Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients.
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Relationships between gene expression and brain wiring in the adult rodent brainA Draft Sequence of the Neandertal GenomeAdvances in autism genetics: on the threshold of a new neurobiologyVoxelwise genome-wide association study (vGWAS)Comment on "Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients"Common circuit defect of excitatory-inhibitory balance in mouse models of autism.Prenatal stress and inhibitory neuron systems: implications for neuropsychiatric disordersChannelopathy pathogenesis in autism spectrum disordersThe molecular basis of cognitive deficits in pervasive developmental disordersTranslational Mouse Models of Autism: Advancing Toward Pharmacological Therapeutics.Slitrk1-deficient mice display elevated anxiety-like behavior and noradrenergic abnormalitiesCAPS-1 promotes fusion competence of stationary dense-core vesicles in presynaptic terminals of mammalian neuronsBehavioural phenotyping assays for mouse models of autismSynaptic proteins and receptors defects in autism spectrum disordersCharacterization of the deleted in autism 1 protein family: implications for studying cognitive disorders.Are Sema5a mutant mice a good model of autism? A behavioral analysis of sensory systems, emotionality and cognition.Annual Research Review: Transgenic mouse models of childhood-onset psychiatric disorders.Uncovering molecular biomarkers that correlate cognitive decline with the changes of hippocampus' gene expression profiles in Alzheimer's disease.Calcium-dependent activator protein for secretion 2 (CAPS2) promotes BDNF secretion and is critical for the development of GABAergic interneuron network.Axonal localization of Ca2+-dependent activator protein for secretion 2 is critical for subcellular locality of brain-derived neurotrophic factor and neurotrophin-3 release affecting proper development of postnatal mouse cerebellum.Alternative splicing variations in mouse CAPS2: differential expression and functional properties of splicing variants.Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.Genome-wide linkage in Utah autism pedigreesTau phosphorylation and cleavage in ethanol-induced neurodegeneration in the developing mouse brain.Bio-collections in autism research.Involvement of ceramide in ethanol-induced apoptotic neurodegeneration in the neonatal mouse brainMaternally inherited genetic variants of CADPS2 are present in autism spectrum disorders and intellectual disability patients.Synaptic signaling and aberrant RNA splicing in autism spectrum disordersDysfunctional gene splicing as a potential contributor to neuropsychiatric disorders.Lack of stress responses to long-term effects of corticosterone in Caps2 knockout mice.A functional polymorphism of the brain derived neurotrophic factor gene and cortical anatomy in autism spectrum disorder.Epigenomic-basis of Preemptive Medicine for Neurodevelopmental DisordersGABA system dysfunction in autism and related disorders: from synapse to symptomsGenetic Evidence for Possible Involvement of the Calcium Channel Gene CACNA1A in Autism Pathogenesis in Chinese Han Population.Ethanol triggers sphingosine 1-phosphate elevation along with neuroapoptosis in the developing mouse brain.Candidate hippocampal biomarkers of susceptibility and resilience to stress in a rat model of depression.Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair Sequencing.The brain-specific RasGEF very-KIND is required for normal dendritic growth in cerebellar granule cells and proper motor coordination.Reduced axonal localization of a Caps2 splice variant impairs axonal release of BDNF and causes autistic-like behavior in mice.Reduction in parvalbumin expression not loss of the parvalbumin-expressing GABA interneuron subpopulation in genetic parvalbumin and shank mouse models of autism
P2860
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P2860
Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients.
description
2007 nî lūn-bûn
@nan
2007 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի մարտին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Autistic-like phenotypes in Ca ...... splicing in autistic patients
@nl
Autistic-like phenotypes in Ca ...... splicing in autistic patients.
@ast
Autistic-like phenotypes in Ca ...... splicing in autistic patients.
@en
type
label
Autistic-like phenotypes in Ca ...... splicing in autistic patients
@nl
Autistic-like phenotypes in Ca ...... splicing in autistic patients.
@ast
Autistic-like phenotypes in Ca ...... splicing in autistic patients.
@en
prefLabel
Autistic-like phenotypes in Ca ...... splicing in autistic patients
@nl
Autistic-like phenotypes in Ca ...... splicing in autistic patients.
@ast
Autistic-like phenotypes in Ca ...... splicing in autistic patients.
@en
P2093
P2860
P50
P921
P3181
P356
P1476
Autistic-like phenotypes in Ca ...... splicing in autistic patients
@en
P2093
Hironobu Ichikawa
Kazuhiko Nakamura
Mika Tanaka
Miwa Washida
Mizuho Nakajima
Norio Mori
Ritsuko Katoh-Semba
Satoshi Shoji
Sevilla D Detera-Wadleigh
Takeo Yoshikawa
P2860
P304
P3181
P356
10.1172/JCI29031
P407
P577
2007-03-22T00:00:00Z