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Lise Lotte Hansen
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wetenschapper
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‡c
investigadora
‡9
ast
|
670
|
|
|
‡a
Author's A nine-nucleotide deletion and splice variation in the coding region of the interferon induced ISG12 gene
|
670
|
|
|
‡a
Author's A role for immunohistochemical detection of BRAF V600E prior to BRAF-inhibitor treatment of malignant melanoma?
|
670
|
|
|
‡a
Author's Allelic imbalance in selected chromosomal regions in ovarian cancer
|
670
|
|
|
‡a
Author's Allelic loss of 16q23.2-24.2 is an independent marker of good prognosis in primary breast cancer
|
670
|
|
|
‡a
Author's Assignment of the human translation termination factor 1
|
670
|
|
|
‡a
Author's Assignment of the human translation termination factor 1 (ETF1) to 5q31.1 and of the proximal marker D5S1995 by radiation hybrid mapping
|
670
|
|
|
‡a
Author's Atheroprotective immunization with malondialdehyde-modified LDL is hapten specific and dependent on advanced MDA adducts: implications for development of an atheroprotective vaccine
|
670
|
|
|
‡a
Author's Author's reply: To PMID 23159593.
|
670
|
|
|
‡a
Author's Chromosome 1q25.3 copy number alterations in primary breast cancers detected by multiplex ligation-dependent probe amplification and allelic imbalance assays and its comparison with fluorescent in situ hybridization assays.
|
670
|
|
|
‡a
Author's Competitive amplification of differentially melting amplicons
|
670
|
|
|
‡a
Author's Competitive amplification of differentially melting amplicons (CADMA) enables sensitive and direct detection of all mutation types by high-resolution melting analysis.
|
670
|
|
|
‡a
Author's Competitive amplification of differentially melting amplicons (CADMA) improves KRAS hotspot mutation testing in colorectal cancer
|
670
|
|
|
‡a
Author's Comprehensive Genome Methylation Analysis in Bladder Cancer: Identification and Validation of Novel Methylated Genes and Application of These as Urinary Tumor Markers
|
670
|
|
|
‡a
Author's Copy number variations alter methylation and parallel IGF2 overexpression in adrenal tumors
|
670
|
|
|
‡a
Author's Effect of the FSH receptor single nucleotide polymorphisms
|
670
|
|
|
‡a
Author's Effect of the FSH receptor single nucleotide polymorphisms (FSHR 307/680) on the follicular fluid hormone profile and the granulosa cell gene expression in human small antral follicles
|
670
|
|
|
‡a
Author's ELMO3: a direct driver of cancer metastasis?
|
670
|
|
|
‡a
Author's Epigenetic changes in myelofibrosis: Distinct methylation changes in the myeloid compartments and in cases with ASXL1 mutations
|
670
|
|
|
‡a
Author's Familial cancer associated with a polymorphism in ARLTS1
|
670
|
|
|
‡a
Author's Genotyping common FSHR polymorphisms based on competitive amplification of differentially melting amplicons (CADMA)
|
670
|
|
|
‡a
Author's Germline mutation in RNASEL predicts increased risk of head and neck, uterine cervix and breast cancer
|
670
|
|
|
‡a
Author's Heterogeneity in the clinical phenotype of TP53 mutations in breast cancer patients
|
670
|
|
|
‡a
Author's High-Resolution Melting Analysis for Mutation Screening of RGSL1, RGS16, and RGS8 in Breast Cancer
|
670
|
|
|
‡a
Author's Hypomethylation and increased expression of the putative oncogene ELMO3 are associated with lung cancer development and metastases formation.
|
670
|
|
|
‡a
Author's Identification and characterization of locus-specific methylation patterns within novel loci undergoing hypermethylation during breast cancer pathogenesis.
|
670
|
|
|
‡a
Author's Identification and validation of highly frequent CpG island hypermethylation in colorectal adenomas and carcinomas
|
670
|
|
|
‡a
Author's Identification of accurate reference genes for RT-qPCR analysis of formalin-fixed paraffin-embedded tissue from primary non-small cell lung cancers and brain and lymph node metastases
|
670
|
|
|
‡a
Author's IGHV1-69-encoded antibodies expressed in chronic lymphocytic leukemia react with malondialdehyde-acetaldehyde adduct, an immunodominant oxidation-specific epitope
|
670
|
|
|
‡a
Author's Improved reproducibility in genome-wide DNA methylation analysis for PAXgene-fixed samples compared with restored formalin-fixed and paraffin-embedded DNA.
