Mutant Mice and Neuroscience: Recommendations Concerning Genetic Background
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Modifying behavioral phenotypes in Fmr1KO mice: genetic background differences reveal autistic-like responses.Gene Targeting Using Homologous Recombination in Embryonic Stem Cells: The Future for Behavior Genetics?Restoration of Sp4 in Forebrain GABAergic Neurons Rescues Hypersensitivity to Ketamine in Sp4 Hypomorphic Mice.A high through-put reverse genetic screen identifies two genes involved in remote memory in miceCrh and Oprm1 mediate anxiety-related behavior and social approach in a mouse model of MECP2 duplication syndromeMolecular mechanism for age-related memory loss: the histone-binding protein RbAp48Differing effects of copper,zinc superoxide dismutase overexpression on neurotoxicity elicited by nitric oxide, reactive oxygen species, and excitotoxinsThe D2 receptor is critical in mediating opiate motivation only in opiate-dependent and withdrawn miceGenetic background changes the pattern of forebrain commissure defects in transgenic mice underexpressing the beta-amyloid-precursor proteinThe Mouse Solitary Odorant Receptor Gene Promoters as Models for the Study of Odorant Receptor Gene ChoiceVulnerability to omega-3 deprivation in a mouse model of NMDA receptor hypofunctionInhibition of protein translation by the DISC1-Boymaw fusion gene from a Scottish family with major psychiatric disorders.Female Mecp2(+/-) mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies.Prolonged Ketamine Effects in Sp4 Hypomorphic Mice: Mimicking Phenotypes of Schizophrenia.Effects of isoflurane on learning and memory functions of wild-type and glutamate transporter type 3 knockout mice.Two genetic loci control syllable sequences of ultrasonic courtship vocalizations in inbred mice.The nucleosome assembly protein TSPYL2 regulates the expression of NMDA receptor subunits GluN2A and GluN2B.NMDA receptor-deficient mice display sexual dimorphism in the onset and severity of behavioural abnormalities.Functional role of the polymorphic 647 T/C variant of ENT1 (SLC29A1) and its association with alcohol withdrawal seizures.A combined pharmacological and genetic approach to investigate the role of orphanin FQ in learning and memory.In search of a depressed mouse: utility of models for studying depression-related behavior in genetically modified mice.Genome engineering via homologous recombination in mouse embryonic stem (ES) cells: an amazingly versatile tool for the study of mammalian biology.The mouse: genetics meets behaviour.EAAC1 gene deletion increases neuronal death and blood brain barrier disruption after transient cerebral ischemia in female miceHippocampal LTP and memory in mouse strains: is there evidence for a causal relationship?Behavioural and physiological characterization of inbred mouse strains: prospects for elucidating the molecular mechanisms of mammalian learning and memory.Behavioral phenotyping enhanced--beyond (environmental) standardization.Replacement of homologous mouse DNA sequence with pathogenic 6-base human CREB1 promoter sequence creates murine model of major depressive disorderEpileptogenesis following Kainic Acid-Induced Status Epilepticus in Cyclin D2 Knock-Out Mice with Diminished Adult NeurogenesisClean thoughts about dirty genes.Nr2e1 regulates retinal lamination and the development of Müller glia, S-cones, and glycineric amacrine cells during retinogenesis.A Knockout Experiment: Disciplinary Divides and Experimental Skill in Animal Behaviour GeneticsRecent advances in transgenic model development for Alzheimer's disease.The role of dietary niacin intake and the adenosine-5'-diphosphate-ribosyl cyclase enzyme CD38 in spatial learning ability: is cyclic adenosine diphosphate ribose the link between diet and behaviour?Environmental standardization: cure or cause of poor reproducibility in animal experiments?Cocaine-induced potentiation of synaptic strength in dopamine neurons: behavioral correlates in GluRA(-/-) mice.Regulation of behaviour by the nuclear receptor TLX.Modeling human disease in rodents by CRISPR/Cas9 genome editing.Novel Sxr(a) ES cell line offers hope for Y chromosome gene-targeted mice.Overexpression of Cu,Zn superoxide dismutase attenuates oxidative inhibition of astrocyte glutamate uptake.
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Mutant Mice and Neuroscience: Recommendations Concerning Genetic Background
description
article
@en
im Oktober 1997 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в жовтні 1997
@uk
name
Mutant Mice and Neuroscience: Recommendations Concerning Genetic Background
@en
Mutant Mice and Neuroscience: Recommendations Concerning Genetic Background
@nl
type
label
Mutant Mice and Neuroscience: Recommendations Concerning Genetic Background
@en
Mutant Mice and Neuroscience: Recommendations Concerning Genetic Background
@nl
prefLabel
Mutant Mice and Neuroscience: Recommendations Concerning Genetic Background
@en
Mutant Mice and Neuroscience: Recommendations Concerning Genetic Background
@nl
P2093
P50
P1433
P1476
Mutant Mice and Neuroscience: Recommendations Concerning Genetic Background
@en
P2093
Alcino J. Silva
Daniel R. Storm
David P. Wolfer
Elizabeth M. Simpson
Hee-Sup Shin
James O. McNamara
Jeanne M. Wehner
John Roder
Karl P. Giese
Michael P. Stryker
P304
P356
10.1016/S0896-6273(00)80958-7
P407
P50
P577
1997-10-01T00:00:00Z