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Identification of mutations in the ribosomal protein L5 (RPL5) and ribosomal protein L11 (RPL11) genes in Czech patients with Diamond-Blackfan anemia

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023736%3A_____%2F09%3A00007623" target="_blank" >RIV/00023736:_____/09:00007623 - isvavai.cz</a>

  • Alternative codes found

    RIV/00064203:_____/09:5375 RIV/00216208:11110/09:3534 RIV/00216208:11130/09:5375 RIV/61989592:15110/09:00009637

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Identification of mutations in the ribosomal protein L5 (RPL5) and ribosomal protein L11 (RPL11) genes in Czech patients with Diamond-Blackfan anemia

  • Original language description

    Diamond-Blackfan anemia (DBA) is a congenital red cell aplasia that is usually diagnosed during early infancy. Apart from defects in red cell maturation, the disorder is also associated with various physical anomalies in 40% of patients. Mutations in theribosomal protein (RP) S19 are found in 25% of patients, while mutations in other proteins of the small ribosomal subunit RPS17 and RPS24 have been found in a fraction of patients. Recently, mutations in RPL5, RPL11 and RPL35a of the large ribosomal subunit have also been reported in several DBA patients.

  • Czech name

    Identifikace mutací v genech pro ribosomální proteiny L5 (RPL5) a L11 u pacientů s Diamondovou-Blackfanovou anémií v ČR

  • Czech description

    Diamondova-Blackfanova anémie (DBA) je vrozená aplasie červených krvinek, která je obvykle diagnostikována během ranného dětství. Kromě postižené maturace červených krvinek je toto onemocnění u 40% pacientů také asociováno s různými fyzickými abnormitami. Mutace v genu pro ribosomální protein (RP) S19 jsou nalézány u 25% pacientů, zatímco mutace v dalších proteinech malé ribosomální podjednotky RPS17 a RPS24 byly nalezeny pouze u malého počtu pacientů.

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/LC06044" target="_blank" >LC06044: Center for Experimental Hematology</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2009

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Human Mutation

  • ISSN

    1059-7794

  • e-ISSN

  • Volume of the periodical

    30

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    6

  • Pages from-to

  • UT code for WoS article

    000264011700007

  • EID of the result in the Scopus database