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A case of carotid body paraganglioma and haemangioblastoma of the spinal cord in a patient with the N131K missense mutation in the VHL gene.
- Published in:
- Neurological Sciences, 2011, v. 32, n. 3, p. 491, doi. 10.1007/s10072-011-0502-y
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- Publication type:
- Article
Genetic testing for hereditary breast cancer in Poland: 1998–2022.
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- Hereditary Cancer in Clinical Practice, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s13053-023-00252-6
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- Publication type:
- Article
Frequency of BRCA1 and BRCA2 mutations in ovarian cancer patients in South-East Poland.
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- Hereditary Cancer in Clinical Practice, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s13053-022-00219-z
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- Publication type:
- Article
Association of recurrent mutations in BRCA1, BRCA2, RAD51C, PALB2, and CHEK2 with the risk of borderline ovarian tumor.
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- Hereditary Cancer in Clinical Practice, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s13053-022-00218-0
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- Publication type:
- Article
Serum selenium level and cancer risk: a nested case-control study.
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- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. 1, doi. 10.1186/s13053-019-0131-7
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- Publication type:
- Article
BRCA1 and BRCA2 mutations in ovarian cancer patients from Belarus: update.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00169-y
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- Publication type:
- Article
Recurrent PALB2 mutations and the risk of cancers of bladder or kidney in Polish population.
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- Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-020-00161-y
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- Publication type:
- Article
Polymorphisms in MMP-1, MMP-2, MMP-7, MMP-13 and MT2A do not contribute to breast, lung and colon cancer risk in polish population.
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- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00147-w
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- Publication type:
- Article
Screening with magnetic resonance imaging, mammography and ultrasound in women at average and intermediate risk of breast cancer.
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- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0064-y
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- Publication type:
- Article
Management of ovarian and endometrial cancers in women belonging to HNPCC carrier families: review of the literature and results of cancer risk assessment in Polish HNPCC families.
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- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0025-2
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- Publication type:
- Article
Large deletion causing von Hippel-Lindau disease and hereditary breast cancer syndrome.
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- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-16
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- Publication type:
- Article
Management of ovarian and endometrial cancers in women belonging to HNPCC carrier families: review of the literature and results of cancer risk assessment in Polish HNPCC families.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 39, doi. 10.1186/s13053-015-0025-2
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- Publication type:
- Article
Optimizing recruitment to a prostate cancer surveillance program among male BRCA1 mutation carriers: invitation by mail or by telephone.
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- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-17
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- Publication type:
- Article
Harnessing Epigenetics for Breast Cancer Therapy: The Role of DNA Methylation, Histone Modifications, and MicroRNA.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 8, p. 7235, doi. 10.3390/ijms24087235
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- Publication type:
- Article
Allelic modification of breast cancer risk in women with an NBN mutation.
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- Breast Cancer Research & Treatment, 2019, v. 178, n. 2, p. 427, doi. 10.1007/s10549-019-05391-w
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- Publication type:
- Article
Age-specific risks of incident, contralateral and ipsilateral breast cancer among 1776 Polish BRCA1 mutation carriers.
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- Breast Cancer Research & Treatment, 2019, v. 174, n. 3, p. 769, doi. 10.1007/s10549-018-05076-w
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- Publication type:
- Article
Germline RECQL mutations are associated with breast cancer susceptibility.
- Published in:
- Nature Genetics, 2015, v. 47, n. 6, p. 643, doi. 10.1038/ng.3284
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- Publication type:
- Article
Lung Cancer Occurrence—Correlation with Serum Chromium Levels and Genotypes.
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- Biological Trace Element Research, 2021, v. 199, n. 4, p. 1228, doi. 10.1007/s12011-020-02240-6
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- Publication type:
- Article
Inherited NBN Mutations and Prostate Cancer Risk and Survival.
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- Cancer Research & Treatment, 2019, v. 51, n. 3, p. 1180, doi. 10.4143/crt.2018.532
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- Publication type:
- Article
Founder Mutations for Early Onset Melanoma as Revealed by Whole Exome Sequencing Suggests That This is Not Associated with the Increasing Incidence of Melanoma in Poland.
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- Cancer Research & Treatment, 2019, v. 51, n. 1, p. 337, doi. 10.4143/crt.2018.157
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- Publication type:
- Article
The Prevalence of Founder Mutations among Individuals from Families with Familial Pancreatic Cancer Syndrome.
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- Cancer Research & Treatment, 2017, v. 49, n. 2, p. 430, doi. 10.4143/crt.2016.217
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- Publication type:
- Article
Prevalence of Germline Mutations in Genes Engaged in DNA Damage Repair by Homologous Recombination in Patients with Triple-Negative and Hereditary Non-Triple-Negative Breast Cancers.
- Published in:
- PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0130393
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- Publication type:
- Article
A Low Selenium Level Is Associated with Lung and Laryngeal Cancers.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0059051
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- Publication type:
- Article
Smoking Related Cancers and Loci at Chromosomes 15q25, 5p15, 6p22.1 and 6p21.33 in the Polish Population.
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- PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0025057
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- Publication type:
- Article
Exploring the Link between Germline and Somatic Genetic Alterations in Breast Carcinogenesis.
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- PLoS ONE, 2010, v. 5, n. 11, p. 1, doi. 10.1371/journal.pone.0014078
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- Publication type:
- Article
Influence of the Levels of Arsenic, Cadmium, Mercury and Lead on Overall Survival in Lung Cancer.
- Published in:
- Biomolecules (2218-273X), 2021, v. 11, n. 8, p. 1160, doi. 10.3390/biom11081160
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- Publication type:
- Article
Cobalt Serum Level as a Biomarker of Cause-Specific Survival among Prostate Cancer Patients.
