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English
Histone modification defects in developmental disorders and cancer
scientific article published on January 2012
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3292885
retrieved
3 November 2017
editorial
0 references
title
Histone modification defects in developmental disorders and cancer
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3292885
retrieved
3 November 2017
author name string
Nicholas C P Cross
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
3292885
retrieved
3 November 2017
language of work or name
English
0 references
publication date
1 January 2012
1 reference
stated in
Europe PubMed Central
PMCID
3292885
retrieved
3 November 2017
number of pages
2
1 reference
based on heuristic
inferred from page(s)
published in
Oncotarget
1 reference
stated in
Europe PubMed Central
PMCID
3292885
retrieved
3 November 2017
volume
3
1 reference
stated in
Europe PubMed Central
PMCID
3292885
retrieved
3 November 2017
page(s)
3-4
1 reference
stated in
Europe PubMed Central
PMCID
3292885
retrieved
3 November 2017
issue
1
1 reference
stated in
Europe PubMed Central
PMCID
3292885
retrieved
3 November 2017
cites work
Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height.
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=3292885
retrieved
27 May 2018
Somatic mutations at EZH2 Y641 act dominantly through a mechanism of selectively altered PRC2 catalytic activity, to increase H3K27 trimethylation
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=3292885
retrieved
27 May 2018
Polycomb group proteins: multi-faceted regulators of somatic stem cells and cancer
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=3292885
retrieved
27 May 2018
Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders
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=3292885
retrieved
27 May 2018
Genomic loss of microRNA-101 leads to overexpression of histone methyltransferase EZH2 in cancer
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=3292885
retrieved
27 May 2018
Identifiers
DOI
10.18632/ONCOTARGET.436
0 references
PMCID
3292885
1 reference
stated in
Europe PubMed Central
PMCID
3292885
retrieved
3 November 2017
PubMed ID
22287508
1 reference
stated in
Europe PubMed Central
PMCID
3292885
retrieved
3 November 2017
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