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Gene|June 14, 1995
Double-differential PCR for gene dosage estimation of erbB oncogenes in benign and cancer tissues and comparison to cellular DNA contentB Brandt, U Vogt, F Harms, et al.The Journal of Clinical Investigation|May 16, 1998
Phenotype-dependent differences in apolipoprotein E metabolism and in cholesterol homeostasis in human monocyte-derived macrophagesP Cullen, A Cignarella, B Brennhausen, et al.Zeitschrift Fur Rheumatologie|August 31, 2019
[Experiences and results from Rheuma-VOR]A Schwarting, M Dreher, G Assmann, et al.Clinical and Experimental Rheumatology|October 24, 2008
A novel system to test for specificity of B cell receptors from tissue of Wegener's granulomatosis patientsJ Voswinkel, A J Kerkdijk, A Mueller, et al.Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|October 1, 1996
Elevated low-density lipoprotein-cholesterol in women with polycystic ovary syndromeS von Eckardstein, A von Eckardstein, H G Bender, et al.Biochimica Et Biophysica Acta|June 13, 1996
Diadenosine polyphosphates regulate cytosolic calcium in human fibroblast cells by interaction with P2x purinoceptors coupled to phospholipase CM Tepel, S Löwe, J R Nofer, et al.European Journal of Clinical Investigation|September 1, 1992
Severe type III hyperlipoproteinemia associated with unusual apolipoprotein E1 phenotype and epsilon 1/'null' genotypeG Feussner, H Funke, W Weng, et al.American Journal of Human Genetics|May 1, 1992
Nonsynonymous polymorphic sites in the apolipoprotein (apo) A-IV gene are associated with changes in the concentration of apo B- and apo A-I-containing lipoproteins in a normal populationA von Eckardstein, H Funke, M Schulte, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|May 1, 1995
Reverse cholesterol transport in plasma of patients with different forms of familial HDL deficiencyA von Eckardstein, Y Huang, S Wu, et al.Journal of Lipid Research|February 1, 1997
The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromesJ A Kuivenhoven, H Pritchard, J Hill, et al.Pageof 38