Construction and characterization of a bacterial clone containing the hemagglutinin gene of the WSN strain (H0N1) of influenza virus
Identifieur interne : 000F27 ( Istex/Corpus ); précédent : 000F26; suivant : 000F28Construction and characterization of a bacterial clone containing the hemagglutinin gene of the WSN strain (H0N1) of influenza virus
Auteurs : Alan R. Davis ; Alan L. Hiti ; Debi P. NayakSource :
- Gene [ 0378-1119 ] ; 1980.
English descriptors
- Teeft :
- Acad, Agarose, Alkaline, Alkaline agarose, Amino, Amino acid sequence, Amino acid sequences, Amino acids, Cdna, Choppin, Crna, Dodecadeoxynucleotide primers, Fowl, Fowl plague virus, Gene, Hemagglutinin, Hon1, Influenza, Influenza virus, Lazarowitz, Natl, Nayak, Neutral agarose, Nick translation, Nuclease, Nucleotide, Nucleotide sequence, Other hon1 viruses, Other influenza, Palese, Peptide, Plasmid, Polymerase, Primer, Proc, Protein sequencing, Proteolytic cleavage, Psti, Reaction mixture, Sequencing, Sodium dodecyl sulfate, Untranslated region, Viral, Virology, Virus, Vrna, Vrna crna.
Abstract
Abstract: A synthetic dodecadeoxynucleotide primer has been used to prepare a double-stranded DNA form of the hemagglutinin (HA) gene of a human influenza virus (WSN strain, HON1). This DNA has been inserted in plasmid pBR322 and cloned in bacterial cells. The insert contains nearly the complete hemagglutinin gene. A restriction map of this insert has been determined and structurally important areas of the HA gene have been sequenced. Amino acid sequences of several regions of the HA protein were deduced from the DNA sequences and compared to the known amino acid sequences of other influenza A viruses. WSN HA shows extensive homology to all influenza A viruses in a few regions, namely the first 17 amino acids of the N-terminus of HA1 (N-terminal polypeptide of HA) and the first 24 amino acids of the N-terminus of HA2 (C-terminal polypeptide of HA). The sequence diverges extensively from other influenza A viruses in most other areas. The sequence of WSN virus HA is similar to that of other H0N1 viruses with the exception of the C-terminus of the HA1 peptide. The change in this area may contribute to some of the unique properties of WSN virus among the HON1 viruses. In addition, WSN HA contains a 17-amino-acid precursor before the N-terminus of HA1 and a single amino acid, arginine, connecting HA1 and HA2.
Url:
DOI: 10.1016/0378-1119(80)90050-5
Links to Exploration step
ISTEX:A49FFC82D563A76282D3D7AB1749501874FB866BLe document en format XML
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Nayak</name><affiliation><mods:affiliation>Department of Microbiology and Immunology, UCLA School of Medicine, Los Angeles, CA 90024 U.S.A.</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Gene</title><title level="j" type="abbrev">GENE</title><idno type="ISSN">0378-1119</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1980">1980</date><biblScope unit="volume">10</biblScope><biblScope unit="issue">3</biblScope><biblScope unit="page" from="205">205</biblScope><biblScope unit="page" to="218">218</biblScope></imprint><idno type="ISSN">0378-1119</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0378-1119</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Acad</term><term>Agarose</term><term>Alkaline</term><term>Alkaline agarose</term><term>Amino</term><term>Amino acid sequence</term><term>Amino acid sequences</term><term>Amino acids</term><term>Cdna</term><term>Choppin</term><term>Crna</term><term>Dodecadeoxynucleotide primers</term><term>Fowl</term><term>Fowl plague virus</term><term>Gene</term><term>Hemagglutinin</term><term>Hon1</term><term>Influenza</term><term>Influenza virus</term><term>Lazarowitz</term><term>Natl</term><term>Nayak</term><term>Neutral agarose</term><term>Nick translation</term><term>Nuclease</term><term>Nucleotide</term><term>Nucleotide sequence</term><term>Other hon1 viruses</term><term>Other