|
🐜
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High proportion of recurrent germline mutations in the BRCA1 gene in breast and ovarian cancer patients from the Prague area
11 auth.
P. Pohlreich,
M. Zikan,
J. Stribrna,
Z. Kleibl,
M. Janatová,
J. Kotlas,
...
J. Židovská,
J. Novotný,
L. Petruželka,
C. Szabo,
B. Matouš
|
6 |
2005 |
6
🐜
|
|
🐜
|
The PALB2 Gene Is a Strong Candidate for Clinical Testing in BRCA1- and BRCA2-Negative Hereditary Breast Cancer
10 auth.
M. Janatová,
Z. Kleibl,
J. Stribrna,
A. Panczak,
K. Veselá,
M. Zimovjanova,
...
P. Kleiblova,
P. Dundr,
J. Soukupová,
P. Pohlreich
|
5 |
2013 |
5
🐜
|
|
🐜
|
Screening for genomic rearrangements in BRCA1 and BRCA2 genes in Czech high-risk breast/ovarian cancer patients: high proportion of population specific alterations in BRCA1 gene
8 auth.
I. Ticha,
Z. Kleibl,
J. Stribrna,
J. Kotlas,
M. Zimovjanova,
M. Matějů,
...
M. Zikan,
P. Pohlreich
|
5 |
2010 |
5
🐜
|
|
🐜
|
Mutations of the BRCA1 Gene in Hereditary Breast and Ovarian Cancer in the Czech Republic
7 auth.
P. Pohlreich,
J. Stribrna,
Z. Kleibl,
M. Zikan,
R. Kalbáčová,
L. Petruželka,
...
B. Konopasek
|
4 |
2003 |
4
🐜
|
|
🐜
|
Expression of human BRCA1Δ17-19 alternative splicing variant with a truncated BRCT domain in MCF-7 cells results in impaired assembly of DNA repair complexes and aberrant DNA damage response.
14 auth.
J. Ševčík,
M. Falk,
L. Macurek,
P. Kleiblova,
F. Lhota,
J. Hojný,
L. Štefančíková,
M. Janatová,
J. Bartek,
J. Stribrna,
...
Z. Hodny,
L. Jezková,
P. Pohlreich,
Z. Kleibl
|
4 |
2013 |
4
🐜
|
|
🐜
|
Mutation Analysis of the RAD51C and RAD51D Genes in High-Risk Ovarian Cancer Patients and Families from the Czech Republic
8 auth.
M. Janatová,
J. Soukupová,
J. Stribrna,
P. Kleiblova,
M. Vočka,
P. Boudová,
...
Z. Kleibl,
P. Pohlreich
|
4 |
2015 |
4
🐜
|
|
🐬
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Multimarker real‐time reverse transcription‐PCR for quantitative detection of melanoma‐associated antigens: a novel possible staging method
P. Arenberger,
M. Arenbergerova,
S. Gkalpakiotis,
J. Lippert,
J. Stribrna,
J. Kremen
|
4 |
2007 |
4
🐬
|
|
🐜
|
Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.
10 auth.
M. Matějů,
J. Stribrna,
M. Zikan,
Z. Kleibl,
M. Janatová,
S. Kormunda,
...
J. Novotný,
P. Souček,
L. Petruželka,
P. Pohlreich
|
3 |
2010 |
3
🐜
|
