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Search results 701 to 760 out of 760 for Ncam2

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Type Details Score
Publication
First Author: William CM
Year: 2017
Journal: J Neurosci
Title: Activity-Dependent Dysfunction in Visual and Olfactory Sensory Systems in Mouse Models of Down Syndrome.
Volume: 37
Issue: 41
Pages: 9880-9888
Publication
First Author: Starbuck JM
Year: 2014
Journal: Am J Med Genet A
Title: Overlapping trisomies for human chromosome 21 orthologs produce similar effects on skull and brain morphology of Dp(16)1Yey and Ts65Dn mice.
Volume: 164A
Issue: 8
Pages: 1981-1990
Publication
First Author: Aldridge K
Year: 2007
Journal: Am J Med Genet A
Title: Differential effects of trisomy on brain shape and volume in related aneuploid mouse models.
Volume: 143A
Issue: 10
Pages: 1060-70
Publication
First Author: Noll C
Year: 2009
Journal: PLoS One
Title: DYRK1A, a novel determinant of the methionine-homocysteine cycle in different mouse models overexpressing this Down-syndrome-associated kinase.
Volume: 4
Issue: 10
Pages: e7540
Publication  
First Author: Kida E
Year: 2013
Journal: Exp Neurol
Title: Long-term running alleviates some behavioral and molecular abnormalities in Down syndrome mouse model Ts65Dn.
Volume: 240
Pages: 178-89
Publication
First Author: Sussan TE
Year: 2008
Journal: Nature
Title: Trisomy represses Apc(Min)-mediated tumours in mouse models of Down's syndrome.
Volume: 451
Issue: 7174
Pages: 73-5
Publication
First Author: Salehi A
Year: 2009
Journal: Sci Transl Med
Title: Restoration of norepinephrine-modulated contextual memory in a mouse model of Down syndrome.
Volume: 1
Issue: 7
Pages: 7ra17
Publication
First Author: Kirsammer G
Year: 2008
Journal: Blood
Title: Highly penetrant myeloproliferative disease in the Ts65Dn mouse model of Down syndrome.
Volume: 111
Issue: 2
Pages: 767-75
Publication
First Author: Jiang Y
Year: 2019
Journal: J Neurosci
Title: Lysosomal Dysfunction in Down Syndrome Is APP-Dependent and Mediated by APP-βCTF (C99).
Volume: 39
Issue: 27
Pages: 5255-5268
Publication  
First Author: Hijazi M
Year: 2013
Journal: Exp Neurol
Title: Overexpression of DYRK1A inhibits choline acetyltransferase induction by oleic acid in cellular models of Down syndrome.
Volume: 239
Pages: 229-34
Publication
First Author: Yang A
Year: 2011
Journal: Cancer Res
Title: Increased survival following tumorigenesis in Ts65Dn mice that model Down syndrome.
Volume: 71
Issue: 10
Pages: 3573-81
Publication
First Author: Roper RJ
Year: 2006
Journal: Proc Natl Acad Sci U S A
Title: Defective cerebellar response to mitogenic Hedgehog signaling in Down [corrected] syndrome mice.
Volume: 103
Issue: 5
Pages: 1452-6
Publication  
First Author: Aziz NM
Year: 2018
Journal: Dis Model Mech
Title: Lifespan analysis of brain development, gene expression and behavioral phenotypes in the Ts1Cje, Ts65Dn and Dp(16)1/Yey mouse models of Down syndrome.
Volume: 11
Issue: 6
Publication
First Author: Richtsmeier JT
Year: 2002
Journal: Am J Med Genet
Title: Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome.
Volume: 107
Issue: 4
Pages: 317-24
Publication
First Author: Blank M
Year: 2011
Journal: J Neurosci
Title: The Down syndrome critical region regulates retinogeniculate refinement.
Volume: 31
Issue: 15
Pages: 5764-76
Publication  
First Author: Ash JA
Year: 2014
Journal: Neurobiol Dis
Title: Maternal choline supplementation improves spatial mapping and increases basal forebrain cholinergic neuron number and size in aged Ts65Dn mice.
Volume: 70
Pages: 32-42
Publication
First Author: Olson LE
Year: 2004
Journal: Science
Title: A chromosome 21 critical region does not cause specific Down syndrome phenotypes.
Volume: 306
Issue: 5696
Pages: 687-90
Publication  
First Author: Kleschevnikov AM
Year: 2017
Journal: Neurobiol Dis
Title: Evidence that increased Kcnj6 gene dose is necessary for deficits in behavior and dentate gyrus synaptic plasticity in the Ts65Dn mouse model of Down syndrome.
Volume: 103
Pages: 1-10
Publication
First Author: Siddiqui A
Year: 2008
Journal: Genes Brain Behav
Title: Molecular responses of the Ts65Dn and Ts1Cje mouse models of Down syndrome to MK-801.
