Personalized Cystic Fibrosis Therapy and Research Center — Raouf S. Amin (CINCINNATI CHILDRENS HOSP MED CTR)
PROJECT SUMMARY – OVERVIEW Cystic Fibrosis results from the absence or dysfunction of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) chloride channel. Defects in CFTR are strongly asso
| Project title | Personalized Cystic Fibrosis Therapy and Research Center |
|---|---|
| Project number | 5P30DK117467-07 |
| PI name | Raouf S. Amin |
| Institution | CINCINNATI CHILDRENS HOSP MED CTR |
| Funding mechanism | P30 |
| Agency | NIDDK |
| Award amount | $944,438 |
| Fiscal year | 2024 |
| Project start | 2018-08-01T00:00:00 |
| Project end | 2025-06-30T00:00:00 |
| Abstract | PROJECT SUMMARY – OVERVIEW Cystic Fibrosis results from the absence or dysfunction of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) chloride channel. Defects in CFTR are strongly asso |
| Key terms | <21+ years old><Address><Adult><Adult Human><Adverse effects><Applications Grants><Assay><Autograft> |
$799/mo
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