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Correction

Correction MEETING SUMMARY: LIPOPROTEIN HETEROGENEITY WORKSHOP 323 Since so many lipoprotein subspecies exist, many in- lytic technique for identifying IDL, LDL, and HDL subspe- vestigators hoped that there could be some unifying ana- cies and that Lindgren's cumulative flotation method was lytic technique and nomenclature. It was suggested that best for both identifying and isolating VLDL subclasses, gradient gel electrophoresis might be the overall best ana- which mostly are too big for the gel technique. Index Terms: lipoproteins • apo B • triglyceride-rich lipoproteins • cholesteryl-rich lipoproteins metabolism • dietary effects • genetics • high density lipoproteins The Editors regret the errors in the figure legends in the articles by Rosenfeld et al. in the January/February issue of Arteriosclerosis. In the first article (Rosenfeld ME, Tsukada T, Gown AM, Ross R. Fatty Streak Initiation in Watanabe Heritable Hyperlipemic and Comparably Hypercholesterolemic Fat-Fed Rabbits), the magnifications should be as follows: Figure 3A. Bar = 100 jam x 36. Figure 12. Bar = 10/*m x 1574. Figure 3B. Bar = 100 fjum x 30. Figure 13. Bar = 100 /im x 250. Figure 14A. Bar = 1 /im x 7181. Figure 4. Bar = 1 ^ m x 4787. Figure 5. Bar = 10 /u,m x 600. Figure 14B. Bar = 1 ^m x 5689. Figure 6. Bar = 1 ^ m x 7041. Figure 15. Bar = 0.1 /-on x 27,329. Figure 7A. Bar = 10 fjum x 720. Figure 16A. Bar = 10 JLUTI X 1575. Figure 7B. Bar = 10/Am x 1000. Figure 16B. Bar = 10 /xm x 1000. Figure 17A. Bar = 1 /xm x 10,806. Figure 8A. Bar = 1 ^ m x 3000. Figure 8B. Bar = 1 /xm x 7000. Figure 17B. Bar = 1 /xm x 15,431. Figure 9. Bar = 1 /urn x 5032. Figure 18. Bar = 1 /xm x 5000. Figure 10A. Bar = 1 ^ m x 7190. Figure 19. Bar =1^m x 5689. Figure 10B. Bar = 1 pm x 8366. Figure 20A. Bar = 1 fxm x 8296. Figure 20B. Bar = 1 ^ m x 9575. Figure 11 A. Bar = 10 /^m x 1478. Figure 11B. Bar = 1 ^ m x 4187. In the second article (Rosenfeld ME, Tsukada T, Chait A, Bierman EL, Gown AM, Ross R. Fatty Streak Expansion and Maturation in Watanabe Heritable Hyperlipemic and Comparably Hypercholesterolemic Fat-Fed Rabbits), the magnifica- tions should be as follows: Figure 4. Bars = 100 /xm x 150. Figure 10A. Bar = 1 /xm x 4000. Figure 5. Bars = 100 /xm x 182. Figure 10B. Bar = 1 /xm x 5075. Figure 6A. Bar = 1 /xm x 3086. Figure 11 A. Bar = 1 ^ m x 1068. Figure 6B. Bar = 1 /xm x 2062. Figure 11B. Bar = 100 fxm x 100. Figure 7A. Bar = 100 /xm x 157. Figure 12A. Bar = 10 pm x 600. Figure 7B. Bar = 100 /tm x 100. Figure 12B. Bar = 10/im x 2400. Figure 8A. Bar = 1 /xm x 2510. Figure 13A. Bar = 100 ^m x 100. Figure 8B. Bar = 1 /xm x 3421. Figure 13B. Bar = 10 /xm x 400. Figure 9A. Bar = 100 /tm x 90. Figure 14. Bar = 1 /xm x 8059. Figure 9B. Bar = 100 /xm x 78. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Arteriosclerosis Wolters Kluwer Health

Correction

Arteriosclerosis , Volume 7 (3) – May 1, 1987
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Copyright
© 1987 by American Heart Association, Inc.
ISSN
0276-5047

