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TP53 mutation
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Somatic TP53 Mutation Mosaicism in a Patient With Li-Fraumeni Syndrome
2009 |
Second Faculty of Medicine
publication
Telomere length in peripheral blood cells of germline TP53 mutation carriers is shorter than that of normal individuals of corresponding age
2007 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
Barrett's esophagus - our experience
2005 |
Second Faculty of Medicine
publication
Increased sperm aneuploidy in two male carriers of germline TP53 mutations
2011 |
Second Faculty of Medicine
publication
Identification of five new families strengthens the link between childhood choroid plexus carcinoma and germline TP53 mutations
2005 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
A Li-Fraumeni syndrome family with retained heterozygosity for a germline TP53 mutation in two tumours
2003 |
Second Faculty of Medicine
publication
Loss of heterozygosity in tumours of carriers of germline TP53 mutations
Publication without faculty affiliation
publication
High frequency of complex TP53 mutations in CNS metastases from breast cancer
2012 |
Third Faculty of Medicine
publication
The TP53 gene promoter is not methylated in families suggestive of Li-Fraumeni syndrome with no germline TP53 mutations
2009 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
A high TP53 mutation burden is a strong predictor of primary refractory mantle cell lymphoma
2020 |
First Faculty of Medicine
publication
A rare tumor and an ethical dilemma in a family with a germline TP53 mutation
2008 |
Second Faculty of Medicine
publication
TP53 mutation variant allele frequency is a potential predictor for clinical outcome of patients with lower-risk myelodysplastic syndromes
2016 |
First Faculty of Medicine
publication
Expression of p53 and TP53 mutational analysis in malignant neoplasms arising in preexisting spiradenoma, cylindroma, and spiradenocylindroma, sporadic or associated with Brooke-Spiegler syndrome
2010 |
Central Library of Charles University
publication
Expression of p53 and TP53 mutational analysis in malignant neoplasms arising in preexisting spiradenoma, cylindroma, and spiradenocylindroma, sporadic or associated with Brooke-Spiegler syndrome
2010 |
Faculty of Medicine in Pilsen
publication
Li-Fraumeni syndrome - a proposal of complex prevention care for carriers of TP53 mutation with total-body MRI
2012 |
Second Faculty of Medicine
publication
A comprehensive study of TP53 mutations in chronic lymphocytic leukemia: analysis of 1287 diagnostic and 1148 follow-up CLL samples
2011 |
Central Library of Charles University, Faculty of Medicine in Hradec Králové
publication
STAT3 and TP53 mutations associate with poor prognosis in anaplastic large cell lymphoma
2021 |
Faculty of Medicine in Hradec Králové
publication
TP53 mutations in myelodysplastic syndrome is significantly correlated with deletion of the long arm 5.chromozomu (5q-) and usually has a negative prognostic value (meaning TP53 examination in the era of lenalidomide)
2013 |
First Faculty of Medicine
publication
Refined criteria for p53 expression in ovarian mucinous tumours are highly concordant with TP53 mutation status, but p53 expression/TP53 status lack prognostic significance
2023 |
Faculty of Medicine in Hradec Králové, First Faculty of Medicine, Faculty of Medicine in Pilsen, Third Faculty of Medicine
publication
Identification of Circulating Tumor DNA for the Early Detection of Small-cell Lung Cancer
2016 |
First Faculty of Medicine
publication
Is there anticipation in the age at onset of cancer in families with Li-Fraumeni syndrome?
2002 |
Second Faculty of Medicine
publication
Analysis of genetic events in 17p13 and 9p21 regions supports predominant monoclonal origin of multifocal and recurrent bladder cancer
2006 |
Second Faculty of Medicine
publication
The Interactions of DNA Repair, Telomere Homeostasis, and p53 Mutational Status in Solid Cancers: Risk, Prognosis, and Prediction
2021 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Detection and Quantification of ctDNA for Longitudinal Monitoring of Treatment in Non-Small Cell Lung Cancer Patients Using a Universal Mutant Detection Assay by Denaturing Capillary Electrophoresis
2022 |
Central Library of Charles University, Faculty of Medicine in Pilsen, Faculty of Science
publication
TP53, EGFR, and KRAS mutations in relation to VHL inactivation and lifestyle risk factors in renal-cell carcinoma from central and eastern Europe
2010 |
First Faculty of Medicine
publication
Li-Fraumeni Syndrome
2003 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
Genomic analysis of head and neck cancer cases from two high incidence regions
2018 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Molecular classification of endometrial cancers translated into practice
2021 |
Faculty of Medicine in Pilsen
publication
Germline mutation in the TP53 gene in uveal melanoma
2018 |
First Faculty of Medicine, Faculty of Physical Education and Sport
publication
Significance of TP53 gene identification in tumour affected families
2003 |
Second Faculty of Medicine