Predicted genetic burden and frequency of phenotype-associated variants in the horse von Durward-Akhurst, S. A., Marlowe, J. L., Schaefer, R. J., Springer, K., Grantham, B., Carey, W. K., Bellone, R. R., Mickelson, J. R., McCue, M. E.

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Genetic Variation and the Distribution of Variant Types in the Horse von Durward-Akhurst, S A, Schaefer, R J, Grantham, B, Carey, W K, Mickelson, J R, McCue, M E

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Identification of a gene variant in the master regulator of lipid metabolism SREBP-1 in a family with a novel form of severe combined hypolipidemia von Kotzka, Jorg, Knebel, Birgit, Janssen, Onno E, Schaefer, J.R, Soufi, M, Jacob, Sylvia, Nitzgen, Ulrike, Muller-Wieland, Dirk

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The convergence-fault mechanism for low-angle boundary formation in single-crystal castings von NAPOLITANO, R. E, SCHAEFER, R. J

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Novel aspects on RANK ligand and osteoprotegerin in osteoporosis and vascular disease von Sattler, A M, Schoppet, M, Schaefer, J R, Hofbauer, L C

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Metabolic basis of high density lipoproteins and apolipoprotein A-I increase by HMG-CoA reductase inhibition in healthy subjects and a patient with coronary artery disease von Schaefer, J.R., Schweer, H., Ikewaki, K., Stracke, H., Seyberth, H.J., Kaffarnik, H., Maisch, B., Steinmetz, A.

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In vivo turnover study demonstrates diminished clearance of lipoprotein(a) in hemodialysis patients von Frischmann, M.E., Kronenberg, F., Trenkwalder, E., Schaefer, J.R., Schweer, H., Dieplinger, B., Koenig, P., Ikewaki, K., Dieplinger, H.

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HDL level or HDL function as the primary target in preventive cardiology von Schaefer, J R

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Computation of dendrites using a phase field model von Wheeler, A.A., Murray, B.T., Schaefer, R.J.

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Congenital Disorder of Glycosylation IId (CDG-IId) - A New Entity: Clinical Presentation with Dandy-Walker Malformation and Myopathy von Peters, V., Penzien, J. M., Reiter, G., Körner, C., Hackler, R., Assmann, B., Fang, J., Schaefer, J. R., Hoffmann, G. F., Heidemann, P. H.

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Delayed catabolism of high density lipoprotein apolipoproteins A-I and A-II in human cholesteryl ester transfer protein deficiency von IKEWAKI, K, RADER, D. J, NAGANO, M, BREWER, H. B, SAKAMOTO, T, NISHIWAKI, M, WAKIMOTO, N, SCHAEFER, J. R, ISHIKAWA, T, FAIRWELL, T, ZECH, L. A, NAKAMURA, H

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Evaluation of apoA-I kinetics in humans using simultaneous endogenous stable isotope and exogenous radiotracer methods von IKEWAKI, K, RADER, D. J, SCHAEFER, J. R, FAIRWELL, T, ZECH, L. A, BREWER, H. B

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Unsaturated fatty acids isolated from human lipoproteins activate protein phosphatase type 2Cβ and induce apoptosis in endothelial cells von Hufnagel, B., Dworak, M., Soufi, M., Mester, Z., Zhu, Y., Schaefer, J.R., Klumpp, S., Krieglstein, J.

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A new case of CDG‐x with stereotyped dystonic hand movements and optic atrophy von Prietsch, V., Peters, V., Hackler, R., Jakobi, R., Assmann, B., Fang, J., Körner, C., Helwig‐Rolig, A., Schaefer, J. R., Hoffmann, G. F.

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Analytical and numerical predictions of dendritic grain envelopes von Gandin, Ch.-A., Schaefer, R.J., Rappax, M.

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Increased Production of HDL ApoA-I in Homozygous Familial Defective ApoB-100 von Schaefer, J R, Winkler, K, Schweer, H, Hoffmann, M M, Soufi, M, Scharnagl, H, Maisch, B, Wieland, H, Steinmetz, A, März, W

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Forty-eight year decline and fragmentation of aspen ( Populus tremuloides) in the South Warner Mountains of California von Di Orio, Aaron P., Callas, Richard, Schaefer, Robert J.

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Homozygous familial hypercholesterolaemia in identical twins von Zschocke, J, Schaefer, JR

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A New Subtype of a Congenital Disorder of Glycosylation (CDG) with Mild Clinical Manifestations von Assmann, B., Hackler, R., Peters, V., Schaefer, J. R., Arndt, T., Mayatepek, E., Jaeken, J., Hoffmann, G. F.

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HDL steady state levels are not affected, but HDL apoA-I turnover is enhanced by Lifibrol in patients with hypercholesterolemia and mixed hyperlipidemia von Winkler, K., Schaefer, J.R., Klima, B., Nuber, C., Friedrich, I., Köster, W., Gierens, H., Scharnagl, H., Soufi, M., Wieland, H., März, W.

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