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Unique mutational profile associated with a loss of TDG expression in the rectal cancer of a patient with a constitutional PMS2 deficiency.
Vasovcak P, Krepelova A, Menigatti M, Puchmajerova A, Skapa P, Augustinakova A, Amann G, Wernstedt A, Jiricny J, Marra G, Wimmer K. Vasovcak P, et al. Among authors: puchmajerova a. DNA Repair (Amst). 2012 Jul 1;11(7):616-23. doi: 10.1016/j.dnarep.2012.04.004. Epub 2012 May 17. DNA Repair (Amst). 2012. PMID: 22608206 Free PMC article.
Mutations in STK11 gene in Czech Peutz-Jeghers patients.
Vasovcák P, Puchmajerová A, Roubalík J, Krepelová A. Vasovcák P, et al. Among authors: puchmajerova a. BMC Med Genet. 2009 Jul 19;10:69. doi: 10.1186/1471-2350-10-69. BMC Med Genet. 2009. PMID: 19615099 Free PMC article.
[Hereditary diffuse gastric cancer].
Puchmajerová A, Vasovčák P, Macháčková E, Foretová L, Křepelová A. Puchmajerová A, et al. Klin Onkol. 2012;25 Suppl:S30-3. Klin Onkol. 2012. PMID: 22920204 Czech.
[Cowden syndrome].
Puchmajerová A, Vasovcák P, Krepelová A, Plevová P. Puchmajerová A, et al. Klin Onkol. 2009;22 Suppl:S56-7. Klin Onkol. 2009. PMID: 19764399 Review. Czech. No abstract available.
[Rhabdoid tumours].
Vasovčák P, Puchmajerová A, Křepelová A. Vasovčák P, et al. Among authors: puchmajerova a. Klin Onkol. 2012;25 Suppl:S27-9. Klin Onkol. 2012. PMID: 22920203 Slovak.
[Birt-Hogg-Dubé syndrome].
Křepelová A, Puchmajerová A, Vasovčák P, Chocholatý M. Křepelová A, et al. Among authors: puchmajerova a. Klin Onkol. 2012;25 Suppl:S18-20. Klin Onkol. 2012. PMID: 22920201 Czech.
37 results