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Importance of homocysteine-induced abnormalities of proteoglycan structure in arteriosclerosis.

作者信息

McCully K S

出版信息

Am J Pathol. 1970 Apr;59(1):181-94.

PMID:4245558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2032855/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/927a/2032855/e73144e67207/amjpathol00567-0218-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/927a/2032855/23f3a5c7aec2/amjpathol00567-0216-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/927a/2032855/4c4c9240a445/amjpathol00567-0216-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/927a/2032855/a988b47a6dcf/amjpathol00567-0217-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/927a/2032855/c2d4337a4dcd/amjpathol00567-0217-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/927a/2032855/8f87a8faed8f/amjpathol00567-0218-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/927a/2032855/e73144e67207/amjpathol00567-0218-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/927a/2032855/23f3a5c7aec2/amjpathol00567-0216-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/927a/2032855/4c4c9240a445/amjpathol00567-0216-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/927a/2032855/a988b47a6dcf/amjpathol00567-0217-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/927a/2032855/c2d4337a4dcd/amjpathol00567-0217-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/927a/2032855/8f87a8faed8f/amjpathol00567-0218-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/927a/2032855/e73144e67207/amjpathol00567-0218-b.jpg

相似文献

1
Importance of homocysteine-induced abnormalities of proteoglycan structure in arteriosclerosis.同型半胱氨酸诱导的蛋白聚糖结构异常在动脉硬化中的重要性。
Am J Pathol. 1970 Apr;59(1):181-94.
2
[Biochemical aspects of some congenital anomalies of the metabolism of sulfur amino acids].
Expos Annu Biochim Med. 1967;28:53-76.
3
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Incorporation of amino acids into fractions of insoluble collagen. Evaluation of metabolic homogeneity of collagen fibres.氨基酸掺入不溶性胶原蛋白组分。胶原蛋白纤维代谢同质性的评估。
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Glycosaminoglycans and sialoproteins in skin aging.皮肤老化中的糖胺聚糖和唾液酸蛋白。
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Deranged B 12 metabolism: studies of fibroblasts grown in tissue culture.维生素B12代谢紊乱：组织培养中生长的成纤维细胞研究
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[Hyperhomocysteinemia, atherosclerosis and arterial and venous thrombosis].[高同型半胱氨酸血症、动脉粥样硬化与动静脉血栓形成]
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Label-free quantification of host cell protein impurity in recombinant hemoglobin materials.无标签定量检测重组血红蛋白制品中宿主细胞蛋白杂质。
Anal Bioanal Chem. 2024 Jan;416(2):387-396. doi: 10.1007/s00216-023-05024-8. Epub 2023 Nov 26.
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Chemical and biomechanical characterization of hyperhomocysteinemic bone disease in an animal model.动物模型中高同型半胱氨酸血症性骨病的化学和生物力学特征
BMC Musculoskelet Disord. 2003 Feb 20;4:2. doi: 10.1186/1471-2474-4-2.
3
Production of arteriosclerosis by homocysteinemia.同型半胱氨酸血症导致动脉硬化

本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
Methyl mercaptan in relation to foetor hepaticus.与肝臭相关的甲硫醇
Biochem J. 1955 Mar;59(3):372-5.
3
SYNTHESIS OF HYDROXYPROLINE IN VITRO BY THE HYDROXYLATION OF PROLINE IN A PRECURSOR OF COLLAGEN.通过在胶原蛋白前体中将脯氨酸羟基化在体外合成羟脯氨酸。
Am J Pathol. 1970 Oct;61(1):1-11.
4
Macromolecular basis for homocystein-induced changes in proteoglycan structure in growth and arteriosclerosis.同型半胱氨酸诱导的生长及动脉硬化中蛋白聚糖结构变化的大分子基础
Am J Pathol. 1972 Jan;66(1):83-96.
5
Homocystinuria. Reduced folate levels during pyridoxine treatment.同型胱氨酸尿症。维生素B6治疗期间叶酸水平降低。
Arch Dis Child. 1973 Jan;48(1):58-62. doi: 10.1136/adc.48.1.58.
6
Inborn errors of metabolism. Vitamin-responsive genetic disease.先天性代谢缺陷。维生素反应性遗传病。
J Clin Pathol Suppl (R Coll Pathol). 1974;8:38-47.
Proc Natl Acad Sci U S A. 1965 Mar;53(3):661-8. doi: 10.1073/pnas.53.3.661.
4
HOMOCYSTINURIA. STUDIES OF 20 FAMILIES WITH 38 AFFECTED MEMBERS.同型胱氨酸尿症。对20个家庭中38名患者的研究。
JAMA. 1965 Aug 30;193:711-9. doi: 10.1001/jama.1965.03090090017003.
5
AMINO-ACID COMPOSITION OF HUMAN DERMAL COLLAGEN.人真皮胶原蛋白的氨基酸组成
Nature. 1965 Jan 16;205:264-6. doi: 10.1038/205264a0.
6
HOMOCYSTINURIA: CLINICAL AND PATHOLOGICAL REVIEW OF TEN CASES.同型胱氨酸尿症：10例临床与病理回顾
J Pediatr. 1965 Mar;66:565-83. doi: 10.1016/s0022-3476(65)80121-4.
7
PARTIAL STRUCTURE OF TWO MAJOR DEGRADATION PRODUCTS FROM THE CROSS-LINKAGES IN ELASTIN.弹性蛋白中交联键产生的两种主要降解产物的部分结构
Nature. 1963 Nov 16;200:651-2. doi: 10.1038/200651a0.
8
HOMOCYSTINURIA: AN ENZYMATIC DEFECT.同型胱氨酸尿症：一种酶缺陷。
Science. 1964 Mar 27;143(3613):1443-5. doi: 10.1126/science.143.3613.1443.
9
HOMOCYSTINURIA: A NEW INBORN ERROR OF METABOLISM ASSOCIATED WITH MENTAL DEFICIENCY.同型胱氨酸尿症：一种与智力缺陷相关的新的先天性代谢紊乱。
Arch Dis Child. 1963 Oct;38(201):425-36. doi: 10.1136/adc.38.201.425.
10
Mucopolysaccharides in the atheromatous aorta.动脉粥样硬化主动脉中的粘多糖。
J Pathol Bacteriol. 1962 Oct;84:405-12. doi: 10.1002/path.1700840214.