Bruton's Tyrosine Kinase Inhibitors. Irreversible to Reversible Covalent Reactive Group Tuning.BindingDB · 2021 · UC San Diego
- BindingDB Entry 50009939: Small Molecule Reversible Inhibitors of Bruton's Tyrosine Kinase (BTK): Structure-Activity Relationships Leading to the Identification of 7-(2-Hydroxypropan-2-yl)-4-[2-methyl-3-(4-oxo-3,4-dihydroquinazolin-3-yl)phenyl]-9H-carbazole-1-carboxamide (BMS-935177).BindingDB · 2021 · UC San Diego
- BindingDB Entry 50010667: Discovery of Branebrutinib (BMS-986195): A Strategy for Identifying a Highly Potent and Selective Covalent Inhibitor Providing Rapid in Vivo Inactivation of Bruton's Tyrosine Kinase (BTK).BindingDB · 2021 · UC San Diego
- BindingDB Entry 50007369: Discovery of 4-Aminoquinoline-3-carboxamide Derivatives as Potent Reversible Bruton's Tyrosine Kinase Inhibitors for the Treatment of Rheumatoid Arthritis.BindingDB · 2021 · UC San Diego