Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4806
|
pubmed:dateCreated |
1987-7-6
|
pubmed:abstractText |
The molecular analysis of genes identified by mutations is a major problem in mammalian genetics. As a step toward this goal, preparative field inversion gel electrophoresis (FIGE) was used to selectively isolate clones from the environment of genetically linked markers, and to select a subset of these clones containing sequences next to specific restriction sites rare in mammalian DNA. This approach has been used to generate a library highly enriched in sequences closely linked to the cystic fibrosis marker met. One clone derived from the end of a Not I restriction fragment containing the met sequence was analyzed in detail and localized within a long range map to a position 300 kilobase pairs 5' of the metD sequence.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
0036-8075
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
5
|
pubmed:volume |
236
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1305-8
|
pubmed:dateRevised |
2007-3-19
|
pubmed:meshHeading |
pubmed-meshheading:3035716-Bacteriophage lambda,
pubmed-meshheading:3035716-Chromosome Mapping,
pubmed-meshheading:3035716-Cloning, Molecular,
pubmed-meshheading:3035716-Cystic Fibrosis,
pubmed-meshheading:3035716-DNA Restriction Enzymes,
pubmed-meshheading:3035716-Electrophoresis,
pubmed-meshheading:3035716-Genetic Markers,
pubmed-meshheading:3035716-Genetic Vectors,
pubmed-meshheading:3035716-Humans,
pubmed-meshheading:3035716-Mutation,
pubmed-meshheading:3035716-Nucleic Acid Hybridization,
pubmed-meshheading:3035716-Repetitive Sequences, Nucleic Acid
|
pubmed:year |
1987
|
pubmed:articleTitle |
Derivation of clones close to met by preparative field inversion gel electrophoresis.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|