(Q22241780)

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Li-fraumeni syndrome

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Li-fraumeni syndrome (English)

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author name string

David Malkin

1

author given names

David

author last names

Malkin

1 reference

PubMed publication ID

7 February 2023

language of work or name

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publication date

April 2011

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1 reference

2

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4

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475-84

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Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

19 March 2017

Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

19 March 2017

Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

19 March 2017

Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

7 April 2017

Tumor spectrum analysis in p53-mutant mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

7 April 2017

Joint effects of germ-line TP53 mutation, MDM2 SNP309, and gender on cancer risk in family studies of Li-Fraumeni syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Effects of MDM2, MDM4 and TP53 codon 72 polymorphisms on cancer risk in a cohort study of carriers of TP53 germline mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Attitude towards pre-implantation genetic diagnosis for hereditary cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Copy number variations and cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Predictive diagnosis of the cancer prone Li-Fraumeni syndrome by accident: new challenges through whole genome array testing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Transactivation of the EGR1 gene contributes to mutant p53 gain of function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Mutant p53 exerts a dominant negative effect by preventing wild-type p53 from binding to the promoter of its target genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

American Society of Clinical Oncology Policy Statement Update: Genetic Testing for Cancer Susceptibility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Germline TP53 mutations and Li-Fraumeni syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Germline p53 mutations in a cohort with childhood sarcoma: sex differences in cancer risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Variable levels of chromosomal instability and mitotic spindle checkpoint defects in breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Molecular mechanisms for genomic disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Development of spontaneous mammary tumors in BALB/c p53 heterozygous mice. A model for Li-Fraumeni syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Anticipated versus actual emotional reactions to disclosure of results of genetic tests for cancer susceptibility: findings from p53 and BRCA1 testing programs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

High metastatic potential in mice inheriting a targeted p53 missense mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Retention of wild-type p53 in tumors from p53 heterozygous mice: reduction of p53 dosage can promote cancer formation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

In vitro analysis of the dominant negative effect of p53 mutants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Chromosome instability is a predominant trait of fibroblasts from Li-Fraumeni families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Tumors associated with p53 germline mutations: a synopsis of 91 families.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Several mutant p53 proteins detected in cancer-prone families with Li-Fraumeni syndrome exhibit transdominant effects on the biochemical properties of the wild-type p53.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Spontaneous and carcinogen-induced tumorigenesis in p53-deficient mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

A possible screening test for inherited p53-related defects based on the apoptotic response of peripheral blood lymphocytes to DNA damage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

A cancer family syndrome in twenty-four kindreds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

High incidence of lung, bone, and lymphoid tumors in transgenic mice overexpressing mutant alleles of the p53 oncogene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Recommendations on predictive testing for germ line p53 mutations among cancer-prone individuals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

Germ-line mutations of the p53 tumor suppressor gene in patients with high risk for cancer inactivate the p53 protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

12 September 2017

A common molecular mechanism underlies two phenotypically distinct 17p13.1 microdeletion syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

27 September 2017

Childhood predictive genetic testing for Li-Fraumeni syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

27 September 2017

Characterization of germline TP53 splicing mutations and their genetic and functional analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

27 September 2017

Germ-line p53 mutations predispose to a wide spectrum of early-onset cancers.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

27 September 2017

Activating mutations in p53 produce a common conformational effect. A monoclonal antibody specific for the mutant form

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

27 September 2017

The p53-deficient mouse: a model for basic and applied cancer studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

27 September 2017

Detailed haplotype analysis at the TP53 locus in p.R337H mutation carriers in the population of Southern Brazil: evidence for a founder effect.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

30 May 2018

Impact of the MDM2 SNP309 and p53 Arg72Pro polymorphism on age of tumour onset in Li-Fraumeni syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

30 May 2018

Sensitivity and predictive value of criteria for p53 germline mutation screening

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

30 May 2018

Absence of germline p16(INK4a) alterations in p53 wild type Li-Fraumeni syndrome families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

30 May 2018

Multiple primary cancers in families with Li-Fraumeni syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

30 May 2018

Who should talk to patients with cancer about genetics?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

30 May 2018

Rhabdomyosarcoma in children: epidemiologic study and identification of a familial cancer syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

