齐尔韦格综合征患者羊水内的脂氧合酶代谢产物 - Suppr

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超能文献

Lipoxygenase metabolites in amniotic fluid of patients with Zellweger syndrome.

作者信息

Mayatepek E, Jakobs C

机构信息

Division of Metabolic Diseases, University Children's Hospital, Heidelberg, Germany.

出版信息

J Inherit Metab Dis. 1998 Jun;21(3):292-4. doi: 10.1023/a:1005340811106.

DOI:10.1023/a:1005340811106

PMID:9686378

Abstract

摘要

相似文献

Lipoxygenase metabolites in amniotic fluid of patients with Zellweger syndrome.齐尔韦格综合征患者羊水内的脂氧合酶代谢产物

J Inherit Metab Dis. 1998 Jun;21(3):292-4. doi: 10.1023/a:1005340811106.

Arachidonate lipoxygenase activity modulating factors in human plasma and amniotic fluid.人血浆和羊水中的花生四烯酸脂氧合酶活性调节因子。

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Prenatal diagnosis of Zellweger syndrome by determination of trihydroxycoprostanic acid in amniotic fluid.

Eur J Pediatr. 1988 Nov;148(2):175-6. doi: 10.1007/BF00445940.

Very long fatty acids in amniotic fluid from a fetus affected with Zellweger syndrome.

Eur J Pediatr. 1989 Apr;148(6):581. doi: 10.1007/BF00441567.

Amniotic fluid lipoxygenase metabolites during spontaneous labor and after RU486 treatment during late pregnancy in rhesus macaques.恒河猴妊娠晚期自然分娩期间及米非司酮治疗后羊水脂氧合酶代谢产物

Prostaglandins. 1990 Jul;40(1):99-105. doi: 10.1016/0090-6980(90)90060-9.

Increased concentrations of arachidonic acid lipoxygenase metabolites in amniotic fluid during parturition.

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Phytanic acid alpha-oxidation in man: identification of 2-hydroxyphytanoyl-CoA lyase, a peroxisomal enzyme with normal activity in Zellweger syndrome.

J Inherit Metab Dis. 2000 Jun;23(4):421-4. doi: 10.1023/a:1005672406773.

Zellweger-like syndrome with detectable hepatic peroxisomes: a variant form of peroxisomal disorder.伴有可检测到的肝过氧化物酶体的泽尔韦格样综合征：过氧化物酶体疾病的一种变异形式。

J Pediatr. 1988 Nov;113(5):841-5. doi: 10.1016/s0022-3476(88)80011-8.

Phytanic acid oxidation in man: identification of a new enzyme catalysing the formation of 2-ketophytanic acid from 2-hydroxyphytanic acid and its deficiency in the Zellweger syndrome.人体内植烷酸氧化：一种催化从2-羟基植烷酸形成2-酮植烷酸的新酶的鉴定及其在齐-韦综合征中的缺乏。

J Inherit Metab Dis. 1995;18(2):201-3. doi: 10.1007/BF00711766.

Cholesterol biosynthesis, peroxisomes and peroxisomal disorders: mevalonate kinase is not only deficient in Zellweger syndrome but also in rhizomelic chondrodysplasia punctata.胆固醇生物合成、过氧化物酶体与过氧化物酶体疾病：甲羟戊酸激酶不仅在泽尔韦格综合征中缺乏，在点状软骨发育不良中也缺乏。

J Inherit Metab Dis. 1998 Jun;21(3):309-12. doi: 10.1023/a:1005353129761.

本文引用的文献

Pre- and postnatal diagnosis of peroxisomal disorders using stable-isotope dilution gas chromatography--mass spectrometry.使用稳定同位素稀释气相色谱 - 质谱法进行过氧化物酶体疾病的产前和产后诊断。

J Inherit Metab Dis. 1995;18 Suppl 1:45-60. doi: 10.1007/BF00711428.

12- and 15-hydroxyeicosatetraenoic acid are excreted in the urine of peroxisome-deficient patients: evidence for peroxisomal metabolism in vivo.

Pediatr Res. 1996 Jan;39(1):146-9. doi: 10.1203/00006450-199601000-00022.

Impaired degradation of leukotrienes in patients with peroxisome deficiency disorders.过氧化物酶体缺乏症患者中白三烯降解受损。

J Clin Invest. 1993 Mar;91(3):881-8. doi: 10.1172/JCI116309.

Leukotrienes: biosynthesis, metabolism, and pathophysiologic significance.白三烯：生物合成、代谢及病理生理学意义

Pediatr Res. 1995 Jan;37(1):1-9. doi: 10.1203/00006450-199501000-00001.

Hydroxyeicosatetraenoic acids (HETEs).羟基二十碳四烯酸（HETEs）。

Prog Lipid Res. 1988;27(4):271-323. doi: 10.1016/0163-7827(88)90009-4.

Hydroxyeicosatetraenoic acid metabolism in cultured human skin fibroblasts. Evidence for peroxisomal beta-oxidation.培养的人皮肤成纤维细胞中羟基二十碳四烯酸的代谢。过氧化物酶体β-氧化的证据。

J Clin Invest. 1990 Apr;85(4):1173-81. doi: 10.1172/JCI114550.

Prenatal diagnosis of inborn errors in peroxisomal beta-oxidation.

Prenat Diagn. 1991 Apr;11(4):253-61. doi: 10.1002/pd.1970110407.

Peroxisomal degradation of leukotrienes by beta-oxidation from the omega-end.白三烯通过ω-端β-氧化途径在过氧化物酶体中的降解

J Biol Chem. 1991 Dec 25;266(36):24763-72.

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