Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q80220526)
Watch
English
Inherited epimutation or a haplotypic basis for the propensity to silence?
scientific article published on 01 May 2007
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17460681
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17460681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
title
Inherited epimutation or a haplotypic basis for the propensity to silence?
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17460681
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17460681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
author name string
Catherine M Suter
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17460681
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17460681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
David I K Martin
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17460681
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17460681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
publication date
1 May 2007
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17460681
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17460681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17460681
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17460681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
volume
39
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17460681
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17460681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17460681
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17460681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
page(s)
573; author reply 576
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17460681
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17460681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng0507-573a
0 references
cites work
Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0507-573A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germline epimutation of MLH1 in individuals with multiple cancers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0507-573A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Extensive but hemiallelic methylation of the hMLH1 promoter region in early-onset sporadic colon cancers with microsatellite instability
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0507-573A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MLH1 Germline Epimutations as a Factor in Hereditary Nonpolyposis Colorectal Cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0507-573A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inheritance of a Cancer-AssociatedMLH1Germ-Line Epimutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0507-573A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The inheritance of epigenetic defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0507-573A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0507-573A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epigenetic variation illustrated by DNA methylation patterns of the fragile-X gene FMR1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0507-573A
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0507-573A
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17460681
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17460681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
PubMed publication ID
17460681
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17460681
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17460681%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
