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Items: 1 to 20 of 113

1.

Clinical consequences of defects in peroxisomal beta-oxidation.

Clayton PT.

Biochem Soc Trans. 2001 May;29(Pt 2):298-305. Review.

PMID:
11356171
2.

Lessons from knockout mice II: Mouse models for peroxisomal disorders with single protein deficiency.

Berger J, Kunze M, Forss-Petter S.

Adv Exp Med Biol. 2003;544:123-34. Review. No abstract available.

PMID:
14713223
3.
4.

[Peroxisomal disorders].

Suzuki Y, Shimozawa N, Imamura A, Kondo N.

Ryoikibetsu Shokogun Shirizu. 2000;(29 Pt 4):452-9. Review. Japanese. No abstract available.

PMID:
11031991
5.

D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder.

Suzuki Y, Jiang LL, Souri M, Miyazawa S, Fukuda S, Zhang Z, Une M, Shimozawa N, Kondo N, Orii T, Hashimoto T.

Am J Hum Genet. 1997 Nov;61(5):1153-62.

6.

Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency.

van Grunsven EG, van Berkel E, Ijlst L, Vreken P, de Klerk JB, Adamski J, Lemonde H, Clayton PT, Cuebas DA, Wanders RJ.

Proc Natl Acad Sci U S A. 1998 Mar 3;95(5):2128-33.

7.

Reinvestigation of peroxisomal 3-ketoacyl-CoA thiolase deficiency: identification of the true defect at the level of d-bifunctional protein.

Ferdinandusse S, van Grunsven EG, Oostheim W, Denis S, Hogenhout EM, IJlst L, van Roermund CW, Waterham HR, Goldfischer S, Wanders RJ.

Am J Hum Genet. 2002 Jun;70(6):1589-93. Epub 2002 Apr 23.

8.

A novel HPLC-based method to diagnose peroxisomal D-bifunctional protein enoyl-CoA hydratase deficiency.

Gloerich J, Denis S, van Grunsven EG, Dacremont G, Wanders RJ, Ferdinandusse S.

J Lipid Res. 2003 Mar;44(3):640-4. Epub 2002 Dec 1.

10.

Evidence for increased oxidative stress in peroxisomal D-bifunctional protein deficiency.

Ferdinandusse S, Finckh B, de Hingh YC, Stroomer LE, Denis S, Kohlschütter A, Wanders RJ.

Mol Genet Metab. 2003 Aug;79(4):281-7.

PMID:
12948743
11.

Prenatal diagnosis of peroxisomal D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency.

Suzuki Y, Zhang Z, Shimozawa N, Muro M, Shono H, Toda S, Miyahara S, Hashimoto T, Usuda N, Ito M, Takashima S, Kondo N.

J Hum Genet. 1999;44(3):143-7.

PMID:
10319576
12.

Induction of peroxisomal lipid metabolism in mice fed a high-fat diet.

Kozawa S, Honda A, Kajiwara N, Takemoto Y, Nagase T, Nikami H, Okano Y, Nakashima S, Shimozawa N.

Mol Med Rep. 2011 Nov-Dec;4(6):1157-62. doi: 10.3892/mmr.2011.560. Epub 2011 Aug 17.

PMID:
21850377
13.

Peroxisomal bifunctional enzyme deficiency.

Watkins PA, Chen WW, Harris CJ, Hoefler G, Hoefler S, Blake DC Jr, Balfe A, Kelley RI, Moser AB, Beard ME, et al.

J Clin Invest. 1989 Mar;83(3):771-7.

14.

Developmental and pathological expression of peroxisomal enzymes: their relationship of D-bifunctional protein deficiency and Zellweger syndrome.

Itoh M, Suzuki Y, Akaboshi S, Zhang Z, Miyabara S, Takashima S.

Brain Res. 2000 Mar 6;858(1):40-7.

PMID:
10700594
15.

Stereochemistry of the peroxisomal branched-chain fatty acid alpha- and beta-oxidation systems in patients suffering from different peroxisomal disorders.

Ferdinandusse S, Rusch H, van Lint AE, Dacremont G, Wanders RJ, Vreken P.

J Lipid Res. 2002 Mar;43(3):438-44.

16.

Aberrant peroxisome morphology in peroxisomal beta-oxidation enzyme deficiencies.

Funato M, Shimozawa N, Nagase T, Takemoto Y, Suzuki Y, Imamura Y, Matsumoto T, Tsukamoto T, Kojidani T, Osumi T, Fukao T, Kondo N.

Brain Dev. 2006 Jun;28(5):287-92. Epub 2006 Jan 10.

PMID:
16376506
17.

Gene expression of peroxisomal beta-oxidation enzymes in rat brain.

Knoll A, Sargueil F, Salles J, Cassagne C, Garbay B.

Brain Res Mol Brain Res. 1999 Dec 10;74(1-2):217-20.

PMID:
10640693
18.

Peroxisomal disorders: overview.

Moser HW, Moser AB.

Ann N Y Acad Sci. 1996 Dec 27;804:427-41. Review. No abstract available.

PMID:
8993562
19.

Enoyl-CoA hydratase deficiency: identification of a new type of D-bifunctional protein deficiency.

van Grunsven EG, Mooijer PA, Aubourg P, Wanders RJ.

Hum Mol Genet. 1999 Aug;8(8):1509-16.

PMID:
10400999
20.

Physiological role of D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein.

Jiang LL, Kurosawa T, Sato M, Suzuki Y, Hashimoto T.

J Biochem. 1997 Mar;121(3):506-13.

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