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Aire-deficient C57BL/6 mice mimicking the common human 13-base pair deletion mutation present with only a mild autoimmune phenotype.
Hubert, François-Xavier; Kinkel, Sarah A; Crewther, Pauline E; Cannon, Ping Z F; Webster, Kylie E; Link, Maire; Uibo, Raivo; O'Bryan, Moira K; Meager, Anthony; Forehan, Simon P; Smyth, Gordon K; Mittaz, Lauréane; Antonarakis, Stylianos E; Peterson, Pärt; Heath, William R; Scott, Hamish S.
Affiliation
  • Hubert FX; Division of Immunology, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
J Immunol ; 182(6): 3902-18, 2009 Mar 15.
Article in En | MEDLINE | ID: mdl-19265170
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Transcription Factors / Mutagenesis, Site-Directed / Polyendocrinopathies, Autoimmune / Molecular Mimicry Type of study: Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Animals / Humans / Male Language: En Journal: J Immunol Year: 2009 Document type: Article Affiliation country: Australia Country of publication: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Transcription Factors / Mutagenesis, Site-Directed / Polyendocrinopathies, Autoimmune / Molecular Mimicry Type of study: Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Animals / Humans / Male Language: En Journal: J Immunol Year: 2009 Document type: Article Affiliation country: Australia Country of publication: United States