ReviewNeuromolecular medicine2004
Gene-targeting technologies for the study of neurological disorders.
Review in Neuromolecular medicine, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
10 citing papers in PubMed.
- Molecular pathways underlying amyloid precursor protein-mediated regulation of adult-born neurons.Neural regeneration research · 2026Article
- RFamide-Related Peptide Neurons Modulate Reproductive Function and Stress Responses.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021Article
- Function and dysfunction of presenilin.Neuro-degenerative diseases · 2014Review
- Monoamine oxidases in development.Cellular and molecular life sciences : CMLS · 2013Review
- Choroid plexus transport: gene deletion studies.Fluids and barriers of the CNS · 2011Article
- Monoamine oxidase a expression is vital for embryonic brain development by modulating developmental apoptosis.The Journal of biological chemistry · 2011Article
- Impaired neurotransmitter release in Alzheimer's and Parkinson's diseases.Neuro-degenerative diseases · 2010Article
- Changes in the expression of genes associated with intraneuronal amyloid-beta and tau in Alzheimer's disease.Journal of Alzheimer's disease : JAD · 2010Article
- Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.Proceedings of the National Academy of Sciences of the United States of America · 2009Article
- Schizophrenia: an integrative approach to modelling a complex disorder.Journal of psychiatry & neuroscience : JPN · 2006Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
Studies using genetic manipulations have proven invaluable in the research of neurological disorders. In the forefront of these approaches is the knockout technology that engineers a targeted gene mutation in mice resulting in inactivation of gene expression. In many cases, important roles of a particular gene in embryonic development have precluded the in vivo study of its function in the adult brain, which is usually the most relevant experimental context for the study of neurological disorders. The conditional knockout technology has provided a tool to overcome this restriction and has been used successfully to generate viable mouse models with gene inactivation patterns in certain regions or cell types of the postnatal brain. This review first describes the methodology of gene targeting in mice, detailing the aspects of designing a targeting vector, introducing it into embryonic stem cells in culture and screening for correct recombination events, and generating chimeric and null mutant mice from the positive clones. It then discusses the special issues and considerations for the generation of conditional knockout mice, including a section about approaches for inducible gene inactivation in the brain and some of their applications. An overview of gene-targeted mouse models that have been used in the study of several neurological disorders, including Alzheimer's disease, Parkinson's disease, Huntington's disease, seizure disorders, and schizophrenia, is also presented. The importance of the results obtained by these models for the understanding of the pathogenic mechanism underlying the disorders is discussed.
Indexed as
Identifiers
15781974What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.