Search
Leader | 00000nz a2200037n 45 0 | ||
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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 |