"Sighted C3H" mice--a tool for analysing the influence of vision on mouse behaviour? - Wikidata - wikimedia - TriplyDB

"Sighted C3H" mice--a tool for analysing the influence of vision on mouse behaviour?

"Sighted C3H" mice--a tool for analysing the influence of vision on mouse behaviour?

http://www.wikidata.org/entity/Q46570840

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Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.Psychophysical testing in rodent models of glaucomatous optic neuropathy Dll1 haploinsufficiency in adult mice leads to a complex phenotype affecting metabolic and immunological processes Dosage of the Abcg1-U2af1 region modifies locomotor and cognitive deficits observed in the Tc1 mouse model of Down syndrome In vivo microscopic voxel-based morphometry with a brain template to characterize strain-specific structures in the mouse brain The App-Runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a Down syndrome mouse model.Specific targeting of the GABA-A receptor α5 subtype by a selective inverse agonist restores cognitive deficits in Down syndrome mice.Chronic Treatment with a Promnesiant GABA-A α5-Selective Inverse Agonist Increases Immediate Early Genes Expression during Memory Processing in Mice and Rectifies Their Expression Levels in a Down Syndrome Mouse Model Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling Down syndrome.Variable phenotypic expressivity in inbred retinal degeneration mouse lines: A comparative study of C3H/HeOu and FVB/N rd1 mice Absence of Neuroplastin-65 Affects Synaptogenesis in Mouse Inner Hair Cells and Causes Profound Hearing Loss.The telomeric part of the human chromosome 21 from Cstb to Prmt2 is not necessary for the locomotor and short-term memory deficits observed in the Tc1 mouse model of Down syndrome Copy number variation influences gene expression and metabolic traits in mice.Presence of the Gpr179(nob5) allele in a C3H-derived transgenic mouse.Mutation of the Na(+)-K(+)-2Cl(-) cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia.Novel missense mutation of uromodulin in mice causes renal dysfunction with alterations in urea handling, energy, and bone metabolism.Correction of cognitive deficits in mouse models of Down syndrome by a pharmacological inhibitor of DYRK1A

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"Sighted C3H" mice--a tool for analysing the influence of vision on mouse behaviour?

http://www.wikidata.org/entity/Q46570840

description

2008 nî lūn-bûn

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2008年の論文

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年學術文章

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2008年學術文章

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name

"Sighted C3H" mice--a tool for analysing the influence of vision on mouse behaviour?

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"Sighted C3H" mice--a tool for analysing the influence of vision on mouse behaviour?

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type

label

"Sighted C3H" mice--a tool for analysing the influence of vision on mouse behaviour?

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"Sighted C3H" mice--a tool for analysing the influence of vision on mouse behaviour?

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prefLabel

"Sighted C3H" mice--a tool for analysing the influence of vision on mouse behaviour?

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"Sighted C3H" mice--a tool for analysing the influence of vision on mouse behaviour?

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P1433

Frontiers in Bioscience

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"Sighted C3H" mice--a tool for analysing the influence of vision on mouse behaviour?

@en

P2093

Anja Schrewe

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Boris Ivandic

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Helmut Fuchs

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Jack Favor

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Johannes Beckers

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Magdalena Kallnik

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Marion Horsch

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Martin Hrabé de Angelis

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Thomas Klopstock

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Wolfgang Wurst

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5810-5823

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scholarly article

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10.2741/3118

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13

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Martin Hrabě de Angelis

Valérie Gailus-Durner

Sabine M. Hölter

P577

2008-05-01T00:00:00Z

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18508624

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