Search Results - "Hanisch, F.G" :: K.UTB vyhledávací portál

A.P.5

by Schessl, J, Bach, E, Rost, S, Feldkirchner, S, Kubny, C, Müller, S, Hanisch, F.G, Kress, W, Schoser, B
Published in Neuromuscular disorders : NMD (01.10.2014)

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P5.53 The C224W FHL1 mutation is causing a protein aggregation disorder of muscle: Two brothers revisited

by Feldkirchner, S, Walter, M.C, Kubny, C, Mueller, S, Kress, W, Hanisch, F.G, Schoser, B, Schessl, J
Published in Neuromuscular disorders : NMD (01.10.2011)

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P5.51 Evaluation of standardized protein pattern of skeletal muscle fibers via laser microdissection

by Feldkirchner, S, Müller, S, Kress, W, Hanisch, F.G, Schoser, B, Schessl, J
Published in Neuromuscular disorders : NMD (01.10.2011)

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A.P.5: Novel recessive myotilin mutation cause severe myofibrillar myopathy

by Schessl, J., Bach, E., Rost, S., Feldkirchner, S., Kubny, C., Müller, S., Hanisch, F.G., Kress, W., Schoser, B.
Published in Neuromuscular disorders : NMD (01.10.2014)

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Structures of neutral O-linked polylactosaminoglycans on human skim milk mucins. A novel type of linearly extended poly-N-acetyllactosamine backbones with Gal beta (1-4GlcNAc beta (1-6)) repeating units

by Hanisch, F.G, Uhlenbruck, G, Peter-Katalinic, J, Egge, H, Dabrowski, J, Dabrowski, U
Published in The Journal of biological chemistry (15.01.1989)

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Inhibition of adhesion of S-fimbriated Escherichia coli to epithelial cells by meconium and feces of breast-fed and formula-fed newborns: mucins are the major inhibitory component

by Schroten, H. (Universitats-Kinderklinik Dusseldorf, Dusseldorf, Germany), Lethen, A, Hanisch, F.G, Plogmann, R, Hacker, J, Nobis-Bosch, R, Wahn, V
Published in Journal of pediatric gastroenterology and nutrition (01.08.1992)

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