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Advances in dermatology
Genotypic Analysis in Primary Cutaneous Lymphomas Using the Standardized Biomed-2 Polymerase Chain Reaction Protocols
Aplicación de los Protocolos de PCR Biomed-2 en el Análisis Genotípico de los Linfomas Cutáneos Primarios
F. Gallardoa,
Autor para correspondencia
FGallardo@imas.imim.es

Correspondence: Servicio de Dermatología, Hospital del Mar, IMAS, Passeig Marítim, 25-29, 08003 Barcelona, Spain.
, B. Bellosillob, S. Serranob, R.M. Pujola
a Servicio de Dermatología, Servicio de Patología, Hospital del Mar, IMAS, Barcelona, Spain
b Laboratorio de Biología Molecular, Servicio de Patología, Hospital del Mar, IMAS, Barcelona, Spain
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        "titulo" => "Aplicaci&#243;n de los Protocolos de PCR Biomed-2 en el An&#225;lisis Genot&#237;pico de los Linfomas Cut&#225;neos Primarios"
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        "titulo" => "Abstract"
        "resumen" => "<p class="elsevierStyleSimplePara elsevierViewall">The European Biomedicine and Health &#40;BIOMED-2&#41; Concerted Action Project BMH4-CT98-3936 has defined standardized protocols for polymerase chain reaction &#40;PCR&#41; amplification of different loci of the T-cell receptor &#40;TCR&#41; and immunoglobulin &#40;Ig&#41; genes with a view to achieving greater sensitivity and specificity in the assessment of clonality of lymphoid neoplasms&#46; To assess T-cell clonality&#44; analysis of TCR&#946; gene and TCR&#948; rearrangements &#40;useful in cases of T&#947;&#948;&#43; cell neoplasms&#41; is proposed alongside that of TCR&#947;&#46; For analysis of B-cell clonality&#44; along with the framework &#40;FR&#41; III segment of the IgH gene&#44; other segments are studied &#40;FRI&#44; FRII&#41; in addition to Ig&#947; and Ig&#954; genes or incomplete DJ rearrangements of the IgH gene and the &#954; deleting element&#46; The results of the amplification are read using automatic reading systems &#40;GeneScan&#41; or using a heteroduplex system&#46;</p>"
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        "resumen" => "<p class="elsevierStyleSimplePara elsevierViewall">El proyecto europeo BIOMED-2 Concerted Action BMH4-CT98-3936 describe protocolos estandarizados de amplificaci&#243;n por reacci&#243;n en cadena de la polimerasa &#40;PCR&#41; de los diferentes <span class="elsevierStyleItalic">loci</span> de los genes del receptor de la c&#233;lula T &#40;TCR&#41; e inmunoglobulinas &#40;Ig&#41; con el objetivo de obtener una mayor sensibilidad y especificidad en el estudio de clonalidad de las neoplasias linfoides&#46; En el estudio de clonalidad T&#44; adem&#225;s del TCR&#947; se propone el estudio adicional de los reordenamientos del gen TCR&#946; y del <span class="elsevierStyleItalic">locus</span> TCR&#948; &#40;&#250;til en casos de neoplasias de c&#233;lulas T&#947;&#948;&#43;&#41;&#46; En el estudio de clonalidad B&#44; junto al segmento FRIII del gen IgH se dise&#241;a el estudio de otros segmentos &#40;FRI&#44; FRII&#41;&#44; as&#237; como de los genes Ig&#955; e Ig&#954; o reordenamientos incompletos DJ del gen IgH y &#954;de &#40;<span class="elsevierStyleItalic">kappa deleting element</span>&#41;&#46; La lectura de los resultados de la amplificaci&#243;n se realiza mediante sistemas automatizados de lectura &#40;GeneScan&#41; o mediante el sistema heterod&#250;plex&#46;</p>"
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        "nota" => "<p class="elsevierStyleNotepara">This study was partly funded by the FIS 03&#47;394 grant from the Spanish Ministry of Health and Consumer Affairs&#46;</p>"
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