influenza</term><term>Palese</term><term>Peptide</term><term>Plasmid</term><term>Polymerase</term><term>Primer</term><term>Proc</term><term>Protein sequencing</term><term>Proteolytic cleavage</term><term>Psti</term><term>Reaction mixture</term><term>Sequencing</term><term>Sodium dodecyl sulfate</term><term>Untranslated region</term><term>Viral</term><term>Virology</term><term>Virus</term><term>Vrna</term><term>Vrna crna</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: A synthetic dodecadeoxynucleotide primer has been used to prepare a double-stranded DNA form of the hemagglutinin (HA) gene of a human influenza virus (WSN strain, HON1). This DNA has been inserted in plasmid pBR322 and cloned in bacterial cells. The insert contains nearly the complete hemagglutinin gene. A restriction map of this insert has been determined and structurally important areas of the HA gene have been sequenced. Amino acid sequences of several regions of the HA protein were deduced from the DNA sequences and compared to the known amino acid sequences of other influenza A viruses. WSN HA shows extensive homology to all influenza A viruses in a few regions, namely the first 17 amino acids of the N-terminus of HA1 (N-terminal polypeptide of HA) and the first 24 amino acids of the N-terminus of HA2 (C-terminal polypeptide of HA). The sequence diverges extensively from other influenza A viruses in most other areas. The sequence of WSN virus HA is similar to that of other H0N1 viruses with the exception of the C-terminus of the HA1 peptide. The change in this area may contribute to some of the unique properties of WSN virus among the HON1 viruses. 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Davis</name><affiliations><json:string>Department of Microbiology and Immunology, UCLA School of Medicine, Los Angeles, CA 90024 U.S.A.</json:string></affiliations></json:item><json:item><name>Alan L. Hiti</name><affiliations><json:string>Department of Microbiology and Immunology, UCLA School of Medicine, Los Angeles, CA 90024 U.S.A.</json:string></affiliations></json:item><json:item><name>Debi P. Nayak</name><affiliations><json:string>Department of Microbiology and Immunology, UCLA School of Medicine, Los Angeles, CA 90024 U.S.A.</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Recombinant DNA</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>dodecadeoxynucleotide primer</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>restriction endonucleases</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>pBR322 plasmid</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>DNA sequence determination</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>bp : base pairs</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>cDNA : complementary DNA</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>HA : hemagglutinin</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>M : matrix proteins</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>NA : neuraminidase</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>NP : nucleoprotein</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>NS : nonstructural protein</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>P : polymerase</value></json:item></subject><arkIstex>ark:/67375/6H6-VH2XB33L-L</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>Full-length article</json:string></originalGenre><abstract>Abstract: A synthetic dodecadeoxynucleotide primer has been used to prepare a double-stranded DNA form of the hemagglutinin (HA) gene of a human influenza virus (WSN strain, HON1). This DNA has been inserted in plasmid pBR322 and cloned in bacterial cells. The insert contains nearly the complete hemagglutinin gene. A restriction map of this insert has been determined and structurally important areas of the HA gene have been sequenced. Amino acid sequences of several regions of the HA protein were deduced from the DNA sequences and compared to the known amino acid sequences of other influenza A viruses. WSN HA shows extensive