Comparative genetic analysis: the utility of mouse genetic systems for studying human monogenic disease
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Summary
This review focuses on the analysis of multiple mutations from chemical mutagenesis projects in a wide variety of genes and the valuable functional information that has been obtained from these studies.
- Type
- article
- Published
- 2007-05-21
- Cited by
- 30
- References
- 139
- Access
- Open access
- OpenAlex
- https://openalex.org/W17514509
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:12868145
Keywords
Message passing, Notation, Factor graph, Representation (politics), Belief propagation
References
- Sequence characterization of ENU-induced mutants of glucose phosphate isomerase in mouse
- Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy.
- Sequence-specific modification of mouse genomic DNA mediated by gene targeting techniques
- Multiple mutations in mouse Chd7 provide models for CHARGE syndrome.
- A new ENU-induced allele of mouse quaking causes severe CNS dysmyelination
- Tissue-specific transgenic and knockout mice.
- Gene therapy for cystic fibrosis lung disease: current status and future perspectives.
- RNA Interference. An Approach to Produce Knockout Organisms and Cell Lines
- Gene disruption in mice: Models of development and disease
- Book Review: The Metabolic Basis of Inherited Disease
- Talking about a revolution: The impact of site-specific recombinases on genetic analyses in mice.
- Efficient gene-driven germ-line point mutagenesis of C57BL/6J mice
- Gene trap mutagenesis in embryonic stem cells.
- Capitalizing on large-scale mouse mutagenesis screens
- Mice without myoglobin
- An allelic series of mutations in Smad2 and Smad4 identified in a genotype-based screen of N-ethyl-N- nitrosourea-mutagenized mouse embryonic stem cells
- Theodosius Dobzhansky's role in the emergence and institutionalization of genetics in Mexico.
- Ethylnitrosourea-induced base pair substitution affects splicing of the mouse gammaE-crystallin encoding gene leading to the expression of a hybrid protein and to a cataract.
- Marker-assisted introgression in backcross breeding programs.
- Functions of mammalian Smad genes as revealed by targeted gene disruption in mice.
Cited by
- Mutations in PI(3,5)P2 Signaling and Neurodegeneration in Mouse and Human.
- Experimental spinal cord stimulation in neuropathic pain models
- Spinal cord stimulation in neuropathic pain technical aspects and effectiveness
- Removing the cloak of invisibility: phenotyping the mouse
- The mouse ascending: perspectives for human-disease models
- The challenges for molecular nutrition research 3: comparative nutrigenomics research as a basis for entering the systems level
- High throughput sequencing approaches to mutation discovery in the mouse
- Optimising experimental design for high-throughput phenotyping in mice: a case study
- Technical approaches for mouse models of human disease
- New insights into behaviour using mouse ENU mutagenesis
- A Targeted Deleterious Allele of the Splicing Factor SCNM1 in the Mouse
- Mouse phenogenomics, toolbox for functional annotation of human genome.
- Interaction between environmental and genetic factors modulates schizophrenic endophenotypes in the Snap-25 mouse mutant blind-drunk
- A new Otogelin ENU mouse model for autosomal-recessive nonsyndromic moderate hearing impairment
- Gut microbial regulation of bile acid metabolism and signaling
- Modèles animaux et pathologies humaines : caractérisation de 3 lignées murines ENU présentant des anomalies du système vestibulaire ou locomoteur
- Roles of PI3-kinase and ARAP2 in regulating glucose metabolism
- The Rate of Adoption of Strategic Marketing Planning (SMP) by the Libyan Commercial Banks (LCBs). An Exploratory Study
- Clinical and pathomorphological characterisation of two diabetic mouse models derived from the Munich ENU mouse mutagenesis project
- Analysis of novel pathways in neurodegeneration using mouse and fly model organisms
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