Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q35121791)
Watch
English
Animal models of mental retardation: from gene to cognitive function.
scientific article
In more languages
default for all languages
No label defined
No description defined
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12732230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12732230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
review article
1 reference
stated in
Europe PubMed Central
title
Animal models of mental retardation: from gene to cognitive function
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12732230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12732230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
author
Igor Branchi
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12732230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12732230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
Zoe Bichler
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12732230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12732230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
Laura Ricceri
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12732230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12732230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
author name string
Joanne Berger-Sweeney
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12732230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12732230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
publication date
1 January 2003
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12732230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12732230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
published in
Neuroscience & Biobehavioral Reviews
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12732230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12732230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
volume
27
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12732230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12732230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
issue
1-2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12732230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12732230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
page(s)
141-153
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12732230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12732230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
cites work
Functional brain development in humans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Behavioral consequences of abnormal cortical development: insights into developmental disabilities
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epidemiology of mental retardation--a Swedish survey.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nonspecific X-linked mental retardation II: the frequency in British Columbia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetics of mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genes responsible for nonspecific mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetics of brain development and malformation syndromes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transgenic and knock-out mouse pups: the growing need for behavioral analysis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic abnormalities in Prader-Willi syndrome and lessons from mouse models.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fragile X syndrome, the Fragile X related proteins, and animal models
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Murine models for Down syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular genetics and animal models in autistic disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Too much of a good thing: mechanisms of gene action in Down syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A physical map of the mouse genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Full house
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Animal models of neurological deficits: how relevant is the rat?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mouse: genetics meets behaviour
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Behavioural phenotyping of mouse mutants
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenomics: fiction or the future?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cognitive and behavioral assessment in experimental stroke research: will it prove useful?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hippocampus-dependent learning and memory is impaired in mice lacking the Ras-guanine-nucleotide releasing factor 1 (Ras-GRF1).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Enrichment induces structural changes and recovery from nonspatial memory deficits in CA1 NMDAR1-knockout mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysing hippocampal function in transgenic mice: an ethological perspective
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Down syndrome: progress in research
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neurobiology of Down's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal neuronal development in the visual cortex of the human fetus and infant with down's syndrome. A quantitative and qualitative Golgi study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A comparison of whole-genome shotgun-derived mouse chromosome 16 and the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Systematic approach to the study of trisomy in the mouse. II
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neurogenesis of the basal forebrain in euploid and trisomy 16 mice: an animal model for developmental disorders in Down syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
On the cause of mental retardation in Down syndrome: extrapolation from full and segmental trisomy 16 mouse models
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Developmental abnormalities and age-related neurodegeneration in a mouse model of Down syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Behavioral assessment of the Ts65Dn mouse, a model for Down syndrome: altered behavior in the elevated plus maze and open field
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Impaired short- and long-term memory in Ts65Dn mice, a model for Down syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hippocampal volume and neuronal number in Ts65Dn mice: a murine model of Down syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alterations of central noradrenergic transmission in Ts65Dn mouse, a model for Down syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ts1Cje, a partial trisomy 16 mouse model for Down syndrome, exhibits learning and behavioral abnormalities
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic dissection of region associated with behavioral abnormalities in mouse models for Down syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
10 years of Genomics, chromosome 21, and Down syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular mapping of twenty-four features of Down syndrome on chromosome 21.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional screening of 2 Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transgenic mice with increased Cu/Zn-superoxide dismutase activity: animal model of dosage effects in Down syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuronal-specific expression of human copper-zinc superoxide dismutase gene in transgenic mice: animal model of gene dosage effects in Down's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Down's syndrome: Abnormal neuromuscular junction in tongue of transgenic mice with elevated levels of human Cu/Zn-superoxide dismutase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neurodevelopmental delay, motor abnormalities and cognitive deficits in transgenic mice overexpressing Dyrk1A (minibrain), a murine model of Down's syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
