| pubmed-article:1734921 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:1734921 | lifeskim:mentions | umls-concept:C0028953 | lld:lifeskim |
| pubmed-article:1734921 | lifeskim:mentions | umls-concept:C0032520 | lld:lifeskim |
| pubmed-article:1734921 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:1734921 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:1734921 | lifeskim:mentions | umls-concept:C2349209 | lld:lifeskim |
| pubmed-article:1734921 | lifeskim:mentions | umls-concept:C1549649 | lld:lifeskim |
| pubmed-article:1734921 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:1734921 | pubmed:dateCreated | 1992-3-12 | lld:pubmed |
| pubmed-article:1734921 | pubmed:abstractText | A method has been developed to allow one to extend the practical limit of oligonucleotide synthesis by coupling the synthesis reaction to a subsequent PCR. Given that DNA synthesizers are capable of producing reasonable yields of oligonucleotides that are 125-150 bases in length, this method could be used to recover the minute amount of full-length product present in mixtures extended well beyond the established limits. This technology could be applied to gene synthesis and mutagenesis. | lld:pubmed |
| pubmed-article:1734921 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1734921 | pubmed:language | eng | lld:pubmed |
| pubmed-article:1734921 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1734921 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:1734921 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1734921 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1734921 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1734921 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1734921 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1734921 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:1734921 | pubmed:issn | 0736-6205 | lld:pubmed |
| pubmed-article:1734921 | pubmed:author | pubmed-author:MillerJ HJH | lld:pubmed |
| pubmed-article:1734921 | pubmed:author | pubmed-author:MichaelsM LML | lld:pubmed |
| pubmed-article:1734921 | pubmed:author | pubmed-author:HsiaoH MHM | lld:pubmed |
| pubmed-article:1734921 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1734921 | pubmed:volume | 12 | lld:pubmed |
| pubmed-article:1734921 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1734921 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1734921 | pubmed:pagination | 44, 46, 48 | lld:pubmed |
| pubmed-article:1734921 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
| pubmed-article:1734921 | pubmed:meshHeading | pubmed-meshheading:1734921-... | lld:pubmed |
| pubmed-article:1734921 | pubmed:meshHeading | pubmed-meshheading:1734921-... | lld:pubmed |
| pubmed-article:1734921 | pubmed:meshHeading | pubmed-meshheading:1734921-... | lld:pubmed |
| pubmed-article:1734921 | pubmed:meshHeading | pubmed-meshheading:1734921-... | lld:pubmed |
| pubmed-article:1734921 | pubmed:meshHeading | pubmed-meshheading:1734921-... | lld:pubmed |
| pubmed-article:1734921 | pubmed:meshHeading | pubmed-meshheading:1734921-... | lld:pubmed |
| pubmed-article:1734921 | pubmed:meshHeading | pubmed-meshheading:1734921-... | lld:pubmed |
| pubmed-article:1734921 | pubmed:meshHeading | pubmed-meshheading:1734921-... | lld:pubmed |
| pubmed-article:1734921 | pubmed:year | 1992 | lld:pubmed |
| pubmed-article:1734921 | pubmed:articleTitle | Using PCR to extend the limit of oligonucleotide synthesis. | lld:pubmed |
| pubmed-article:1734921 | pubmed:affiliation | Department of Microbiology and Molecular Genetics, University of California, Los Angeles 90024. | lld:pubmed |
| pubmed-article:1734921 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:1734921 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
