Search Results - "Ruegg, M.A"

M.I.3 The role of laminins in myomatrix assembly and skeletal muscle stability by Ruegg, M.A, Meinen, S, Maier, G, Lin, S, Yurchenco, P.G

“…The basement membrane of skeletal muscle (myomatrix) consists of a complex network of highly glycosylated proteins. Important components of the myomatrix are…”
Get full text

M.I.1 Mechanism of laminin assembly: Insight for structural repairs of MDC1A by Yurchenco, P.D, Crosson, S, McKee, K.K, Ruegg, M.A

“…Laminins play a key role in the assembly of sarcolemmal basement membranes by establishing anchors to the cell surface and underlying cytoskeleton, by…”
Get full text

G.P.212 by Meinen, S, Maier, G, Chauhan, M, Lin, S, McKee, K.K, Crosson, S.C, Yurchenco, P.D, Ruegg, M.A

“…The basement membrane surrounding skeletal muscle fibers (myomatrix) and its binding to the sarcolemma is important for the structural stability of muscle. The…”
Get full text

P34-20 Low MuSK expression in disease susceptible muscles in MuSK+experimental autoimmune myasthenia gravis (EAMG) by Punga, A.R, Lin, S, Ruegg, M.A

Get full text

M.P.4.07 Reverse protein arrays for efficient protein diagnosis of muscular dystrophies in less than 10 mg muscle tissue by Escher, C.A, Lochmüller, H, Walter, M.C, Ehrat, M, Reimann, J, Ruegg, M.A, Gygax, D

Get full text

T.P.6.03 Restoring cell-basal lamina interaction to rescue tissue degeneration in congenital muscular dystrophy by Porrello, E, Domi, T, Capotondo, A, Triolo, D, Sampaolesi, M, Brunelli, S, Comi, G, Ruegg, M.A, Cossu, G, Biffi, A, Quattrini, A, Previtali, S.C

Get full text

EM.P.1.04 Treatment approaches in laminin-α2-deficient congenital muscular dystrophy (MDC1A) by Meinen, S, Lin, S, Rüegg, M.A

Get full text

G.P.212: Mechanisms and therapeutic approaches to counteract MDC1A: The role of laminin self-assembly and linkage to muscle membrane by Meinen, S., Maier, G., Chauhan, M., Lin, S., McKee, K.K., Crosson, S.C., Yurchenco, P.D., Ruegg, M.A.

“…The basement membrane surrounding skeletal muscle fibers (myomatrix) and its binding to the sarcolemma is important for the structural stability of muscle. The…”
Get full text

T.P.3.03 TREAT-NMD-Activity 7: Accelerate preclinical phase of new therapeutic treatment development by Willmann, R, Rüegg, M.A, Fairclough, R, Davies, K.E, Possekel, S, Meier, T

Get full text

M.P.4.07 Reverse protein arrays for efficient protein diagnosis of muscular dystrophies in less than 10mg muscle tissue by Escher, C.A., Lochmüller, H., Walter, M.C., Ehrat, M., Reimann, J., Ruegg, M.A., Gygax, D.

Get full text

Laminin α2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice by Guo, L.T., Zhang, X.U., Kuang, W., Xu, H., Liu, L.A., Vilquin, J.-T., Miyagoe-Suzuki, Y., Takeda, S., Ruegg, M.A., Wewer, U.M., Engvall, E.

“…Deficiency of laminin α2 is the cause of one of the most severe muscular dystrophies in humans and other species. It is not yet clear how particular mutations…”
Get full text

Mouse models of α-synucleinopathy and Lewy pathology by Sommer, B, Barbieri, S, Hofele, K, Wiederhold, K.-H, Probst, A, Mistl, C, Danner, S, Kauffmann, S, Spooren, W, Tolnay, M, Bilbe, G, van der Putten, H, Kafmann, S, Caromi, P, Ruegg, M.A

“…The discovery of two missense mutations (A53T and A30P) in the gene encoding the presynaptic protein α-synuclein (αSN) that are genetically linked to rare…”
Get full text