High-level expression of the Mnb/Dyrk1A gene in brain and heart during rat early development.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mnb/Dyrk1A is transiently expressed and asymmetrically segregated in neural progenitor cells at the transition to neurogenic divisions.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The kinase DYRK phosphorylates protein-synthesis initiation factor eIF2Bepsilon at Ser539 and the microtubule-associated protein tau at Thr212: potential role for DYRK as a glycogen synthase kinase 3-priming kinase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The kinase DYRK1A phosphorylates the transcription factor FKHR at Ser329 in vitro, a novel in vivo phosphorylation site
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Protein kinase Dyrk1 activates cAMP response element-binding protein during neuronal differentiation in hippocampal progenitor cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dyrk1A haploinsufficiency affects viability and causes developmental delay and abnormal brain morphology in mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mouse brain transcriptome by SAGE: differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Correlative Memory Deficits, Abeta Elevation, and Amyloid Plaques in Transgenic Mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuron loss in APP transgenic mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alzheimer-type neuropathology in transgenic mice overexpressing V717F β-amyloid precursor protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neurobehavioral development, adult openfield exploration and swimming navigation learning in mice with a modified beta-amyloid precursor protein gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Overexpression of a calcium-binding protein, S100 beta, in astrocytes alters synaptic plasticity and impairs spatial learning in transgenic mice.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rett syndrome: review of biological abnormalities.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rett syndrome and the MECP2 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neurobiology of Rett syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rett syndrome: a disorder affecting early brain growth
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neurobiology of Rett syndrome: a genetic disorder of synapse development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prevalence of fragile X syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Absence of expression of the FMR-1 gene in fragile X syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization and localization of the FMR-1 gene product associated with fragile X syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
FMR1 gene and fragile X syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biology of the fragile X mental retardation protein, an RNA-binding protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mildly impaired water maze performance in male Fmr1 knockout mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
(Over)correction of FMR1 deficiency with YAC transgenics: behavioral and physical features
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fragile X mouse: strain effects of knockout phenotype and evidence suggesting deficient amygdala function.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transgenic mouse model for the fragile X syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Behavioral and neuroanatomical characterization of the Fmr1 knockout mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assessing the effects of the 129/Sv genetic background on swimming navigation learning in transgenic mutants: a study using mice with a modified beta-amyloid precursor protein gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dendritic anomalies in disorders associated with mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Doublecortin is required in mice for lamination of the hippocampus but not the neocortex.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
In search of the MRX genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked non-specific mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Impaired conditioned fear and enhanced long-term potentiation in Fmr2 knock-out mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Non-specific X-linked semidominant mental retardation by mutations in a Rab GDP-dissociation inhibitor.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in GDI1 are responsible for X-linked non-specific mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion of the mental retardation gene Gdi1 impairs associative memory and alters social behavior in mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Synaptic regulation of protein synthesis and the fragile X protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Impaired learning and motor behavior in heterozygous Pafah1b1 (Lis1) mutant mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neural consequences of environmental enrichment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Enrichment enhances spatial memory and increases synaptophysin levels in aged female mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Environmental enrichment inhibits spontaneous apoptosis, prevents seizures and is neuroprotective
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Delaying the onset of Huntington's in mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Differential clinical and motor control function in a pair of monozygotic twins with Huntington's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternal care, hippocampal synaptogenesis and cognitive development in rats.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Infantile experience and resistance to physiological stress.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human brain malformations and their lessons for neuronal migration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Serotonin1A receptor acts during development to establish normal anxiety-like behaviour in the adult
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Zic2 regulates the kinetics of neurulation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Targeted mutagenesis of Lis1 disrupts cortical development and LIS1 homodimerization
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The DNA sequence of human chromosome 21
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Critical Periods of Vulnerability for the Developing Nervous System: Evidence from Humans and Animal Models
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chronology of neuron development: animal studies and their clinical implications.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparative aspects of the brain growth spurt
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0149-7634%2803%2900016-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0149-7634(03)00016-2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12732230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12732230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
PubMed publication ID
12732230
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12732230
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12732230%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
ResearchGate publication ID
10773684
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