Mutations in the Yeast LCB1 and LCB2Genes, Including Those Corresponding to the Hereditary Sensory Neuropathy Type I Mutations, Dominantly Inactivate Serine Palmitoyltransferase
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference34 articles.
1. SPTLC1 is mutated in hereditary sensory neuropathy, type 1
2. Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I
3. Roles of lipid rafts in membrane transport
4. Ceramide in the eukaryotic stress response
5. Enzymes of Sphingolipid Metabolism: From Modular to Integrative Signaling
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