VIAF

Virtual International Authority File

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Leader     00000nz a2200037n 45 0
001     WKP|Q57044933  (VIAF cluster)  (Authority/Source Record)
003     WKP
005     20241121000327.0
008     241121nneanz||abbn n and d
035 ‎‡a  (WKP)Q57044933‏
024 ‎‡a  0000-0002-9961-4293‏ ‎‡2  orcid‏
024 ‎‡a  7202838151‏ ‎‡2  scopus‏
035 ‎‡a  (OCoLC)Q57044933‏
100 0 ‎‡a  Linda M Peters‏ ‎‡c  researcher‏ ‎‡9  en‏
375 ‎‡a  2‏ ‎‡2  iso5218‏
400 0 ‎‡a  Linda M Peters‏ ‎‡c  wetenschapper‏ ‎‡9  nl‏
670 ‎‡a  Author's A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1.‏
670 ‎‡a  Author's Development of a qPCR Method to Measure Mitochondrial and Genomic DNA Damage with Application to Chemotherapy-Induced DNA Damage and Cryopreserved Cells‏
670 ‎‡a  Author's Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function‏
670 ‎‡a  Author's Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse‏
670 ‎‡a  Author's Signatures from tissue-specific MPSS libraries identify transcripts preferentially expressed in the mouse inner ear.‏
909 ‎‡a  (orcid) 0000000299614293‏ ‎‡9  1‏
909 ‎‡a  (scopus) 7202838151‏ ‎‡9  1‏
919 ‎‡a  locusforautosomaldominantprogressivenonsyndromichearinglossdfna27isonchromosome4q12131‏ ‎‡A  A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1.‏ ‎‡9  1‏
919 ‎‡a  developmentofaqpcrmethodtomeasuremitochondrialandgenomicdnadamagewithapplicationtochemotherapyinduceddnadamageandcryopreservedcells‏ ‎‡A  Development of a qPCR Method to Measure Mitochondrial and Genomic DNA Damage with Application to Chemotherapy-Induced DNA Damage and Cryopreserved Cells‏ ‎‡9  1‏
919 ‎‡a  dominantandrecessivedeafnesscausedbymutationsofanovelgenetmc1requiredforcochlearhaircellfunction‏ ‎‡A  Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function‏ ‎‡9  1‏
919 ‎‡a  mutationsingrxcr1arethebasisforinnereardysfunctioninthepirouettemouse‏ ‎‡A  Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse‏ ‎‡9  1‏
919 ‎‡a  signaturesfromtissuespecificmpsslibrariesidentifytranscriptspreferentiallyexpressedinthemouseinnerear‏ ‎‡A  Signatures from tissue-specific MPSS libraries identify transcripts preferentially expressed in the mouse inner ear.‏ ‎‡9  1‏
946 ‎‡a  a‏ ‎‡9  1‏
996 ‎‡2  DNB|1097760286
996 ‎‡2  NTA|23468044X
996 ‎‡2  SZ|1097760286
996 ‎‡2  LC|n 2005032760
996 ‎‡2  NTA|067905374
996 ‎‡2  NTA|073983578
996 ‎‡2  LC|no2023051114
996 ‎‡2  ISNI|0000000460003449
996 ‎‡2  ISNI|0000000451684799
996 ‎‡2  ISNI|0000000392873409
996 ‎‡2  NTA|407740783
996 ‎‡2  NTA|426491157
996 ‎‡2  ISNI|0000000397172337
996 ‎‡2  LC|no2023076536
996 ‎‡2  NTA|315863986
996 ‎‡2  NTA|074397788
996 ‎‡2  NTA|282418954
996 ‎‡2  ISNI|0000000049288472
996 ‎‡2  NTA|237395355
996 ‎‡2  BAV|495_333908
996 ‎‡2  LC|no2009189237
996 ‎‡2  NTA|07184435X
996 ‎‡2  ISNI|000000005457617X
996 ‎‡2  ISNI|0000000388453022
996 ‎‡2  ISNI|000000039576075X
996 ‎‡2  J9U|987007393022505171
996 ‎‡2  LC|n 95034208
996 ‎‡2  LC|nr 96037135
996 ‎‡2  B2Q|0000801600
996 ‎‡2  DNB|105105732
996 ‎‡2  LIH|LNB:3_y_M;=B_f_
996 ‎‡2  LNB|LNC10-000108065
996 ‎‡2  NTA|072645881
996 ‎‡2  DNB|135909724
996 ‎‡2  LC|nb2013019667
996 ‎‡2  NUKAT|n 2012109918
996 ‎‡2  LC|n 93000625
996 ‎‡2  DNB|1051384419
996 ‎‡2  ISNI|0000000067222709
996 ‎‡2  ISNI|0000000119117880
996 ‎‡2  CAOONL|ncf10909014
996 ‎‡2  RERO|A022897208
996 ‎‡2  LC|n 80062543
996 ‎‡2  ISNI|0000000425396013
996 ‎‡2  LC|n 82096736
996 ‎‡2  ISNI|000000002149723X
996 ‎‡2  DNB|135164540
996 ‎‡2  LC|no2018010828
996 ‎‡2  NTA|272748188
997 ‎‡a  0 0 lived 0 0‏ ‎‡9  1‏