Showing results (1-10 of 12) with videos related to
Sort By:
Pageof 2
The Biochemical Journal|March 1, 1984
Specificity studies on the oligosaccharide neuraminidase of human fibroblastsK Mendla, M CantzThe European Journal of Neuroscience|May 1, 2001
Protein kinase Calpha and beta1 isoforms are regulators of alpha-secretory proteolytic processing of amyloid precursor protein in vivoS Rossner, K Mendla, R Schliebs, et al.Pediatric Research|March 1, 1984
Partial deficiency of glycoprotein neuraminidase in some patients with Morquio disease type AJ Glössl, H Kresse, K Mendla, et al.Life Sciences|January 1, 1997
Muscarinic M1 receptor agonists increase the secretion of the amyloid precursor protein ectodomainD M Müller, K Mendla, S A Farber, et al.The Biochemical Journal|February 15, 1988
Defective lysosomal release of glycoprotein-derived sialic acid in fibroblasts from patients with sialic acid storage diseaseK Mendla, J Baumkötter, C Rosenau, et al.Neuroscience Letters|April 11, 1997
Dependence of cerebrospinal fluid Tau protein levels on apolipoprotein E4 allele frequency in patients with Alzheimer's diseaseS Golombowski, F Müller-Spahn, H Romig, et al.The European Journal of Neuroscience|September 21, 2000
Constitutive overactivation of protein kinase C in guinea pig brain increases alpha-secretory APP processing without decreasing beta-amyloid generationS Rossner, M Beck, T Stahl, et al.Human Genetics|January 1, 1985
N-Acetylneuraminic acid storage diseaseJ Baumkötter, M Cantz, K Mendla, et al.European Journal of Drug Metabolism and Pharmacokinetics|July 1, 1994
Medicinal chemistry of muscarinic agonists for the treatment of dementia disordersE Cereda, A Brambilla, A Ezhaya, et al.Prenatal Diagnosis|November 1, 1986
Prenatal diagnosis and confirmation of infantile sialic acid storage diseaseE Vamos, J Libert, N Elkhazen, et al.Pageof 2