Abstract

MEETING SUMMARY: LIPOPROTEIN HETEROGENEITY WORKSHOP 323 Since so many lipoprotein subspecies exist, many in- lytic technique for identifying IDL, LDL, and HDL subspe- vestigators hoped that there could be some unifying ana- cies and that Lindgren's cumulative flotation method was lytic technique and nomenclature. It was suggested that best for both identifying and isolating VLDL subclasses, gradient gel electrophoresis might be the overall best ana- which mostly are too big for the gel technique. Index Terms: lipoproteins • apo B • triglyceride-rich lipoproteins • cholesteryl-rich lipoproteins metabolism • dietary effects • genetics • high density lipoproteins The Editors regret the errors in the figure legends in the articles by Rosenfeld et al. in the January/February issue of Arteriosclerosis. In the first article (Rosenfeld ME, Tsukada T, Gown AM, Ross R. Fatty Streak Initiation in Watanabe Heritable Hyperlipemic and Comparably Hypercholesterolemic Fat-Fed Rabbits), the magnifications should be as follows: Figure 3A. Bar = 100 jam x 36. Figure 12. Bar = 10/*m x 1574. Figure 3B. Bar = 100 fjum x 30. Figure 13. Bar = 100 /im x 250. Figure 14A. Bar = 1 /im x 7181. Figure 4. Bar = 1 ^ m x 4787. Figure 5. Bar = 10 /u,m x 600. Figure 14B. Bar = 1 ^m x 5689. Figure 6. Bar = 1 ^ m x 7041. Figure 15. Bar = 0.1 /-on x 27,329. Figure 7A. Bar = 10 fjum x 720. Figure 16A. Bar = 10 JLUTI X 1575. Figure 7B. Bar = 10/Am x 1000. Figure 16B. Bar = 10 /xm x 1000. Figure 17A. Bar = 1 /xm x 10,806. Figure 8A. Bar = 1 ^ m x 3000. Figure 8B. Bar = 1 /xm x 7000. Figure 17B. Bar = 1 /xm x 15,431. Figure 9. Bar = 1 /urn x 5032. Figure 18. Bar = 1 /xm x 5000. Figure 10A. Bar = 1 ^ m x 7190. Figure 19. Bar =1^m x 5689. Figure 10B. Bar = 1 pm x 8366. Figure 20A. Bar = 1 fxm x 8296. Figure 20B. Bar = 1 ^ m x 9575. Figure 11 A. Bar = 10 /^m x 1478. Figure 11B. Bar = 1 ^ m x 4187. In the second article (Rosenfeld ME, Tsukada T, Chait A, Bierman EL, Gown AM, Ross R. Fatty Streak Expansion and Maturation in Watanabe Heritable Hyperlipemic and Comparably Hypercholesterolemic Fat-Fed Rabbits), the magnifica- tions should be as follows: Figure 4. Bars = 100 /xm x 150. Figure 10A. Bar = 1 /xm x 4000. Figure 5. Bars = 100 /xm x 182. Figure 10B. Bar = 1 /xm x 5075. Figure 6A. Bar = 1 /xm x 3086. Figure 11 A. Bar = 1 ^ m x 1068. Figure 6B. Bar = 1 /xm x 2062. Figure 11B. Bar = 100 fxm x 100. Figure 7A. Bar = 100 /xm x 157. Figure 12A. Bar = 10 pm x 600. Figure 7B. Bar = 100 /tm x 100. Figure 12B. Bar = 10/im x 2400. Figure 8A. Bar = 1 /xm x 2510. Figure 13A. Bar = 100 ^m x 100. Figure 8B. Bar = 1 /xm x 3421. Figure 13B. Bar = 10 /xm x 400. Figure 9A. Bar = 100 /tm x 90. Figure 14. Bar = 1 /xm x 8059. Figure 9B. Bar = 100 /xm x 78.

Journal

Arteriosclerosis – Wolters Kluwer Health

Published: May 1, 1987

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