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ASXL genes and RUNX1: an intimate connection?
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
25170110
retrieved
31 July 2017
title
ASXL genes and RUNX1: an intimate connection?
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
25170110
retrieved
31 July 2017
author
Klaus H Metzeler
object named as
Klaus H Metzeler
series ordinal
1
0 references
language of work or name
English
0 references
publication date
1 August 2014
1 reference
stated in
Europe PubMed Central
PubMed ID
25170110
retrieved
31 July 2017
published in
Blood
1 reference
stated in
Europe PubMed Central
PubMed ID
25170110
retrieved
31 July 2017
volume
124
1 reference
stated in
Europe PubMed Central
PubMed ID
25170110
retrieved
31 July 2017
issue
9
1 reference
stated in
Europe PubMed Central
PubMed ID
25170110
retrieved
31 July 2017
page(s)
1382-1383
1 reference
stated in
Europe PubMed Central
PubMed ID
25170110
retrieved
31 July 2017
cites work
Frequent ASXL2 mutations in acute myeloid leukemia patients with t(8;21)/RUNX1-RUNX1T1 chromosomal translocations.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4148754
retrieved
5 July 2018
The landscape of somatic mutations in epigenetic regulators across 1,000 paediatric cancer genomes.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4148754
retrieved
5 July 2018
Core-binding factor acute myeloid leukemia: can we improve on HiDAC consolidation?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4148754
retrieved
5 July 2018
Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4148754
retrieved
5 July 2018
Functional and cancer genomics of ASXL family members
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4148754
retrieved
5 July 2018
RUNX1 mutations are associated with poor outcome in younger and older patients with cytogenetically normal acute myeloid leukemia and with distinct gene and MicroRNA expression signatures
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4148754
retrieved
5 July 2018
Acquired mutations in ASXL1 in acute myeloid leukemia: prevalence and prognostic value
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4148754
retrieved
5 July 2018
ASXL1 mutations identify a high-risk subgroup of older patients with primary cytogenetically normal AML within the ELN Favorable genetic category
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4148754
retrieved
5 July 2018
Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4148754
retrieved
28 October 2018
High number of additional genetic lesions in acute myeloid leukemia with t(8;21)/RUNX1-RUNX1T1: frequency and impact on clinical outcome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25170110
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1182/BLOOD-2014-07-586073
1 reference
stated in
Europe PubMed Central
PubMed ID
25170110
retrieved
31 July 2017
PMCID
4148754
1 reference
stated in
Europe PubMed Central
PubMed ID
25170110
retrieved
31 July 2017
PubMed ID
25170110
1 reference
stated in
Europe PubMed Central
PubMed ID
25170110
retrieved
31 July 2017
ResearchGate publication ID
265176121
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