Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2022 Dec 2;16:4127–4138. doi: 10.2147/DDDT.S393122

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© 2022 Kang et al.

This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).

PMC Copyright notice

Gross view of skin lesions from rosacea-like mice model. (A) The back skin performance of mice injected intradermally with LL-37 or 0.9% normal saline and injected intraperitoneally with thalidomide or 0.9% normal saline. Images were captured before each injection (Scale Bar=5mm). (B) The severity of the rosacea-like phenotype was assessed based on the area of lesions (n=5 for each group). With the extension of LL-37 induction time, the area of dorsal skin lesions gradually increased, while that with the intraperitoneal injection of thalidomide was significantly reduced compared with 0.9% normal saline.