homology to all influenza A viruses in a few regions, namely the first 17 amino acids of the N-terminus of HA1 (N-terminal polypeptide of HA) and the first 24 amino acids of the N-terminus of HA2 (C-terminal polypeptide of HA). The sequence diverges extensively from other influenza A viruses in most other areas. The sequence of WSN virus HA is similar to that of other H0N1 viruses with the exception of the C-terminus of the HA1 peptide. The change in this area may contribute to some of the unique properties of WSN virus among the HON1 viruses. In addition, WSN HA contains a 17-amino-acid precursor before the N-terminus of HA1 and a single amino acid, arginine, connecting HA1 and HA2.</abstract><qualityIndicators><score>9.652</score><pdfWordCount>5955</pdfWordCount><pdfCharCount>35107</pdfCharCount><pdfVersion>1.4</pdfVersion><pdfPageCount>14</pdfPageCount><pdfPageSize>540 x 742 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractWordCount>221</abstractWordCount><abstractCharCount>1325</abstractCharCount><keywordCount>13</keywordCount></qualityIndicators><title>Construction and characterization of a bacterial clone containing the hemagglutinin gene of the WSN strain (H0N1) of influenza virus</title><pmid><json:string>6254839</json:string></pmid><pii><json:string>0378-1119(80)90050-5</json:string></pii><genre><json:string>research-article</json:string></genre><serie><title>Proc. Natl. Acad. Sci. 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Heyneker</json:string><json:string>Lys Arg</json:string><json:string>David Goeddel</json:string><json:string>Val Arg</json:string><json:string>Dennis Kleid</json:string><json:string>Gin Asn</json:string><json:string>Lys Asn</json:string><json:string>Val Asn</json:string><json:string>Ala Gly</json:string><json:string>Gin Phe</json:string><json:string>Ala Ser</json:string><json:string>City</json:string><json:string>Gin Gin</json:string><json:string>Val Ala</json:string><json:string>Met Cys</json:string><json:string>Val Cys</json:string><json:string>Debi</json:string><json:string>Ala Ala</json:string><json:string>Ala Thr</json:string><json:string>Val Glu</json:string><json:string>Lys Taq</json:string><json:string>Met Val</json:string><json:string>Lys Val</json:string><json:string>Val Val</json:string></persName><placeName><json:string>IN</json:string><json:string>Mannheim</json:string><json:string>CA</json:string><json:string>St. Petersburg</json:string><json:string>FL</json:string><json:string>Indianapolis</json:string></placeName><ref_url></ref_url><ref_bibl><json:string>Sanger et al., 1977</json:string><json:string>Bolivar et al., 1977</json:string><json:string>Sleigh et al., 1979a,b</json:string><json:string>Sanger and Coulson, 1978</json:string><json:string>McDonell et al., 1977</json:string><json:string>Lazarowitz and Choppin, 1975</json:string><json:string>Klenk et al., 1975</json:string><json:string>McGeoch et al., 1976</json:string><json:string>Wickens et al., 1978</json:string><json:string>Palese and Schuhnan, 1976</json:string><json:string>Skehel and Waterfield, 1975</json:string><json:string>Lazarowitz et al., 1973a</json:string><json:string>Clewell, 1972</json:string><json:string>Waterfield et al.</json:string><json:string>Efstratiadis et al., 1976</json:string><json:string>Maxam and Gilbert, 1977</json:string><json:string>Efstratiadis et al. (1976)</json:string><json:string>Waterfield et al., 1979</json:string><json:string>Palese, 1977</json:string><json:string>Robertson et al., 1979</json:string><json:string>Landy and Ross, 1977</json:string><json:string>Berk and Sharpe, 1978</json:string><json:string>Nayak and Baluda, 1967</json:string><json:string>Nayak et al., 1978</json:string><json:string>Chang et al., 1978</json:string><json:string>Janda et ah, 1979</json:string><json:string>Barry and Mahy, 1979</json:string><json:string>Porter et al., 1979</json:string><json:string>Crea et al., 1978</json:string><json:string>Emtage et al., 1979</json:string><json:string>Air, 