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Novel MUC1 variant identified by massively parallel sequencing explains interstitial kidney disease in a large Dutch family

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F23%3A10465391" target="_blank" >RIV/00216208:11110/23:10465391 - isvavai.cz</a>

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=pyVlNFuluO" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=pyVlNFuluO</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.kint.2023.02.021" target="_blank" >10.1016/j.kint.2023.02.021</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Novel MUC1 variant identified by massively parallel sequencing explains interstitial kidney disease in a large Dutch family

  • Original language description

    Chronic kidney disease (CKD) can be caused by various systemic and kidney disorders with overlapping or nonspecific clinical presentations. Despite a thorough diagnostic workup, the primary cause of CKD remains uncertain in 20% to 35% of affected individuals. Recent studies have demonstrated that massively parallel sequencing (MPS) can be a useful additional tool in the diagnostic workup of patients with unexplained CKD, providing a molecular diagnosis in 11% to 56% of cases. Establishing the correct diagnosis through MPS may not only have therapeutic consequences but may also improve detection of extrarenal manifestations (reverse phenotyping), improve genetic counseling of patients and their relatives, and influence donor selection for (living-related) transplantation. Here, we describe a large Dutch family with interstitial kidney disease of unknown origin in whom we identified a novel frameshift mutation in the MUC1 gene, encoding mucin 1, using an MPS-based multigene panel.

  • 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

    30101 - Human genetics

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)

Others

  • Publication year

    2023

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Kidney International

  • ISSN

    0085-2538

  • e-ISSN

    1523-1755

  • Volume of the periodical

    103

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    4

  • Pages from-to

    986-989

  • UT code for WoS article

    000985430900001

  • EID of the result in the Scopus database

    2-s2.0-85152114710