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Archives of Pharmacal Research
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December 7, 2006
Sphingosine kinase assay system with fluorescent detection in high performance liquid chromatography
You-Xun Jin, Hwan-Soo Yoo, Akio Kihara, et al.
Brain & Development
|
December 16, 2019
Novel biallelic FA2H mutations in a Japanese boy with fatty acid hydroxylase-associated neurodegeneration
Masahiro Kawaguchi, Takayuki Sassa, Hiroyuki Kidokoro, et al.
Biochimica Et Biophysica Acta
|
September 24, 2015
Histological analyses by matrix-assisted laser desorption/ionization-imaging mass spectrometry reveal differential localization of sphingomyelin molecular species regulated by particular ceramide synthase in mouse brains
Masayuki Sugimoto, Yoichi Shimizu, Takeshi Yoshioka, et al.
Molecular Biology of the Cell
|
December 4, 2015
A role of the sphingosine-1-phosphate (S1P)-S1P receptor 2 pathway in epithelial defense against cancer (EDAC)
Sayaka Yamamoto, Yuta Yako, Yoichiro Fujioka, et al.
Analytical Biochemistry
|
June 11, 2008
A sphingosine kinase activity assay using direct infusion electrospray ionization tandem mass spectrometry
You-Xun Jin, Lian Hua Shi, Hwan-Soo Yoo, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 12, 2014
Integrin α9 on lymphatic endothelial cells regulates lymphocyte egress
Koyu Ito, Junko Morimoto, Akio Kihara, et al.
Brain & Development
|
April 5, 2022
Hypomyelinating spastic dyskinesia and ichthyosis caused by a homozygous splice site mutation leading to exon skipping in ELOVL1
Taiko Takahashi, Sevcan Mercan, Takayuki Sassa, et al.
Journal of Cell Science
|
April 13, 2019
The very-long-chain fatty acid elongase Elo2 rescues lethal defects associated with loss of the nuclear barrier function in fission yeast cells
Yasuha Kinugasa, Yasuhiro Hirano, Megumi Sawai, 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 atrophy
Noomi Mueller, Takayuki Sassa, Susanne Morales-Gonzalez, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 10, 2015
Essential role of the cytochrome P450 CYP4F22 in the production of acylceramide, the key lipid for skin permeability barrier formation
Yusuke Ohno, Shota Nakamichi, Aya Ohkuni, et al.
Page
of 16
Search research articles
Search
Showing results (131-140 of 154) with videos related to
Sort By:
Page
of 16
Archives of Pharmacal Research
|
December 7, 2006
Sphingosine kinase assay system with fluorescent detection in high performance liquid chromatography
You-Xun Jin, Hwan-Soo Yoo, Akio Kihara, et al.
Brain & Development
|
December 16, 2019
Novel biallelic FA2H mutations in a Japanese boy with fatty acid hydroxylase-associated neurodegeneration
Masahiro Kawaguchi, Takayuki Sassa, Hiroyuki Kidokoro, et al.
Biochimica Et Biophysica Acta
|
September 24, 2015
Histological analyses by matrix-assisted laser desorption/ionization-imaging mass spectrometry reveal differential localization of sphingomyelin molecular species regulated by particular ceramide synthase in mouse brains
Masayuki Sugimoto, Yoichi Shimizu, Takeshi Yoshioka, et al.
Molecular Biology of the Cell
|
December 4, 2015
A role of the sphingosine-1-phosphate (S1P)-S1P receptor 2 pathway in epithelial defense against cancer (EDAC)
Sayaka Yamamoto, Yuta Yako, Yoichiro Fujioka, et al.
Analytical Biochemistry
|
June 11, 2008
A sphingosine kinase activity assay using direct infusion electrospray ionization tandem mass spectrometry
You-Xun Jin, Lian Hua Shi, Hwan-Soo Yoo, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 12, 2014
Integrin α9 on lymphatic endothelial cells regulates lymphocyte egress
Koyu Ito, Junko Morimoto, Akio Kihara, et al.
Brain & Development
|
April 5, 2022
Hypomyelinating spastic dyskinesia and ichthyosis caused by a homozygous splice site mutation leading to exon skipping in ELOVL1
Taiko Takahashi, Sevcan Mercan, Takayuki Sassa, et al.
Journal of Cell Science
|
April 13, 2019
The very-long-chain fatty acid elongase Elo2 rescues lethal defects associated with loss of the nuclear barrier function in fission yeast cells
Yasuha Kinugasa, Yasuhiro Hirano, Megumi Sawai, 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 atrophy
Noomi Mueller, Takayuki Sassa, Susanne Morales-Gonzalez, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 10, 2015
Essential role of the cytochrome P450 CYP4F22 in the production of acylceramide, the key lipid for skin permeability barrier formation
Yusuke Ohno, Shota Nakamichi, Aya Ohkuni, et al.
Page
of 16