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

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

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

http://www.wikidata.org/entity/Q34145842

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A Comprehensive Review of Pediatric Tumors and Associated Cancer Predisposition Syndromes.Impact of neonatal screening and surveillance for the TP53 R337H mutation on early detection of childhood adrenocortical tumors.Childhood adrenocortical tumours: a review.An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma.Survey of familial glioma and role of germline p16INK4A/p14ARF and p53 mutation Two hits revisited again Tumor protein p53 (TP53) testing and Li-Fraumeni syndrome : current status of clinical applications and future directions.Population prevalence of hereditary breast cancer phenotypes and implementation of a genetic cancer risk assessment program in southern Brazil Inherited germline TP53 mutation encodes a protein with an aberrant C-terminal motif in a case of pediatric adrenocortical tumor Risk assessment and management of high risk familial breast cancer.Pediatric adrenocortical tumors: what they can tell us on adrenal development and comparison with adult adrenal tumors.TP53-Associated Pediatric Malignancies.Clinical and molecular aspects of adrenocortical tumourigenesis.Intronic TP53 Germline Sequence Variants Modify the Risk in German Breast/Ovarian Cancer Families.Referral for cancer genetics consultation: a review and compilation of risk assessment criteria Elevated breast cancer risk among mothers of a population-based series of 2668 children with cancer.Adrenocortical carcinoma: clinical outcomes and prognosis of 330 patients at a tertiary care center Germline TP53 Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family Registry Adrenocortical stem and progenitor cells: implications for adrenocortical carcinoma Towards an understanding of the role of p53 in adrenocortical carcinogenesis.Development of adrenal cortex zonation.Epidemiology and genetics of childhood cancer.Adrenocortical tumors and hyperplasias in childhood--etiology, genetics, clinical presentation and therapy.DNA methylation patterns of candidate genes regulated by thymine DNA glycosylase in patients with TP53 germline mutations.Prevalence and functional consequence of TP53 mutations in pediatric adrenocortical carcinoma: a children's oncology group study.Interplay between human papilloma virus infection and p53 gene alterations in head and neck squamous cell carcinoma of an Indian patient population.An identical, complex TP53 mutation arising independently in two unrelated families with diverse cancer profiles: the complexity of interpreting cancer risk in carriers.Malignant transformation and new primary tumours after therapeutic radiation for benign disease: substantial risks in certain tumour prone syndromes Prevalence of germline TP53 mutations in a prospective series of unselected patients with adrenocortical carcinoma P53 germline mutations in childhood cancers and cancer risk for carrier individuals Immunohistochemical analysis of expression and allelotype of mismatch repair genes (hMLH1 and hMSH2) in bladder cancer.Genomic alterations associated with loss of heterozygosity for TP53 in Li-Fraumeni syndrome fibroblasts.Mutations of the BRCA1 and BRCA2 genes in patients with bilateral breast cancer.Li-Fraumeni syndrome: report of a clinical research workshop and creation of a research consortium Adrenocortical carcinoma is a lynch syndrome-associated cancer p53: a molecular marker for the detection of cancer.Update on tumours of the adrenal cortex, phaeochromocytoma and extra-adrenal paraganglioma.Early occurrence of lung adenocarcinoma and breast cancer after radiotherapy of a chest wall sarcoma in a patient with a de novo germline mutation in TP53.Mutations in the p53 Tumor Suppressor Gene: Important Milestones at the Various Steps of Tumorigenesis Genetics and epigenetics of adrenocortical tumors.

P2860

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P2860

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

http://www.wikidata.org/entity/Q34145842

description

1999 nî lūn-bûn

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1999 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1999 թվականի հոտեմբերին հրատարակված գիտական հոդված

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1999年の論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年论文

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name

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

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

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

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

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

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

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prefLabel

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

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

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

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American Journal of Human Genetics

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

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P2093

A M Kelsey

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D G Evans

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G Forster

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G McGown

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G P Margison

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M Harris

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M Thorncroft

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P2860

'Touchdown' PCR to circumvent spurious priming during gene amplification

A comprehensive genetic map of the human genome based on 5,264 microsatellites

Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms

Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype

Simultaneous adrenocortical carcinoma and ganglioneuroblastoma in a child with Turner syndrome and germline p53 mutation.

An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53.

Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma.

A cancer family syndrome in twenty-four kindreds.

Molecular etiology of low-penetrance retinoblastoma in two pedigrees.

Deletion of RB exons 24 and 25 causes low-penetrance retinoblastoma

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995-1006

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10.1086/302575

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4

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65

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10486318

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