Kleibl Z - Search Results

1

Contribution of Massive Parallel Sequencing to Diagnosis of Hereditary Ovarian Cancer in the Czech Republic.

Soukupová J, Lhotová K, Zemánková P, Vočka M, Janatová M, Stolařová L, Borecká M, Kleiblová P, Macháčková E, Foretová L, Koudová M, Lhota F, Tavandzis S, Zikán M, Stránecký V, Veselá K, Panczak A, Kotlas J, Kleibl Z. Soukupová J, et al. Among authors: kleibl z. Klin Onkol. 2019 Summer;32(Supplementum2):72-78. doi: 10.14735/amko2019S72. Klin Onkol. 2019. PMID: 31409082 English.

2

Mutations of the BRCA1 gene in hereditary breast and ovarian cancer in the Czech Republic.

Pohlreich P, Stríbrná J, Kleibl Z, Zikán M, Kalbácová R, Petruzelka L, Konopásek B. Pohlreich P, et al. Among authors: kleibl z. Med Princ Pract. 2003 Jan-Mar;12(1):23-9. doi: 10.1159/000068163. Med Princ Pract. 2003. PMID: 12566964 Free article.

3

[Hereditary predisposition for the development of breast and ovarian carcinoma].

Zikán M, Jancárková N, Pohlreich P, Matous B, Kleibl Z, Stríbrná J, Zivný J. Zikán M, et al. Among authors: kleibl z. Cas Lek Cesk. 2004;143(1):26-30. Cas Lek Cesk. 2004. PMID: 15061115 Review. Czech.

4

The CHEK2 c.1100delC germline mutation rarely contributes to breast cancer development in the Czech Republic.

Kleibl Z, Novotny J, Bezdickova D, Malik R, Kleiblova P, Foretova L, Petruzelka L, Ilencikova D, Cinek P, Pohlreich P. Kleibl Z, et al. Breast Cancer Res Treat. 2005 Mar;90(2):165-7. doi: 10.1007/s10549-004-4023-8. Breast Cancer Res Treat. 2005. PMID: 15803363

5

High proportion of recurrent germline mutations in the BRCA1 gene in breast and ovarian cancer patients from the Prague area.

Pohlreich P, Zikan M, Stribrna J, Kleibl Z, Janatova M, Kotlas J, Zidovska J, Novotny J, Petruzelka L, Szabo C, Matous B. Pohlreich P, et al. Among authors: kleibl z. Breast Cancer Res. 2005;7(5):R728-36. doi: 10.1186/bcr1282. Epub 2005 Jul 19. Breast Cancer Res. 2005. PMID: 16168118 Free PMC article.

6

Novel complex genomic rearrangement of the BRCA1 gene.

Zikan M, Pohlreich P, Stribrna J, Kleibl Z, Cibula D. Zikan M, et al. Among authors: kleibl z. Mutat Res. 2008 Jan 1;637(1-2):205-8. doi: 10.1016/j.mrfmmm.2007.08.002. Epub 2007 Aug 7. Mutat Res. 2008. PMID: 17868747

7

Analysis of CHEK2 FHA domain in Czech patients with sporadic breast cancer revealed distinct rare genetic alterations.

Kleibl Z, Havranek O, Novotny J, Kleiblova P, Soucek P, Pohlreich P. Kleibl Z, et al. Breast Cancer Res Treat. 2008 Nov;112(1):159-64. doi: 10.1007/s10549-007-9838-7. Epub 2007 Dec 4. Breast Cancer Res Treat. 2008. PMID: 18058223

8

Long-term BRCA1 down-regulation by small hairpin RNAs targeting the 3' untranslated region.

Vondruskova E, Malik R, Sevcik J, Kleiblova P, Kleibl Z. Vondruskova E, et al. Among authors: kleibl z. Neoplasma. 2008;55(2):130-7. Neoplasma. 2008. PMID: 18237251

9

Contribution of mutations in ATM to breast cancer development in the Czech population.

Soukupova J, Dundr P, Kleibl Z, Pohlreich P. Soukupova J, et al. Among authors: kleibl z. Oncol Rep. 2008 Jun;19(6):1505-10. Oncol Rep. 2008. PMID: 18497957

10

[Prerequisites for preimplantation genetic diagnosis (PGD in carriers of mutations responsible for hereditary cancers].

Hüttelová R, Kleibl Z, Rezátová J, Krutílková V, Foretová L, Novotný J, Kotlas J, Zikán M, Pohlreich P. Hüttelová R, et al. Among authors: kleibl z. Klin Onkol. 2009;22 Suppl:S69-74. Klin Onkol. 2009. PMID: 19764403 Czech.

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