(Q57266809)

1

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Robert D Alston

2

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Richard JQ McNally

3

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Anna M Kelsey

5

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Martin Harris

6

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Osborn B Eden

7

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Jennifer M Varley

https://scigraph.springernature.com/pub.10.1038/sj.onc.1204621

8

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language of work or name

English

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publication date

August 2001

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published in

Oncogene

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volume

20

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issue

34

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page(s)

4621-4628

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exact match

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cites work

The descriptive epidemiology of malignant cystosarcoma phyllodes tumors of the breast

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

Cancer phenotype correlates with constitutional TP53 genotype in families with the Li-Fraumeni syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

Linkage studies in a Li-Fraumeni family with increased expression of p53 protein but no germline mutation in p53.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

Constitutional p53 mutations associated with brain tumors in young adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

Germline p53 mutations are frequently detected in young children with rhabdomyosarcoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

Wilms' tumor in the Li-Fraumeni cancer family syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

Germline p53 gene mutations in subsets of glioma patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

Incidence of germ-line p53 mutations in patients with gliomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

Constitutional p53 mutation in a non-Li-Fraumeni cancer family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

Secondary breast cancer in patients presenting with osteosarcoma: possible involvement of germline p53 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

Li-Fraumeni syndrome--a molecular and clinical review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

Astrocytomas and choroid plexus tumors in two families with identical p53 germline mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

Genetic basis of drug sensitivity in human testis tumour cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

Germline mutations of p53 but not p16/CDKN2 or PTEN/MMAC1 tumor suppressor genes predispose to gliomas. The ANOCEF Group. Association des NeuroOncologues d'Expression Française.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

Comprehensive mutational scanning of the p53 coding region by two- dimensional gene scanning

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

Exclusion of a p53 germline mutation in a classic Li-Fraumeni syndrome family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

7 January 2021

Are germ cell tumors part of the Li-Fraumeni cancer family syndrome?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

7 January 2021

Malignant melanoma in families of children with osteosarcoma, chondrosarcoma, and adrenal cortical carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

7 January 2021

Germ-line TP53 mutations in Finnish cancer families exhibiting features of the Li-Fraumeni syndrome and negative for BRCA1 and BRCA2

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

7 January 2021

Familial Brain Tumour Syndrome Associated with a p53 Germline Deletion of Codon 236

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

7 January 2021

SBLA syndrome revisited

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

7 January 2021

Detection of novel germ-line p53 mutations in diverse-cancer-prone families identified by selecting patients with childhood adrenocortical carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

7 January 2021

Novel p53 splice site mutations in three families with Li-Fraumeni syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

7 January 2021

High frequency of germline p53 mutations in childhood adrenocortical cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204621

7 January 2021