|
670
|
|
|
‡a
Author's Increased sensitivity of KRAS mutation detection by high-resolution melting analysis of COLD-PCR products
|
670
|
|
|
‡a
Author's LOH rather than genotypes ofTP53codon 72 is associated with disease-free survival in primary breast cancer
|
670
|
|
|
‡a
Author's Methylation of cancer related genes in tumor and peripheral blood DNA from the same breast cancer patient as two independent events
|
670
|
|
|
‡a
Author's Molecular genetic analysis of easily accessible breast tumour DNA, purified from tissue left over from hormone receptor measurement
|
670
|
|
|
‡a
Author's Mutations and polymorphisms in the pyruvate dehydrogenase E1 alpha gene
|
670
|
|
|
‡a
Author's No difference in the frequency of locus-specific methylation in the peripheral blood DNA of women diagnosed with breast cancer and age-matched controls.
|
670
|
|
|
‡a
Author's Polymorphisms in the human X-linked pyruvate dehydrogenase E1 alpha gene
|
670
|
|
|
‡a
Author's Publisher Correction: Epigenetic changes in myelofibrosis: Distinct methylation changes in the myeloid compartments and in cases with ASXL1 mutations
|
670
|
|
|
‡a
Author's Pyruvate dehydrogenase deficiency caused by a 33 base pair duplication in the PDH E1 alpha subunit.
|
670
|
|
|
‡a
Author's Pyruvate dehydrogenase deficiency caused by a 5 base pair duplication in the E1 alpha subunit
|
670
|
|
|
‡a
Author's Refined localization of the pyruvate dehydrogenase E1 alpha gene
|
670
|
|
|
‡a
Author's Refined localization of the pyruvate dehydrogenase E1 alpha gene (PDHA1) by linkage analysis
|
670
|
|
|
‡a
Author's Sensitive and fast mutation detection by solid phase chemical cleavage
|
670
|
|
|
‡a
Author's Size matters: Associations between the androgen receptor CAG repeat length and the intrafollicular hormone milieu.
|
670
|
|
|
‡a
Author's The influence of DNA degradation in formalin-fixed, paraffin-embedded (FFPE) tissue on locus-specific methylation assessment by MS-HRM
|
670
|
|
|
‡a
Author's The role of innate immunity in atherogenesis
|
670
|
|
|
‡a
Author's TP53 mutation is an independent prognostic marker for poor outcome in both node-negative and node-positive breast cancer
|
670
|
|
|
‡a
Author's X-linked pyruvate dehydrogenase E1 alpha subunit deficiency in heterozygous females: variable manifestation of the same mutation
|
909
|
|
|
‡a
(orcid) 0000000179152506
‡9
1
|
919
|
|
|
‡a
effectofthefshreceptorsinglenucleotidepolymorphismsfshr307680onthefollicularfluidhormoneprofileandthegranulosacellgeneexpressioninhumansmallantralfollicles
‡A
Effect of the FSH receptor single nucleotide polymorphisms (FSHR 307/680) on the follicular fluid hormone profile and the granulosa cell gene expression in human small antral follicles
‡9
1
|
919
|
|
|
‡a
mutationsandpolymorphismsinthepyruvatedehydrogenasee1alphagene
‡A
Mutations and polymorphisms in the pyruvate dehydrogenase E1 alpha gene
‡9
1
|
919
|
|
|
‡a
moleculargeneticanalysisofeasilyaccessiblebreasttumourdnapurifiedfromtissueleftoverfromhormonereceptormeasurement
‡A
Molecular genetic analysis of easily accessible breast tumour DNA, purified from tissue left over from hormone receptor measurement
‡9
1
|
919
|
|
|
‡a
effectofthefshreceptorsinglenucleotidepolymorphisms
‡A
Effect of the FSH receptor single nucleotide polymorphisms
‡9
1
|
919
|
|
|
‡a
comprehensivegenomemethylationanalysisinbladdercanceridentificationandvalidationofnovelmethylatedgenesandapplicationoftheseasurinarytumormarkers
‡A
Comprehensive Genome Methylation Analysis in Bladder Cancer: Identification and Validation of Novel Methylated Genes and Application of These as Urinary Tumor Markers
‡9
1
|
919
|
|
|
‡a
polymorphismsinthehuman10linkedpyruvatedehydrogenasee1alphagene
‡A
Polymorphisms in the human X-linked pyruvate dehydrogenase E1 alpha gene
‡9
1
|
919
|
|
|
‡a
publishercorrectionepigeneticchangesinmyelofibrosisdistinctmethylationchangesinthemyeloidcompartmentsandincaseswithasxl1mutations
‡A
Publisher Correction: Epigenetic changes in myelofibrosis: Distinct methylation changes in the myeloid compartments and in cases with ASXL1 mutations
‡9
1
|
919
|
|
|
‡a
copynumbervariationsaltermethylationandparalleligf2overexpressioninadrenaltumors
‡A
Copy number variations alter methylation and parallel IGF2 overexpression in adrenal tumors
‡9
1
|
919
|
|
|
‡a
chromosome1q253copynumberalterationsinprimarybreastcancersdetectedbymultiplexligationdependentprobeamplificationandallelicimbalanceassaysanditscomparisonwithfluorescentinsituhybridizationassays
‡A
Chromosome 1q25.3 copy number alterations in primary breast cancers detected by multiplex ligation-dependent probe amplification and allelic imbalance assays and its comparison with fluorescent in situ hybridization assays.
