Source:http://linkedlifedata.com/resource/pubmed/id/10500292
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
1999-11-5
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pubmed:abstractText |
Dysfunctional immunoglobulins (Igs) that are prone to aggregation are unavoidably generated by the diverse repertoire of B cells. Here, Fred Stevens and Yair Argon analyse the patterns of mutations that lead to pathological Igs, account for non-random mutations in human Ig sequences and suggest the exertion of selective forces, which contribute to determining and limiting the Ig repertoire.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0167-5699
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
451-7
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:10500292-B-Lymphocytes,
pubmed-meshheading:10500292-Humans,
pubmed-meshheading:10500292-Immunoglobulin Light Chains,
pubmed-meshheading:10500292-Models, Molecular,
pubmed-meshheading:10500292-Mutation,
pubmed-meshheading:10500292-Paraproteinemias,
pubmed-meshheading:10500292-Protein Folding
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pubmed:year |
1999
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pubmed:articleTitle |
Pathogenic light chains and the B-cell repertoire.
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pubmed:affiliation |
Biosciences Division, Argonne National Laboratory, Argonne, IL, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Review,
Research Support, Non-U.S. Gov't
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