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Matrix (Stuttgart, Germany)|March 1, 1989
Ehlers-Danlos syndrome type VI with normal lysyl hydroxylase activity cannot be explained by a defect in cellular uptake of ascorbic acidP M Royce, U Moser, B SteinmannSchweizer Archiv Fur Tierheilkunde|September 4, 2010
[Benefit of clinical and laboratory parameters for the diagnosis of endometritis in dairy cows]M Hässig, B Steinmann, M M WittenbrinkThe Journal of Biological Chemistry|January 15, 1991
Cyclosporin A slows collagen triple-helix formation in vivo: indirect evidence for a physiologic role of peptidyl-prolyl cis-trans-isomeraseB Steinmann, P Bruckner, A Superti-FurgaPlos One|May 19, 2010
Repeated and time-correlated morphological convergence in cave-dwelling harvestmen (Opiliones, Laniatores) from Montane Western North AmericaShahan Derkarabetian, David B Steinmann, Marshal HedinThe Journal of Biological Chemistry|July 5, 1986
Clinical variability of osteogenesis imperfecta reflecting molecular heterogeneity: cysteine substitutions in the alpha 1(I) collagen chain producing lethal and mild formsB Steinmann, A Nicholls, F M PopePlant Foods for Human Nutrition (Dordrecht, Netherlands)|January 1, 1993
Early effects and the possible mechanism of the effect of Concanavalin A (con A) and Phaseolus vulgaris lectin (PHA-P) on intestinal absorption of calcium and sucroseR Ayyagari, M Raghunath, B S RaoNutritional Neuroscience|July 15, 2016
Probable Basis of Altered BBB Nutrient Transport in the Offspring of Severely Hypothyroid DamsS B Sundari, M Rupalatha, M RaghunathMethods of Information in Medicine|December 14, 2005
Marfan syndrome--a diagnostic challenge caused by phenotypic and genetic heterogeneityC Baumgartner, G Mátyás, B Steinmann, et al.Helvetica Paediatrica Acta|April 1, 1977
Uridine diphosphate galactose 4'-epimerase deficiency. IV. Report of eight cases in three familiesR Gitzelmann, B Steinmann, B Mitchell, et al.Connective Tissue Research|January 1, 1993
Normal production, nature, and extent of intracellular degradation of newly synthesized collagen in fibroblasts from a patient with prolidase deficiencyV H Rao, P M Royce, B SteinmannPageof 23