Leader
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00000nz a2200037n 45 0 |
001
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WKP|Q57320695
(VIAF cluster)
(Authority/Source Record)
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WKP |
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20241121000211.0 |
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(WKP)Q57320695
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0000-0001-8779-2060
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orcid
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035
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(OCoLC)Q57320695
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100
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0 |
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‡a
David I Wilson
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es
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ast
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375
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1
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iso5218
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400
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ডেভিড আই উইলসন
‡9
bn
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0 |
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David I. Wilson
‡c
researcher (ORCID 0000-0001-8779-2060)
‡9
en
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400
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0 |
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‡a
David I Wilson
‡c
onderzoeker
‡9
nl
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670
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‡a
Author's ADAM33 expression in asthmatic airways and human embryonic lungs
|
670
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‡a
Author's Beta cell differentiation during early human pancreas development
|
670
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‡a
Author's Beta-cell differentiation during human development does not rely on nestin-positive precursors: implications for stem cell-derived replacement therapy
|
670
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‡a
Author's BRCA1 EXON 11, a CERES (composite regulatory element of splicing) element involved in splice regulation
|
670
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‡a
Author's BRCA1 exon 11 alternative splicing, multiple functions and the association with cancer.
|
670
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|
‡a
Author's Centriolar association of ALMS1 and likely centrosomal functions of the ALMS motif-containing proteins C10orf90 and KIAA1731
|
670
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‡a
Author's Characterization and multipotentiality of human fetal femur-derived cells: implications for skeletal tissue regeneration
|
670
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‡a
Author's Characterization of ciliated bronchial epithelium 1, a ciliated cell-associated gene induced during mucociliary differentiation
|
670
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‡a
Author's Differences between human and mouse alpha-fetoprotein expression during early development
|
670
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‡a
Author's Ectopic SOX9 mediates extracellular matrix deposition characteristic of organ fibrosis
|
670
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‡a
Author's Epigenetic regulation during fetal femur development: DNA methylation matters.
|
670
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‡a
Author's Evaluating Human Embryonic Germ Cells: Concord and Conflict as Pluripotent Stem Cells
|
670
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‡a
Author's Evidence for centriolar satellite localization of CDK1 and cyclin B2.
|
670
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|
‡a
Author's Evidence for reciliation of RPE1 cells in late G1 phase, and ciliary localisation of cyclin B1.
|
670
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‡a
Author's Expression and localisation of thymosin beta-4 in the developing human early fetal heart
|
670
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|
‡a
Author's Expression profiles of SF-1, DAX1, and CYP17 in the human fetal adrenal gland: potential interactions in gene regulation
|
670
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‡a
Author's FRA2A is a CGG repeat expansion associated with silencing of AFF3
|
670
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|
|
‡a
Author's Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes
|
670
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|
‡a
Author's Hepatic differentiation of murine embryonic stem cells
|
670
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|
‡a
Author's Human embryo and early fetus research
|
670
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|
‡a
Author's Human embryonic germ cells for future neuronal replacement therapy
|
670
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|
‡a
Author's Human endothelial and foetal femur-derived stem cell co-cultures modulate osteogenesis and angiogenesis.
|
670
|
|
|
‡a
Author's In humans, early cortisol biosynthesis provides a mechanism to safeguard female sexual development
|
670
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|
|
‡a
Author's In vitro expression of NGN3 identifies RAB3B as the predominant Ras-associated GTP-binding protein 3 family member in human islets
|
670
|
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|
‡a
Author's In vitro fertilization improves childhood growth and metabolism.
|
670
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|
‡a
Author's Induction of a disintegrin and metalloprotease 33 during embryonic lung development and the influence of IL-13 or maternal allergy
|
670
|
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|
‡a
Author's Long-range evolutionary constraints reveal cis-regulatory interactions on the human X chromosome
|
670
|
|
|
‡a
Author's MicroRNA-146a regulates human foetal femur derived skeletal stem cell differentiation by down-regulating SMAD2 and SMAD3.
