Associated Papers
CERT1 mutations perturb human development by disrupting sphingolipid homeostasis.
Gehin C et al.
The Journal of Clinical Investigation, 2023
Involvement of a Cluster of Basic Amino Acids in Phosphorylation-Dependent Functional Repression of the Ceramide Transport Protein CERT.
Goto A et al.
International Journal of Molecular Sciences, 2022
Intellectual disability-associated gain-of-function mutations in CERT1 that encodes the ceramide transport protein CERT.
Murakami H et al.
Plos One, 2020
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