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12 886 (0,161s)

Result

Atypical Teratoid/Rhabdoid Tumors Are Comprised of Three Epigenetic Subgroups with Distinct Enhancer Landscapes

Atypical teratoid/rhabdoid tumor (ATRT) is one of the most common brain tumors favorably to current treatments, suggesting molecular inter-tumor heterogeneity, tumor location, and type of...

FD - Onkologie a hematologie

  • 2016
  • Jx
  • Link
Result

Rhabdoid tumours

Rhabdoid tumors (RT) are rare highly malignant tumors. They are part of the embryonic types of tumors and therefore occur in early childhood (between ages of 0?2. These tumors are composed of rhabdoid<...

FD - Onkologie a hematologie

  • 2012
  • Jx
  • Link
Result

Tazemetostat in the therapy of pediatric INI1-negative malignant rhabdoid tumors

patients with primary atypical teratoid rhabdoid tumor (AT/RT, a rhabdoid tumor atypical teratoid rhabdoid tumor. The treatment combined metronomic therapy...

Other natural sciences

  • 2023
  • Jimp
  • Link
Result

Poorly differentiated chordoma with SMARCB1/INI1 loss: a distinct molecular entity with dismal prognosis

Chordomas are tumors of the skull base and spine thought to arise from remnants of the notochord. Expression of cytokeratins and S100 is frequent and nuclear expression of brachyury, a transcription factor important for axial development, ha...

FD - Onkologie a hematologie

  • 2016
  • Jx
  • Link
Result

Atypical Teratoid/Rhabdoid Tumor (AT/RT) With Molecular Features of Pleomorphic Xanthoastrocytoma

Atypical teratoid/rhabdoid tumor (AT/RT) is a highly malignant central nervous system tumor predominantly occurring in infants that may also arise in older children and adults. Rare secondary AT/RT develop...

Oncology

  • 2021
  • Jimp
  • Link
Result

Spinal cord atypical teratoid/rhabdoid tumors in children: Clinical, genetic, and outcome characteristics in a representative European cohort

Background Case reports have portrayed spinal cord atypical teratoid/rhabdoid tumor (spATRT) as an aggressive form of ATRT. We conducted a retrospective European and the group of extradural malignant rhabdoid

Oncology

  • 2020
  • Jimp
  • Link
Result

Cribriform neuroepithelial tumor: molecular characterization of a SMARCB1-deficient non-rhabdoid tumor with favorable long-term outcome

Rhabdoid phenotype and loss of SMARCB1 expression in a brain tumor are characteristic features of atypical teratoid/rhabdoid tumors (ATRT). Rare non-rhabdoid brain tumors showing...

Oncology

  • 2017
  • Jimp
  • Link
Result

Two cases of CNS atypical theratoid rhabdoid tumor and review of literature

The authors declare they have no potential conflicts of interest concerning drugs, products, or services used in the study. The Editorial Board declares that the manuscript met the ICMJE ?uniform requirements? for biomedical papers....

Clinical neurology

  • 2017
  • Jimp
  • Link
Result

Tyrosinase immunohistochemistry can be employed for the diagnosis of atypical teratoid/rhabdoid tumours of the tyrosinase subgroup (ATRT-TYR)

Atypical teratoid/rhabdoid tumour (ATRT) is a malignant brain tumour mainly occurring in young children. Mutations of chromatin remodelling complex member SMARCB1/INI1 or (rarely) SMARCA4/BRG1 are the sole recurrent genetic...

Oncology

  • 2020
  • Jimp
  • Link
Result

Age and DNA methylation subgroup as potential independent risk factors for treatment stratification in children with atypical teratoid/rhabdoid tumors

(including markers for stratification) for patients with atypical teratoid/rhabdoid tumors (ATRTs). The European Rhabdoid Registry (EU-RHAB) recruits uniformly treated) were determined using DNA methylati...

Oncology

  • 2020
  • Jimp
  • Link
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