|
670
|
|
|
‡a
Author's Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome
|
670
|
|
|
‡a
Author's Narrowing the critical region within 11q24-qter for hypoplastic left heart and identification of a candidate gene, JAM3, expressed during cardiogenesis
|
670
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|
‡a
Author's Nek2 localises to the distal portion of the mother centriole/basal body and is required for timely cilium disassembly at the G2/M transition.
|
670
|
|
|
‡a
Author's Novel SOX9 expression during human pancreas development correlates to abnormalities in Campomelic dysplasia.
|
670
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|
|
‡a
Author's Phospholamban and sarcolipin are maintained in the endoplasmic reticulum by retrieval from the ER-Golgi intermediate compartment
|
670
|
|
|
‡a
Author's Probing the epigenetic regulation of HIF-1α transcription in developing tissue.
|
670
|
|
|
‡a
Author's Rare variants in NR2F2 cause congenital heart defects in humans
|
670
|
|
|
‡a
Author's RBFOX2 protein domains and cellular activities.
|
670
|
|
|
‡a
Author's Regionally-derived cell populations and skeletal stem cells from human foetal femora exhibit specific osteochondral and multi-lineage differentiation capacity in vitro and ex vivo
|
670
|
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|
‡a
Author's Science, medicine, and the future: Genetics and cardiovascular risk.
|
670
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|
|
‡a
Author's Separation of the PROX1 gene from upstream conserved elements in a complex inversion/translocation patient with hypoplastic left heart.
|
670
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|
|
‡a
Author's Soluble ADAM33 initiates airway remodeling to promote susceptibility for allergic asthma in early life
|
670
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|
‡a
Author's Stem cell marker TRA-1-60 is expressed in foetal and adult kidney and upregulated in tubulo-interstitial disease
|
670
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|
‡a
Author's Subcellular localization of ALMS1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes
|
670
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|
|
‡a
Author's The early human germ cell lineage does not express SOX2 during in vivo development or upon in vitro culture.
|
670
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|
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‡a
Author's The soluble form of a disintegrin and metalloprotease 33 promotes angiogenesis: implications for airway remodeling in asthma.
|
670
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|
|
‡a
Author's Transcriptional regulation of the Alström syndrome gene ALMS1 by members of the RFX family and Sp1
|
670
|
|
|
‡a
Author's Two children with subtelomeric 11q deletions: a description and interpretation of their clinical presentations and molecular genetic findings.
|
909
|
|
|
‡a
(orcid) 0000000187792060
‡9
1
|
919
|
|
|
‡a
transcriptionalregulationofthealstromsyndromegenealms1bymembersoftherfxfamilyandsp1
‡A
Transcriptional regulation of the Alström syndrome gene ALMS1 by members of the RFX family and Sp1
‡9
1
|
919
|
|
|
‡a
solubleformofadisintegrinandmetalloprotease33promotesangiogenesisimplicationsforairwayremodelinginasthma
‡A
The soluble form of a disintegrin and metalloprotease 33 promotes angiogenesis: implications for airway remodeling in asthma.
‡9
1
|
919
|
|
|
‡a
earlyhumangermcelllineagedoesnotexpresssox2duringinvivodevelopmentoruponinvitroculture
‡A
The early human germ cell lineage does not express SOX2 during in vivo development or upon in vitro culture.
‡9
1
|
919
|
|
|
‡a
subcellularlocalizationofalms1supportsinvolvementofcentrosomeandbasalbodydysfunctioninthepathogenesisofobesityinsulinresistanceandtype2diabetes
‡A
Subcellular localization of ALMS1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes
‡9
1
|
919
|
|
|
‡a
stemcellmarkertra160isexpressedinfoetalandadultkidneyandupregulatedintubulointerstitialdisease
‡A
Stem cell marker TRA-1-60 is expressed in foetal and adult kidney and upregulated in tubulo-interstitial disease
‡9
1
|
919
|
|
|
‡a
solubleadam33initiatesairwayremodelingtopromotesusceptibilityforallergicasthmainearlylife
‡A
Soluble ADAM33 initiates airway remodeling to promote susceptibility for allergic asthma in early life
‡9
1
|
919
|
|
|
‡a
separationoftheprox1genefromupstreamconservedelementsinacomplexinversiontranslocationpatientwithhypoplasticleftheart
‡A
Separation of the PROX1 gene from upstream conserved elements in a complex inversion/translocation patient with hypoplastic left heart.
