Skip to main content
NCBI home page
Journal of Clinical Pathology. Supplement (Association of Clinical Pathologists) logoLink to Journal of Clinical Pathology. Supplement (Association of Clinical Pathologists)
. 1973;5:38–42. doi: 10.1136/jcp.s1-5.1.38

The pathogenesis of atherosclerosis.

C W Adams
PMCID: PMC1436089  PMID: 4270163

Full text

PDF
38

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ADAMS C. W. ARTERIOSCLEROSIS IN MAN, OTHER MAMMALS AND BIRDS. Biol Rev Camb Philos Soc. 1964 Aug;39:372–423. doi: 10.1111/j.1469-185x.1964.tb01163.x. [DOI] [PubMed] [Google Scholar]
  2. ADAMS C. W., BAYLISS O. B., IBRAHIM M. Z. A hypothesis to explain the accumulation of cholesterol in atherosclerosis. Lancet. 1962 Apr 28;1(7235):890–892. doi: 10.1016/s0140-6736(62)91914-1. [DOI] [PubMed] [Google Scholar]
  3. ADAMS C. W., BAYLISS O. B., IBRAHIM M. Z., WEBSTER M. W., Jr PHOSPHOLIPIDS IN ATHEROSCLEROSIS: THE MODIFICATION OF THE CHOLESTEROL GRANULOMA BY PHOSPHOLIPID. J Pathol Bacteriol. 1963 Oct;86:431–436. doi: 10.1002/path.1700860217. [DOI] [PubMed] [Google Scholar]
  4. Abdulla Y. H., Adams C. W., Bayliss O. B. Relative absence of triglycerides in coronary atherosclerotic lesions. J Atheroscler Res. 1969 Sep-Oct;10(2):149–152. doi: 10.1016/s0368-1319(69)80003-7. [DOI] [PubMed] [Google Scholar]
  5. Abdulla Y. H., Adams C. W., Morgan R. S. Connective-tissue reactions to implantation of purified sterol, sterol esters, phosphoglycerides, glycerides and free fatty acids. J Pathol Bacteriol. 1967 Jul;94(1):63–71. doi: 10.1002/path.1700940109. [DOI] [PubMed] [Google Scholar]
  6. Adams C. W., Abdulla Y. H., Bayliss O. B. Entry of esterified cholesterol into foam cells. Atherosclerosis. 1971 Jan-Feb;13(1):111–119. doi: 10.1016/0021-9150(71)90012-8. [DOI] [PubMed] [Google Scholar]
  7. Adams C. W., Bayliss O. B., Abdulla Y. H., Mahler F. R., Root M. A. Lipase, esterase and triglyceride in the aging human aorta. J Atheroscler Res. 1969 Jan-Feb;9(1):87–102. doi: 10.1016/s0368-1319(69)80070-0. [DOI] [PubMed] [Google Scholar]
  8. Adams C. W., Bayliss O. B. The relationship between diffuse intimal thickening, medial enzyme failure and intimal lipid deposition in various human arteries. J Atheroscler Res. 1969 Nov-Dec;10(3):327–339. doi: 10.1016/s0368-1319(69)80036-0. [DOI] [PubMed] [Google Scholar]
  9. Adams C. W. Lipids, lipoproteins and atherosclerotic lesions. Proc R Soc Med. 1971 Sep;64(9):902–905. doi: 10.1177/003591577106400912. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Adams C. W., Morgan R. S., Bayliss O. B. The differential entry of [125-I] albumin into mildly and severely atheromatous rabbit aortas. Atherosclerosis. 1970 Jan-Feb;11(1):119–124. doi: 10.1016/0021-9150(70)90010-9. [DOI] [PubMed] [Google Scholar]
  11. Adams C. W., Morgan R. S. The effect of saturated and polyunsaturated lecithins on the resorption of 4-14-C-cholesterol from subcutaneous implants. J Pathol Bacteriol. 1967 Jul;94(1):73–76. doi: 10.1002/path.1700940110. [DOI] [PubMed] [Google Scholar]
  12. Armstrong M. L., Megan M. B. Lipid depletion in atheromatous coronary arteries in rhesus monkeys after regression diets. Circ Res. 1972 Jun;30(6):675–680. doi: 10.1161/01.res.30.6.675. [DOI] [PubMed] [Google Scholar]
  13. BOETTCHER C. J. CHEMICAL CONSTITUENTS OF HUMAN ATHEROSCLEROTIC LESIONS. Proc R Soc Med. 1964 Sep;57:792–795. doi: 10.1177/003591576405700911. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Bihari-Varga M., Végh M. Quantitative studies on the complexes formed between aortic mucopolysaccharides and serum lipoproteins. Biochim Biophys Acta. 1967 Oct 2;144(2):202–210. doi: 10.1016/0005-2760(67)90150-6. [DOI] [PubMed] [Google Scholar]
  15. Björkerud S., Bondjers G. Endothelial integrity and viability in the aorta of the normal rabbit and rat as evaluated with dye exclusion tests and interference contrast microscopy. Atherosclerosis. 1972 May-Jun;15(3):285–300. doi: 10.1016/0021-9150(72)90019-6. [DOI] [PubMed] [Google Scholar]
