(Q43711843)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

title

TP53 mutations in myelodysplastic syndrome are strongly correlated with aberrations of chromosome 5, and correlate with adverse prognosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

main subject

myelodysplastic syndrome

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

author name string

Austin G Kulasekararaj

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Alexander E Smith

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Azim M Mohamedali

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Pramila Krishnamurthy

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Nicholas C Lea

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Joop Gäken

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Coralie Pennaneach

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Robin Ireland

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Barbara Czepulkowski

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Sabine Pomplun

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Judith C Marsh

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

Ghulam J Mufti

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

language of work or name

English

0 references

publication date

9 January 2013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

British Journal of Haematology

21 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

volume

160

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

page(s)

660-672

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

The genetic basis of myelodysplastic syndromes.

21 February 2020

cites work

1 reference

Clinical effect of point mutations in myelodysplastic syndromes

21 January 2018

1 reference

TP53 gene mutation is frequent in patients with acute myeloid leukemia and complex karyotype, and is associated with very poor prognosis.

21 January 2018

1 reference

Haploinsufficiency for ribosomal protein genes causes selective activation of p53 in human erythroid progenitor cells

21 January 2018

1 reference

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders

21 January 2018

1 reference

Comprehensive assessment of genetic and molecular features predicting outcome in patients with chronic lymphocytic leukemia: results from the US Intergroup Phase III Trial E2997.

21 January 2018

1 reference

Reversal of p53 epigenetic silencing in multiple myeloma permits apoptosis by a p53 activator

21 January 2018

1 reference

Detection of large-scale variation in the human genome

21 January 2018

1 reference

TP53 mutations in low-risk myelodysplastic syndromes with del(5q) predict disease progression.

21 January 2018

1 reference

TP53 mutations in myeloid malignancies are either homozygous or hemizygous due to copy number-neutral loss of heterozygosity or deletion of 17p.

21 January 2018

1 reference

Overexpression of p53 mRNA in colorectal cancer and its relationship to p53 gene mutation

21 January 2018

1 reference

The NCBI dbGaP database of genotypes and phenotypes

21 January 2018

1 reference

Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms

21 January 2018

1 reference

Recurring mutations found by sequencing an acute myeloid leukemia genome

21 January 2018

1 reference

RAS, FMS and p53 mutations and poor clinical outcome in myelodysplasias: a 10-year follow-up.

21 January 2018

1 reference

Differential prognostic effect of IDH1 versus IDH2 mutations in myelodysplastic syndromes: a Mayo Clinic study of 277 patients

21 January 2018

1 reference

Next-generation sequencing of the TET2 gene in 355 MDS and CMML patients reveals low-abundance mutant clones with early origins, but indicates no definite prognostic value

21 January 2018

1 reference

Loss of heterozygosity on chromosome 5q in ovarian cancer is frequently accompanied by TP53 mutation and identifies a tumour suppressor gene locus at 5q13.1-21.

21 January 2018

1 reference

Next-generation sequencing of cancer genomes: back to the future.

21 January 2018

1 reference

Recurrent DNMT3A mutations in patients with myelodysplastic syndromes

21 January 2018

1 reference

Clonal architecture of secondary acute myeloid leukemia

21 January 2018

1 reference

Frequent pathway mutations of splicing machinery in myelodysplasia

21 January 2018

1 reference

Clinical application and proposal for modification of the International Working Group (IWG) response criteria in myelodysplasia

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/BJH.12203

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23297687%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

1 reference