P53 germline mutations in childhood cancers and cancer risk for carrier individuals - Wikidata - wikimedia - TriplyDB

P53 germline mutations in childhood cancers and cancer risk for carrier individuals

P53 germline mutations in childhood cancers and cancer risk for carrier individuals

http://www.wikidata.org/entity/Q36621004

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Genetic causes of cancer predisposition in children and adolescents Somatic mutagenesis in autoimmunity Solid tumor second primary neoplasms: who is at risk, what can we do?p53 Proteoforms and Intrinsic Disorder: An Illustration of the Protein Structure-Function Continuum Concept Genetics, genomics, and cancer risk assessment: State of the Art and Future Directions in the Era of Personalized Medicine Realizing the promise of cancer predisposition genes.An information-theoretic analysis of genetics, gender and age in cancer patients Identification of a novel germ-line mutation in the TP53 gene in a Mexican family with Li-Fraumeni syndrome.Germline mutations and polymorphisms in the origins of cancers in women.The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations.Childhood adrenocortical tumours: a review.Single-nucleotide polymorphisms in the p53 signaling pathway.Map making in the 21st century: charting breast cancer susceptibility pathways in rodent models.An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma.Effects of measured susceptibility genes on cancer risk in family studies.Evaluation of a decision aid for families considering p53 genetic counseling and testing.Clinical management of hereditary breast cancer syndromes.Late onset Li-Fraumeni Syndrome with bilateral breast cancer and other malignancies: case report and review of the literature.Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion.Regular surveillance for Li-Fraumeni Syndrome: advice, adherence and perceived benefits.Joint effects of germ-line TP53 mutation, MDM2 SNP309, and gender on cancer risk in family studies of Li-Fraumeni syndrome.Tumor protein p53 (TP53) testing and Li-Fraumeni syndrome : current status of clinical applications and future directions.10 rare tumors that warrant a genetics referral.Hereditary cancer risk assessment: essential tools for a better approach.siRNA screening identifies differences in the Fanconi anemia pathway in BALB/c-Trp53+/- with susceptibility versus C57BL/6-Trp53+/- mice with resistance to mammary tumors.Breast cancer in young women Contralateral risk-reducing mastectomy: review of risk factors and risk-reducing strategies.Multiplex genetic cancer testing identifies pathogenic mutations in TP53 and CDH1 in a patient with bilateral breast and endometrial adenocarcinoma.Lobular breast cancer: incidence and genetic and non-genetic risk factors.The MDM2 promoter polymorphism SNP309T-->G and the risk of uterine leiomyosarcoma, colorectal cancer, and squamous cell carcinoma of the head and neck Germline TP53 mutational spectrum in French Canadians with breast cancer.The benefit and burden of cancer screening in Li-Fraumeni syndrome: a case report Primed for cancer: Li Fraumeni Syndrome and the pre-cancerous niche Cancer susceptibility syndromes in children in the area of broad clinical use of massive parallel sequencing.Prevalence and functional consequence of TP53 mutations in pediatric adrenocortical carcinoma: a children's oncology group study.Familial aggregation of urinary tract and bone tumors: searching for a syndrome.Using a family history questionnaire to identify adult patients with increased genetic risk for sarcoma.p53 and disease: when the guardian angel fails.Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour.Prevalence of germline TP53 mutations in a prospective series of unselected patients with adrenocortical carcinoma

P2860

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P2860

P53 germline mutations in childhood cancers and cancer risk for carrier individuals

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P53 germline mutations in childhood cancers and cancer risk for carrier individuals

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P53 germline mutations in childhood cancers and cancer risk for carrier individuals

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P53 germline mutations in childhood cancers and cancer risk for carrier individuals

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P53 germline mutations in childhood cancers and cancer risk for carrier individuals

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P53 germline mutations in childhood cancers and cancer risk for carrier individuals

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P53 germline mutations in childhood cancers and cancer risk for carrier individuals

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P53 germline mutations in childhood cancers and cancer risk for carrier individuals

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Abel A

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Frébourg T

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P2860

Mutation and cancer: statistical study of retinoblastoma

Are there low-penetrance TP53 Alleles? evidence from childhood adrenocortical tumors

A cancer family syndrome in twenty-four kindreds.

Germline mutations in the TP53 gene.

A simple p53 functional assay for screening cell lines, blood, and tumors.

Li-Fraumeni syndrome--a molecular and clinical review.

Segregation analysis of cancer in families of childhood soft-tissue-sarcoma patients.

Germ-line p53 mutations in 15 families with Li-Fraumeni syndrome.

The Li-Fraumeni syndrome: from clinical epidemiology to molecular genetics.

A constitutional de novo mutation in exon 8 of the p53 gene in a patient with multiple primary malignancies.

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