- Published in:
- Cancers, 2024, v. 16, n. 15, p. 2618, doi. 10.3390/cancers16152618
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- Publication type:
- Article
Risk of Second Primary Thyroid Cancer in Women with Breast Cancer.
- Published in:
- Cancers, 2022, v. 14, n. 4, p. 957, doi. 10.3390/cancers14040957
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- Article
Blood Arsenic Levels as a Marker of Breast Cancer Risk among BRCA1 Carriers.
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- Cancers, 2021, v. 13, n. 13, p. 3345, doi. 10.3390/cancers13133345
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- Publication type:
- Article
Recurrent Mutations in BRCA1 , BRCA2 , RAD51C , PALB2 and CHEK2 in Polish Patients with Ovarian Cancer.
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- Cancers, 2021, v. 13, n. 4, p. 849, doi. 10.3390/cancers13040849
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- Article
CA125 and Ovarian Cancer: A Comprehensive Review.
- Published in:
- Cancers, 2020, v. 12, n. 12, p. 3730, doi. 10.3390/cancers12123730
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- Publication type:
- Article
Prevalence of Recurrent Mutations Predisposing to Breast Cancer in Early-Onset Breast Cancer Patients from Poland.
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- Cancers, 2020, v. 12, n. 8, p. 2321, doi. 10.3390/cancers12082321
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- Publication type:
- Article
BARD1 is a Low/Moderate Breast Cancer Risk Gene: Evidence Based on an Association Study of the Central European p.Q564X Recurrent Mutation.
- Published in:
- Cancers, 2019, v. 11, n. 6, p. 740, doi. 10.3390/cancers11060740
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- Publication type:
- Article
Blood molybdenum level as a marker of cancer risk on BRCA1 carriers.
- Published in:
- Hereditary Cancer in Clinical Practice, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s13053-024-00291-7
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- Publication type:
- Article
Germline CHEK2 mutations and colorectal cancer risk: different effects of a missense and truncating mutations?
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 2, p. 237, doi. 10.1038/sj.ejhg.5201734
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- Publication type:
- Article
Germline CHEK2 mutations and colorectal cancer risk: different effects of a missense and truncating mutations?
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- 2007
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- Correction Notice
Germline fumarate hydratase mutations in patients with ovarian mucinous cystadenoma.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 7, p. 880, doi. 10.1038/sj.ejhg.5201630
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- Publication type:
- Article
A high frequency of BRCA2 gene mutations in Polish families with ovarian and stomach cancer.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 12, p. 955, doi. 10.1038/sj.ejhg.5201064
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- Publication type:
- Article
Survival of bladder or renal cancer in patients with CHEK2 mutations.
- Published in:
- PLoS ONE, 2021, v. 16, n. 9, p. 1, doi. 10.1371/journal.pone.0257132
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- Publication type:
- Article
Polymorphisms in nucleotide excision repair genes and susceptibility to colorectal cancer in the Polish population.
- Published in:
- Molecular Biology Reports, 2015, v. 42, n. 3, p. 755, doi. 10.1007/s11033-014-3824-z
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- Publication type:
- Article
Large <i>BRCA1</i> and <i>BRCA2</i> genomic rearrangements in Polish high-risk breast and ovarian cancer families.
- Published in:
- Molecular Biology Reports, 2013, v. 40, n. 12, p. 6619, doi. 10.1007/s11033-013-2775-0
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- Publication type:
- Article
Predictors of survival for breast cancer patients with a <italic>BRCA1</italic> mutation.
- Published in:
- Breast Cancer Research & Treatment, 2018, v. 168, n. 2, p. 513, doi. 10.1007/s10549-017-4605-x
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- Publication type:
- Article
Prospective evaluation of alcohol consumption and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers.
- Published in:
- Breast Cancer Research & Treatment, 2015, v. 151, n. 2, p. 435, doi. 10.1007/s10549-015-3393-4
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- Publication type:
- Article
Double heterozygotes among breast cancer patients analyzed for BRCA1, CHEK2, ATM, NBN/NBS1, and BLM germ-line mutations.
- Published in:
- 2014
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- Publication type:
- Report
The HOXB13 p.Gly84Glu mutation is not associated with the risk of breast cancer.
- Published in:
- 2012
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- Publication type:
- Report
Different CHEK2 germline mutations are associated with distinct immunophenotypic molecular subtypes of breast cancer.
- Published in:
- Breast Cancer Research & Treatment, 2012, v. 132, n. 3, p. 937, doi. 10.1007/s10549-011-1635-7
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- Publication type:
- Article
A nonsense mutation (E1978X) in the ATM gene is associated with breast cancer.
- Published in:
- 2010
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- Publication type:
- Report
Synergistic interaction of variants in CHEK2 and BRCA2 on breast cancer risk.
- Published in:
- Breast Cancer Research & Treatment, 2009, v. 117, n. 1, p. 161, doi. 10.1007/s10549-008-0249-1
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- Publication type:
- Article
Genetic contribution to all cancers: the first demonstration using the model of breast cancers from Poland stratified by age at diagnosis and tumour pathology.
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- Breast Cancer Research & Treatment, 2009, v. 114, n. 1, p. 121, doi. 10.1007/s10549-008-9974-8
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- Publication type:
- Article
Smoking and the risk of breast cancer in BRCA1 and BRCA2 carriers: an update.
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- Breast Cancer Research & Treatment, 2009, v. 114, n. 1, p. 127, doi. 10.1007/s10549-008-9977-5
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- Publication type:
- Article