107 related articles for article (PubMed ID: 7668838)
21. Pristanic acid does not accumulate in peroxisomal acyl-CoA oxidase deficiency: evidence for a distinct peroxisomal pristanyl-CoA oxidase.
ten Brink HJ; Poll-The BT; Saudubray JM; Wanders RJ; Jakobs C
J Inherit Metab Dis; 1991; 14(5):681-4. PubMed ID: 1779614
[TBL] [Abstract][Full Text] [Related]
22. Peroxisome proliferator-activated receptor alpha-responsive genes induced in the newborn but not prenatal liver of peroxisomal fatty acyl-CoA oxidase null mice.
Cook WS; Jain S; Jia Y; Cao WQ; Yeldandi AV; Reddy JK; Rao MS
Exp Cell Res; 2001 Aug; 268(1):70-6. PubMed ID: 11461119
[TBL] [Abstract][Full Text] [Related]
23. Peroxisomal beta-oxidation of polyunsaturated long chain fatty acids in human fibroblasts. The polyunsaturated and the saturated long chain fatty acids are retroconverted by the same acyl-CoA oxidase.
Christensen E; Woldseth B; Hagve TA; Poll-The BT; Wanders RJ; Sprecher H; Stokke O; Christophersen BO
Scand J Clin Lab Invest Suppl; 1993; 215():61-74. PubMed ID: 8327852
[TBL] [Abstract][Full Text] [Related]
24. 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
Biochem Biophys Res Commun; 1996 Dec; 229(1):205-10. PubMed ID: 8954107
[TBL] [Abstract][Full Text] [Related]
25. [Peroxisomal D-bifunctional enzyme deficiency. A case report].
Chávez-Torres R; Ruiz-Chávez J; Ruiz-Cruz E; Juárez-Naranjo E; Campos-Campos L; Villanueva-Padrón L; Horta-Martínez A; Montes-Castillo Mde L; Monroy-Hernández V; Hernández-Caballero E
Rev Med Inst Mex Seguro Soc; 2008; 46(4):445-8. PubMed ID: 19213219
[TBL] [Abstract][Full Text] [Related]
26. A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy).
Poll-The BT; Roels F; Ogier H; Scotto J; Vamecq J; Schutgens RB; Wanders RJ; van Roermund CW; van Wijland MJ; Schram AW
Am J Hum Genet; 1988 Mar; 42(3):422-34. PubMed ID: 2894756
[TBL] [Abstract][Full Text] [Related]
27. 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; 858(1):40-7. PubMed ID: 10700594
[TBL] [Abstract][Full Text] [Related]
28. Neuronal migration abnormality in peroxisomal bifunctional enzyme defect.
Kaufmann WE; Theda C; Naidu S; Watkins PA; Moser AB; Moser HW
Ann Neurol; 1996 Feb; 39(2):268-71. PubMed ID: 8967760
[TBL] [Abstract][Full Text] [Related]
29. Molecular organization of peroxisomal enzymes: protein-protein interactions in the membrane and in the matrix.
Makkar RS; Contreras MA; Paintlia AS; Smith BT; Haq E; Singh I
Arch Biochem Biophys; 2006 Jul; 451(2):128-40. PubMed ID: 16781659
[TBL] [Abstract][Full Text] [Related]
30. A sensitive assay of acyl-coenzyme A oxidase by coupling with beta-oxidation multienzyme complex.
Souri M; Aoyama T; Hashimoto T
Anal Biochem; 1994 Sep; 221(2):362-7. PubMed ID: 7810878
[TBL] [Abstract][Full Text] [Related]
31. Pseudo-Zellweger syndrome: deficiencies in several peroxisomal oxidative activities.
Goldfischer S; Collins J; Rapin I; Neumann P; Neglia W; Spiro AJ; Ishii T; Roels F; Vamecq J; Van Hoof F
J Pediatr; 1986 Jan; 108(1):25-32. PubMed ID: 2868085
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Altered phospholipid molecular species and glycolipid composition in brain, liver and fibroblasts of Zellweger syndrome.
Miyazaki C; Saitoh M; Itoh M; Yamashita S; Miyagishi M; Takashima S; Moser AB; Iwamori M; Mizuguchi M
Neurosci Lett; 2013 Sep; 552():71-5. PubMed ID: 23933200
[TBL] [Abstract][Full Text] [Related]
34. Central nervous system malformations and white matter changes in pseudo-neonatal adrenoleukodystrophy.
Kyllerman M; Blomstrand S; Månsson JE; Conradi NG; Hindmarsh T
Neuropediatrics; 1990 Nov; 21(4):199-201. PubMed ID: 2290480
[TBL] [Abstract][Full Text] [Related]
35. Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease.
Baumgartner MR; Verhoeven NM; Jakobs C; Roels F; Espeel M; Martinez M; Rabier D; Wanders RJ; Saudubray JM
Neurology; 1998 Nov; 51(5):1427-32. PubMed ID: 9818873
[TBL] [Abstract][Full Text] [Related]
36. 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
Pediatr Res; 1989 May; 25(5):548-52. PubMed ID: 2717271
[TBL] [Abstract][Full Text] [Related]
37. Phytanic acid oxidase deficiency in childhood.
Wise GA; Duffy BJ; Mitchell JD; Pollard AC; Poulos A; Pollard J
Clin Exp Neurol; 1985; 21():289-99. PubMed ID: 3843227
[TBL] [Abstract][Full Text] [Related]
38. Reinvestigation of trihydroxycholestanoic acidemia reveals a peroxisome biogenesis disorder.
Gootjes J; Skovby F; Christensen E; Wanders RJ; Ferdinandusse S
Neurology; 2004 Jun; 62(11):2077-81. PubMed ID: 15184617
[TBL] [Abstract][Full Text] [Related]
39. Peroxisomal beta-oxidation defect with detectable peroxisomes: a case with neonatal onset and progressive course.
Barth PG; Wanders RJ; Schutgens RB; Bleeker-Wagemakers EM; van Heemstra D
Eur J Pediatr; 1990 Jul; 149(10):722-6. PubMed ID: 2209666
[TBL] [Abstract][Full Text] [Related]
40. D-bifunctional protein deficiency: a cause of neonatal onset seizures and hypotonia.
Nascimento J; Mota C; Lacerda L; Pacheco S; Chorão R; Martins E; Garrido C
Pediatr Neurol; 2015 May; 52(5):539-43. PubMed ID: 25882080
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