‡9
1
|
919
|
|
|
‡a
regionallyderivedcellpopulationsandskeletalstemcellsfromhumanfoetalfemoraexhibitspecificosteochondralandmultilineagedifferentiationcapacityinvitroandexvivo
‡A
Regionally-derived cell populations and skeletal stem cells from human foetal femora exhibit specific osteochondral and multi-lineage differentiation capacity in vitro and ex vivo
‡9
1
|
919
|
|
|
‡a
rbfox2proteindomainsandcellularactivities
‡A
RBFOX2 protein domains and cellular activities.
‡9
1
|
919
|
|
|
‡a
rarevariantsinnr2f2causecongenitalheartdefectsinhumans
‡A
Rare variants in NR2F2 cause congenital heart defects in humans
‡9
1
|
919
|
|
|
‡a
phospholambanandsarcolipinaremaintainedintheendoplasmicreticulumbyretrievalfromtheergolgiintermediatecompartment
‡A
Phospholamban and sarcolipin are maintained in the endoplasmic reticulum by retrieval from the ER-Golgi intermediate compartment
‡9
1
|
919
|
|
|
‡a
novelsox9expressionduringhumanpancreasdevelopmentcorrelatestoabnormalitiesincampomelicdysplasia
‡A
Novel SOX9 expression during human pancreas development correlates to abnormalities in Campomelic dysplasia.
‡9
1
|
919
|
|
|
‡a
nek2localisestothedistalportionofthemothercentriolebasalbodyandisrequiredfortimelyciliumdisassemblyattheg21000transition
‡A
Nek2 localises to the distal portion of the mother centriole/basal body and is required for timely cilium disassembly at the G2/M transition.
‡9
1
|
919
|
|
|
‡a
mutationofalms1alargegenewithatandemrepeatencoding47aminoacidscausesalstromsyndrome
‡A
Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome
‡9
1
|
919
|
|
|
‡a
microrna146aregulateshumanfoetalfemurderivedskeletalstemcelldifferentiationbydownregulatingsmad2andsmad3
‡A
MicroRNA-146a regulates human foetal femur derived skeletal stem cell differentiation by down-regulating SMAD2 and SMAD3.
‡9
1
|
919
|
|
|
‡a
longrangeevolutionaryconstraintsrevealcisregulatoryinteractionsonthehuman10chromosome
‡A
Long-range evolutionary constraints reveal cis-regulatory interactions on the human X chromosome
‡9
1
|
919
|
|
|
‡a
inductionofadisintegrinandmetalloprotease33duringembryoniclungdevelopmentandtheinfluenceofil13ormaternalallergy
‡A
Induction of a disintegrin and metalloprotease 33 during embryonic lung development and the influence of IL-13 or maternal allergy
‡9
1
|
919
|
|
|
‡a
invitrofertilizationimproveschildhoodgrowthandmetabolism
‡A
In vitro fertilization improves childhood growth and metabolism.
‡9
1
|
919
|
|
|
‡a
invitroexpressionofngn3identifiesrab3basthepredominantrasassociatedgtpbindingprotein3familymemberinhumanislets
‡A
In vitro expression of NGN3 identifies RAB3B as the predominant Ras-associated GTP-binding protein 3 family member in human islets
‡9
1
|
919
|
|
|
‡a
inhumansearlycortisolbiosynthesisprovidesamechanismtosafeguardfemalesexualdevelopment
‡A
In humans, early cortisol biosynthesis provides a mechanism to safeguard female sexual development
‡9
1
|
919
|
|
|
‡a
humanendothelialandfoetalfemurderivedstemcellcoculturesmodulateosteogenesisandangiogenesis
‡A
Human endothelial and foetal femur-derived stem cell co-cultures modulate osteogenesis and angiogenesis.
