P53 germline mutations in childhood cancers and cancer risk for carrier individuals (Q36621004)

15 August 2017

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

1 reference

Brigitte Bressac-de Paillerets

15 August 2017

object named as

Bressac-de Paillerets B

1 reference

15 August 2017

Chompret A

1 reference

15 August 2017

Brugières L

1 reference

15 August 2017

Ronsin M

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15 August 2017

Gardes M

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15 August 2017

Dessarps-Freichey F

1 reference

15 August 2017

Abel A

1 reference

15 August 2017

Hua D

1 reference

15 August 2017

Ligot L

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15 August 2017

Dondon MG

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15 August 2017

Frébourg T

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15 August 2017

Lemerle J

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15 August 2017

Bonaïti-Pellié C

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15 August 2017

Feunteun J

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15 August 2017

language of work or name

English

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publication date

1 June 2000

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British Journal of Cancer

15 August 2017

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15 August 2017

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15 August 2017

1 reference

15 August 2017

1932-1937

1 reference

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

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

Li-Fraumeni syndrome – a molecular and clinical review

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

Germline mutations in the TP53 gene

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

A previously undescribed mutation within the tetramerisation domain of TP53 in a family with Li-Fraumeni syndrome.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

p53 and the Li-Fraumeni syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

ARCAD: a method for estimating age-dependent disease risk associated with mutation carrier status from family data

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

Mutation and cancer: statistical study of retinoblastoma

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

A cancer family syndrome in twenty-four kindreds

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

Follow-up study of twenty-four families with Li-Fraumeni syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

Radiation and genetic factors in the risk of second malignant neoplasms after a first cancer in childhood

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

Prevalence and spectrum of germline mutations of the p53 gene among patients with sarcoma

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

[Hereditary p53 mutation in a patient with multiple tumors: significance for genetic counseling].

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

Germ-line mutations of TP53 in Li-Fraumeni families: an extended study of 39 families

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

Constitutional mutation in exon 8 of the p53 gene in a patient with multiple primary tumours: molecular and immunohistochemical findings

21 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2363254

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

21 October 2018

1 reference

12 December 2020

Splice-site mutation of the p53 gene in a family with hereditary breast-ovarian cancer

1 reference

12 December 2020

Germline mutations of the p53 tumor suppressor gene in children with osteosarcoma

1 reference

12 December 2020

A method for estimating cancer risk in p53 mutation carriers

1 reference

12 December 2020

A de novo p53 germline mutation affecting codon 151 in a six year old child with multiple tumors

1 reference

12 December 2020

Two functional assays employed to detect an unusual mutation in the oligomerisation domain of p53 in a Li-Fraumeni like family

1 reference

12 December 2020

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

1 reference

12 December 2020

Screening for germ line p53 mutations in children with malignant tumors and a family history of cancer

1 reference

12 December 2020

A novel germline p53 splicing mutation in a pediatric patient with a second malignant neoplasm

1 reference

12 December 2020

Identifiers

DOI

10.1054/BJOC.2000.1167

1 reference

Dimensions Publication ID

15 August 2017

0 references

1 reference

15 August 2017

PubMed publication ID

10864200

1 reference