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   <subfield code="a">An improved RT-PCR method for the detection of killer-cell immunoglobulin-like receptor (KIR) transcripts</subfield>
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   <subfield code="c">[A. Thompson, A. van der Slik, F. Koning, J. van Bergen]</subfield>
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   <subfield code="a">Killer cell immunoglobulin-like receptors (KIRs) are expressed on human natural killer (NK) cells and a proportion of T cells. As the specificity of these NK and T cells is, at least in part, determined by the combination of KIRs they express, it is important to be able to determine the KIR expression pattern of NK and T cell clones to understand their function. However, for most KIR genes, specific reagents to detect expression are currently either unavailable or sensitive to allelic variations. In this study, a reverse transcriptase-polymerase chain reaction (RT-PCR) that uses new primer sets for the gene-specific detection of KIR transcripts is presented and validated. The key advantage of this RT-PCR method over previously published ones is that it was designed to detect transcripts of all confirmed allelic variants of the KIR genes, while remaining gene-specific.</subfield>
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   <subfield code="a">Killer-cell immunoglobulin-like receptor (KIR)</subfield>
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   <subfield code="a">Thompson</subfield>
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   <subfield code="u">Department of Immunmohematology and Blood Transfusion, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands</subfield>
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   <subfield code="a">van der Slik</subfield>
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   <subfield code="a">van Bergen</subfield>
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   <subfield code="g">58/11(2006-11-01), 865-872</subfield>
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