Volume: 7
Issue: 7
Pages: 810-20
Publication  
First Author: Nguyen TL
Year: 2018
Journal: Dis Model Mech
Title: Correction of cognitive deficits in mouse models of Down syndrome by a pharmacological inhibitor of DYRK1A.
Volume: 11
Issue: 9
Publication
First Author: Lane AA
Year: 2014
Journal: Nat Genet
Title: Triplication of a 21q22 region contributes to B cell transformation through HMGN1 overexpression and loss of histone H3 Lys27 trimethylation.
Volume: 46
Issue: 6
Pages: 618-23
Publication
First Author: Singh N
Year: 2016
Journal: Dev Dyn
Title: Chronic up-regulation of sonic hedgehog has little effect on postnatal craniofacial morphology of euploid and trisomic mice.
Volume: 245
Issue: 2
Pages: 114-22
Publication
First Author: Olson LE
Year: 2004
Journal: Dev Dyn
Title: Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes.
Volume: 230
Issue: 3
Pages: 581-9
Publication
First Author: Duchon A
Year: 2021
Journal: Hum Mol Genet
Title: Multi-influential genetic interactions alter behaviour and cognition through six main biological cascades in Down syndrome mouse models.
Volume: 30
Issue: 9
Pages: 771-788
Publication
First Author: Colombi I
Year: 2024
Journal: iScience
Title: Heterogeneous subpopulations of GABA(A)R-responding neurons coexist across neuronal network scales and developmental stages in health and disease.
Volume: 27
Issue: 4
Pages: 109438
Publication
First Author: Herault Y
Year: 2017
Journal: Dis Model Mech
Title: Rodent models in Down syndrome research: impact and future opportunities.
Volume: 10
Issue: 10
Pages: 1165-1186
Genotype
Symbol: Ts(17<16>)65Dn/? Del(16Cbr1-Fam3b)1Rhr/?
Background: involves: 129S6/SvEvTac * C57BL/6 * DBA/2J
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Tbx5/Tbx5<+> Ts(17<16>)65Dn/?
Background: involves: C3H * C57BL/6
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Brwd1/Brwd1<+> Ts(17<16>)65Dn/?
Background: involves: C3H/HeJ * C57BL/6J * DBA/2J
Zygosity: cx
Has Mutant Allele: true
Genotype
Symbol: Del(17Scaf8-Pde10a)2Yey/+ Ts(17<16>)65Dn/?
Background: involves: 129S7/SvEvBrd * DBA/2J
Zygosity: cx
Has Mutant Allele: true
Publication
First Author: Adorno M
Year: 2013
Journal: Nature
Title: Usp16 contributes to somatic stem-cell defects in Down's syndrome.
Volume: 501
Issue: 7467
Pages: 380-4
Publication
First Author: Guedj F
Year: 2012
Journal: Neurobiol Dis
Title: DYRK1A: a master regulatory protein controlling brain growth.
Volume: 46
Issue: 1
Pages: 190-203
Publication
First Author: Laguna A
Year: 2013
Journal: Hum Mol Genet
Title: Triplication of DYRK1A causes retinal structural and functional alterations in Down syndrome.
Volume: 22
Issue: 14
Pages: 2775-84
Publication  
First Author: Lisgaras CP
Year: 2023
Journal: Neurobiol Dis
Title: Interictal spikes in Alzheimer's disease: Preclinical evidence for dominance of the dentate gyrus and cholinergic control by the medial septum.
Volume: 187
Pages: 106294
Publication
First Author: Forejt J
Year: 2003
Journal: Comp Funct Genomics
Title: Segmental trisomy of mouse chromosome 17: introducing an alternative model of Down's syndrome.
Volume: 4
Issue: 6
Pages: 647-52
Publication
First Author: Rachidi M
Year: 2007
Journal: Neurosci Res
Title: Mental retardation in Down syndrome: from gene dosage imbalance to molecular and cellular mechanisms.
Volume: 59
Issue: 4
Pages: 349-69
Publication  
First Author: Souchet B
Year: 2014
Journal: Neurobiol Dis
Title: Excitation/inhibition balance and learning are modified by Dyrk1a gene dosage.
Volume: 69
Pages: 65-75
Publication
First Author: Li H
Year: 2016
Journal: Genetics
Title: Penetrance of Congenital Heart Disease in a Mouse Model of Down Syndrome Depends on a Trisomic Potentiator of a Disomic Modifier.
Volume: 203
Issue: 2
Pages: 763-70
Publication
First Author: Davisson M
Year: 2007
Journal: Hum Reprod
Title: Impact of trisomy on fertility and meiosis in male mice.
Volume: 22
Issue: 2
Pages: 468-76
Publication
First Author: Gao Y
Year: 2023
Journal: Cell
Title: β2-microglobulin functions as an endogenous NMDAR antagonist to impair synaptic function.