1979</json:string><json:string>Porter et al., 19790</json:string><json:string>Seeburg et al., 1977</json:string><json:string>Sleigh et al., 1979b</json:string><json:string>Skehel and Hay, 1978</json:string><json:string>Desselberger et al., 1980</json:string><json:string>Klenow and Henningsen, 1970</json:string><json:string>Sleigh et al., 1979</json:string><json:string>Davis et al., 1980</json:string><json:string>Laver and Kilbourne, 1966</json:string><json:string>Palese et al., 1977</json:string><json:string>Porter et al., 1978</json:string><json:string>Curtiss et al., 1977</json:string><json:string>Desselberger et al., 1979</json:string><json:string>Ward and Dopheide, 1979</json:string><json:string>Plotch and Krug, 1978</json:string><json:string>Accepted February 25th, 1980</json:string><json:string>Davis and Nayak, 1979</json:string><json:string>Rigby et al., 1977</json:string></ref_bibl><bibl></bibl></unitex></namedEntities><ark><json:string>ark:/67375/6H6-VH2XB33L-L</json:string></ark><categories><wos><json:string>1 - 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This DNA has been inserted in plasmid pBR322 and cloned in bacterial cells. The insert contains nearly the complete hemagglutinin gene. A restriction map of this insert has been determined and structurally important areas of the HA gene have been sequenced. Amino acid sequences of several regions of the HA protein were deduced from the DNA sequences and compared to the known amino acid sequences of other influenza A viruses. WSN HA shows extensive homology to all influenza A viruses in a few regions, namely the first 17 amino acids of the N-terminus of HA1 (N-terminal polypeptide of HA) and the first 24 amino acids of the N-terminus of HA2 (C-terminal polypeptide of HA). The sequence diverges extensively from other influenza A viruses in most other areas. The sequence of WSN virus HA is similar to that of other H0N1 viruses with the exception of the C-terminus of the HA1 peptide. The change in this area may contribute to some of the unique properties of WSN virus among the HON1 viruses. In addition, WSN HA contains a 17-amino-acid precursor before the N-terminus of HA1 and a single amino acid, arginine, connecting HA1 and HA2.</p></abstract><textClass><keywords scheme="keyword"><list><head>Keywords</head><item><term>Recombinant DNA</term></item><item><term>dodecadeoxynucleotide primer</term></item><item><term>restriction endonucleases</term></item><item><term>pBR322 plasmid</term></item><item><term>DNA sequence determination</term></item></list></keywords></textClass><textClass><keywords scheme="keyword"><list><head>Abbreviations</head><item><term>bp</term><term>base pairs</term></item><item><term>cDNA</term><term>complementary DNA</term></item><item><term>HA</term><term>hemagglutinin</term></item><item><term>M</term><term>matrix proteins</term></item><item><term>NA</term><term>neuraminidase</term></item><item><term>NP</term><term>nucleoprotein</term></item><item><term>NS</term><term>nonstructural protein</term></item><item><term>P</term><term>polymerase</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="1980">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-VH2XB33L-L/fulltext.txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Elsevier, elements deleted: tail"><istex:xmlDeclaration>version="1.0" encoding="utf-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//ES//DTD journal article DTD version 4.5.2//EN//XML" URI="art452.dtd" name="istex:docType"></istex:docType><istex:document><converted-article version="4.5.2" docsubtype="fla"><item-info><jid>GENE</jid><aid>80900505</aid><ce:pii>0378-1119(80)90050-5</ce:pii><ce:doi>10.1016/0378-1119(80)90050-5</ce:doi><ce:copyright type="unknown" year="1980"></ce:copyright></item-info><head><ce:title>Construction and characterization of a bacterial clone containing the hemagglutinin gene of the WSN strain (H0N1) of influenza virus</ce:title><ce:author-group><ce:author><ce:given-name>Alan R.