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Iscience|October 8, 2021
Erratum: Diverse meibum lipids produced by Awat1 and Awat2 are important for stabilizing tear film and protecting the ocular surfaceMegumi Sawai, Keisuke Watanabe, Kana Tanaka, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|August 8, 2018
Neural symptoms in a gene knockout mouse model of Sjögren-Larsson syndrome are associated with a decrease in 2-hydroxygalactosylceramideTsukasa Kanetake, Takayuki Sassa, Koki Nojiri, et al.
Iscience|June 11, 2021
Diverse meibum lipids produced by Awat1 and Awat2 are important for stabilizing tear film and protecting the ocular surfaceMegumi Sawai, Keisuke Watanabe, Kana Tanaka, et al.
The Journal of Biological Chemistry|August 9, 2017
The 3-hydroxyacyl-CoA dehydratases HACD1 and HACD2 exhibit functional redundancy and are active in a wide range of fatty acid elongation pathwaysMegumi Sawai, Yukiko Uchida, Yusuke Ohno, et al.
The Journal of Dermatology|January 25, 2021
Comprehensive stratum corneum ceramide profiling reveals reduced acylceramides in ichthyosis patient with CERS3 mutationsMoe Yamamoto, Takayuki Sassa, Yuki Kyono, et al.
Journal of Dermatological Science|August 16, 2022
Ceramide profiling of stratum corneum in Sjögren-Larsson syndromeAyami Arai, Takuya Takeichi, Hiroyuki Wakamoto, et al.
Plos One|July 5, 2013
Cooperative Synthesis of Ultra Long-Chain Fatty Acid and Ceramide during Keratinocyte DifferentiationYukiko Mizutani, Hui Sun, Yusuke Ohno, et al.
Cell|September 10, 2009
The F-BAR domain of srGAP2 induces membrane protrusions required for neuronal migration and morphogenesisSabrice Guerrier, Jaeda Coutinho-Budd, Takayuki Sassa, et al.
Journal of Medical Genetics|November 30, 2018
De novo mutation in <i>ELOVL1</i> causes ichthyosis, <i>acanthosis nigricans</i>, hypomyelination, spastic paraplegia, high frequency deafness and optic atrophyNoomi Mueller, Takayuki Sassa, Susanne Morales-Gonzalez, et al.
Brain & Development|April 5, 2022
Hypomyelinating spastic dyskinesia and ichthyosis caused by a homozygous splice site mutation leading to exon skipping in ELOVL1Taiko Takahashi, Sevcan Mercan, Takayuki Sassa, et al.
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