Important notice for the users!

 

IDbases have been moved to Lund University and are available at

http://structure.bmc.lu.se/idbase/

They will remain for a while in this old address and will be removed in the future.

 

 

 

- databases for immunodeficiency-causing mutations

   ORAI1base
   Mutation registry for  Severe combined immunodeficiency


ORAI1base mutation publications

[2009] [2006]

Search PubMed latest citations for ORAI1 mutations

    2009

  • 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
    J Allergy Clin Immunol 2009(6): 1311-1318.e7 [PubMed abstract].

    2006

  • A mutation in Orai1 causes immune deficiency by abrogating CRAC channel function.
    Feske S, Gwack Y, Prakriya M, Srikanth S, Puppel SH, Tanasa B, Hogan PG, Lewis RS, Daly M, Rao A
    Nature 2006(7090): 179-85 [PubMed abstract].

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Last modified 16.06.2011