Hiroko Hama
Affiliations: | Medical University of South Carolina, Charleston, SC, United States |
Area:
Biochemistry, Neuroscience BiologyGoogle:
"Hiroko Hama"Mean distance: 53433
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Publications
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| Kota V, Hama H. (2014) 2'-Hydroxy ceramide in membrane homeostasis and cell signaling. Advances in Biological Regulation. 54: 223-30 |
| Scheid I, Maruani A, Huguet G, et al. (2013) Heterozygous FA2H mutations in autism spectrum disorders. Bmc Medical Genetics. 14: 124 |
| Kota V, Dhople VM, Fullbright G, et al. (2013) 2′-hydroxy C16-ceramide induces apoptosis-associated proteomic changes in C6 glioma cells Journal of Proteome Research. 12: 4366-4375 |
| Kota V, Szulc ZM, Hama H. (2012) Identification of C(6) -ceramide-interacting proteins in D6P2T Schwannoma cells. Proteomics. 12: 2179-84 |
| Dan P, Edvardson S, Bielawski J, et al. (2011) 2-Hydroxylated sphingomyelin profiles in cells from patients with mutated fatty acid 2-hydroxylase. Lipids in Health and Disease. 10: 84 |
| Potter KA, Kern MJ, Fullbright G, et al. (2011) Central nervous system dysfunction in a mouse model of FA2H deficiency. Glia. 59: 1009-21 |
| Kruer MC, Paisán-Ruiz C, Boddaert N, et al. (2010) Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA). Annals of Neurology. 68: 611-8 |
| Hama H. (2010) Fatty acid 2-Hydroxylation in mammalian sphingolipid biology. Biochimica Et Biophysica Acta. 1801: 405-14 |
| Alderson NL, Hama H. (2009) Fatty acid 2-hydroxylase regulates cAMP-induced cell cycle exit in D6P2T schwannoma cells. Journal of Lipid Research. 50: 1203-8 |
| Edvardson S, Hama H, Shaag A, et al. (2008) Mutations in the fatty acid 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystonia. American Journal of Human Genetics. 83: 643-8 |