Tier 3 — preclinical
NAD+ repletion improves muscle function in muscular dystrophy and counters global PARylation
Science translational medicine
2016
8; 361; 361ra139
Bibliography
- PubMed
- PMID 27798264
- PubMed Central
- PMC5535761
- Funding
- Indexed grant support includes NIA NIH HHS, NIAMS NIH HHS. The complete funding declaration is not specified in the accessible abstract.
- Competing interests
- A complete competing-interest declaration is not specified in the accessible publication information.
Study snapshot
| Design | Preclinical animal study with supporting assays as applicable |
|---|---|
| Model | Mice, C. elegans and human transcript datasets |
| Sample | Mouse and worm muscular-dystrophy models; supporting human transcript data |
| Intervention | Dietary NR and NAD+ pathway analysis |
| Duration | Model-specific disease experiments |
| Endpoints | Model-specific physiological outcomes; Biochemical or functional measures reported in the study |
What the study showed, in plain terms
Key findings
What this study can and cannot tell us
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