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TP53 gene
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publication
TP53 gene mutations are rare in nondysplastic Barrett's esophagus
2006 |
Second Faculty of Medicine
publication
Significance of TP53 gene identification in tumour affected families
2003 |
Second Faculty of Medicine
publication
TP53 gene mutations are rare in nondysplastic Barrett´s esophagus
2006 |
First Faculty of Medicine
publication
TP53 gene mutations are rare in nondysplastic Barrett´s esophagus
2006 |
Faculty of Physical Education and Sport
publication
Importance of promoter methylation of GATA4 and TP53 genes in endometrioid carcinoma of endometrium
2014 |
First Faculty of Medicine, Faculty of Medicine in Hradec Králové
publication
TP53 gene mutation in Barrett´s exophagus
Publication without faculty affiliation
publication
Germline mutation in the TP53 gene in uveal melanoma
2018 |
First Faculty of Medicine, Faculty of Physical Education and Sport
publication
Mutations and polymorphisms in TP53 gene-an overview on the role in colorectal cancer
2012 |
First Faculty of Medicine
publication
Somatic Mutations in Exon 7 of the TP53 Gene in Index Colorectal Lesions Are Associated with the Early Occurrence of Metachronous Adenoma
2022 |
Central Library of Charles University, First Faculty of Medicine, Faculty of Science
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, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Genotype and Haplotype Analyses of TP53 Gene in Breast Cancer Patients: Association with Risk and Clinical Outcomes
2015 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Genotype and haplotype analysis of TP53 gene and the risk of pancreatic cancer: an association study in the Czech Republic
2010 |
Central Library of Charles University, First Faculty of Medicine, Second Faculty of Medicine
publication
Cutaneous hidradenocarcinoma: A clinicopathological, immunohistochemical, and molecular biologic study of 14 cases, including Her2/neu gene expression/amplification, TP53 gene mutation analysis, and t(11;19) translocation
2009 |
Central Library of Charles University
publication
Cutaneous hidradenocarcinoma: A clinicopathological, immunohistochemical, and molecular biologic study of 14 cases, including Her2/neu gene expression/amplification, TP53 gene mutation analysis, and t(11;19) translocation
2009 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
No association between the TP53 codon 72 polymorphism and risk or prognosis of Hodgkin and non-Hodgkin lymphoma
2011 |
Central Library of Charles University, First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
publication
Cases of LiFraumeni syndrome: diagnostic and preventive possibilities
2006 |
Second Faculty of Medicine
publication
Acquired uniparental disomy in bone-marrow cells of patients with myelodysplastic syndrome and complex karyotype
2015 |
First Faculty of Medicine
publication
Cutaneous hidradenocarcinoma: A clinicopathological, immunohistochemical, and molecular biologic study of 14 cases, including Her2/neu gene expression/amplification, TP53 gene mutation analysis, and t(11;19) translocation
2009 |
Faculty of Medicine in Pilsen
publication
Copy number neutral loss of heterozygosity at 17p and homozygous mutations of TP53 are associated with complex chromosomal aberrations in patients newly diagnosed with myelodysplastic syndromes
2016 |
First Faculty of Medicine
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
Increased sperm aneuploidy in two male carriers of germline TP53 mutations
2011 |
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
Genotype and haplotype analysis of cell cycle genes in sporadic colorectal cancer in the Czech Republic
2009 |
First Faculty of Medicine, Second Faculty of Medicine, Third 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
Markers of progression and development of metastases in ovarian carcinomas estimated using gene expression profiles
2015 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Medicine in Pilsen
publication
A rare tumor and an ethical dilemma in a family with a germline TP53 mutation
2008 |
Second Faculty of Medicine
publication
A girl with neurofibromatosis type 1, atypical autism and mosaic ring chromosome 17
2007 |
Second Faculty of Medicine
publication
Circulating tumor DNA detection in head and neck cancer: evaluation of two different detection approaches
2017 |
First Faculty of Medicine
publication
Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia
2012 |
Second Faculty of Medicine
publication
Treatment of Chronic Lymphocytic Leukemia with TP53 Aberrations
2015 |
Faculty of Medicine in Pilsen