VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q42767488 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241221010711.0
008 241221nneanz||abbn n and d
035 ‎‡a (WKP)Q42767488‏
024 ‎‡a 0000-0001-5301-675X‏ ‎‡2 orcid‏
035 ‎‡a (OCoLC)Q42767488‏
100 0 ‎‡a Jonathan Peter Warner‏ ‎‡9 ast‏ ‎‡9 es‏ ‎‡9 sl‏
375 ‎‡a 1‏ ‎‡2 iso5218‏
400 0 ‎‡a Jonathan Peter Warner‏ ‎‡c researcher‏ ‎‡9 en‏
400 0 ‎‡a Jonathan Peter Warner‏ ‎‡c wetenschapper‏ ‎‡9 nl‏
670 ‎‡a Author's A general method for the detection of large CAG repeat expansions by fluorescent PCR‏
670 ‎‡a Author's A human parthenogenetic chimaera.‏
670 ‎‡a Author's A new polymerase chain reaction‏
670 ‎‡a Author's A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes‏
670 ‎‡a Author's A novel atypical 22q11.2 distal deletion in father and son.‏
670 ‎‡a Author's A single allele from the polymorphic CCG rich sequence immediately 3' to the unstable CAG trinucleotide in the IT15 cDNA shows almost complete disequilibrium with Huntington's disease chromosomes in the Scottish population‏
670 ‎‡a Author's A study of the Huntington's disease associated trinucleotide repeat in the Scottish population.‏
670 ‎‡a Author's Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridization using a cosmid contig‏
670 ‎‡a Author's BRCA1 5382insC mutation in sporadic and familial breast and ovarian carcinoma in Scotland‏
670 ‎‡a Author's Chromosomal organisation of a repeated gene cluster expressed in mammalian stages of Leishmania‏
670 ‎‡a Author's Co-localization of the ketohexokinase and glucokinase regulator genes to a 500-kb region of Chromosome 2p23‏
670 ‎‡a Author's Discriminative stimulus properties of delta9-tetrahydrocannabinol‏
670 ‎‡a Author's Discriminative stimulus properties of delta9-tetrahydrocannabinol (THC) in C57Bl/6J mice‏
670 ‎‡a Author's Divergent effects of cannabidiol on the discriminative stimulus and place conditioning effects of Delta(9)-tetrahydrocannabinol‏
670 ‎‡a Author's Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28.‏
670 ‎‡a Author's Human glucokinase regulatory protein (GCKR): cDNA and genomic cloning, complete primary structure, and chromosomal localization.‏
670 ‎‡a Author's Improved PCR based methods for detecting C9orf72 hexanucleotide repeat expansions.‏
670 ‎‡a Author's Molecular genetics of the human glucokinase regulator-fructokinase‏
670 ‎‡a Author's Molecular genetics of the human glucokinase regulator-fructokinase (GCKR-KHK) region of chromosome 2p23.‏
670 ‎‡a Author's Organization of the human glucokinase regulator gene GCKR‏
670 ‎‡a Author's P67L: a cystic fibrosis allele with mild effects found at high frequency in the Scottish population.‏
670 ‎‡a Author's Spinocerebellar ataxia type 8 in Scotland: frequency, neurological, neuropsychological and neuropsychiatric findings‏
670 ‎‡a Author's Spinocerebellar ataxia type 8 in Scotland: genetic and clinical features in seven unrelated cases and a review of published reports.‏
670 ‎‡a Author's Structural analysis of the human ret proto-oncogene using exon trapping.‏
670 ‎‡a Author's Targeted sequencing of the Paget's disease associated 14q32 locus identifies several missense coding variants in RIN3 that predispose to Paget's disease of bone.‏
670 ‎‡a Author's The ASP1 gene of Saccharomyces cerevisiae, encoding the intracellular isozyme of L-asparaginase‏
909 ‎‡a (orcid) 000000015301675x‏ ‎‡9 1‏
919 ‎‡a brca15382inscmutationinsporadicandfamilialbreastandovariancarcinomainscotland‏ ‎‡A BRCA1 5382insC mutation in sporadic and familial breast and ovarian carcinoma in Scotland‏ ‎‡9 1‏
919 ‎‡a colocalizationoftheketohexokinaseandglucokinaseregulatorgenestoa500kbregionofchromosome2p23‏ ‎‡A Co-localization of the ketohexokinase and glucokinase regulator genes to a 500-kb region of Chromosome 2p23‏ ‎‡9 1‏
919 ‎‡a discriminativestimuluspropertiesofdelta9tetrahydrocannabinol‏ ‎‡A Discriminative stimulus properties of delta9-tetrahydrocannabinol‏ ‎‡9 1‏
919 ‎‡a discriminativestimuluspropertiesofdelta9tetrahydrocannabinolthcinc57bl6jmice‏ ‎‡A Discriminative stimulus properties of delta9-tetrahydrocannabinol (THC) in C57Bl/6J mice‏ ‎‡9 1‏
919 ‎‡a divergenteffectsofcannabidiolonthediscriminativestimulusandplaceconditioningeffectsofdelta9tetrahydrocannabinol‏ ‎‡A Divergent effects of cannabidiol on the discriminative stimulus and place conditioning effects of Delta(9)-tetrahydrocannabinol‏ ‎‡9 1‏
919 ‎‡a emerydreifussmusculardystrophylinkagetomarkersindistalxq28‏ ‎‡A Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28.‏ ‎‡9 1‏
