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Page 1
R93W mutation in Orai1 causes impaired calcium influx in platelets.
Bergmeier W, Oh-Hora M, McCarl CA, Roden RC, Bray PF, Feske S. Bergmeier W, et al. Among authors: feske s. Blood. 2009 Jan 15;113(3):675-8. doi: 10.1182/blood-2008-08-174516. Epub 2008 Oct 24. Blood. 2009. PMID: 18952890 Free PMC article.
STIM1 mutation associated with a syndrome of immunodeficiency and autoimmunity.
Picard C, McCarl CA, Papolos A, Khalil S, Lüthy K, Hivroz C, LeDeist F, Rieux-Laucat F, Rechavi G, Rao A, Fischer A, Feske S. Picard C, et al. Among authors: feske s. N Engl J Med. 2009 May 7;360(19):1971-80. doi: 10.1056/NEJMoa0900082. N Engl J Med. 2009. PMID: 19420366 Free PMC article.
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.
211 results