</ce:given-name><ce:surname>Davis</ce:surname></ce:author><ce:author><ce:given-name>Alan L.</ce:given-name><ce:surname>Hiti</ce:surname></ce:author><ce:author><ce:given-name>Debi P.</ce:given-name><ce:surname>Nayak</ce:surname></ce:author><ce:affiliation><ce:textfn>Department of Microbiology and Immunology, UCLA School of Medicine, Los Angeles, CA 90024 U.S.A.</ce:textfn></ce:affiliation></ce:author-group><ce:date-received day="1" month="2" year="1980"></ce:date-received><ce:date-accepted day="25" month="2" year="1980"></ce:date-accepted><ce:abstract><ce:section-title>Abstract</ce:section-title><ce:abstract-sec><ce:simple-para>A synthetic dodecadeoxynucleotide primer has been used to prepare a double-stranded DNA form of the hemagglutinin (HA) gene of a human influenza virus (WSN strain, HON1). This DNA has been inserted in plasmid pBR322 and cloned in bacterial cells. The insert contains nearly the complete hemagglutinin gene. A restriction map of this insert has been determined and structurally important areas of the HA gene have been sequenced. Amino acid sequences of several regions of the HA protein were deduced from the DNA sequences and compared to the known amino acid sequences of other influenza A viruses. WSN HA shows extensive homology to all influenza A viruses in a few regions, namely the first 17 amino acids of the N-terminus of HA1 (N-terminal polypeptide of HA) and the first 24 amino acids of the N-terminus of HA2 (C-terminal polypeptide of HA). The sequence diverges extensively from other influenza A viruses in most other areas. The sequence of WSN virus HA is similar to that of other H0N1 viruses with the exception of the C-terminus of the HA1 peptide. The change in this area may contribute to some of the unique properties of WSN virus among the HON1 viruses. In addition, WSN HA contains a 17-amino-acid precursor before the N-terminus of HA1 and a single amino acid, arginine, connecting HA1 and HA2.</ce:simple-para></ce:abstract-sec></ce:abstract><ce:keywords><ce:section-title>Keywords</ce:section-title><ce:keyword><ce:text>Recombinant DNA</ce:text></ce:keyword><ce:keyword><ce:text>dodecadeoxynucleotide primer</ce:text></ce:keyword><ce:keyword><ce:text>restriction endonucleases</ce:text></ce:keyword><ce:keyword><ce:text>pBR322 plasmid</ce:text></ce:keyword><ce:keyword><ce:text>DNA sequence determination</ce:text></ce:keyword></ce:keywords><ce:keywords class="abr"><ce:section-title>Abbreviations</ce:section-title><ce:keyword><ce:text>bp</ce:text><ce:keyword><ce:text>base pairs</ce:text></ce:keyword></ce:keyword><ce:keyword><ce:text>cDNA</ce:text><ce:keyword><ce:text>complementary DNA</ce:text></ce:keyword></ce:keyword><ce:keyword><ce:text>HA</ce:text><ce:keyword><ce:text>hemagglutinin</ce:text></ce:keyword></ce:keyword><ce:keyword><ce:text>M</ce:text><ce:keyword><ce:text>matrix proteins</ce:text></ce:keyword></ce:keyword><ce:keyword><ce:text>NA</ce:text><ce:keyword><ce:text>neuraminidase</ce:text></ce:keyword></ce:keyword><ce:keyword><ce:text>NP</ce:text><ce:keyword><ce:text>nucleoprotein</ce:text></ce:keyword></ce:keyword><ce:keyword><ce:text>NS</ce:text><ce:keyword><ce:text>nonstructural protein</ce:text></ce:keyword></ce:keyword><ce:keyword><ce:text>P</ce:text><ce:keyword><ce:text>polymerase</ce:text></ce:keyword></ce:keyword></ce:keywords></head></converted-article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo><title>Construction and characterization of a bacterial clone containing the hemagglutinin gene of the WSN strain (H0N1) of influenza virus</title></titleInfo><titleInfo type="alternative" contentType="CDATA"><title>Construction and characterization of a bacterial clone containing the hemagglutinin gene of the WSN strain (H0N1) of influenza virus</title></titleInfo><name type="personal"><namePart type="given">Alan R.</namePart><namePart type="family">Davis</namePart><affiliation>Department of Microbiology and Immunology, UCLA School of Medicine, Los Angeles, CA 90024 U.S.A.