  16. Constantinides P., Robinson M. Ultrastructural injury of arterial endothelium. II. Effects of vasoactive amines. Arch Pathol. 1969 Aug;88(2):106–112. [PubMed] [Google Scholar]
  17. DAWBER T. R., KANNEL W. B., REVOTSKIE N., KAGAN A. The epidemiology of coronary heart disease--the Framingham enquiry. Proc R Soc Med. 1962 Apr;55:265–271. doi: 10.1177/003591576205500403. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. DUGUID J. B. The arterial lining. Lancet. 1952 Aug 2;2(6727):207–208. doi: 10.1016/s0140-6736(52)91543-2. [DOI] [PubMed] [Google Scholar]
  19. French J. E. Atherosclerosis in relation to the structure and function of the arterial intima, with special reference to th endothelium. Int Rev Exp Pathol. 1966;5:253–353. [PubMed] [Google Scholar]
  20. Fry D. L. Acute vascular endothelial changes associated with increased blood velocity gradients. Circ Res. 1968 Feb;22(2):165–197. doi: 10.1161/01.res.22.2.165. [DOI] [PubMed] [Google Scholar]
  21. GERO S., GERGELY J., DEVENYI T., JAKAB L., SZEKELY J., VIRAG S. Role of mucoid substances of the aorta in the deposition of lipids. Nature. 1960 Jul 9;187:152–153. doi: 10.1038/187152a0. [DOI] [PubMed] [Google Scholar]
  22. GERO S., GERGELY J., JAKAB L., SZEKELY J., VIRAG S. Comparative immunoelectrophoretic studies on homogenates of aorta, pulmonary arteries and inferior vena cava of atherosclerotic individuals. J Atheroscler Res. 1961 Jan-Feb;1:88–91. doi: 10.1016/s0368-1319(61)80059-8. [DOI] [PubMed] [Google Scholar]
  23. HEPTINSTALL R. H., BARKLEY H., PORTER K. A. The relative roles of blood cholesterol level and blood pressure level in the production of experimental aortic atheroma in rabbits. Angiology. 1958 Apr;9(2):84–87. doi: 10.1177/000331975800900206. [DOI] [PubMed] [Google Scholar]
  24. Hoff H. F. Effect of hypoxia on phosphoesterases, oxidative and glycolytic enzymes in the rabbit common carotid artery. A histochemical study. Histochemie. 1970;23(3):244–253. doi: 10.1007/BF00306426. [DOI] [PubMed] [Google Scholar]
  25. KIRK J. E., LAURSEN T. J. Diffusion coefficients of various solutes for human aortic tissue, with special reference to variation to tissue permeability with age. J Gerontol. 1955 Jul;10(3):288–302. doi: 10.1093/geronj/10.3.288. [DOI] [PubMed] [Google Scholar]
  26. Kao V. C., Wissler R. W. A study of the immunohistochemical localization of serum lipoproteins and other plasma proteins in human atherosclerotic lesions. Exp Mol Pathol. 1965 Oct;4(5):465–479. doi: 10.1016/0014-4800(65)90011-0. [DOI] [PubMed] [Google Scholar]
  27. Lofland H. B., Jr, St Clair R. W., Clarkson T. B., Bullock B. C., Lehner N. D. Atherosclerosis in Cebus monkeys. II. Arterial metabolism. Exp Mol Pathol. 1968 Aug;9(1):57–70. doi: 10.1016/0014-4800(68)90050-6. [DOI] [PubMed] [Google Scholar]
  28. McMILLAN G. C., HORLICK L., DUFF G. L. Cholesterol content of aorta in relation to severity of atherosclerosis; studies during progression and retrogression of experimental lesions. AMA Arch Pathol. 1955 Mar;59(3):285–290. [PubMed] [Google Scholar]
  29. NEWMAN H. A., ZILVERSMIT D. B. Quantitative aspects of cholesterol flux in rabbit atheromatous lesions. J Biol Chem. 1962 Jul;237:2078–2084. [PubMed] [Google Scholar]
  30. Newman D. L., Gosling R. G., Bowden N. L. Changes in aortic distensibility and area ratio with the development of atherosclerosis. Atherosclerosis. 1971 Sep-Oct;14(2):231–240. doi: 10.1016/0021-9150(71)90052-9. [DOI] [PubMed] [Google Scholar]
  31. Newman H. A., Zilversmit D. B. Uptake and release of cholesterol by rabbit atheromatous lesions. Circ Res. 1966 Mar;18(3):293–302. doi: 10.1161/01.res.18.3.293. [DOI] [PubMed] [Google Scholar]
  32. Nilsson A., Zilversmit D. B. Fate of intravenously administered particulate and lipoprotein cholesterol in the rat. J Lipid Res. 1972 Jan;13(1):32–38. [PubMed] [Google Scholar]