Volume: 186
Issue: 5
Pages: 1026-1038.e20
Publication
First Author: Caldwell ALM
Year: 2022
Journal: Nat Neurosci
Title: Aberrant astrocyte protein secretion contributes to altered neuronal development in multiple models of neurodevelopmental disorders.
Volume: 25
Issue: 9
Pages: 1163-1178
Publication    
First Author: Zorrilla de San Martin J
Year: 2020
Journal: Elife
Title: Alterations of specific cortical GABAergic circuits underlie abnormal network activity in a mouse model of Down syndrome.
Volume: 9
Publication
First Author: Zhu PJ
Year: 2019
Journal: Science
Title: Activation of the ISR mediates the behavioral and neurophysiological abnormalities in Down syndrome.
Volume: 366
Issue: 6467
Pages: 843-849
Publication
First Author: Wiseman FK
Year: 2009
Journal: Hum Mol Genet
Title: Down syndrome--recent progress and future prospects.
Volume: 18
Issue: R1
Pages: R75-83
Publication
First Author: Fedoriw AM
Year: 2015
Journal: Development
Title: Key mediators of somatic ATR signaling localize to unpaired chromosomes in spermatocytes.
Volume: 142
Issue: 17
Pages: 2972-80
Publication
First Author: Peiris H
Year: 2016
Journal: PLoS Genet
Title: A Syntenic Cross Species Aneuploidy Genetic Screen Links RCAN1 Expression to β-Cell Mitochondrial Dysfunction in Type 2 Diabetes.
Volume: 12
Issue: 5
Pages: e1006033
Publication
First Author: Peng S
Year: 2009
Journal: J Neurosci
Title: Decreased brain-derived neurotrophic factor depends on amyloid aggregation state in transgenic mouse models of Alzheimer's disease.
Volume: 29
Issue: 29
Pages: 9321-9
Publication    
First Author: Schill EM
Year: 2019
Journal: JCI Insight
Title: Down syndrome mouse models have an abnormal enteric nervous system.
Volume: 5
Publication
First Author: Bhutta MF
Year: 2013
Journal: Mamm Genome
Title: Surveying the Down syndrome mouse model resource identifies critical regions responsible for chronic otitis media.
Volume: 24
Issue: 11-12
Pages: 439-45
Publication
First Author: Raveau M
Year: 2012
Journal: PLoS Genet
Title: The App-Runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a Down syndrome mouse model.
Volume: 8
Issue: 5
Pages: e1002724
Publication
First Author: Xing Z
Year: 2023
Journal: Hum Mol Genet
Title: Dissection of a Down syndrome-associated trisomy to separate the gene dosage-dependent and -independent effects of an extra chromosome.
Volume: 32
Issue: 13
Pages: 2205-2218
Publication
First Author: Adorno M
Year: 2018
Journal: Sci Rep
Title: Usp16 modulates Wnt signaling in primary tissues through Cdkn2a regulation.
Volume: 8
Issue: 1
Pages: 17506
Publication
First Author: Liu H
Year: 2023
Journal: PLoS Biol
Title: DSCAM gene triplication causes excessive GABAergic synapses in the neocortex in Down syndrome mouse models.
Volume: 21
Issue: 4
Pages: e3002078
Publication
First Author: Gao FJ
Year: 2021
Journal: Acta Neuropathol Commun
Title: Forebrain Shh overexpression improves cognitive function and locomotor hyperactivity in an aneuploid mouse model of Down syndrome and its euploid littermates.
Volume: 9
Issue: 1
Pages: 137
Publication
First Author: Levine S
Year: 2009
Journal: Exp Mol Pathol
Title: Systemic pathology in aged mouse models of Down's syndrome and Alzheimer's disease.
Volume: 86
Issue: 1
Pages: 18-22
Publication
First Author: Sheppard K
Year: 2022
Journal: Cell Rep
Title: Stride-level analysis of mouse open field behavior using deep-learning-based pose estimation.
Volume: 38
Issue: 2
Pages: 110231
Publication
First Author: Zhang L
Year: 2012
Journal: Bioeng Bugs
Title: Genetic analysis of Down syndrome facilitated by mouse chromosome engineering.
Volume: 3
Issue: 1
Pages: 8-12
Publication
First Author: Gupta M
Year: 2016
Journal: Mamm Genome
Title: Mouse models of Down syndrome: gene content and consequences.
Volume: 27
Issue: 11-12
Pages: 538-555
Publication
First Author: Salehi A
Year: 2006
Journal: Neuron
Title: Increased App expression in a mouse model of Down's syndrome disrupts NGF transport and causes cholinergic neuron degeneration.
Volume: 51
Issue: 1
Pages: 29-42
Publication
First Author: Roubertoux PL
Year: 2017
Journal: Behav Genet
Title: Differential Brain, Cognitive and Motor Profiles Associated with Partial Trisomy. Modeling Down Syndrome in Mice.
Volume: 47
Issue: 3
Pages: 305-322