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Immunological Reviews|March 18, 2009
Bruton's tyrosine kinase (Btk): function, regulation, and transformation with special emphasis on the PH domainAbdalla J Mohamed, Liang Yu, Carl-Magnus Bäckesjö, et al.
FEBS Letters|August 18, 1997
Missense mutations affecting a conserved cysteine pair in the TH domain of BtkM Vihinen, B F Nore, P T Mattsson, et al.
Bulletin Du Cancer|November 12, 2009
[Family members integration in patients' care in haematology units: a new application of proximology.]E Amblard-Manhès, M-C Fedor, B Belgacem, et al.
Immunological Reviews|January 22, 2005
Bruton's tyrosine kinase: cell biology, sequence conservation, mutation spectrum, siRNA modifications, and expression profilingJessica M Lindvall, K Emelie M Blomberg, Jouni Väliaho, et al.
Retina (Philadelphia, Pa.)|January 22, 2025
THE HETEROGENEOUS PRESENTATIONS OF DE NOVO AND RECURRENT OCULAR INFLAMMATION AFTER COVID-19 VACCINATION : A Multicenter Report and a Review of the LiteratureSruthi Arepalli, Laura Kopplin, Edmund Tsui, et al.
BMC Surgery|March 25, 2014
Longitudinal plication--a surgical strategy for complete rectal prolapse managementSeerwan H S Qaradaghy, Taher A H Hawramy, Beston F Nore, et al.
Frontiers in Cellular and Infection Microbiology|July 26, 2021
Plasma LOX-Products and Monocyte Signaling Is Reduced by Adjunctive Cyclooxygenase-2 Inhibitor in a Phase I Clinical Trial of Tuberculosis PatientsMarthe Jøntvedt Jørgensen, Kristin G Nore, Hans Christian D Aass, et al.
Toxicology and Applied Pharmacology|May 4, 2019
Enrichment of genes associated with squamous differentiation in cancer initiating cells isolated from urothelial cells transformed by the environmental toxicant arseniteZachary E Hoggarth, Danyelle B Osowski, Andrea Slusser-Nore, et al.
Journal of Agricultural and Food Chemistry|October 17, 2017
Characterization and Degradation of Pectic Polysaccharides in Cocoa PulpEsther Meersman, Nore Struyf, Clare Kyomugasho, et al.
Pediatrics|January 31, 1998
Mutation screening of the BTK gene in 56 families with X-linked agammaglobulinemia (XLA): 47 unique mutations without correlation to clinical courseE Holinski-Feder, M Weiss, O Brandau, et al.
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