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PRECLINICAL PUBLICATION · 2013

Impaired wound repair in adult endoglin heterozygous mice associated with lower NO bioavailability.

Mouse / Wound

Evidence by therapy association

Study details and outcomes are extracted in the context of a specific intervention. Separate associations are retained rather than silently merged.

PMID 23765132 ↗2013Reported benefit

Impaired wound repair in adult endoglin heterozygous mice associated with lower NO bioavailability.

MouseWoundC57BL/6 endoglin heterozygous null (Eng+/-) and wild-type littermatesFemale

Model: Cutaneous full-thickness skin wound in endoglin heterozygous null mice with reepithelialisation followed for up to 8 days; acute 12-O-tetradecanoylphorbol-13-acetate stimulation used as a separate hyperplasia challenge

Wound area was larger in endoglin heterozygous mice from 2 to 8 days after injury with closure delayed by 1 to 2 days, and the nitric oxide donor LA-803 accelerated wound closure in endoglin heterozygous mice with no effect in normal littermates

Extraction: extract · Supplied extraction confidence: 0.6. Machine-extracted fields require source verification.