‡9
1
|
919
|
|
|
‡a
humanembryonicgermcellsforfutureneuronalreplacementtherapy
‡A
Human embryonic germ cells for future neuronal replacement therapy
‡9
1
|
919
|
|
|
‡a
humanembryoandearlyfetusresearch
‡A
Human embryo and early fetus research
‡9
1
|
919
|
|
|
‡a
hepaticdifferentiationofmurineembryonicstemcells
‡A
Hepatic differentiation of murine embryonic stem cells
‡9
1
|
919
|
|
|
‡a
genomewidednamethylationanalysisofpatientswithimprintingdisordersidentifiesdifferentiallymethylatedregionsassociatedwithnovelcandidateimprintedgenes
‡A
Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes
‡9
1
|
919
|
|
|
‡a
fra2aisacggrepeatexpansionassociatedwithsilencingofaff3
‡A
FRA2A is a CGG repeat expansion associated with silencing of AFF3
‡9
1
|
919
|
|
|
‡a
expressionprofilesofsf1dax1andcyp17inthehumanfetaladrenalglandpotentialinteractionsingeneregulation
‡A
Expression profiles of SF-1, DAX1, and CYP17 in the human fetal adrenal gland: potential interactions in gene regulation
‡9
1
|
919
|
|
|
‡a
expressionandlocalisationofthymosinbeta4inthedevelopinghumanearlyfetalheart
‡A
Expression and localisation of thymosin beta-4 in the developing human early fetal heart
‡9
1
|
919
|
|
|
‡a
narrowingthecriticalregionwithin11q24qterforhypoplasticleftheartandidentificationofacandidategenejam3expressedduringcardiogenesis
‡A
Narrowing the critical region within 11q24-qter for hypoplastic left heart and identification of a candidate gene, JAM3, expressed during cardiogenesis
‡9
1
|
919
|
|
|
‡a
evidenceforreciliationofrpe1cellsinlateg1phaseandciliarylocalisationofcyclinb1
‡A
Evidence for reciliation of RPE1 cells in late G1 phase, and ciliary localisation of cyclin B1.
‡9
1
|
919
|
|
|
‡a
evidenceforcentriolarsatellitelocalizationofcdk1andcyclinb2
‡A
Evidence for centriolar satellite localization of CDK1 and cyclin B2.
‡9
1
|
919
|
|
|
‡a
evaluatinghumanembryonicgermcellsconcordandconflictaspluripotentstemcells
‡A
Evaluating Human Embryonic Germ Cells: Concord and Conflict as Pluripotent Stem Cells
‡9
1
|
919
|
|
|
‡a
probingtheepigeneticregulationofhif1αtranscriptionindevelopingtissue
‡A
Probing the epigenetic regulation of HIF-1α transcription in developing tissue.
‡9
1
|
919
|
|
|
‡a
epigeneticregulationduringfetalfemurdevelopmentdnamethylationmatters
‡A
Epigenetic regulation during fetal femur development: DNA methylation matters.
‡9
1
|
919
|
|
|
‡a
ectopicsox9mediatesextracellularmatrixdepositioncharacteristicoforganfibrosis
‡A
Ectopic SOX9 mediates extracellular matrix deposition characteristic of organ fibrosis
‡9
1
|
919
|
|
|
‡a
differencesbetweenhumanandmousealphafetoproteinexpressionduringearlydevelopment
‡A
Differences between human and mouse alpha-fetoprotein expression during early development
‡9
1
|
919
|
|
|
‡a
sciencemedicineandthefuturegeneticsandcardiovascularrisk
‡A
Science, medicine, and the future: Genetics and cardiovascular risk.
‡9
1
|
919
|
|
|
‡a
characterizationofciliatedbronchialepithelium1aciliatedcellassociatedgeneinducedduringmucociliarydifferentiation
‡A
Characterization of ciliated bronchial epithelium 1, a ciliated cell-associated gene induced during mucociliary differentiation
‡9
1
|
919
|
|
|
‡a
characterizationandmultipotentialityofhumanfetalfemurderivedcellsimplicationsforskeletaltissueregeneration
‡A
Characterization and multipotentiality of human fetal femur-derived cells: implications for skeletal tissue regeneration
‡9
1
|
919
|
|
|
‡a
centriolarassociationofalms1andlikelycentrosomalfunctionsofthealmsmotifcontainingproteinsc10orf90andkia
‡A
Centriolar association of ALMS1 and likely centrosomal functions of the ALMS motif-containing proteins C10orf90 and KIAA1731
‡9
1
|
919
|
|
|
‡a
brca1exon11alternativesplicingmultiplefunctionsandtheassociationwithcancer
‡A
BRCA1 exon 11 alternative splicing, multiple functions and the association with cancer.