‡9
1
|
919
|
|
|
‡a
identificationofaccuratereferencegenesforrtqpcranalysisofformalinfixedparaffinembeddedtissuefromprimarynonsmallcelllungcancersandbrainandlymphnodemetastases
‡A
Identification of accurate reference genes for RT-qPCR analysis of formalin-fixed paraffin-embedded tissue from primary non-small cell lung cancers and brain and lymph node metastases
‡9
1
|
919
|
|
|
‡a
ighv169encodedantibodiesexpressedinchroniclymphocyticleukemiareactwithmalondialdehydeacetaldehydeadductanimmunodominantoxidationspecificepitope
‡A
IGHV1-69-encoded antibodies expressed in chronic lymphocytic leukemia react with malondialdehyde-acetaldehyde adduct, an immunodominant oxidation-specific epitope
‡9
1
|
919
|
|
|
‡a
pyruvatedehydrogenasedeficiencycausedbya33basepairduplicationinthepdhe1alphasubunit
‡A
Pyruvate dehydrogenase deficiency caused by a 33 base pair duplication in the PDH E1 alpha subunit.
‡9
1
|
919
|
|
|
‡a
pyruvatedehydrogenasedeficiencycausedbya5basepairduplicationinthee1alphasubunit
‡A
Pyruvate dehydrogenase deficiency caused by a 5 base pair duplication in the E1 alpha subunit
‡9
1
|
919
|
|
|
‡a
refinedlocalizationofthepyruvatedehydrogenasee1alphagene
‡A
Refined localization of the pyruvate dehydrogenase E1 alpha gene
‡9
1
|
919
|
|
|
‡a
refinedlocalizationofthepyruvatedehydrogenasee1alphagenepdha1bylinkageanalysis
‡A
Refined localization of the pyruvate dehydrogenase E1 alpha gene (PDHA1) by linkage analysis
‡9
1
|
919
|
|
|
‡a
improvedreproducibilityingenomewidednamethylationanalysisforpaxgenefixedsamplescomparedwithrestoredformalinfixedandparaffinembeddeddna
‡A
Improved reproducibility in genome-wide DNA methylation analysis for PAXgene-fixed samples compared with restored formalin-fixed and paraffin-embedded DNA.
‡9
1
|
919
|
|
|
‡a
identificationandcharacterizationoflocusspecificmethylationpatternswithinnovellociundergoinghypermethylationduringbreastcancerpathogenesis
‡A
Identification and characterization of locus-specific methylation patterns within novel loci undergoing hypermethylation during breast cancer pathogenesis.
‡9
1
|
919
|
|
|
‡a
increasedsensitivityofkrasmutationdetectionbyhighresolutionmeltinganalysisofcoldpcrproducts
‡A
Increased sensitivity of KRAS mutation detection by high-resolution melting analysis of COLD-PCR products
‡9
1
|
919
|
|
|
‡a
lohratherthangenotypesoftp53codon72isassociatedwithdiseasefreesurvivalinprimarybreastcancer
‡A
LOH rather than genotypes ofTP53codon 72 is associated with disease-free survival in primary breast cancer
‡9
1
|
919
|
|
|
‡a
methylationofcancerrelatedgenesintumorandperipheralblooddnafromthesamebreastcancerpatientas2independentevents
‡A
Methylation of cancer related genes in tumor and peripheral blood DNA from the same breast cancer patient as two independent events
‡9
1
|
919
|
|
|
‡a
sensitiveandfastmutationdetectionbysolidphasechemicalcleavage
‡A
Sensitive and fast mutation detection by solid phase chemical cleavage
‡9
1
|
919
|
|
|
‡a
sizemattersassociationsbetweentheandrogenreceptorcagrepeatlengthandtheintrafollicularhormonemilieu
‡A
Size matters: Associations between the androgen receptor CAG repeat length and the intrafollicular hormone milieu.
