Moser HW - Search Results

1

Peroxisomal L-pipecolic acid oxidation is deficient in liver from Zellweger syndrome patients.

Mihalik SJ, Moser HW, Watkins PA, Danks DM, Poulos A, Rhead WJ. Mihalik SJ, et al. Among authors: moser hw. Pediatr Res. 1989 May;25(5):548-52. doi: 10.1203/00006450-198905000-00024. Pediatr Res. 1989. PMID: 2717271

2

Phytanoyl-CoA hydroxylase is present in human liver, located in peroxisomes, and deficient in Zellweger syndrome: direct, unequivocal evidence for the new, revised pathway of phytanic acid alpha-oxidation in humans.

Jansen GA, Mihalik SJ, Watkins PA, Moser HW, Jakobs C, Denis S, Wanders RJ. Jansen GA, et al. Among authors: moser hw. Biochem Biophys Res Commun. 1996 Dec 4;229(1):205-10. doi: 10.1006/bbrc.1996.1781. Biochem Biophys Res Commun. 1996. PMID: 8954107 Free article.

3

The 22-kD peroxisomal integral membrane protein in Zellweger syndrome--presence, abundance, and association with a peroxisomal thiolase precursor protein.

Gärtner J, Chen WW, Kelley RI, Mihalik SJ, Moser HW. Gärtner J, et al. Among authors: moser hw. Pediatr Res. 1991 Feb;29(2):141-6. doi: 10.1203/00006450-199102000-00007. Pediatr Res. 1991. PMID: 1673025

4

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.

5

Peroxisomal integral membrane proteins in livers of patients with Zellweger syndrome, infantile Refsum's disease and X-linked adrenoleukodystrophy.

Small GM, Santos MJ, Imanaka T, Poulos A, Danks DM, Moser HW, Lazarow PB. Small GM, et al. Among authors: moser hw. J Inherit Metab Dis. 1988;11(4):358-71. doi: 10.1007/BF01800425. J Inherit Metab Dis. 1988. PMID: 2468817

6

Adrenoleukodystrophy and other peroxisomal disorders that affect the nervous system, including new observations on L-pipecolic acid oxidase in primates.

Moser HW, Mihalik SJ, Watkins PA. Moser HW, et al. Brain Dev. 1989;11(2):80-90. doi: 10.1016/s0387-7604(89)80074-9. Brain Dev. 1989. PMID: 2653074 Free article. Review.

7

Presence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome).

Lazarow PB, Fujiki Y, Small GM, Watkins P, Moser H. Lazarow PB, et al. Proc Natl Acad Sci U S A. 1986 Dec;83(23):9193-6. doi: 10.1073/pnas.83.23.9193. Proc Natl Acad Sci U S A. 1986. PMID: 3538019 Free PMC article.

8

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.

9

Peroxisomal beta-oxidation enzyme proteins in adrenoleukodystrophy: distinction between X-linked adrenoleukodystrophy and neonatal adrenoleukodystrophy.

Chen WW, Watkins PA, Osumi T, Hashimoto T, Moser HW. Chen WW, et al. Among authors: moser hw. Proc Natl Acad Sci U S A. 1987 Mar;84(5):1425-8. doi: 10.1073/pnas.84.5.1425. Proc Natl Acad Sci U S A. 1987. PMID: 3469675 Free PMC article.

10

Characterization of phytanoyl-Coenzyme A hydroxylase in human liver and activity measurements in patients with peroxisomal disorders.

Jansen GA, Mihalik SJ, Watkins PA, Jakobs C, Moser HW, Wanders RJ. Jansen GA, et al. Among authors: moser hw. Clin Chim Acta. 1998 Mar 23;271(2):203-11. doi: 10.1016/s0009-8981(97)00259-3. Clin Chim Acta. 1998. PMID: 9565335 Free article.

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