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Page 1
Changes on chromosome 11p15.5 as specific marker for embryonal rhabdomyosarcoma?
Vicha A, Jencova P, Novakova-Kodetova D, Stolova L, Voriskova D, Vyletalova K, Broz P, Drahokoupilova E, Guha A, Kopecká M, Krskova L. Vicha A, et al. Among authors: jencova p. Genes Chromosomes Cancer. 2023 Dec;62(12):732-739. doi: 10.1002/gcc.23194. Epub 2023 Aug 2. Genes Chromosomes Cancer. 2023. PMID: 37530573
A rational approach to the CNS tumors diagnostics.
Krsková L, Šípalová B, Němečková T, Strnadová M, Kalendová T, Kalfusová A, Alexandra, Malkusová, Šandová M, Koblížek M, Balko J, Vícha A, Brož P, Jenčová P, Štolová L, Dagmar, Voříšková, Belhajová M, Zápotocký M, Sumerauer D, Zámečník J. Krsková L, et al. Among authors: jencova p. Cesk Patol. 2022 Fall;58(3):135-137. Cesk Patol. 2022. PMID: 36224035 English.
Methylation pattern in the diagnosis and prognosis of brain cancer.
Vícha A, Štolová L, Jenčová P, Zápotocký M, Sumerauer D, Mišove A, Koblížek M, Brož P, Zámečník J, Kynčl M, Libý P, Krsková L. Vícha A, et al. Among authors: jencova p. Cesk Patol. 2021 Summer;57(3):154-160. Cesk Patol. 2021. PMID: 34551564 English.
An unusual fusion gene EML4-ALK in a patient with congenital mesoblastic nephroma.
Misove A, Vicha A, Zapotocky M, Malis J, Balko J, Nemeckova T, Szabova J, Kyncl M, Novakova-Kodetova D, Stolova L, Jencova P, Broz P, Krskova L. Misove A, et al. Among authors: jencova p. Genes Chromosomes Cancer. 2021 Dec;60(12):837-840. doi: 10.1002/gcc.22990. Epub 2021 Aug 22. Genes Chromosomes Cancer. 2021. PMID: 34378283
Rare IDH1 variants are common in pediatric hemispheric diffuse astrocytomas and frequently associated with Li-Fraumeni syndrome.
Sumerauer D, Krskova L, Vicha A, Misove A, Mamatjan Y, Jencova P, Vlckova M, Slamova L, Vanova K, Liby P, Taborsky J, Koblizek M, Klubal R, Kyncl M, Zadeh G, Stary J, Zamecnik J, Ramaswamy V, Zapotocky M. Sumerauer D, et al. Among authors: jencova p. Acta Neuropathol. 2020 Apr;139(4):795-797. doi: 10.1007/s00401-019-02118-5. Epub 2020 Jan 3. Acta Neuropathol. 2020. PMID: 31897644 No abstract available.
Interference of bone marrow CD56+ mesenchymal stromal cells in minimal residual disease investigation of neuroblastoma and other CD45- /CD56+ pediatric malignancies using flow cytometry.
Theodorakos I, Paterakis G, Papadakis V, Vicha A, Topakas G, Jencova P, Karchilaki E, Taparkou A, Tsagarakis NJ, Polychronopoulou S. Theodorakos I, et al. Among authors: jencova p. Pediatr Blood Cancer. 2019 Aug;66(8):e27799. doi: 10.1002/pbc.27799. Epub 2019 May 7. Pediatr Blood Cancer. 2019. PMID: 31066205
[Identifying the Importance of MT-3 Expression for Neuroblastoma Cells].
Eckschlager T, Vícha A, Jenčová P, Merlos R, Dostálová S, Buchtelová H, Strmiska V, Michálek P, Heger Z, Adam V. Eckschlager T, et al. Among authors: jencova p. Klin Onkol. 2018 Spring;31(Supplementum1):145-147. Klin Onkol. 2018. PMID: 29808689 Czech.
Comparative gene expression profiling of human metallothionein-3 up-regulation in neuroblastoma cells and its impact on susceptibility to cisplatin.
Merlos Rodrigo MA, Dostalova S, Buchtelova H, Strmiska V, Michalek P, Krizkova S, Vicha A, Jencova P, Eckschlager T, Stiborova M, Heger Z, Adam V. Merlos Rodrigo MA, et al. Among authors: jencova p. Oncotarget. 2017 Dec 16;9(4):4427-4439. doi: 10.18632/oncotarget.23333. eCollection 2018 Jan 12. Oncotarget. 2017. PMID: 29435113 Free PMC article.
Absence of BRAF mutation in pheochromocytoma and paraganglioma.
Vosecka T, Vicha A, Zelinka T, Jencova P, Pacak K, Duskova J, Benes J, Guha A, Stanek L, Kohoutova M, Musil Z. Vosecka T, et al. Among authors: jencova p. Neoplasma. 2017;64(2):278-282. doi: 10.4149/neo_2017_215. Neoplasma. 2017. PMID: 28043156 Free PMC article.