The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Lentiviral-mediated silencing of SOD1 through RNA interference retards disease onset and progression in a mouse model of ALS
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Cites
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Converging Mechanisms in ALS and FTD: Disrupted RNA and Protein Homeostasis
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Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons
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Molecular biology of amyotrophic lateral sclerosis: insights from genetics
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Antisense oligonucleotide therapy for neurodegenerative disease
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Antisense Oligonucleotide Therapies for Neurodegenerative Diseases
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Amyotrophic lateral sclerosis: translating genetic discoveries into therapies
Akçimen, F., Lopez, E. R., Landers, J. E., Nath, A., Chiò, A., Chia, R., & Traynor, B. J. (2023) · Nature Reviews Genetics · doi:10.1038/s41576-023-00592-y · Cited by 234
In vivo genome editing improves motor function and extends survival in a mouse model of ALS
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Metadata
- Authors
- Raoul, C., Abbas-Terki, T., Bensadoun, J.-C., Guillot, S., Haase, G., Szulc, J., Henderson, C. E., & Aebischer, P.
- Venue
- Nature Medicine
- Published
- 2005-03-13
- Volume
- 11
- Issue
- 4
- Pages
- 423-428
- ISSN
- 1078-8956 (ISSN-L)
- 1546-170X
- OpenAlex
- W1979837223
- Cited by
- 464
- References
- 2
- FWCI
- 31.06
- Type
- journal article
- Language
- en
- Open access
- green
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