  33. PAGE I. H. Atherosclerosis; an introduction. Circulation. 1954 Jul;10(1):1–27. doi: 10.1161/01.cir.10.1.1. [DOI] [PubMed] [Google Scholar]
  34. Rothblat G. H., Kritchevsky D. The excretion of free and ester cholesterol by tissue culture cells: studies with L5178Y and L-cells. Biochim Biophys Acta. 1967 Oct 2;144(2):423–429. doi: 10.1016/0005-2760(67)90172-5. [DOI] [PubMed] [Google Scholar]
  35. SPAIN D. M., ARISTIZABAL N. Rabbit local tissue response to triglycerides, cholesterol, and its ester. Arch Pathol. 1962 Jan;73:82–85. [PubMed] [Google Scholar]
  36. STEIN Y., STEIN O., SHAPIRO B. Enzymic pathways of glyceride and phospholipid synthesis in aortic homogenates. Biochim Biophys Acta. 1963 Feb 19;70:33–42. doi: 10.1016/0006-3002(63)90716-9. [DOI] [PubMed] [Google Scholar]
  37. Scott P. J., Hurley P. J. The distribution of radio-iodinated serum albumin and low-density lipoprotein in tissues and the arterial wall. Atherosclerosis. 1970 Jan-Feb;11(1):77–103. doi: 10.1016/0021-9150(70)90008-0. [DOI] [PubMed] [Google Scholar]
  38. Smith E. B., Evans P. H., Downham M. D. Lipid in the aortic intima. The correlation of morphological and chemical characteristics. J Atheroscler Res. 1967 Mar-Apr;7(2):171–186. doi: 10.1016/s0368-1319(67)80079-6. [DOI] [PubMed] [Google Scholar]
  39. Smith E. B., Slater R. S., Chu P. K. The lipids in raised fatty and fibrous lesions in human aorta. A comparison of the changes at different stages of development. J Atheroscler Res. 1968 May-Jun;8(3):399–419. doi: 10.1016/s0368-1319(68)80097-3. [DOI] [PubMed] [Google Scholar]
  40. Smith E. B., Slater R. S. Relationship between low-density lipoprotein in aortic intima and serum-lipid levels. Lancet. 1972 Feb 26;1(7748):463–469. doi: 10.1016/s0140-6736(72)90122-5. [DOI] [PubMed] [Google Scholar]
  41. Smith E. B., Slater R. The chemical and immunological assay of low density lipoproteins extracted from human aortic intima. Atherosclerosis. 1970 May-Jun;11(3):417–438. doi: 10.1016/0021-9150(70)90021-3. [DOI] [PubMed] [Google Scholar]
  42. St Clair R. W., Lofland H. B., Jr, Clarkson T. B. Composition and synthesis of fatty acids in atherosclerotic aortas of the pigeon. J Lipid Res. 1968 Nov;9(6):739–747. [PubMed] [Google Scholar]
  43. WOLINSKY H., GLAGOV S. STRUCTURAL BASIS FOR THE STATIC MECHANICAL PROPERTIES OF THE AORTIC MEDIA. Circ Res. 1964 May;14:400–413. doi: 10.1161/01.res.14.5.400. [DOI] [PubMed] [Google Scholar]
  44. Walton K. W., Williamson N. Histological and immunofluorescent studies on the evolution of the human atheromatous plaque. J Atheroscler Res. 1968 Jul-Aug;8(4):599–624. doi: 10.1016/s0368-1319(68)80020-1. [DOI] [PubMed] [Google Scholar]
  45. Woolf N., Pilkington T. R. The immunohistochemical demonstration of lipoproteins in vessel walls. J Pathol Bacteriol. 1965 Oct;90(2):459–463. doi: 10.1002/path.1700900213. [DOI] [PubMed] [Google Scholar]
  46. Wright H. P. Areas of mitosis in aortic endothelium of guinea-pigs. J Pathol. 1971 Sep;105(1):65–67. doi: 10.1002/path.1711050110. [DOI] [PubMed] [Google Scholar]
  47. Wright H. P. Mitosis patterns in aortic endothelium. Atherosclerosis. 1972 Jan-Feb;15(1):93–100. doi: 10.1016/0021-9150(72)90042-1. [DOI] [PubMed] [Google Scholar]
  48. ZEMPLENYI T. Enzymes of the arterial wall. J Atheroscler Res. 1962 Jan-Apr;2:2–24. doi: 10.1016/s0368-1319(62)80048-9. [DOI] [PubMed] [Google Scholar]
  49. ZILVERSMIT D. B., SHORE M. L., ACKERMAN R. F. The origin of aortic phospholipid in rabbit atheromatosis. Circulation. 1954 Apr;9(4):581–585. doi: 10.1161/01.cir.9.4.581. [DOI] [PubMed] [Google Scholar]
  50. Zilversmit D. B. Cholesterol flux in the atherosclerotic plaque. Ann N Y Acad Sci. 1968 Nov 21;149(2):710–724. doi: 10.1111/j.1749-6632.1968.tb53830.x. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Clinical Pathology. Supplement (Ass. Clin. Path.) are provided here courtesy of BMJ Publishing Group

RESOURCES