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Renal cell carcinoma with areas mimicking renal angiomyoadenomatous tumor/clear cell papillary renal cell carcinoma

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11140%2F13%3A10138948" target="_blank" >RIV/00216208:11140/13:10138948 - isvavai.cz</a>

  • Alternative codes found

    RIV/00669806:_____/13:10138948

  • Result on the web

    <a href="http://ac.els-cdn.com/S0046817712004479/1-s2.0-S0046817712004479-main.pdf?_tid=7ffbc3a2-08a4-11e3-a6a1-00000aab0f02&acdnat=1376899016_081aa406806f0005cb0b36992fcf1e78" target="_blank" >http://ac.els-cdn.com/S0046817712004479/1-s2.0-S0046817712004479-main.pdf?_tid=7ffbc3a2-08a4-11e3-a6a1-00000aab0f02&acdnat=1376899016_081aa406806f0005cb0b36992fcf1e78</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.humpath.2012.11.019" target="_blank" >10.1016/j.humpath.2012.11.019</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Renal cell carcinoma with areas mimicking renal angiomyoadenomatous tumor/clear cell papillary renal cell carcinoma

  • Original language description

    We present a cohort of 8 renal carcinomas that displayed a variable (5%-95% extent) light microscopic appearance of renal angiomyoadenomatous tumor/clear cell papillary renal cell carcinoma (RAT/CCPRCC) without fulfilling the criteria for these tumors. All but 1 case predominantly (75%-95% extent) showed histopathologic features of conventional clear cell renal cell carcinoma. In 5 of 7 cases with mostly conventional clear renal cell carcinoma (CRCC) morphology, a diagnosis of CRCC was supported by themolecular genetic findings (presence of von Hippel-Lindau tumor suppressor [VHL] mutation and/or VHL promoter methylation and/or loss of heterozygosity [LOH] for 3p). Of the other 2 cases with predominantly characteristic CRCC morphology, 1 tumor did notreveal any VHL mutation, VHL promoter methylation, or LOH for 3p, and both chromosomes 7 and 17 were disomic, whereas the other tumor displayed polysomy for chromosomes 7 and 17 and no VHL mutation, VHL promoter methylation, or LOH for 3

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    FP - Other medical fields

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/NT12010" target="_blank" >NT12010: Assesment of genetic changes in angiogenesis in different subtypes of renal tumours</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2013

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Human Pathology

  • ISSN

    0046-8177

  • e-ISSN

  • Volume of the periodical

    44

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    9

  • Pages from-to

    1412-1420

  • UT code for WoS article

    000321225000025

  • EID of the result in the Scopus database