Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q24650396)
Watch
English
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
title
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
main subject
Rett syndrome
0 references
BDNF
0 references
author
Helen Leonard
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
Nicholas de Klerk
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
John Christodoulou
series ordinal
8
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
author name string
B Ben Zeev
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
A Bebbington
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
G Ho
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
E Gak
series ordinal
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
M Vecsler
series ordinal
7
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
language of work or name
English
0 references
publication date
1 April 2009
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
published in
Neurology
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
volume
72
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
issue
14
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
page(s)
1242-1247
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
cites work
MeCP2, a key contributor to neurological disease, activates and represses transcription
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=2677489
retrieved
7 April 2017
Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett 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=2677489
retrieved
7 April 2017
Neurotrophins: roles in neuronal development and function
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=2677489
retrieved
7 April 2017
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
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=2677489
retrieved
7 April 2017
The story of Rett syndrome: from clinic to neurobiology
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=2677489
retrieved
7 April 2017
Phenotypic manifestations of MECP2 mutations in classical and atypical Rett 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=2677489
retrieved
7 April 2017
DNA Methylation-Related Chromatin Remodeling in Activity-Dependent Bdnf Gene Regulation
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=2677489
retrieved
7 April 2017
Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2
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=2677489
retrieved
7 April 2017
The BDNF val66met polymorphism affects activity-dependent secretion of BDNF and human memory and hippocampal function
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=2677489
retrieved
7 April 2017
Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett 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=2677489
retrieved
28 September 2017
Investigating genotype-phenotype relationships in Rett syndrome using an international data set.
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=2677489
retrieved
28 September 2017
Association between brain-derived neurotrophic factor Val66Met gene polymorphism and progressive brain volume changes in schizophrenia
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=2677489
retrieved
28 September 2017
Brain-derived neurotrophic factor expression and respiratory function improve after ampakine treatment in a mouse model of Rett 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=2677489
retrieved
28 September 2017
BDNF Val66Met variant and age of onset in schizophrenia.
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=2677489
retrieved
28 September 2017
Seizures in Rett syndrome: an overview from a one-year calendar study
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=2677489
retrieved
28 September 2017
No association between polymorphisms in the BDNF gene and age at onset in Huntington 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=2677489
retrieved
28 September 2017
Predictors of seizure onset in Rett 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=2677489
retrieved
28 September 2017
Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation.
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=2677489
retrieved
28 September 2017
X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett 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=2677489
retrieved
28 September 2017
Describing the phenotype in Rett syndrome using a population database
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=2677489
retrieved
28 September 2017
The methyl-CpG-binding protein MeCP2 links DNA methylation to histone methylation
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=2677489
retrieved
28 September 2017
Neurotrophins and activity-dependent plasticity
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=2677489
retrieved
28 September 2017
Neurotrophic factors and synaptic plasticity
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=2677489
retrieved
28 September 2017
Guidelines for reporting clinical features in cases with MECP2 mutations.
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=2677489
retrieved
30 May 2018
Cortical degeneration in the absence of neurotrophin signaling: dendritic retraction and neuronal loss after removal of the receptor TrkB.
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=2677489
retrieved
30 May 2018
The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett 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=2677489
retrieved
28 November 2018
Role of BDNF Val66Met functional polymorphism in Alzheimer's disease-related depression.
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=2677489
retrieved
28 November 2018
Elucidating the role of brain-derived neurotrophic factor in the brain.
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=2677489
retrieved
28 November 2018
Neurophysiological and genetic distinctions between pure and comorbid anxiety 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=2677489
retrieved
28 November 2018
Temporal grey matter reductions in bipolar disorder are associated with the BDNF Val66Met 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=2677489
retrieved
28 November 2018
Investigating the role of the brain-derived neurotrophic factor (BDNF) val66met variant in obsessive-compulsive disorder (OCD).
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=2677489
retrieved
28 November 2018
The diagnosis of autism in a female: could it be Rett 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=2677489
retrieved
28 November 2018
Brain-derived neurotrophic factor (BDNF) gene and rapid-cycling bipolar disorder: family-based association study
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=2677489
retrieved
28 November 2018
The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression
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=2677489
retrieved
28 November 2018
Variant brain-derived neurotrophic factor (BDNF) (Met66) alters the intracellular trafficking and activity-dependent secretion of wild-type BDNF in neurosecretory cells and cortical neurons.
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=2677489
retrieved
28 November 2018
Refining the phenotype of common mutations in Rett 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=2677489
retrieved
28 November 2018
Epilepsy in a representative series of Rett 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=2677489
retrieved
28 November 2018
Rett syndrome: characterization of seizures versus non-seizures
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/19349604
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Influence of mutation type and location on phenotype in 123 patients with Rett syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/19349604
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1212/01.WNL.0000345664.72220.6A
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
PMC publication ID
2677489
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
PubMed publication ID
19349604
1 reference
stated in
Europe PubMed Central
PMC publication ID
2677489
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19349604%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
ResearchGate publication ID
24260651
0 references
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
