Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2001-10-3
pubmed:abstractText
One of the most powerful tools that the molecular biology revolution has given us is the ability to turn genes on and off at our discretion. In the mouse, this has been accomplished by using binary systems in which gene expression is dependent on the interaction of two components, resulting in either transcriptional transactivation or DNA recombination. During recent years, these systems have been used to analyse complex and multi-staged biological processes, such as embryogenesis and cancer, with unprecedented precision. Here, I review these systems and discuss certain studies that exemplify the advantages and limitations of each system.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Cre recombinase, http://linkedlifedata.com/resource/pubmed/chemical/DNA Nucleotidyltransferases, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/FLP recombinase, http://linkedlifedata.com/resource/pubmed/chemical/Fungal Proteins, http://linkedlifedata.com/resource/pubmed/chemical/GAL4 protein, S cerevisiae, http://linkedlifedata.com/resource/pubmed/chemical/Integrases, http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Saccharomyces cerevisiae Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Tetracycline, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/Viral Proteins, http://linkedlifedata.com/resource/pubmed/chemical/tetracycline resistance-encoding...
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1471-0056
pubmed:author
pubmed:issnType
Print
pubmed:volume
2
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
743-55
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:11584291-Animals, pubmed-meshheading:11584291-Cell Lineage, pubmed-meshheading:11584291-DNA Nucleotidyltransferases, pubmed-meshheading:11584291-DNA-Binding Proteins, pubmed-meshheading:11584291-Embryonic and Fetal Development, pubmed-meshheading:11584291-Forecasting, pubmed-meshheading:11584291-Fungal Proteins, pubmed-meshheading:11584291-Gene Expression Regulation, pubmed-meshheading:11584291-Gene Expression Regulation, Developmental, pubmed-meshheading:11584291-Genetic Techniques, pubmed-meshheading:11584291-Integrases, pubmed-meshheading:11584291-Mice, pubmed-meshheading:11584291-Mice, Knockout, pubmed-meshheading:11584291-Mice, Transgenic, pubmed-meshheading:11584291-Organ Specificity, pubmed-meshheading:11584291-Promoter Regions, Genetic, pubmed-meshheading:11584291-Recombination, Genetic, pubmed-meshheading:11584291-Repressor Proteins, pubmed-meshheading:11584291-Saccharomyces cerevisiae, pubmed-meshheading:11584291-Saccharomyces cerevisiae Proteins, pubmed-meshheading:11584291-Tetracycline, pubmed-meshheading:11584291-Transcription Factors, pubmed-meshheading:11584291-Transcriptional Activation, pubmed-meshheading:11584291-Transgenes, pubmed-meshheading:11584291-Viral Proteins
pubmed:year
2001
pubmed:articleTitle
Conditional control of gene expression in the mouse.
pubmed:affiliation
Section of Genetics of Vertebrate Development, Laboratory of Cancer and Developmental Biology, National Cancer Institute-Frederick Cancer Research and Development Center, Frederick, Maryland 21702-1201, USA. mlewandoski@ncifcrf.gov
pubmed:publicationType
Journal Article, Review