‡9
1
|
919
|
|
|
‡a
brca1exon11acerescompositeregulatoryelementofsplicingelementinvolvedinspliceregulation
‡A
BRCA1 EXON 11, a CERES (composite regulatory element of splicing) element involved in splice regulation
‡9
1
|
919
|
|
|
‡a
betacelldifferentiationduringhumandevelopmentdoesnotrelyonnestinpositiveprecursorsimplicationsforstemcellderivedreplacementtherapy
‡A
Beta-cell differentiation during human development does not rely on nestin-positive precursors: implications for stem cell-derived replacement therapy
‡9
1
|
919
|
|
|
‡a
2childrenwithsubtelomeric11qdeletionsadescriptionandinterpretationoftheirclinicalpresentationsandmoleculargeneticfindings
‡A
Two children with subtelomeric 11q deletions: a description and interpretation of their clinical presentations and molecular genetic findings.
‡9
1
|
919
|
|
|
‡a
betacelldifferentiationduringearlyhumanpancreasdevelopment
‡A
Beta cell differentiation during early human pancreas development
‡9
1
|
919
|
|
|
‡a
adam33expressioninasthmaticairwaysandhumanembryoniclungs
‡A
ADAM33 expression in asthmatic airways and human embryonic lungs
‡9
1
|
943
|
|
|
‡a
173x
‡A
1731
‡9
1
|
946
|
|
|
‡a
b
‡9
1
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996
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LC|n 2010000469
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LC|n 97803514
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LC|n 2012005735
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NUKAT|n 99044213
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NSK|000602500
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PTBNP|200207
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J9U|987007448422405171
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N6I|vtls002516130
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SUDOC|14788294X
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LC|no 00008364
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BIBSYS|90670044
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RERO|A016399774
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SELIBR|286832
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LC|no2017022391
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NDL|00554263
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PLWABN|9810622616605606
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SUDOC|230863698
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CAOONL|ncf10302200
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J9U|987007275110705171
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NTA|172171954
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J9U|987007600933505171
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BLBNB|000515051
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J9U|987007297567905171
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NTA|071982582
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JPG|500004727
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BNF|10713834
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BNF|13329233
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LC|nb2017006150
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SUDOC|141083883
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BIBSYS|9007634
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DE633|pe30010478
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CAOONL|ncf10431110
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LC|n 81073315
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BNF|12420395
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NUKAT|n 2017217798
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DNB|1157193188
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ISNI|0000000116031942
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NKC|xx0035843
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SUDOC|033219656
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BIBSYS|11070802
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J9U|987011289244805171
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DNB|118083341
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SUDOC|264701852
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BNF|18161795
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NDL|01162170
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LC|no2006062240
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ISNI|000000007100654X
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NTA|073388351
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NII|DA04478278
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BIBSYS|1483107588118
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J9U|987012881134405171
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DNB|139134069
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J9U|987007376324205171
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NTA|375197656
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CAOONL|ncf11499911
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RERO|A025241563
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PTBNP|1571401
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ISNI|000000004058745X
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BNF|14036816
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ISNI|000000008392417X
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W2Z|1533887398036
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ISNI|0000000082016874
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NTA|201947595
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CAOONL|ncf11321833
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BNF|15994435
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LC|n 2006185053
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LC|no2020067363
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BNF|18065689
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CAOONL|ncf12107611
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LC|no2019137032
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LC|n 80104445
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J9U|987007424863105171
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LC|no2016143602
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SUDOC|182491854
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CAOONL|ncf10578327
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SUDOC|255023898
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BIBSYS|3093308
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NUKAT|n 2005019342
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LC|nb2014010545
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NTA|332483096
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LC|nb2023001843
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RERO|A012532244
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997
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0 0 lived 0 0
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1
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