Search
Leader | 00000nz a2200037n 45 0 | ||
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001 | WKP|Q59840436 (VIAF cluster) (Authority/Source Record) | ||
003 | WKP | ||
005 | 20241121000214.0 | ||
008 | 241121nneanz||abbn n and d | ||
035 | ‡a (WKP)Q59840436 | ||
024 | ‡a 0000-0002-7241-9607 ‡2 orcid | ||
035 | ‡a (OCoLC)Q59840436 | ||
100 | 0 | ‡a Ngoc B Lu-Nguyen ‡c researcher ORCID ID = 0000-0002-7241-9607 ‡9 en | |
400 | 0 | ‡a Ngoc B Lu-Nguyen ‡c wetenschapper ‡9 nl | |
670 | ‡a Author's Combination Antisense Treatment for Destructive Exon Skipping of Myostatin and Open Reading Frame Rescue of Dystrophin in Neonatal mdx Mice. | ||
670 | ‡a Author's Efficient Expression of Igf-1 from Lentiviral Vectors Protects In Vitro but Does Not Mediate Behavioral Recovery of a Parkinsonian Lesion in Rats. | ||
670 | ‡a Author's Functional Rescue of Dystrophin Deficiency in Mice Caused by Frameshift Mutations Using Campylobacter jejuni Cas9 | ||
670 | ‡a Author's Intrastriatal Delivery of Integration-Deficient Lentiviral Vectors in a Rat Model of Parkinson's Disease. | ||
670 | ‡a Author's Systemic Antisense Therapeutics for Dystrophin and Myostatin Exon Splice Modulation Improve Muscle Pathology of Adult mdx Mice | ||
670 | ‡a Author's Targeting TGFβ Signaling to Address Fibrosis Using Antisense Oligonucleotides | ||
670 | ‡a Author's Transgenic expression of human glial cell line-derived neurotrophic factor from integration-deficient lentiviral vectors is neuroprotective in a rodent model of Parkinson's disease | ||
909 | ‡a (orcid) 0000000272419607 ‡9 1 | ||
919 | ‡a efficientexpressionofigf1fromlentiviralvectorsprotectsinvitrobutdoesnotmediatebehavioralrecoveryofaparkinsonianlesioninrats ‡A Efficient Expression of Igf-1 from Lentiviral Vectors Protects In Vitro but Does Not Mediate Behavioral Recovery of a Parkinsonian Lesion in Rats. ‡9 1 | ||
919 | ‡a targetingtgfβsignalingtoaddressfibrosisusingantisenseoligonucleotides ‡A Targeting TGFβ Signaling to Address Fibrosis Using Antisense Oligonucleotides ‡9 1 | ||
919 | ‡a systemicantisensetherapeuticsfordystrophinandmyostatinexonsplicemodulationimprovemusclepathologyofadult1510mice ‡A Systemic Antisense Therapeutics for Dystrophin and Myostatin Exon Splice Modulation Improve Muscle Pathology of Adult mdx Mice ‡9 1 | ||
919 | ‡a intrastriataldeliveryofintegrationdeficientlentiviralvectorsinaratmodelofparkinsonsdisease ‡A Intrastriatal Delivery of Integration-Deficient Lentiviral Vectors in a Rat Model of Parkinson's Disease. ‡9 1 | ||
919 | ‡a functionalrescueofdystrophindeficiencyinmicecausedbyframeshiftmutationsusingcampylobacterjejunicas9 ‡A Functional Rescue of Dystrophin Deficiency in Mice Caused by Frameshift Mutations Using Campylobacter jejuni Cas9 ‡9 1 | ||
919 | ‡a combinationantisensetreatmentfordestructiveexonskippingofmyostatinandopenreadingframerescueofdystrophininneonatal1510mice ‡A Combination Antisense Treatment for Destructive Exon Skipping of Myostatin and Open Reading Frame Rescue of Dystrophin in Neonatal mdx Mice. ‡9 1 | ||
919 | ‡a transgenicexpressionofhumanglialcelllinederivedneurotrophicfactorfromintegrationdeficientlentiviralvectorsisneuroprotectiveinarodentmodelofparkinsonsdisease ‡A Transgenic expression of human glial cell line-derived neurotrophic factor from integration-deficient lentiviral vectors is neuroprotective in a rodent model of Parkinson's disease ‡9 1 | ||
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997 | ‡a 0 0 lived 0 0 ‡9 1 |