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Intermittent acute porphyria. Clinical and biochemical studies of disordered heme biosynthesis.

作者信息

Meyer U A

出版信息

Enzyme. 1973;16(1):334-42.

PMID:4791052
Abstract
摘要

相似文献

1
Intermittent acute porphyria. Clinical and biochemical studies of disordered heme biosynthesis.间歇性急性卟啉病。血红素生物合成紊乱的临床与生化研究。
Enzyme. 1973;16(1):334-42.
2
Acute intermittent porphyria: studies of the enzymatic basis of disordered haem biosynthesis.
S Afr Med J. 1971 Sep 25:108-11.
3
Enzymatic defects in hepatic porphyria. Preliminary observations in patients with porphyria cutanea tarda and variegate porphyria.
Enzyme. 1973;16(1):354-66.
4
Endocrine-gene interaction in the pathogenesis of acute intermittent porphyria.急性间歇性卟啉病发病机制中的内分泌-基因相互作用。
Res Publ Assoc Res Nerv Ment Dis. 1974;53:225-37.
5
Intermittent acute porphyria: the enzymatic defect.间歇性急性卟啉症:酶缺陷
Res Publ Assoc Res Nerv Ment Dis. 1974;53:211-24.
6
Hepatic porphyrias: new findings on the nature of metabolic defects.肝性卟啉病:代谢缺陷本质的新发现
Prog Liver Dis. 1976;5:280-93.
7
Decreased red cell uroporphyrinogen I synthetase activity in intermittent acute porphyria.间歇性急性卟啉病中红细胞尿卟啉原I合成酶活性降低。
J Clin Invest. 1972 Oct;51(10):2530-6. doi: 10.1172/JCI107068.
8
[Intermittent acuteporphyria. Clinical significance of reduced activity of uroporphyrinogen-I-synthetase].[间歇性急性卟啉病。尿卟啉原-I-合成酶活性降低的临床意义]
Schweiz Med Wochenschr. 1974 Dec 14;104(50):1874-7.
9
Hereditary hepatic porphyrias.遗传性肝卟啉症
Fed Proc. 1973 Jun;32(6):1649-55.
10
[Biosynthesis of heme: regulation; hereditary and experimental porphyrias].[血红素的生物合成:调节;遗传性和实验性卟啉症]
Expos Annu Biochim Med. 1980;34:45-80.

引用本文的文献

1
Heme synthetase deficiency in human protoporphyria. Demonstration of the defect in liver and cultured skin fibroblasts.人类原卟啉症中的血红素合成酶缺乏症。肝脏和培养的皮肤成纤维细胞中缺陷的证明。
J Clin Invest. 1975 Nov;56(5):1139-48. doi: 10.1172/JCI108189.
2
Studies in porphyria. IV. Expression of the gene defect of acute intermittent porphyria in cultured human skin fibroblasts and amniotic cells: prenatal diagnosis of the porphyric trait.卟啉症研究。IV. 急性间歇性卟啉症基因缺陷在培养的人皮肤成纤维细胞和羊水中的表达:卟啉性状的产前诊断。
J Exp Med. 1975 Sep 1;142(3):722-31. doi: 10.1084/jem.142.3.722.
3
Perspectives in acute intermittent porphyria.
急性间歇性卟啉症的研究视角
Indian J Pediatr. 1976 Jul;43(342):204-7. doi: 10.1007/BF02751598.
4
Study of factors causing excess protoporphyrin accumulation in cultured skin fibroblasts from patients with protoporphyria.原卟啉病患者培养皮肤成纤维细胞中原卟啉过度蓄积的影响因素研究。
J Clin Invest. 1977 Dec;60(6):1354-61. doi: 10.1172/JCI108895.
5
Studies in porphyria. VII. Induction of uroporphyrinogen-I synthase and expression of the gene defect of acute intermittent porphyria in mitogen-stimulated human lymphocytes.卟啉症的研究。VII. 促有丝分裂原刺激的人淋巴细胞中尿卟啉原-I合酶的诱导及急性间歇性卟啉症基因缺陷的表达
J Clin Invest. 1978 Feb;61(2):499-508. doi: 10.1172/JCI108961.
6
Heme content of normal and porphyric cultured skin fibroblasts.
Biochem Genet. 1977 Dec;15(11-12):1061-70. doi: 10.1007/BF00484497.
7
Enzymatic defects of hereditary porphyrias: an explanation of dominance at the molecular level.
Hum Genet. 1977 Dec 23;39(3):261-76. doi: 10.1007/BF00295419.