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Recurrent inversion events at 17q21.31 microdeletion locus are linked to the MAPT H2 haplotype
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scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3202913
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20606400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 February 2020
title
Recurrent inversion events at 17q21.31 microdeletion locus are linked to the MAPT H2 haplotype
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3202913
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20606400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 February 2020
author
Lisenka Vissers
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
3202913
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20606400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 February 2020
Joris A Veltman
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
3202913
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20606400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 February 2020
author name string
P N Rao
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
3202913
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20606400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 February 2020
W Li
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
3202913
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20606400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 February 2020
R A Ophoff
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMCID
3202913
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20606400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 February 2020
language of work or name
English
0 references
publication date
6 July 2010
1 reference
stated in
Europe PubMed Central
PMCID
3202913
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20606400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 February 2020
published in
Cytogenetics and Genome Research
1 reference
stated in
Europe PubMed Central
PMCID
3202913
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20606400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 February 2020
volume
129
1 reference
stated in
Europe PubMed Central
PMCID
3202913
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20606400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 February 2020
page(s)
275-279
1 reference
stated in
Europe PubMed Central
PMCID
3202913
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20606400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 February 2020
issue
4
1 reference
stated in
Europe PubMed Central
PMCID
3202913
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20606400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 February 2020
cites work
Evolutionary toggling of the MAPT 17q21.31 inversion region
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=3202913
retrieved
7 April 2017
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome
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=3202913
retrieved
7 April 2017
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability
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=3202913
retrieved
7 April 2017
A common inversion under selection in Europeans
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=3202913
retrieved
7 April 2017
Genomic rearrangements and sporadic disease
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=3202913
retrieved
27 September 2017
Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease
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=3202913
retrieved
27 September 2017
A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.
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=3202913
retrieved
27 September 2017
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome
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=3202913
retrieved
27 September 2017
Evidence suggesting that Homo neanderthalensis contributed the H2 MAPT haplotype to Homo sapiens
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=3202913
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27 September 2017
A genome-wide survey of segmental duplications that mediate common human genetic variation of chromosomal architecture
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202913
retrieved
27 September 2017
A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.
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=3202913
retrieved
27 September 2017
The H1c haplotype at the MAPT locus is associated with Alzheimer's disease.
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=3202913
retrieved
28 November 2018
Genetic evidence for the involvement of tau in progressive supranuclear palsy
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3202913
retrieved
28 November 2018
Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20606400
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Visualization of MAPT inversion on stretched chromosomes of tau-negative frontotemporal dementia patients
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20606400
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Genomic inversions of human chromosome 15q11-q13 in mothers of Angelman syndrome patients with class II (BP2/3) deletions
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20606400
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1159/000315901
1 reference
stated in
Europe PubMed Central
PMCID
3202913
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20606400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 February 2020
PMCID
3202913
1 reference
stated in
Europe PubMed Central
PMCID
3202913
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20606400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 February 2020
PubMed ID
20606400
1 reference
stated in
Europe PubMed Central
PMCID
3202913
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20606400%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 February 2020
ResearchGate publication ID
45097363
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