185 related articles for article (PubMed ID: 3242571)
1. [Peroxisomal disorders--clinical and biochemical studies].
Shimozawa N; Suzuki Y; Yamaguchi S; Shimizu N; Orii T
No To Hattatsu; 1988 Nov; 20(6):480-91. PubMed ID: 3242571
[No Abstract] [Full Text] [Related]
2. Peroxisomal beta-oxidation: enzymology and molecular biology.
Hashimoto T
Ann N Y Acad Sci; 1996 Dec; 804():86-98. PubMed ID: 8993538
[No Abstract] [Full Text] [Related]
3. Peroxisomal disorders: overview.
Moser HW; Moser AB
Ann N Y Acad Sci; 1996 Dec; 804():427-41. PubMed ID: 8993562
[No Abstract] [Full Text] [Related]
4. Functions and organization of peroxisomal beta-oxidation.
Mannaerts GP; van Veldhoven PP
Ann N Y Acad Sci; 1996 Dec; 804():99-115. PubMed ID: 8993539
[No Abstract] [Full Text] [Related]
5. Substrate stereospecificities of rat liver peroxisomal 3-hydroxyacyl-CoA dehydrogenases.
Dieuaide M; Novikov DK; Carchon H; Van Veldhoven PP; Mannaerts GP
Ann N Y Acad Sci; 1996 Dec; 804():680-1. PubMed ID: 8993593
[No Abstract] [Full Text] [Related]
6. Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis.
Wanders RJ; van Roermund CW; Brul S; Schutgens RB; Tager JM
J Inherit Metab Dis; 1992; 15(3):385-8. PubMed ID: 1357231
[No Abstract] [Full Text] [Related]
7. A bifunctional protein with deficient enzymic activity: identification of a new peroxisomal disorder using novel methods to measure the peroxisomal beta-oxidation enzyme activities.
Wanders RJ; van Roermund CW; Schelen A; Schutgens RB; Tager JM; Stephenson JB; Clayton PT
J Inherit Metab Dis; 1990; 13(3):375-9. PubMed ID: 2122104
[No Abstract] [Full Text] [Related]
8. Regulation of rat hepatic peroxisomal enoyl-CoA hydratase-3-hydroxyacyl-CoA dehydrogenase bifunctional enzyme by thyroid hormone.
Takeda T; Ichikawa K; Miyamoto T; Kobayashi M; Nishii Y; Suzuki S; Sakurai A; Hashizume K
Biochem Biophys Res Commun; 1992 May; 185(1):211-6. PubMed ID: 1599458
[TBL] [Abstract][Full Text] [Related]
9. Recombinant 2-enoyl-CoA hydratase derived from rat peroxisomal multifunctional enzyme 2: role of the hydratase reaction in bile acid synthesis.
Qin YM; Haapalainen AM; Conry D; Cuebas DA; Hiltunen JK; Novikov DK
Biochem J; 1997 Dec; 328 ( Pt 2)(Pt 2):377-82. PubMed ID: 9371691
[TBL] [Abstract][Full Text] [Related]
10. Purification, properties, and immunocytochemical localization of human liver peroxisomal enoyl-CoA hydratase/3-hydroxyacyl-CoA dehydrogenase.
Reddy MK; Usuda N; Reddy MN; Kuczmarski ER; Rao MS; Reddy JK
Proc Natl Acad Sci U S A; 1987 May; 84(10):3214-8. PubMed ID: 3106963
[TBL] [Abstract][Full Text] [Related]
11. Peroxisomal bifunctional enzyme deficiency.
Watkins PA; Chen WW; Harris CJ; Hoefler G; Hoefler S; Blake DC; Balfe A; Kelley RI; Moser AB; Beard ME
J Clin Invest; 1989 Mar; 83(3):771-7. PubMed ID: 2921319
[TBL] [Abstract][Full Text] [Related]
12. Induction of the three peroxisomal beta-oxidation enzymes is synergistically regulated by dexamethasone and fatty acids, and counteracted by insulin in Morris 7800C1 hepatoma cells in culture.
Sørensen HN; Gautik KM; Bremer J; Spydevold O
Eur J Biochem; 1992 Sep; 208(3):705-11. PubMed ID: 1356767
[TBL] [Abstract][Full Text] [Related]
13. Peroxisomal bifunctional enzyme deficiency with associated retinal findings.
Al-Hazzaa SA; Ozand PT
Ophthalmic Genet; 1997 Jun; 18(2):93-9. PubMed ID: 9228246
[TBL] [Abstract][Full Text] [Related]
14. Deficient activities and proteins of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome.
Suzuki Y; Orii T; Mori M; Tatibana M; Hashimoto T
Clin Chim Acta; 1986 Apr; 156(2):191-6. PubMed ID: 3519003
[TBL] [Abstract][Full Text] [Related]
15. [Peroxisomal disorders].
Suzuki Y; Shimozawa N; Imamura A; Kondo N
Ryoikibetsu Shokogun Shirizu; 2000; (29 Pt 4):452-9. PubMed ID: 11031991
[No Abstract] [Full Text] [Related]
16. Bifunctional protein deficiency: complementation within the same group suggesting differential enzyme defects and clues to the underlying basis.
Van Grunsven EG; van Berkel E; Lemonde H; Clayton PT; Wanders RJ
J Inherit Metab Dis; 1998 Jun; 21(3):298-301. PubMed ID: 9686380
[No Abstract] [Full Text] [Related]
17. Molecular analysis of peroxisomal beta-oxidation enzymes in infants with peroxisomal disorders indicates heterogeneity of the primary defect.
Guerroui S; Aubourg P; Chen WW; Hashimoto T; Scotto J
Biochem Biophys Res Commun; 1989 May; 161(1):242-51. PubMed ID: 2471528
[TBL] [Abstract][Full Text] [Related]
18. Evidence that multifunctional protein 2, and not multifunctional protein 1, is involved in the peroxisomal beta-oxidation of pristanic acid.
Dieuaide-Noubhani M; Asselberghs S; Mannaerts GP; Van Veldhoven PP
Biochem J; 1997 Jul; 325 ( Pt 2)(Pt 2):367-73. PubMed ID: 9230115
[TBL] [Abstract][Full Text] [Related]
19. Biochemical findings in a series of Australian patients with isolated defects in peroxisomal beta-oxidation.
Paton BC; Sharp PC; Poulos A
Ann N Y Acad Sci; 1996 Dec; 804():750-1. PubMed ID: 8993614
[No Abstract] [Full Text] [Related]
20. 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. PubMed ID: 11992265
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]