TP53 mutations in myelodysplastic syndrome are strongly correlated with aberrations of chromosome 5, and correlate with adverse prognosis. (Q43711843)

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scientific article published on 9 January 2013

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English	TP53 mutations in myelodysplastic syndrome are strongly correlated with aberrations of chromosome 5, and correlate with adverse prognosis.	scientific article published on 9 January 2013

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Europe PubMed Central

PubMed publication ID

23297687

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

retrieved

21 February 2020

title

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

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stated in

Europe PubMed Central

PubMed publication ID

23297687

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

retrieved

21 February 2020

main subject

myelodysplastic syndrome

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inferred from title

author

Syed A Mian

series ordinal

3

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Europe PubMed Central

PubMed publication ID

23297687

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

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21 February 2020

author name string

Austin G Kulasekararaj

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1

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Europe PubMed Central

PubMed publication ID

23297687

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

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21 February 2020

Alexander E Smith

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2

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PubMed publication ID

23297687

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

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21 February 2020

Azim M Mohamedali

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4

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Europe PubMed Central

PubMed publication ID

23297687

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

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21 February 2020

Pramila Krishnamurthy

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5

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PubMed publication ID

23297687

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21 February 2020

Nicholas C Lea

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6

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PubMed publication ID

23297687

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21 February 2020

Joop Gäken

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7

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PubMed publication ID

23297687

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21 February 2020

Coralie Pennaneach

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8

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PubMed publication ID

23297687

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21 February 2020

Robin Ireland

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9

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PubMed publication ID

23297687

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

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21 February 2020

Barbara Czepulkowski

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10

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PubMed publication ID

23297687

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21 February 2020

Sabine Pomplun

series ordinal

11

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Europe PubMed Central

PubMed publication ID

23297687

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

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21 February 2020

Judith C Marsh

series ordinal

12

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Europe PubMed Central

PubMed publication ID

23297687

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

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21 February 2020

Ghulam J Mufti

series ordinal

13

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Europe PubMed Central

PubMed publication ID

23297687

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

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21 February 2020

language of work or name

English

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publication date

9 January 2013

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Europe PubMed Central

PubMed publication ID

23297687

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retrieved

21 February 2020

published in

British Journal of Haematology

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PubMed publication ID

23297687

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

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21 February 2020

volume

160

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Europe PubMed Central

PubMed publication ID

23297687

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21 February 2020

issue

5

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Europe PubMed Central

PubMed publication ID

23297687

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21 February 2020

page(s)

660-672

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Europe PubMed Central

PubMed publication ID

23297687

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21 February 2020

cites work

The genetic basis of myelodysplastic syndromes.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

Clinical effect of point mutations in myelodysplastic syndromes

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

Detection of large-scale variation in the human genome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

TP53 Mutations in Low-Risk Myelodysplastic Syndromes With del(5q) Predict Disease Progression

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

The NCBI dbGaP database of genotypes and phenotypes

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

Recurring mutations found by sequencing an acute myeloid leukemia genome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

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.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

Recurrent DNMT3A mutations in patients with myelodysplastic syndromes

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

Clonal architecture of secondary acute myeloid leukemia

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

Frequent pathway mutations of splicing machinery in myelodysplasia

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FBJH.12203

retrieved

21 January 2018

Identifiers

DOI

10.1111/BJH.12203

1 reference

stated in

Europe PubMed Central

PubMed publication ID

23297687

reference URL

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

retrieved

21 February 2020

PubMed publication ID

23297687

1 reference

stated in

Europe PubMed Central

PubMed publication ID

23297687

reference URL

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

retrieved

21 February 2020

 

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