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J D Capra

Researcher at University of Texas Southwestern Medical Center

Publications -  70
Citations -  5044

J D Capra is an academic researcher from University of Texas Southwestern Medical Center. The author has contributed to research in topics: Antigen & Antibody. The author has an hindex of 37, co-authored 70 publications receiving 4998 citations. Previous affiliations of J D Capra include Southampton General Hospital & University of Alberta Hospital.

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Journal ArticleDOI

Analysis of somatic mutation in five B cell subsets of human tonsil.

TL;DR: It is found that the somatic mutation machinery is activated only after B cells reach the germinal center and become centroblasts (Bm3), and the analysis of Ig variable region transcripts from the different subpopulations confirms that the pathway of B cell differentiation from virgin B cell throughout the gerMinal center up to the memory compartment can be traced with phenotypic markers.
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Analysis of HLA-DQ genotypes and susceptibility in insulin-dependent diabetes mellitus

TL;DR: It is concluded that the presence of the HLA Class II antigen DQw1.2 is strongly protective against the development of IDDM, and that complete HLA-DQ typing is necessary for accurate assessment of susceptibility to IDDM.
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Initial characterization of monoclonal antibodies against human monocytes

TL;DR: Initial chemical characterization of the monocyte antigen recognized by two of these antibodies is presented, and it is suggested that this molecule is a single polypeptide chain with an apparent molecular weight of 200,000.
Journal Article

VH restriction among human cold agglutinins. The VH4-21 gene segment is required to encode anti-I and anti-i specificities.

TL;DR: Although the VH4-21 gene segment is essential for cold agglutinin activity, the other genetic elements that contribute to the V region of the antibody molecules can be extremely diverse and the structural information provided in this report sharply restricts the requirement for encoding pathogenic cold agglusiveness activity to one of the components of the H chain V region.
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The smaller human VH gene families display remarkably little polymorphism.

TL;DR: The nucleotide sequence of 30 distinct human VH gene segments from the VHIV, VHV and VHVI gene families are reported to provide evidence that at least some human Vh gene segments are remarkably stable.