Linked Life Data

2818653

Source:http://linkedlifedata.com/resource/pubmed/id/2818653

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
1989-12-8
pubmed:abstractText
We have developed a technique for restriction nuclease sites mapping in genomic DNA cloned into phage lambda vectors. Synthetic oligonucleotides homologous to the vector sequences and adjacent to the cloning site were used as hybridisation probes for indirect end labelling procedure. In addition, a number of oligonucleotides homologous to the sequences of tumour necrosis factor genes were used for mapping from the internal sites. As a result, a map of 35 kb genomic region on the chromosome 17 inside major histocompatibility complex and surrounding mouse tumour necrosis factor genes was constructed.
pubmed:language
rus
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0132-3423
pubmed:author
pubmed:issnType
Print
pubmed:volume
15
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
990-3
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed:year
1989
pubmed:articleTitle
[Mapping the genome locus containing genes for mouse tumor necrosis factor by means of hybridization end labelling with the use of synthetic oligonucleotides].
pubmed:publicationType
Journal Article, English Abstract