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Diseases caused by mutations in ORAI1 and STIM1.
Lacruz RS, Feske S. Lacruz RS, et al. Among authors: feske s. Ann N Y Acad Sci. 2015 Nov;1356(1):45-79. doi: 10.1111/nyas.12938. Epub 2015 Oct 15. Ann N Y Acad Sci. 2015. PMID: 26469693 Free PMC article. Review.
ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia.
McCarl CA, Picard C, Khalil S, Kawasaki T, Röther J, Papolos A, Kutok J, Hivroz C, Ledeist F, Plogmann K, Ehl S, Notheis G, Albert MH, Belohradsky BH, Kirschner J, Rao A, Fischer A, Feske S. McCarl CA, et al. Among authors: feske s. J Allergy Clin Immunol. 2009 Dec;124(6):1311-1318.e7. doi: 10.1016/j.jaci.2009.10.007. J Allergy Clin Immunol. 2009. PMID: 20004786 Free PMC article.
CRAC channelopathies.
Feske S. Feske S. Pflugers Arch. 2010 Jul;460(2):417-35. doi: 10.1007/s00424-009-0777-5. Epub 2010 Jan 29. Pflugers Arch. 2010. PMID: 20111871 Free PMC article. Review.
Immunodeficiency due to mutations in ORAI1 and STIM1.
Feske S, Picard C, Fischer A. Feske S, et al. Clin Immunol. 2010 May;135(2):169-82. doi: 10.1016/j.clim.2010.01.011. Epub 2010 Mar 1. Clin Immunol. 2010. PMID: 20189884 Free PMC article. Review.
205 results