178 related articles for article (PubMed ID: 24122089)
1. Molecular species of phospholipids with very long chain fatty acids in skin fibroblasts of Zellweger syndrome.
Hama K; Nagai T; Nishizawa C; Ikeda K; Morita M; Satoh N; Nakanishi H; Imanaka T; Shimozawa N; Taguchi R; Inoue K; Yokoyama K
Lipids; 2013 Dec; 48(12):1253-67. PubMed ID: 24122089
[TBL] [Abstract][Full Text] [Related]
2. Very-long-chain polyunsaturated fatty acids accumulate in phosphatidylcholine of fibroblasts from patients with Zellweger syndrome and acyl-CoA oxidase1 deficiency.
Abe Y; Honsho M; Nakanishi H; Taguchi R; Fujiki Y
Biochim Biophys Acta; 2014 Apr; 1841(4):610-9. PubMed ID: 24418004
[TBL] [Abstract][Full Text] [Related]
3. Detection of unusual very-long-chain fatty acid and ether lipid derivatives in the fibroblasts and plasma of patients with peroxisomal diseases using liquid chromatography-mass spectrometry.
Takashima S; Toyoshi K; Itoh T; Kajiwara N; Honda A; Ohba A; Takemoto S; Yoshida S; Shimozawa N
Mol Genet Metab; 2017 Mar; 120(3):255-268. PubMed ID: 28089346
[TBL] [Abstract][Full Text] [Related]
4. Profiling and Imaging of Phospholipids in Brains of Abcd1-Deficient Mice.
Hama K; Fujiwara Y; Morita M; Yamazaki F; Nakashima Y; Takei S; Takashima S; Setou M; Shimozawa N; Imanaka T; Yokoyama K
Lipids; 2018 Jan; 53(1):85-102. PubMed ID: 29469952
[TBL] [Abstract][Full Text] [Related]
5. Molecular species of phosphatidylcholine containing very long chain fatty acids in human brain: enrichment in X-linked adrenoleukodystrophy brain and diseases of peroxisome biogenesis brain.
Sharp P; Johnson D; Poulos A
J Neurochem; 1991 Jan; 56(1):30-7. PubMed ID: 1702833
[TBL] [Abstract][Full Text] [Related]
6. Analysis of very long-chain fatty acids using electrospray ionization mass spectrometry.
Valianpour F; Selhorst JJ; van Lint LE; van Gennip AH; Wanders RJ; Kemp S
Mol Genet Metab; 2003 Jul; 79(3):189-96. PubMed ID: 12855224
[TBL] [Abstract][Full Text] [Related]
7. Very long-chain fatty acids in peroxisomal disease.
Poulos A; Beckman K; Johnson DW; Paton BC; Robinson BS; Sharp P; Usher S; Singh H
Adv Exp Med Biol; 1992; 318():331-40. PubMed ID: 1378993
[TBL] [Abstract][Full Text] [Related]
8. Immunochemical and biochemical studies of fatty acid oxidation in fibroblasts of Zellweger and X-linked adrenoleukodystrophy patients.
Reubsaet FA; Veerkamp JH; Brückwilder ML; Trijbels JM; Hashimoto T; Monnens LA
Biochim Biophys Acta; 1991 Jun; 1083(3):305-9. PubMed ID: 2049396
[TBL] [Abstract][Full Text] [Related]
9. Profiles of very-long-chain fatty acids in plasma, fibroblasts, and blood cells in Zellweger syndrome, X-linked adrenoleukodystrophy, and rhizomelic chondrodysplasia punctata.
Schutgens RB; Bouman IW; Nijenhuis AA; Wanders RJ; Frumau ME
Clin Chem; 1993 Aug; 39(8):1632-7. PubMed ID: 8353949
[TBL] [Abstract][Full Text] [Related]
10. Localization of nervonic acid beta-oxidation in human and rodent peroxisomes: impaired oxidation in Zellweger syndrome and X-linked adrenoleukodystrophy.
Sandhir R; Khan M; Chahal A; Singh I
J Lipid Res; 1998 Nov; 39(11):2161-71. PubMed ID: 9799802
[TBL] [Abstract][Full Text] [Related]
11. The Zellweger syndrome: deficient conversion of docosahexaenoic acid (22:6(n-3)) to eicosapentaenoic acid (20:5(n-3)) and normal delta 4-desaturase activity in cultured skin fibroblasts.
Grønn M; Christensen E; Hagve TA; Christophersen BO
Biochim Biophys Acta; 1990 May; 1044(2):249-54. PubMed ID: 2140517
[TBL] [Abstract][Full Text] [Related]
12. Fatty acid synthesis from [2-14C]acetate in normal and peroxisome-deficient (Zellweger) fibroblasts.
Poulos A; Usher S; Paton BC
Lipids; 1993 Feb; 28(2):97-102. PubMed ID: 8441343
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Chinese patients with adrenoleukodystrophy and Zellweger spectrum disorder presenting with hereditary spastic paraplegia.
Chen YJ; Wang MW; Dong EL; Lin XH; Wang N; Zhang ZQ; Lin X; Chen WJ
Parkinsonism Relat Disord; 2019 Aug; 65():256-260. PubMed ID: 31227335
[TBL] [Abstract][Full Text] [Related]
15. Identification and Characterization of Phospholipids with Very Long Chain Fatty Acids in Brewer's Yeast.
Řezanka T; Kolouchová I; Gharwalová L; Palyzová A; Sigler K
Lipids; 2017 Dec; 52(12):1007-1017. PubMed ID: 28905226
[TBL] [Abstract][Full Text] [Related]
16. Detection of Characteristic Phosphatidylcholine Containing Very Long Chain Fatty Acids in Cerebrospinal Fluid from Patients with X-Linked Adrenoleukodystrophy.
Fujitani N; Saito M; Akashi T; Morita M; So T; Oka K
Biol Pharm Bull; 2022; 45(11):1725-1727. PubMed ID: 36328509
[TBL] [Abstract][Full Text] [Related]
17. Physiological significance of fatty acid elongation system in adrenoleukodystrophy.
Koike R; Tsuji S; Ohno T; Suzuki Y; Orii T; Miyatake T
J Neurol Sci; 1991 Jun; 103(2):188-94. PubMed ID: 1880537
[TBL] [Abstract][Full Text] [Related]
18. The deficient degradation of synthetic 2- and 3-methyl-branched fatty acids in fibroblasts from patients with peroxisomal disorders.
Van Veldhoven PP; Huang S; Eyssen HJ; Mannaerts GP
J Inherit Metab Dis; 1993; 16(2):381-91. PubMed ID: 7692128
[TBL] [Abstract][Full Text] [Related]
19. Structure and lipid distribution of polyenoic very-long-chain fatty acids in the brain of peroxisome-deficient patients (Zellweger syndrome).
Sharp P; Poulos A; Fellenberg A; Johnson D
Biochem J; 1987 Nov; 248(1):61-7. PubMed ID: 3435449
[TBL] [Abstract][Full Text] [Related]
20. Phytanic acid and very long chain fatty acids in genetic peroxisomal disorders.
Molzer B; Kainz-Korschinsky M; Sundt-Heller R; Bernheimer H
J Clin Chem Clin Biochem; 1989 May; 27(5):309-14. PubMed ID: 2474624
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