</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Alan L.</namePart><namePart type="family">Hiti</namePart><affiliation>Department of Microbiology and Immunology, UCLA School of Medicine, Los Angeles, CA 90024 U.S.A.</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Debi P.</namePart><namePart type="family">Nayak</namePart><affiliation>Department of Microbiology and Immunology, UCLA School of Medicine, Los Angeles, CA 90024 U.S.A.</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="Full-length article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-1JC4F85T-7">research-article</genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1980</dateIssued><copyrightDate encoding="w3cdtf">1980</copyrightDate></originInfo><language><languageTerm type="code" authority="iso639-2b">eng</languageTerm><languageTerm type="code" authority="rfc3066">en</languageTerm></language><abstract lang="en">Abstract: A synthetic dodecadeoxynucleotide primer has been used to prepare a double-stranded DNA form of the hemagglutinin (HA) gene of a human influenza virus (WSN strain, HON1). This DNA has been inserted in plasmid pBR322 and cloned in bacterial cells. The insert contains nearly the complete hemagglutinin gene. A restriction map of this insert has been determined and structurally important areas of the HA gene have been sequenced. Amino acid sequences of several regions of the HA protein were deduced from the DNA sequences and compared to the known amino acid sequences of other influenza A viruses. WSN HA shows extensive homology to all influenza A viruses in a few regions, namely the first 17 amino acids of the N-terminus of HA1 (N-terminal polypeptide of HA) and the first 24 amino acids of the N-terminus of HA2 (C-terminal polypeptide of HA). The sequence diverges extensively from other influenza A viruses in most other areas. The sequence of WSN virus HA is similar to that of other H0N1 viruses with the exception of the C-terminus of the HA1 peptide. The change in this area may contribute to some of the unique properties of WSN virus among the HON1 viruses. In addition, WSN HA contains a 17-amino-acid precursor before the N-terminus of HA1 and a single amino acid, arginine, connecting HA1 and HA2.</abstract><subject><genre>Keywords</genre><topic>Recombinant DNA</topic><topic>dodecadeoxynucleotide primer</topic><topic>restriction endonucleases</topic><topic>pBR322 plasmid</topic><topic>DNA sequence determination</topic></subject><subject><genre>Abbreviations</genre><topic>bp : base pairs</topic><topic>cDNA : complementary DNA</topic><topic>HA : hemagglutinin</topic><topic>M : matrix proteins</topic><topic>NA : neuraminidase</topic><topic>NP : nucleoprotein</topic><topic>NS : nonstructural protein</topic><topic>P : polymerase</topic></subject><relatedItem type="host"><titleInfo><title>Gene</title></titleInfo><titleInfo type="abbreviated"><title>GENE</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1980</dateIssued></originInfo><identifier type="ISSN">0378-1119</identifier><identifier type="PII">S0378-1119(00)X0451-9</identifier><part><date>1980</date><detail type="volume"><number>10</number><caption>vol.</caption></detail><detail type="issue"><number>3</number><caption>no.</caption></detail><extent unit="issue-pages"><start>185</start><end>289</end></extent><extent unit="pages"><start>205</start><end>218</end></extent></part></relatedItem><identifier type="istex">A49FFC82D563A76282D3D7AB1749501874FB866B</identifier><identifier type="ark">ark:/67375/6H6-VH2XB33L-L</identifier><identifier type="DOI">10.1016/0378-1119(80)90050-5</identifier><identifier type="PII">0378-1119(80)90050-5</identifier><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-HKKZVM7B-M">elsevier</recordContentSource></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/ark:/67375/6H6-VH2XB33L-L/record.json</uri></json:item></metadata></istex></record>Pour manipuler ce document sous Unix (Dilib)
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