(Q37588167)

21 August 2017

Identification of TP53 as an acute lymphocytic leukemia susceptibility gene through exome sequencing (English)

1 reference

acute lymphocytic leukemia

21 August 2017

0 references

1 reference

1 reference

3

Donna M Muzny

1 reference

21 August 2017

1

Bradford C Powell

1 reference

21 August 2017

8

Richard A Gibbs

1 reference

21 August 2017

Lichun Jiang

2

1 reference

21 August 2017

Lisa R Treviño

4

1 reference

21 August 2017

Zoann E Dreyer

5

1 reference

21 August 2017

Louise C Strong

6

1 reference

21 August 2017

David A Wheeler

7

1 reference

21 August 2017

Sharon E Plon

9

1 reference

21 August 2017

19 December 2012

1 reference

21 August 2017

Pediatric Blood Cancer

1 reference

21 August 2017

60

1 reference

21 August 2017

6

1 reference

21 August 2017

E1-3

1 reference

An integrative variant analysis suite for whole exome next-generation sequencing data

21 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3926299

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3926299

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3926299

Fast and accurate long-read alignment with Burrows-Wheeler transform

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3926299

The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3926299

Polymorphisms in p53 and the p53 pathway: roles in cancer susceptibility and response to treatment

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3926299

NCBI Reference Sequences: current status, policy and new initiatives

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3926299

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3926299

The vertebrate genome annotation (Vega) database

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3926299

Outcome of treatment in children with hypodiploid acute lymphoblastic leukemia

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3926299

Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: lessons from recent developments in the IARC TP53 database

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3926299

Absence of hereditary p53 mutations in 10 familial leukemia pedigrees

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3926299

Directed evolution of p53 variants with altered DNA-binding specificities by in vitro compartmentalization.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3926299

Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3926299

Beyond Li Fraumeni Syndrome: clinical characteristics of families with p53 germline mutations.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3926299

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

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3926299

Absence of germline p53 mutations in familial lymphoma

1 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23255406

12 December 2020

inferred from PubMed ID database lookup

2009 Version of the Chompret Criteria for Li Fraumeni Syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23255406

12 December 2020

inferred from PubMed ID database lookup

Familial and metachronous malignant lymphoma: absence of constitutional p53 mutations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23255406

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1002/PBC.24417

1 reference

release_5khz7c3ifjahlgvawwmdmxbn4a

21 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/5khz7c3ifjahlgvawwmdmxbn4a

24 November 2022

mapped directly with Wikidata item

1 reference

21 August 2017

1 reference