- The Prevalence of Founder Mutations among Individuals from Families with Familial Pancreatic Cancer Syndrome
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Lener MR, Kashyap A, Kluźniak , Cybulski C, Soluch A, Pietrzak S, Huzarski T, Gronwald J, Lubiński
- KMID: 2378115
- Cancer Res Treat.
- 2017 Apr;49(2):430-436.
- doi: 10.4143/crt.2016.217
PURPOSE: Familial pancreatic cancer describes families with at least two first-degree relatives with pancreatic cancer that do not fulfil the criteria of other inherited tumor syndromes with increased risks of... -
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- Inherited NBN Mutations and Prostate Cancer Risk and Survival
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Rusak B, Kluźniak , Wokołorczykv D, Stempa K, Kashyap A, Gronwald J, Huzarski T, Dębniak T, Jakubowska A, Masojć B, Akbari MR, Narodv SA, Lubiński , Cybulski C, The Polish Hereditary Prostate Cancer Consortium
- KMID: 2454309
- Cancer Res Treat.
- 2019 Jul;51(3):1180-1187.
- doi: 10.4143/crt.2018.532
PURPOSE: The purpose of this study was to establish the contribution of four founder alleles of NBN to prostate cancer risk and cancer survival. MATERIALS AND METHODS: Five thousand one hundred... -
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- Serum Concentrations of Selenium and Copper in Patients Diagnosed with Pancreatic Cancer
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Lener MR, Scott RJ, Wiechowska-Kozłowska A, Serrano-Fernández P, Baszuk P, Jaworska-Bieniek K, Sukiennicki G, Marciniak , Muszyńska M, Kładny J, Gromowski , Kaczmarek , Jakubowska A, Lubiński
- KMID: 2344079
- Cancer Res Treat.
- 2016 Jul;48(3):1056-1064.
- doi: 10.4143/crt.2015.282
PURPOSE: Understanding of the etiology and pathogenesis of pancreatic cancer (PaCa) is still insufficient. This study evaluated the associations between concentrations of selenium (Se) and copper (Cu) in the serum... -
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- 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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Dębniak T, Scott RJ, Lea RA, Górski B, Masojć B, Cybulski C, Kram A, Maleszka R, Gromowski , Paszkowska-Szczur K, Kashyap A, Lener MR, Malińska , Rogoża E, Murawa D, Rudnicka H, Deptuła J, Lubiński
- KMID: 2437624
- Cancer Res Treat.
- 2019 Jan;51(1):337-344.
- doi: 10.4143/crt.2018.157
PURPOSE: Germline mutations within melanoma susceptibility genes are present only in minority of melanoma patients and it is expected that additional genes will be discovered with next generation sequence technology... -
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