Generation of iPSC lines from hereditary spastic paraplegia 56 (SPG56) patients and family members carrying CYP2U1 mutations
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,General Medicine
Reference6 articles.
1. CYP2U1, a novel human thymus- and brain-specific cytochrome P450, catalyzes omega- and (omega-1)-hydroxylation of fatty acids;Chuang;J. Biol. Chem.,2004
2. CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56;Durand;Hum. Mutat.,2018
3. Xenobiotic-metabolizing enzymes and transporters in the normal human brain: regional and cellular mapping as a basis for putative roles in cerebral function;Dutheil;Drug Metab. Dispos.,2009
4. Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms;Fink;Acta Neuropathol.,2013
5. Characterization and tissue distribution of a novel human cytochrome P450-CYP2U1;Karlgren;Biochem. Biophys. Res. Commun.,2004
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