919 ‎‡a humanglucokinaseregulatoryproteingckrcdnaandgenomiccloningcompleteprimarystructureandchromosomallocalization‏ ‎‡A Human glucokinase regulatory protein (GCKR): cDNA and genomic cloning, complete primary structure, and chromosomal localization.‏ ‎‡9 1‏
919 ‎‡a improvedpcrbasedmethodsfordetectingc9orf72hexanucleotiderepeatexpansions‏ ‎‡A Improved PCR based methods for detecting C9orf72 hexanucleotide repeat expansions.‏ ‎‡9 1‏
919 ‎‡a moleculargeneticsofthehumanglucokinaseregulatorfructokinase‏ ‎‡A Molecular genetics of the human glucokinase regulator-fructokinase‏ ‎‡9 1‏
919 ‎‡a moleculargeneticsofthehumanglucokinaseregulatorfructokinasegckrkhkregionofchromosome2p23‏ ‎‡A Molecular genetics of the human glucokinase regulator-fructokinase (GCKR-KHK) region of chromosome 2p23.‏ ‎‡9 1‏
919 ‎‡a organizationofthehumanglucokinaseregulatorgenegckr‏ ‎‡A Organization of the human glucokinase regulator gene GCKR‏ ‎‡9 1‏
919 ‎‡a p67lacysticfibrosisallelewithmildeffectsfoundathighfrequencyinthescottishpopulation‏ ‎‡A P67L: a cystic fibrosis allele with mild effects found at high frequency in the Scottish population.‏ ‎‡9 1‏
919 ‎‡a spinocerebellarataxiatype8inscotlandfrequencyneurologicalneuropsychologicalandneuropsychiatricfindings‏ ‎‡A Spinocerebellar ataxia type 8 in Scotland: frequency, neurological, neuropsychological and neuropsychiatric findings‏ ‎‡9 1‏
919 ‎‡a spinocerebellarataxiatype8inscotlandgeneticandclinicalfeaturesin7unrelatedcasesandareviewofpublishedreports‏ ‎‡A Spinocerebellar ataxia type 8 in Scotland: genetic and clinical features in seven unrelated cases and a review of published reports.‏ ‎‡9 1‏
919 ‎‡a structuralanalysisofthehumanretprotooncogeneusingexontrapping‏ ‎‡A Structural analysis of the human ret proto-oncogene using exon trapping.‏ ‎‡9 1‏
919 ‎‡a targetedsequencingofthepagetsdiseaseassociated14q32locusidentifiesseveralmissensecodingvariantsinrin3thatpredisposetopagetsdiseaseofbone‏ ‎‡A Targeted sequencing of the Paget's disease associated 14q32 locus identifies several missense coding variants in RIN3 that predispose to Paget's disease of bone.‏ ‎‡9 1‏
919 ‎‡a asp1geneofsaccharomycescerevisiaeencodingtheintracellularisozymeof50asparaginase‏ ‎‡A The ASP1 gene of Saccharomyces cerevisiae, encoding the intracellular isozyme of L-asparaginase‏ ‎‡9 1‏
919 ‎‡a newpolymerasechainreactionpcrassayforthetrinucleotiderepeatthatisunstableandexpandedonhuntingtonsdiseasechromosomes‏ ‎‡A A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes‏ ‎‡9 1‏
919 ‎‡a chromosomalorganisationofarepeatedgeneclusterexpressedinmammalianstagesofleishmania‏ ‎‡A Chromosomal organisation of a repeated gene cluster expressed in mammalian stages of Leishmania‏ ‎‡9 1‏
919 ‎‡a newpolymerasechainreaction‏ ‎‡A A new polymerase chain reaction‏ ‎‡9 1‏
919 ‎‡a humanparthenogeneticchimaera‏ ‎‡A A human parthenogenetic chimaera.‏ ‎‡9 1‏
919 ‎‡a generalmethodforthedetectionoflargecagrepeatexpansionsbyfluorescentpcr‏ ‎‡A A general method for the detection of large CAG repeat expansions by fluorescent PCR‏ ‎‡9 1‏
919 ‎‡a novelatypical22q112distaldeletioninfatherandson‏ ‎‡A A novel atypical 22q11.2 distal deletion in father and son.‏ ‎‡9 1‏
919 ‎‡a singleallelefromthepolymorphicccgrichsequenceimmediately3totheunstablecagtrinucleotideintheit15cdnashowsalmostcompletedisequilibriumwithhuntingtonsdiseasechromosomesinthescottishpopulation‏ ‎‡A A single allele from the polymorphic CCG rich sequence immediately 3' to the unstable CAG trinucleotide in the IT15 cDNA shows almost complete disequilibrium with Huntington's disease chromosomes in the Scottish population‏ ‎‡9 1‏
919 ‎‡a studyofthehuntingtonsdiseaseassociatedtrinucleotiderepeatinthescottishpopulation‏ ‎‡A A study of the Huntington's disease associated trinucleotide repeat in the Scottish population.‏ ‎‡9 1‏
919 ‎‡a analysisofchromosome21copynumberinunculturedamniocytesbyfluorescenceinsituhybridizationusingacosmidcontig‏ ‎‡A Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridization using a cosmid contig‏ ‎‡9 1‏
946 ‎‡a b‏ ‎‡9 1‏
996 ‎‡2 PLWABN|9813224645305606‏
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996 ‎‡2 PTBNP|1547727‏
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996 ‎‡2 CAOONL|ncf11462576‏
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996 ‎‡2 PLWABN|9810694033005606‏
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997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