Abstract
The circulating and tissue-bound forms of follistatin (FST315 and FST288, respectively) modulate the actions of activins. FST knockout (KO/null) mice, lacking both isoforms, die perinatally with defects in lung, skin, and the musculoskeletal system. Using constructs of the human FST gene engineered to enable expression of each isoform under the control of natural regulatory elements, transgenic mouse lines were created and crossed with FST null mice to attempt to rescue the neonatal lethality.........
| Original language | English |
|---|---|
| Pages (from-to) | 415 - 429 |
| Number of pages | 14 |
| Journal | Molecular Endocrinology |
| Volume | 22 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 2008 |
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