‡9
1
|
919
|
|
|
‡a
hypomethylationandincreasedexpressionoftheputativeoncogeneelmo3areassociatedwithlungcancerdevelopmentandmetastasesformation
‡A
Hypomethylation and increased expression of the putative oncogene ELMO3 are associated with lung cancer development and metastases formation.
‡9
1
|
919
|
|
|
‡a
highresolutionmeltinganalysisformutationscreeningofrgsl1rgs16andrgs8inbreastcancer
‡A
High-Resolution Melting Analysis for Mutation Screening of RGSL1, RGS16, and RGS8 in Breast Cancer
‡9
1
|
919
|
|
|
‡a
roleofinnateimmunityinatherogenesis
‡A
The role of innate immunity in atherogenesis
‡9
1
|
919
|
|
|
‡a
tp53mutationisanindependentprognosticmarkerforpooroutcomeinbothnodenegativeandnodepositivebreastcancer
‡A
TP53 mutation is an independent prognostic marker for poor outcome in both node-negative and node-positive breast cancer
‡9
1
|
919
|
|
|
‡a
assignmentofthehumantranslationterminationfactor1etf1to5q311andoftheproximalmarkerd5s1995byradiationhybridmapping
‡A
Assignment of the human translation termination factor 1 (ETF1) to 5q31.1 and of the proximal marker D5S1995 by radiation hybrid mapping
‡9
1
|
919
|
|
|
‡a
heterogeneityintheclinicalphenotypeoftp53mutationsinbreastcancerpatients
‡A
Heterogeneity in the clinical phenotype of TP53 mutations in breast cancer patients
‡9
1
|
919
|
|
|
‡a
assignmentofthehumantranslationterminationfactor1
‡A
Assignment of the human translation termination factor 1
‡9
1
|
919
|
|
|
‡a
germlinemutationinrnaselpredictsincreasedriskofheadandneckuterinecervixandbreastcancer
‡A
Germline mutation in RNASEL predicts increased risk of head and neck, uterine cervix and breast cancer
‡9
1
|
919
|
|
|
‡a
genotypingcommonfshrpolymorphismsbasedoncompetitiveamplificationofdifferentiallymeltingampliconscadma
‡A
Genotyping common FSHR polymorphisms based on competitive amplification of differentially melting amplicons (CADMA)
‡9
1
|
919
|
|
|
‡a
influenceofdnadegradationinformalinfixedparaffinembeddedffpetissueonlocusspecificmethylationassessmentbymshrm
‡A
The influence of DNA degradation in formalin-fixed, paraffin-embedded (FFPE) tissue on locus-specific methylation assessment by MS-HRM
‡9
1
|
919
|
|
|
‡a
alleliclossof16q232242isanindependentmarkerofgoodprognosisinprimarybreastcancer
‡A
Allelic loss of 16q23.2-24.2 is an independent marker of good prognosis in primary breast cancer
‡9
1
|
919
|
|
|
‡a
allelicimbalanceinselectedchromosomalregionsinovariancancer
‡A
Allelic imbalance in selected chromosomal regions in ovarian cancer
‡9
1
|
919
|
|
|
‡a
roleforimmunohistochemicaldetectionofbrafv600epriortobrafinhibitortreatmentofmalignantmelanoma
‡A
A role for immunohistochemical detection of BRAF V600E prior to BRAF-inhibitor treatment of malignant melanoma?
