Biology Reference
In-Depth Information
Romeo, V., 2012. Myotonic dystrophy Type 1 or Steinert's disease. Adv. Exp. Med. Biol.
724, 239-257.
Rosales, X.Q., Tsao, C.Y., 2012. Childhood onset of limb-girdle muscular dystrophy.
Pediatr. Neurol. 46, 13-23.
Round, J.M., Jones, D.A., Edwards, R.H., 1982. A flexible microprocessor system for the
measurement of cell size. J. Clin. Pathol. 35, 620-624.
Rowan, S.L., Rygiel, K., Purves-Smith, F.M., Solbak, N.M., Turnbull, D.M.,
Hepple, R.T., 2012. Denervation causes fiber atrophy and myosin heavy chain
co-expression in senescent skeletal muscle. PLoS One 7, e29082.
Ruegg, S., Lehky Hagen, M., Hohl, U., Kappos, L., Fuhr, P., Plasilov, M., Muller, H.,
Heinimann, K., 2005. Oculopharyngeal muscular dystrophy—an under-diagnosed dis-
order? Swiss Med. Wkly. 135, 574-586.
Ryall, J.G., Schertzer, J.D., Alabakis, T.M., Gehrig, S.M., Plant, D.R., Lynch, G.S., 2008.
Intramuscular beta2-agonist administration enhances early regeneration and functional
repair in rat skeletal muscle after myotoxic injury. J. Appl. Physiol. 105, 165-172.
Sakuma, K., Yamaguchi, A., 2012. Sarcopenia and cachexia: the adaptations of negative reg-
ulators of skeletal muscle mass. J. Cachexia Sarcopenia Muscle 3, 77-94.
Samaha, F.J., Guth, L., Albers, R.W., 1970. Phenotypic differences between the actomyosin
ATPase of the three fiber types of mammalian skeletal muscle. Exp. Neurol. 26,
120-125.
Sandona, D., Desaphy, J.F., Camerino, G.M., Bianchini, E., Ciciliot, S., Danieli-Betto, D.,
Dobrowolny, G., Furlan, S., Germinario, E., Goto, K., Gutsmann, M., Kawano, F.,
Nakai, N., Ohira, T., Ohno, Y., Picard, A., Salanova, M., Schiffl, G., Blottner, D.,
Musaro, A., Ohira, Y., Betto, R., Conte, D., Schiaffino, S., 2012. Adaptation of mouse
skeletal muscle to long-term microgravity in the MDS mission. PLoS One 7, e33232.
Schiaffino, S., 2010. Fibre types in skeletal muscle: a personal account. Acta Physiol (Oxf.)
199, 451-463.
Schiaffino, S., Bormioli, S.P., 1973. Adaptive changes in developing rat skeletal muscle in
response to functional overload. Exp. Neurol. 40, 126-137.
Schiaffino, S., Reggiani, C., 2011. Fiber types in mammalian skeletal muscles. Physiol. Rev.
91, 1447-1531.
Schiaffino, S., Hanzlikova, V., Pierobon, S., 1970. Relations between structure and function
in rat skeletal muscle fibers. J. Cell Biol. 47, 107-119.
Schiaffino, S., Gorza, L., Sartore, S., Saggin, L., Ausoni, S., Vianello, M., Gundersen, K.,
Lomo, T., 1989. Three myosin heavy chain isoforms in type 2 skeletal muscle fibres.
J. Muscle Res. Cell Motil. 10, 197-205.
Schneider, C.A., Rasband, W.S., Eliceiri, K.W., 2012. NIH Image to ImageJ: 25 years of
image analysis. Nat. Methods 9, 671-675.
Schrauwen-Hinderling, V.B., Hesselink, M.K., Schrauwen, P., Kooi, M.E., 2006. Intra-
myocellular lipid content in human skeletal muscle. Obesity (Silver Spring) 14, 357-367.
Schubert, W., Sotgia, F., Cohen, A.W., Capozza, F., Bonuccelli, G., Bruno, C., Minetti, C.,
Bonilla, E., Dimauro, S., Lisanti, M.P., 2007. Caveolin-1(-/-)- and caveolin-2(-/-)-
deficient mice both display numerous skeletal muscle abnormalities, with tubular aggre-
gate formation. Am. J. Pathol. 170, 316-333.
Selcen, D., 2010. Myofibrillar myopathies. Curr. Opin. Neurol. 23, 477-481.
Sheard, P.W., Bewick, G.S., Woolley, A.G., Shaw, J., Fisher, L., Fong, S.W., Duxson, M.J.,
2010. Investigation of neuromuscular abnormalities in neurotrophin-3-deficient mice.
Eur. J. Neurosci. 31, 29-41.
Shelley, P., Martin-Gronert, M.S., Rowlerson, A., Poston, L., Heales, S.J., Hargreaves, I.P.,
McConnell, J.M., Ozanne, S.E., Fernandez-Twinn, D.S., 2009. Altered skeletal muscle
insulin signaling and mitochondrial complex II-III linked activity in adult offspring of
obese mice. Am. J. Physiol. Regul. Integr. Comp. Physiol. 297, R675-R681.
Search WWH ::




Custom Search