|
1.
|
原著
|
Swim-up method is superior to density gradient centrifugation for preserving sperm DNA integrity during sperm processing 2024/01/29
|
|
2.
|
原著
|
Impairment of spatial memory accuracy improved by Cbr1 copy number resumption and GABAB receptor-dependent enhancement of synaptic inhibition in Down syndrome model mice. 2020/08/25
|
|
3.
|
原著
|
Perturbation of the immune cells and prenatal neurogenesis by the triplication of the Erg gene in mouse models of Down syndrome. 2020/01
|
|
4.
|
原著
|
Impaired cortico-striatal excitatory transmission triggers epilepsy. 2019/04/23
|
|
5.
|
原著
|
Alterations of in vivo CA1 network activity in Dp(16)1Yey Down syndrome model mice. 2018/02/27
|
|
6.
|
原著
|
DYRK1A-haploinsufficiency in mice causes autistic-like features and febrile seizures. 2018/02
|
|
7.
|
原著
|
Potentiation of excitatory synaptic transmission ameliorates aggression in mice with Stxbp1 haploinsufficiency. 2017/12/15
|
|
8.
|
原著
|
Ts1Cje Down syndrome model mice exhibit environmental stimuli-triggered locomotor hyperactivity and sociability concurrent with increased flux through central dopamine and serotonin metabolism. 2017/07
|
|
9.
|
原著
|
Brain ventriculomegaly in Down syndrome mice is caused by Pcp4 dose-dependent cilia dysfunction. 2017/03/01
|
|
10.
|
原著
|
Enlarged brain ventricles and impaired neurogenesis in the Ts1Cje and Ts2Cje mouse models of Down syndrome. 2010/05
|
|
11.
|
原著
|
Central respiratory failure in a mouse model depends on the genetic background of the host. 2010
|
|
12.
|
原著
|
Loss of pre-inspiratory neuron synchroneity in mice with DSCAM deficiency. 2010
|
|
13.
|
原著
|
Increased lipid peroxidation in Down's syndrome mouse models. 2009/09
|
|
14.
|
原著
|
DSCAM deficiency causes loss of pre-inspiratory neuron synchroneity and perinatal death. 2009/03/04
|
|
15.
|
原著
|
Association study between the Down syndrome cell adhesion molecule (DSCAM) gene and bipolar disorder. 2008/02
|
|
16.
|
原著
|
Mitochondrial dysfunction and tau hyperphosphorylation in Ts1Cje, a mouse model for Down syndrome. 2006/09/15
|
|
17.
|
原著
|
Transcriptional profiling of a mouse model for Lafora disease reveals dysregulation of genes involved in the expression and modification of proteins. 2005/10/21
|
|
18.
|
原著
|
Dosage-dependent over-expression of genes in the trisomic region of Ts1Cje mouse model for Down syndrome. 2004/07/01
|
|
19.
|
原著
|
Targeted disruption of the Epm2a gene causes formation of Lafora inclusion bodies, neurodegeneration, ataxia, myoclonus epilepsy and impaired behavioral response in mice. 2002/05/15
|
|
20.
|
原著
|
R133C and R168X mutations in Japanese Rett syndrome patients: a caution for misdiagnosis. 2001/12
|
|
21.
|
原著
|
Dscam is associated with axonal and dendritic features of neuronal cells. 2001/11/01
|
|
22.
|
原著
|
Mutation screening for Japanese Lafora's disease patients: identification of novel sequence variants in the coding and upstream regulatory regions of EPM2A gene. 2001/10
|
|
23.
|
原著
|
T-STAR gene: fine mapping in the candidate region for childhood absence epilepsy on 8q24 and mutational analysis in patients. 2001/08
|
|
24.
|
原著
|
Cloning and functional characterization of DSCAML1, a novel DSCAM-like cell adhesion molecule that mediates homophilic intercellular adhesion. 2001/07/20
|
|
25.
|
原著
|
Regional and developmental expression of Epm2a gene and its evolutionary conservation. 2001/05/25
|
|
26.
|
原著
|
DSCAM, a highly conserved gene in mammals, expressed in differentiating mouse brain. 2001/03/02
|
|
27.
|
原著
|
Childhood absence epilepsy in 8q24: refinement of candidate region and construction of physical map. 2000/09/15
|
|
28.
|
原著
|
Distinct transcriptional regulation and phylogenetic divergence of human LEFTY genes. 2000/05
|
|
29.
|
原著
|
Assignment of the gene GRM1 coding for metabotropic glutamate receptor 1 to human chromosome band 6q24 by in situ hybridization. 2000
|
|
30.
|
原著
|
Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome. 2000
|
|
31.
|
原著
|
An alternative splicing form of phosphatidylserine-specific phospholipase A1 that exhibits lysophosphatidylserine-specific lysophospholipase activity in humans. 1999/04/16
|
|
32.
|
原著
|
Isolation and characterization of mouse homologue for the human epilepsy gene, EPM2A. 1999/04/02
|
|
33.
|
原著
|
The human CC chemokine TECK (SCYA25) maps to chromosome 19p13.2. 1998/07/15
|
|
34.
|
原著
|
Mouse and human SHPS-1: molecular cloning of cDNAs and chromosomal localization of genes. 1997/02/03
|
|
10件表示
|
|
全件表示(34件)
|