‡9
1
|
919
|
|
|
‡a
9nucleotidedeletionandsplicevariationinthecodingregionoftheinterferoninducedisg12gene
‡A
A nine-nucleotide deletion and splice variation in the coding region of the interferon induced ISG12 gene
‡9
1
|
919
|
|
|
‡a
competitiveamplificationofdifferentiallymeltingamplicons
‡A
Competitive amplification of differentially melting amplicons
‡9
1
|
919
|
|
|
‡a
familialcancerassociatedwithapolymorphisminarlts1
‡A
Familial cancer associated with a polymorphism in ARLTS1
‡9
1
|
919
|
|
|
‡a
atheroprotectiveimmunizationwithmalondialdehydemodifiedldlishaptenspecificanddependentonadvancedmdaadductsimplicationsfordevelopmentofanatheroprotectivevaccine
‡A
Atheroprotective immunization with malondialdehyde-modified LDL is hapten specific and dependent on advanced MDA adducts: implications for development of an atheroprotective vaccine
‡9
1
|
919
|
|
|
‡a
10linkedpyruvatedehydrogenasee1alphasubunitdeficiencyinheterozygousfemalesvariablemanifestationofthesamemutation
‡A
X-linked pyruvate dehydrogenase E1 alpha subunit deficiency in heterozygous females: variable manifestation of the same mutation
‡9
1
|
919
|
|
|
‡a
epigeneticchangesinmyelofibrosisdistinctmethylationchangesinthemyeloidcompartmentsandincaseswithasxl1mutations
‡A
Epigenetic changes in myelofibrosis: Distinct methylation changes in the myeloid compartments and in cases with ASXL1 mutations
‡9
1
|
919
|
|
|
‡a
competitiveamplificationofdifferentiallymeltingampliconscadmaenablessensitiveanddirectdetectionofallmutationtypesbyhighresolutionmeltinganalysis
‡A
Competitive amplification of differentially melting amplicons (CADMA) enables sensitive and direct detection of all mutation types by high-resolution melting analysis.
‡9
1
|
919
|
|
|
‡a
authorsreplytopmid23159593
‡A
Author's reply: To PMID 23159593.
‡9
1
|
919
|
|
|
‡a
identificationandvalidationofhighlyfrequentcpgislandhypermethylationincolorectaladenomasandcarcinomas
‡A
Identification and validation of highly frequent CpG island hypermethylation in colorectal adenomas and carcinomas
‡9
1
|
919
|
|
|
‡a
competitiveamplificationofdifferentiallymeltingampliconscadmaimproveskrashotspotmutationtestingincolorectalcancer
‡A
Competitive amplification of differentially melting amplicons (CADMA) improves KRAS hotspot mutation testing in colorectal cancer
‡9
1
|
919
|
|
|
‡a
nodifferenceinthefrequencyoflocusspecificmethylationintheperipheralblooddnaofwomendiagnosedwithbreastcancerandagematchedcontrols
‡A
No difference in the frequency of locus-specific methylation in the peripheral blood DNA of women diagnosed with breast cancer and age-matched controls.
‡9
1
|
919
|
|
|
‡a
elmo3adirectdriverofcancermetastasis
‡A
ELMO3: a direct driver of cancer metastasis?
‡9
1
|
946
|
|
|
‡a
a
‡9
1
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996
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JPG|500143948
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LC|no2018149094
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LIH|LNB:_b_JI;=BL
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996
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LC|n 2009076198
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BIBSYS|90352800
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ISNI|0000000046276003
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DNB|138521514
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LC|no2022063672
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ISNI|000000008138355X
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NSK|000237616
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DBC|87097968981905
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BIBSYS|90527065
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DBC|87097919246965
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DBC|87097919374548
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ISNI|0000000075874862
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NII|DA08304086
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NTA|086635972
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DBC|87097992424014
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DBC|87097968095379
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PLWABN|9812829524505606
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BIBSYS|97014629
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BIBSYS|90252333
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ISNI|0000000481256621
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DBC|87097968392217
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J9U|987008729297805171
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DBC|87097962785063
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DNB|1066611726
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RERO|A009049384
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LC|no2023130984
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NKC|jo20191026817
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DBC|870979138790738
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DNB|1058349015
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LC|no2002033061
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LC|n 2012026586
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DBC|87097962614773
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LC|n 98004925
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BIBSYS|1060368
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DBC|87097968537487
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BIBSYS|13048593
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DBC|87097968162661
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BNC|981058612191206706
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ISNI|0000000054721488
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SUDOC|074543482
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DBC|87097968392349
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PLWABN|9810642824105606
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NTA|071377255
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SUDOC|26606647X
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LC|nb2005009130
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RERO|A003346564
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BIBSYS|14010479
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DBC|87097969843093
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BIBSYS|1642068437332
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DNB|1057533122
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BIBSYS|99067533
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BIBSYS|1052930
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DNB|11899719X
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BIBSYS|11037701
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996
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LC|no2016072911
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DBC|87097968397685
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DBC|87097919105393
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996
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BIBSYS|4001150
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BIBSYS|15041231
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996
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W2Z|1479731351118
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996
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DNB|1347887954
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996
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LC|nr 94007889
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996
|
|
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BIBSYS|5092983
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996
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|
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J9U|987012469332105171
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996
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DBC|87097968397693
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996
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NTA|072277211
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LC|no2020027067
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SUDOC|157037851
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|
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W2Z|1642068437332
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996
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DBC|87097946414977
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996
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DBC|87097968392330
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DNB|116332476
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ISNI|0000000117288627
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ISNI|0000000444841530
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DBC|87097939373084
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996
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ISNI|0000000513307754
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DBC|87097969978487
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996
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LC|n 2024064242
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PLWABN|9813276154405606
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NTA|442538472
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BIBSYS|41894
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996
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LC|n 97051174
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W2Z|4029290
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DNB|1158262981
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NTA|432212833
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LC|nb2004310268
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W2Z|13057607
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996
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|
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CAOONL|ncf10163810