30 May 2018

TP53 PIN3 and MDM2 SNP309 polymorphisms as genetic modifiers in the Li-Fraumeni syndrome: impact on age at first diagnosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

Genetic counseling can influence the course of a suspected familial cancer syndrome patient: from a case of Li-Fraumeni like syndrome with a germline mutation in the TP53 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

Psychological functioning in persons considering genetic counseling and testing for Li-Fraumeni syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

F18-fluorodeoxyglucose-positron emission tomography/computed tomography screening in Li-Fraumeni syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

Constitutional CHEK2 mutations are associated with a decreased risk of lung and laryngeal cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

Detection of R337H, a germline TP53 mutation predisposing to multiple cancers, in asymptomatic women participating in a breast cancer screening program in Southern Brazil

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

Younger age of cancer initiation is associated with shorter telomere length in Li-Fraumeni syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

The single-nucleotide polymorphism 309 in the MDM2 gene contributes to the Li-Fraumeni syndrome and related phenotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

MDM2 SNP309 Accelerates Tumor Formation in a Gender-Specific and Hormone-Dependent Manner

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian families.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

Penetrance of adrenocortical tumours associated with the germline TP53 R337H mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

Gain of function of a p53 hot spot mutation in a mouse model of Li-Fraumeni syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

Li-Fraumeni and related syndromes: correlation between tumor type, family structure, and TP53 genotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

Is there anticipation in the age at onset of cancer in families with Li-Fraumeni syndrome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

A novel mechanism of tumorigenesis involving pH-dependent destabilization of a mutant p53 tetramer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

p53, CHK2, and CHK1 genes in Finnish families with Li-Fraumeni syndrome: further evidence of CHK2 in inherited cancer predisposition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

Detection of 11 germline inactivating TP53 mutations and absence of TP63 and HCHK2 mutations in 17 French families with Li-Fraumeni or Li-Fraumeni-like syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

p53 compound heterozygosity in a severely affected child with Li-Fraumeni syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

Exclusion of the genes CDKN2 and PTEN as causative gene defects in Li-Fraumeni syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

DNA damage-associated dysregulation of the cell cycle and apoptosis control in cells with germ-line p53 mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

A detailed study of loss of heterozygosity on chromosome 17 in tumours from Li – Fraumeni patients carrying a mutation to the TP53 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

Tumour incidence, spectrum and ploidy in mice with a large deletion in the p53 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135649

29 November 2018

Telomere length in peripheral blood cells of germline TP53 mutation carriers is shorter than that of normal individuals of corresponding age

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening hCHK2 for Mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Statement of the American Society of Clinical Oncology: genetic testing for cancer susceptibility, Adopted on February 20, 1996

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasms

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychologic aspects of cancer genetic testing: a research update for clinicians

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enhanced proliferative potential in culture of cells from p53-deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a novel PTEN intronic deletion in Li-Fraumeni syndrome and its effect on RNA processing

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germ line BAX alterations are infrequent in Li-Fraumeni syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

2009 Version of the Chompret Criteria for Li Fraumeni Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of Li–Fraumeni syndrome and Li–Fraumeni-like families for germline mutations in Bcl10

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Professionals assess the acceptability of preimplantation genetic diagnosis and prenatal diagnosis for managing inherited predisposition to cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening patients for heterozygous p53 mutations using a functional assay in yeast

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Opinion: Comparative biology of mouse versus human cells: modelling human cancer in mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prediction of pathogenic mutations in patients with early-onset breast cancer by family history

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Statement of the American Society of Human Genetics on genetic testing for breast and ovarian cancer predisposition

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Founder effect for the highly prevalent R337H mutation of tumor suppressor p53 in Brazilian patients with adrenocortical tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis, preimplantation genetic diagnosis, and cancer: was Hamlet wrong?

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A functional screen for germ line p53 mutations based on transcriptional activation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome stability, in the absence of apoptosis, is critical for suppression of tumorigenesis in Trp53 mutant mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early detection of adrenocortical carcinoma in a child with Li-Fraumeni syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutant p53 gain of function in two mouse models of Li-Fraumeni syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Joint effects of germ-line p53 mutation and sex on cancer risk in Li-Fraumeni syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of a third Li-Fraumeni syndrome predisposition locus to human chromosome 1q23

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1177/1947601911413466

1 reference

Consolidated OpenCitations Corpus – April 2017

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OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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