Hama H - Search Results

1

Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA).

Kruer MC, Paisán-Ruiz C, Boddaert N, Yoon MY, Hama H, Gregory A, Malandrini A, Woltjer RL, Munnich A, Gobin S, Polster BJ, Palmeri S, Edvardson S, Hardy J, Houlden H, Hayflick SJ. Kruer MC, et al. Among authors: hama h. Ann Neurol. 2010 Nov;68(5):611-8. doi: 10.1002/ana.22122. Ann Neurol. 2010. PMID: 20853438 Free PMC article.

2

2-Hydroxylated sphingomyelin profiles in cells from patients with mutated fatty acid 2-hydroxylase.

Dan P, Edvardson S, Bielawski J, Hama H, Saada A. Dan P, et al. Among authors: hama h. Lipids Health Dis. 2011 May 20;10:84. doi: 10.1186/1476-511X-10-84. Lipids Health Dis. 2011. PMID: 21599921 Free PMC article.

3

Mutations in the fatty acid 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystonia.

Edvardson S, Hama H, Shaag A, Gomori JM, Berger I, Soffer D, Korman SH, Taustein I, Saada A, Elpeleg O. Edvardson S, et al. Among authors: hama h. Am J Hum Genet. 2008 Nov;83(5):643-8. doi: 10.1016/j.ajhg.2008.10.010. Am J Hum Genet. 2008. PMID: 19068277 Free PMC article.

4

Heterozygous FA2H mutations in autism spectrum disorders.

Scheid I, Maruani A, Huguet G, Leblond CS, Nygren G, Anckarsäter H, Beggiato A, Rastam M, Amsellem F, Gillberg IC, Elmaleh M, Leboyer M, Gillberg C, Betancur C, Coleman M, Hama H, Cook EH, Bourgeron T, Delorme R. Scheid I, et al. Among authors: hama h. BMC Med Genet. 2013 Dec 3;14:124. doi: 10.1186/1471-2350-14-124. BMC Med Genet. 2013. PMID: 24299421 Free PMC article.

5

FA2H-dependent fatty acid 2-hydroxylation in postnatal mouse brain.

Alderson NL, Maldonado EN, Kern MJ, Bhat NR, Hama H. Alderson NL, et al. Among authors: hama h. J Lipid Res. 2006 Dec;47(12):2772-80. doi: 10.1194/jlr.M600362-JLR200. Epub 2006 Sep 23. J Lipid Res. 2006. PMID: 16998236 Free article.

6

Fatty acid 2-Hydroxylation in mammalian sphingolipid biology.

Hama H. Hama H. Biochim Biophys Acta. 2010 Apr;1801(4):405-14. doi: 10.1016/j.bbalip.2009.12.004. Epub 2009 Dec 21. Biochim Biophys Acta. 2010. PMID: 20026285 Free PMC article. Review.

7

Central nervous system dysfunction in a mouse model of FA2H deficiency.

Potter KA, Kern MJ, Fullbright G, Bielawski J, Scherer SS, Yum SW, Li JJ, Cheng H, Han X, Venkata JK, Khan PA, Rohrer B, Hama H. Potter KA, et al. Among authors: hama h. Glia. 2011 Jul;59(7):1009-21. doi: 10.1002/glia.21172. Epub 2011 Apr 13. Glia. 2011. PMID: 21491498 Free PMC article.

8

The human FA2H gene encodes a fatty acid 2-hydroxylase.

Alderson NL, Rembiesa BM, Walla MD, Bielawska A, Bielawski J, Hama H. Alderson NL, et al. Among authors: hama h. J Biol Chem. 2004 Nov 19;279(47):48562-8. doi: 10.1074/jbc.M406649200. Epub 2004 Aug 27. J Biol Chem. 2004. PMID: 15337768 Free article.

9

Regulation of telomere length by fatty acid elongase 3 in yeast. Involvement of inositol phosphate metabolism and Ku70/80 function.

Ponnusamy S, Alderson NL, Hama H, Bielawski J, Jiang JC, Bhandari R, Snyder SH, Jazwinski SM, Ogretmen B. Ponnusamy S, et al. Among authors: hama h. J Biol Chem. 2008 Oct 10;283(41):27514-27524. doi: 10.1074/jbc.M802980200. Epub 2008 Aug 11. J Biol Chem. 2008. PMID: 18694931 Free PMC article.

10

A novel method for the measurement of in vitro fatty acid 2-hydroxylase activity by gas chromatography-mass spectrometry.

Alderson NL, Walla MD, Hama H. Alderson NL, et al. Among authors: hama h. J Lipid Res. 2005 Jul;46(7):1569-75. doi: 10.1194/jlr.D500013-JLR200. Epub 2005 May 1. J Lipid Res. 2005. PMID: 15863841 Free article.

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