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Search results 201 to 215 out of 215 for Eif4h

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0.018s
Type Details Score
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
Publication      
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
Allele
Name: eukaryotic translation initiation factor 4H; endonuclease-mediated mutation 1, Shanghai Model Organisms Center
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
Strain
Attribute String: coisogenic, endonuclease-mediated mutation, mutant strain
Allele
Name: deletion, Chr 5, Uta Francke 1
Allele Type: Targeted
Attribute String: Null/knockout
Strain
Attribute String: mutant stock, targeted mutation, deletion
Genotype
Symbol: Del(5Gtf2i-Limk1)1Uta/+
Background: involves: 129S7/SvEvBrd * C57BL/6J
Zygosity: ht
Has Mutant Allele: true
Genotype
Symbol: Del(5Gtf2i-Limk1)1Uta/? Del(5Limk1-Trim50)2Uta/?
Background: involves: 129S7/SvEvBrd * C57BL/6J
Zygosity: cx
Has Mutant Allele: true
Publication  
First Author: Screen M
Year: 2024
Journal: Life Sci Alliance
Title: RNA helicase EIF4A1-mediated translation is essential for the GC response.
Volume: 7
Issue: 2
Publication
First Author: Campuzano V
Year: 2012
Journal: PLoS Genet
Title: Reduction of NADPH-oxidase activity ameliorates the cardiovascular phenotype in a mouse model of Williams-Beuren Syndrome.
Volume: 8
Issue: 2
Pages: e1002458
Publication
First Author: Goergen CJ
Year: 2011
Journal: J Vasc Res
Title: Induced chromosome deletion in a Williams-Beuren syndrome mouse model causes cardiovascular abnormalities.
Volume: 48
Issue: 2
Pages: 119-29
Publication
First Author: Borralleras C
Year: 2015
Journal: Mol Ther
Title: Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams-Beuren Syndrome.
Volume: 23
Issue: 11
Pages: 1691-1699
Publication
First Author: Li HH
Year: 2009
Journal: EMBO Mol Med
Title: Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice.
Volume: 1
Issue: 1
Pages: 50-65
Publication
First Author: Davenport CM
Year: 2022
Journal: Cell
Title: Innate frequency-discrimination hyperacuity in Williams-Beuren syndrome mice.
Volume: 185
Issue: 21
Pages: 3877-3895.e21