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996
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|
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BIBSYS|15330
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|
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DBC|87097969558844
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LC|no2008094050
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BIBSYS|4074370
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LC|n 79021676
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J9U|987007299340405171
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|
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DNB|171740688
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J9U|987007461441705171
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996
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ISNI|0000000365440077
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DBC|87097919103080
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|
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SELIBR|199332
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|
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ISNI|0000000055541972
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NUKAT|n 02062614
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CAOONL|ncf10224782
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996
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|
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BIBSYS|99058370
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996
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|
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LC|n 2008077474
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|
|
|
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DBC|87097968159482
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996
|
|
|
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W2Z|90352800
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996
|
|
|
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KRNLK|KAC200912469
|
996
|
|
|
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J9U|987012749347805171
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996
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|
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NUKAT|n 2011113262
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996
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ISNI|0000000432733778
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|
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BIBSYS|7033936
|
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|
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BIBSYS|4050397
|
996
|
|
|
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BIBSYS|90860850
|
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|
|
|
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DBC|87097968397499
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996
|
|
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LC|n 86098146
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|
|
|
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SUDOC|167648799
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996
|
|
|
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LC|n 96120945
|
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|
|
|
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BIBSYS|1067479
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996
|
|
|
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DBC|87097969308783
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996
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|
|
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RERO|A027724363
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996
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|
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DNB|1017190879
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|
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BIBSYS|1092817
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DBC|87097948651216
|
996
|
|
|
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DNB|117123385X
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996
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|
|
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BIBSYS|4105981
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|
|
|
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ISNI|0000000074862448
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|
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BIBSYS|90951274
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996
|
|
|
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SUDOC|198594895
|
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|
|
|
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BNE|XX1416308
|
996
|
|
|
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DNB|116455527
|
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|
|
|
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DBC|870979137453207
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996
|
|
|
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BIBSYS|97014459
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996
|
|
|
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NUKAT|n 2012244313
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|
|
|
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ISNI|0000000481144005
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|
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RERO|A027526758
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|
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ISNI|0000000035058836
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BIBSYS|11039731
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BIBSYS|5058070
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NUKAT|n 2004039797
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BIBSYS|13004455
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996
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|
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BIBSYS|99015626
|
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|
|
|
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ISNI|0000000486324283
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|
|
|
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ISNI|0000000485672956
|
996
|
|
|
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NUKAT|n 2019214201
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996
|
|
|
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CAOONL|ncf11633927
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996
|
|
|
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LC|n 85119693
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ISNI|0000000082137553
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BIBSYS|4107229
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DBC|87097968085063
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996
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|
|
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DBC|87097968397707
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996
|
|
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ISNI|0000000035252399
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|
|
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LC|n 2023052458
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|
|
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DNB|1293523380
|
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|
|
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BIBSYS|9050658
|
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|
|
|
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LC|n 2012052969
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|
|
|
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BIBSYS|11003874
|
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|
|
|
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DBC|87097946660838
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996
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|
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BNF|15087099
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|
|
|
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BIBSYS|3013801
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|
|
|
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DBC|87097969267815
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996
|
|
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DBC|870979135444774
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996
|
|
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BIBSYS|4029290
|
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|
|
|
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BIBSYS|90744000
|
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|
|
|
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LC|n 88178932
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|
|
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LC|no2008096853
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996
|
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BIBSYS|3112817
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|
|
|
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BIBSYS|11056662
|
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|
|
|
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DNB|134612973
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996
|
|
|
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BIBSYS|1045032
|
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|
|
|
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PLWABN|9813318184605606
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997
|
|
|
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0 0 lived 0 0
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1
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