Search Results - "Janatova, M."
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Hereditary truncating mutations of DNA repair and other genes in BRCA1/BRCA2/PALB2-negatively tested breast cancer patients
Published in Clinical genetics (01-10-2016)“…Hereditary breast cancer comprises a minor but clinically meaningful breast cancer (BC) subgroup. Mutations in the major BC‐susceptibility genes are important…”
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Thermovision: a new diagnostic method for orofacial pain?
Published in Journal of pain research (01-01-2018)“…Infrared thermography can be used to obtain more complete information about a patient's condition. The method can be used in various medical applications for…”
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RE: frameshift variant FANCLc.1096_1099dupATTA is not associated with high breast cancer risk
Published in Clinical genetics (01-10-2016)Get full text
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Functional evaluation of breast cancer case-associated non-coding variants in BRCA1/2
Published in European journal of cancer (1990) (01-07-2016)Get full text
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Identification of pancreatic cancer susceptibility genes in the Czech Republic
Published in European journal of cancer (1990) (01-07-2016)Get full text
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CHEK2 gene analysis in 1020 high-risk breast and ovarian cancer patients in the Czech Republic
Published in European journal of cancer (1990) (01-07-2016)Get full text
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Mutation analysis of the PALB2 gene in unselected pancreatic cancer patients in the Czech Republic
Published in Cancer genetics (01-05-2016)“…Abstract Pancreatic ductal adenocarcinoma (PDAC) has the worst prognosis among common solid cancer diagnoses. It has been shown that up to 10% of PDAC cases…”
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1156 A High Prevalence of PALB2 Mutations Among Familial Breast Cancer Patients in the Czech Republic
Published in European journal of cancer (1990) (01-07-2012)Get full text
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328: Identification and quantification of BRCA1 splicing variants
Published in European journal of cancer (1990) (01-07-2014)Get full text
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967: Hereditary variants of genes coding for TP53 and its regulators (CHK2 and WIP1) in high-risk breast cancer patients
Published in European journal of cancer (1990) (01-07-2014)Get full text
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959: Identification of pathogenic mutations in RAD51 paralogs in BRCA1/2-negative ovarian cancer patients in the Czech Republic
Published in European journal of cancer (1990) (01-07-2014)Get full text
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1131 POSTER PALB2 Mutations in Familial Breast Cancer in the Czech Republic
Published in European journal of cancer (1990) (2011)Get full text
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419 USER-based Approach for Identification of BRCA1 Alternative Splicing Variants
Published in European journal of cancer (1990) (01-07-2012)Get full text
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418 Alternative Splicing Variants BRCA1Δ14-15 and Δ17-19 Differentially Impair the DNA Double Strand Break Response of MCF-7 Cells
Published in European journal of cancer (1990) (01-07-2012)Get full text
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Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers
Published in Neoplasma (2010)“…The two major susceptibility genes, BRCA1 and BRCA2, are involved in hereditary breast and ovarian cancer syndrome. Early detection of mutation carriers has…”
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805 Alterations in BRCA1, BRCA2, TP53 and ATM genes in sporadic breast tumours
Published in European journal of cancer supplements (2010)Get full text
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The role of alterations in BRCA1, BRCA2, TP53 and ATM genes in sporadic breast tumors
Published in European journal of cancer supplements (2008)Get full text
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Microsatellite markers in breast cancer studies
Published in Prague medical report (2004)“…Microsatellites are tandem repeats of simple polymorphic sequences randomly distributed in non-coding regions of DNA. They can be used in cancer genetics and…”
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