A RAG1 mutation found in Omenn syndrome causes coding flank hypersensitivity: a novel mechanism for antigen receptor repertoire restriction
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Human RAG mutations: biochemistry and clinical implicationsBase flipping in V(D)J recombination: insights into the mechanism of hairpin formation, the 12/23 rule, and the coordination of double-strand breaksA systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency.Characterization of T and B cell repertoire diversity in patients with RAG deficiencyHypomorphic Rag1 mutations alter the pre-immune repertoire at early stages of lymphoid development.
P2860
A RAG1 mutation found in Omenn syndrome causes coding flank hypersensitivity: a novel mechanism for antigen receptor repertoire restriction
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on September 2008
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
A RAG1 mutation found in Omenn ...... eceptor repertoire restriction
@en
A RAG1 mutation found in Omenn ...... ceptor repertoire restriction.
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type
label
A RAG1 mutation found in Omenn ...... eceptor repertoire restriction
@en
A RAG1 mutation found in Omenn ...... ceptor repertoire restriction.
@nl
prefLabel
A RAG1 mutation found in Omenn ...... eceptor repertoire restriction
@en
A RAG1 mutation found in Omenn ...... ceptor repertoire restriction.
@nl
P2093
P2860
P1476
A RAG1 mutation found in Omenn ...... eceptor repertoire restriction
@en
P2093
Catherine P Lu
David B Roth
Serre-Yu Wong
P2860
P304
P356
10.4049/JIMMUNOL.181.6.4124
P407
P577
2008-09-01T00:00:00Z