(Q34740986)

4 August 2017

title

NRAS mutations with low allele burden have independent prognostic significance for patients with lower risk myelodysplastic syndromes (English)

1 reference

4 August 2017

D M Murphy

1

1 reference

4 August 2017

R Bejar

2

1 reference

4 August 2017

K Stevenson

3

1 reference

4 August 2017

D Neuberg

4

1 reference

4 August 2017

Y Shi

5

1 reference

4 August 2017

C Cubrich

6

1 reference

4 August 2017

K Richardson

7

1 reference

4 August 2017

P Eastlake

8

1 reference

4 August 2017

G Garcia-Manero

9

1 reference

4 August 2017

H Kantarjian

10

1 reference

4 August 2017

B L Ebert

11

1 reference

4 August 2017

G Mike Makrigiorgos

12

1 reference

4 August 2017

publication date

27 May 2013

1 reference

4 August 2017

1 reference

4 August 2017

volume

27

1 reference

4 August 2017

issue

10

1 reference

4 August 2017

page(s)

2077-2081

1 reference

https://scigraph.springernature.com/pub.10.1038/leu.2013.160

4 August 2017

exact match

0 references

cites work

COLD-PCR enrichment of rare cancer mutations prior to targeted amplicon resequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967719

Clinical effect of point mutations in myelodysplastic syndromes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967719

NCCN Clinical Practice Guidelines in Oncology: myelodysplastic syndromes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967719

Unraveling the molecular pathophysiology of myelodysplastic syndromes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967719

Ice-COLD-PCR enables rapid amplification and robust enrichment for low-abundance unknown DNA mutations

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967719

The genetic basis of myelodysplastic syndromes.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967719

COLD-PCR-enhanced high-resolution melting enables rapid and selective identification of low-level unknown mutations

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967719

Clonal heterogeneity in the 5q- syndrome: p53 expressing progenitors prevail during lenalidomide treatment and expand at disease progression

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967719

COLD-PCR: a new platform for highly improved mutation detection in cancer and genetic testing

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967719

PCR-based methods for the enrichment of minority alleles and mutations

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967719

Replacing PCR with COLD-PCR enriches variant DNA sequences and redefines the sensitivity of genetic testing

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3967719

Pathophysiology and treatment of the myelodysplastic syndrome with isolated 5q deletion

7 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FLEU.2013.160

Acquisition of FLT3 or N-ras mutations is frequently associated with progression of myelodysplastic syndrome to acute myeloid leukemia

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FLEU.2013.160

NRAS, FLT3 and TP53 mutations in patients with myelodysplastic syndrome and a del(5q)

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23708912

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic aberrations in the development and subsequent progression of myelodysplastic syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23708912

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/LEU.2013.160

1 reference

Dimensions Publication ID

4 August 2017

0 references

1 reference

4 August 2017

1 reference