Moser AB - Search Results

1

Very long-chain acyl-CoA synthetase 3 mediates onco-sphingolipid metabolism in malignant glioma.

Kolar EA, Shi X, Clay EM, Moser AB, Lal B, Nirujogi RS, Pandey A, Bandaru VVR, Laterra J, Pei Z, Watkins PA. Kolar EA, et al. Among authors: moser ab. Med Res Arch. 2021 May;9(5):2433. doi: 10.18103/mra.v9i5.2433. Epub 2021 May 25. Med Res Arch. 2021. PMID: 34395855 Free PMC article.

2

A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy.

Heinzer AK, Watkins PA, Lu JF, Kemp S, Moser AB, Li YY, Mihalik S, Powers JM, Smith KD. Heinzer AK, et al. Among authors: moser ab. Hum Mol Genet. 2003 May 15;12(10):1145-54. doi: 10.1093/hmg/ddg126. Hum Mol Genet. 2003. PMID: 12719378

3

Drug discovery for X-linked adrenoleukodystrophy: An unbiased screen for compounds that lower very long-chain fatty acids.

Moser AB, Liu Y, Shi X, Schrifl U, Hiebler S, Fatemi A, Braverman NE, Steinberg SJ, Watkins PA. Moser AB, et al. J Cell Biochem. 2021 Oct;122(10):1337-1349. doi: 10.1002/jcb.30014. Epub 2021 May 30. J Cell Biochem. 2021. PMID: 34056752 Free PMC article.

4

Peroxisomal disorders: complementation analysis using beta-oxidation of very long chain fatty acids.

McGuinness MC, Moser AB, Moser HW, Watkins PA. McGuinness MC, et al. Among authors: moser hw, moser ab. Biochem Biophys Res Commun. 1990 Oct 15;172(1):364-9. doi: 10.1016/s0006-291x(05)80218-9. Biochem Biophys Res Commun. 1990. PMID: 2222480 Free article.

5

Peroxisomal very long chain fatty acid beta-oxidation activity is determined by the level of adrenodeukodystrophy protein (ALDP) expression.

Braiterman LT, Watkins PA, Moser AB, Smith KD. Braiterman LT, et al. Among authors: moser ab. Mol Genet Metab. 1999 Feb;66(2):91-9. doi: 10.1006/mgme.1998.2789. Mol Genet Metab. 1999. PMID: 10068511 Free article.

6

Peroxisomal straight-chain Acyl-CoA oxidase and D-bifunctional protein are essential for the retroconversion step in docosahexaenoic acid synthesis.

Su HM, Moser AB, Moser HW, Watkins PA. Su HM, et al. Among authors: moser hw, moser ab. J Biol Chem. 2001 Oct 12;276(41):38115-20. doi: 10.1074/jbc.M106326200. Epub 2001 Aug 10. J Biol Chem. 2001. PMID: 11500517 Free article.

7

Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies.

Watkins PA, McGuinness MC, Raymond GV, Hicks BA, Sisk JM, Moser AB, Moser HW. Watkins PA, et al. Among authors: moser hw, moser ab. Ann Neurol. 1995 Sep;38(3):472-7. doi: 10.1002/ana.410380322. Ann Neurol. 1995. PMID: 7668838

8

Adrenoleukodystrophy and Zellweger syndrome.

Moser HW, Moser AB, Chen WW, Watkins PA. Moser HW, et al. Among authors: moser ab. Prog Clin Biol Res. 1990;321:511-35. Prog Clin Biol Res. 1990. PMID: 2183241 Review. No abstract available.

9

Complementation analysis of patients with intact peroxisomes and impaired peroxisomal beta-oxidation.

McGuinness MC, Moser AB, Poll-The BT, Watkins PA. McGuinness MC, et al. Among authors: moser ab. Biochem Med Metab Biol. 1993 Apr;49(2):228-42. doi: 10.1006/bmmb.1993.1025. Biochem Med Metab Biol. 1993. PMID: 8484962 Free article.

10

A mouse model for X-linked adrenoleukodystrophy.

Lu JF, Lawler AM, Watkins PA, Powers JM, Moser AB, Moser HW, Smith KD. Lu JF, et al. Among authors: moser hw, moser ab. Proc Natl Acad Sci U S A. 1997 Aug 19;94(17):9366-71. doi: 10.1073/pnas.94.17.9366. Proc Natl Acad Sci U S A. 1997. PMID: 9256488 Free PMC article.

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