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Disruption of the Sjögren-Larsson Syndrome Gene Aldh3a2 in Mice Increases Keratinocyte Growth and Retards Skin Barrier Recovery

The fatty aldehyde dehydrogenase (FALDH) ALDH3A2 is the causative gene of Sjögren Larsson syndrome (SLS). To date, the molecular mechanism underlying the symptoms characterizing SLS has been poorly understood. Using Aldh3a2(−/−) mice, we found here that Aldh3a2 was the major FALDH active in undiffer...

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Publicado en:J Biol Chem
Autores principales: Naganuma, Tatsuro, Takagi, Shuyu, Kanetake, Tsukasa, Kitamura, Takuya, Hattori, Satoko, Miyakawa, Tsuyoshi, Sassa, Takayuki, Kihara, Akio
Formato: Artigo
Lenguaje:Inglês
Publicado: American Society for Biochemistry and Molecular Biology 2016
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4882436/
https://ncbi.nlm.nih.gov/pubmed/27053112
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M116.714030
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