Macháčková E - 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: machackova e. Klin Onkol. 2019 Summer;32(Supplementum2):72-78. doi: 10.14735/amko2019S72. Klin Onkol. 2019. PMID: 31409082 English.

2

A high occurrence of BRCA1 and BRCA2 mutations among Czech hereditary breast and breast-ovarian cancer families.

Machácková E, Foretová L, Navrátilová M, Valík D, Claes K, Messiaen L. Machácková E, et al. Cas Lek Cesk. 2000 Oct 11;139(20):635-7. Cas Lek Cesk. 2000. PMID: 11192759

3

Novel germline BRCA1 and BRCA2 mutations in breast and breast/ovarian cancer families from the Czech Republic.

Machackova E, Damborsky J, Valik D, Foretova L. Machackova E, et al. Hum Mutat. 2001 Dec;18(6):545. doi: 10.1002/humu.1232. Hum Mutat. 2001. PMID: 11748848

4

Differentiating pathogenic mutations from polymorphic alterations in the splice sites of BRCA1 and BRCA2.

Claes K, Poppe B, Machackova E, Coene I, Foretova L, De Paepe A, Messiaen L. Claes K, et al. Among authors: machackova e. Genes Chromosomes Cancer. 2003 Jul;37(3):314-20. doi: 10.1002/gcc.10221. Genes Chromosomes Cancer. 2003. PMID: 12759930

5

BRCA1 and BRCA2 mutations in women with familial or early-onset breast/ovarian cancer in the Czech Republic.

Foretova L, Machackova E, Navratilova M, Pavlu H, Hruba M, Lukesova M, Valik D. Foretova L, et al. Among authors: machackova e. Hum Mutat. 2004 Apr;23(4):397-8. doi: 10.1002/humu.9226. Hum Mutat. 2004. PMID: 15024741

6

High occurrence of BRCA1 intragenic rearrangements in hereditary breast and ovarian cancer syndrome in the Czech Republic.

Vasickova P, Machackova E, Lukesova M, Damborsky J, Horky O, Pavlu H, Kuklova J, Kosinova V, Navratilova M, Foretova L. Vasickova P, et al. Among authors: machackova e. BMC Med Genet. 2007 Jun 11;8:32. doi: 10.1186/1471-2350-8-32. BMC Med Genet. 2007. PMID: 17561994 Free PMC article.

7

Spectrum and characterisation of BRCA1 and BRCA2 deleterious mutations in high-risk Czech patients with breast and/or ovarian cancer.

Machackova E, Foretova L, Lukesova M, Vasickova P, Navratilova M, Coene I, Pavlu H, Kosinova V, Kuklova J, Claes K. Machackova E, et al. BMC Cancer. 2008 May 20;8:140. doi: 10.1186/1471-2407-8-140. BMC Cancer. 2008. PMID: 18489799 Free PMC article.

8

[Limitations of genetic testing in oncology].

Foretová L, Navrátilová M, Machácková E. Foretová L, et al. Among authors: machackova e. Klin Onkol. 2009;22 Suppl:S65-8. Klin Onkol. 2009. PMID: 19764402 Review. Czech.

9

Genetic and preventive services for hereditary breast and ovarian cancer in the czech republic.

Foretova L, Petrakova K, Palacova M, Kalabova R, Navratilova M, Lukesova M, Vasickova P, Machackova E, Kleibl Z, Pohlreich P. Foretova L, et al. Among authors: machackova e. Hered Cancer Clin Pract. 2006 Nov 15;4(1):3-6. doi: 10.1186/1897-4287-4-1-3. Hered Cancer Clin Pract. 2006. PMID: 20222996 Free PMC article.

10

The AIB1 gene polyglutamine repeat length polymorphism and the risk of breast cancer development.

Kleibl Z, Havranek O, Kormunda S, Novotny J, Foretova L, Machackova E, Soukupova J, Janatova M, Tavandzis S, Pohlreich P. Kleibl Z, et al. Among authors: machackova e. J Cancer Res Clin Oncol. 2011 Feb;137(2):331-8. doi: 10.1007/s00432-010-0889-5. Epub 2010 Apr 27. J Cancer Res Clin Oncol. 2011. PMID: 20422428

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