Mutation of CERKL, a Novel Human Ceramide Kinase Gene, Causes Autosomal Recessive Retinitis Pigmentosa (RP26)

The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools

Julie Thompson · Nucleic Acids Research · 1997 · 39.2K citations · Full text

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Online Mendelian Inheritance in Man 'OMIM'.

Sangeeta Amladi · PubMed · 2007 · 870 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I

Jennifer L. Dawkins, D J Hulme, Sonal Brahmbhatt et al. · Nature Genetics · 2001 · 422 citations

Life Sciences, Genetics, Molecular Genetics +9

Ceramide Kinase, a Novel Lipid Kinase

Masako Sugiura, Keita Kono, Hong Liu et al. · Journal of Biological Chemistry · 2002 · 297 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +9

Ceramide Kinase Mediates Cytokine- and Calcium Ionophore-induced Arachidonic Acid Release

Benjamin J. Pettus, Alicja Bielawska, Sarah Spiegel et al. · Journal of Biological Chemistry · 2003 · 212 citations · Full text

Life Sciences, Biochemistry, Cell Biology +17