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English
Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patients.
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
title
Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patients
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
main subject
myotonic dystrophy
1 reference
based on heuristic
inferred from title
author
Corrado Angelini
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
Giuseppe Novelli
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
Bruno Dallapiccola
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
Massimo Gennarelli
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
author name string
M Pavoni
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
P Amicucci
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
E Menegazzo
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
G Zelano
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
publication date
1 June 1999
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
published in
Neuromuscular Disorders
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
volume
9
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
page(s)
215-219
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
cites work
Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An unstable triplet repeat in a gene related to myotonic muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
GAA instability in Friedreich's Ataxia shares a common, DNA-directed and intraallelic mechanism with other trinucleotide diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeats
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of the CTG repeat expansion in congenital myotonic dystrophy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myotonic dystrophy: molecular windows on a complex etiology
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myotonic dystrophy: will the real gene please step forward!
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHP.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Triplet repeat expansion in myotonic dystrophy alters the adjacent chromatin structure
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of large CTG repeat expansions in myotonic dystrophy alleles using PCR
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterisation of expression of mDMAHP, a homeodomain-encoding gene at the murine DM locus.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistance.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Small increase in triplet repeat length of cerebellum from patients with myotonic dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myotonic dystrophy as a brain disorder.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900003-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0960-8966(99)00003-6
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
PubMed ID
10399747
1 reference
stated in
Europe PubMed Central
PubMed ID
10399747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10399747%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
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