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Multiple productive IGH rearrangements denote oligoclonality even in immunophenotypically monoclonal CLL

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F18%3A00068192" target="_blank" >RIV/65269705:_____/18:00068192 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14110/18:00102140

  • Result on the web

    <a href="http://www.nature.com/articles/leu2017274" target="_blank" >http://www.nature.com/articles/leu2017274</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1038/leu.2017.274" target="_blank" >10.1038/leu.2017.274</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Multiple productive IGH rearrangements denote oligoclonality even in immunophenotypically monoclonal CLL

  • Original language description

    In our systematic study of CLL cases with multiple productive IGH rearrangements (MP-IGH CLL),3 we previously showed that one-third of them exhibit two CLL populations with distinct immunophenotypes. We also pointed to the presence of multiple clones as a likely cause of MP-IGH detection even in cases with an immunophenotypically monoclonal disease, on the basis of IGK, IGL and incomplete IGH gene rearrangement analyses. Still, the underlying biological cause of MP-IGHs possibly involves lack of allelic exclusion4 or IGHV gene replacement.5 The extent to which these mechanisms are involved in MP-IGH CLL cases with homogeneous immunophenotype is still not known, and the lack of conclusive evidence hinders further research on CLL oligoclonality. To clarify this phenomenon, we performed extensive analysis of clonality in MP-IGH CLL combining conventional methods (Sanger sequencing, IGH fragment analysis), immunophenotyping, single-cell analysis (SCA), and next-generation sequencing (NGS).

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30204 - Oncology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Leukemia

  • ISSN

    0887-6924

  • e-ISSN

  • Volume of the periodical

    32

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    3

  • Pages from-to

    234-236

  • UT code for WoS article

    000419771800027

  • EID of the result in the Scopus database