Automated Methods for the Analysis of Skeletal Muscle Fiber Size and Metabolic Type - International Review of Cell and Molecular Biology - page 317

Fidzianska, A., Kaminska, A., 1995. Neural cell adhesion molecule (N-CAM) as a marker of
muscle tissue alternations. Review of the literature and own observations. Folia Neuro-
pathol. 33, 125-128.
Filosto, M., Tomelleri, G., Tonin, P., Scarpelli, M., Vattemi, G., Rizzuto, N., Padovani, A.,
Simonati, A., 2007. Neuropathology of mitochondrial diseases. Biosci. Rep. 27, 23-30.
Fitts, R.H., Riley, D.R., Widrick, J.J., 2000. Physiology of a microgravity environment
invited review: microgravity and skeletal muscle. J. Appl. Physiol. 89, 823-839.
Fitts, R.H., Riley, D.R., Widrick, J.J., 2001. Functional and structural adaptations of skeletal
muscle to microgravity. J. Exp. Biol. 204, 3201-3208.
Folland, J.P., Williams, A.G., 2007. The adaptations to strength training: morphological and
neurological contributions to increased strength. Sports Med. 37, 145-168.
Franceschini, A., Szklarczyk, D., Frankild, S., Kuhn, M., Simonovic, M., Roth, A., Lin, J.,
Minguez, P., Bork, P., von Mering, C., Jensen, L.J., 2013. STRING v9.1: protein-
protein interaction networks, with increased coverage and integration. Nucleic Acids
Res. 41, D808-D815.
Friedmann-Bette, B., Bauer, T., Kinscherf, R., Vorwald, S., Klute, K., Bischoff, D.,
Muller, H., Weber, M.A., Metz, J., Kauczor, H.U., Bartsch, P., Billeter, R., 2010.
Effects of strength training with eccentric overload on muscle adaptation in male athletes.
Eur. J. Appl. Physiol. 108, 821-836.
Garton, F., Seto, J.T., North, K.N., Yang, N., 2010. Validation of an automated computa-
tional method for skeletal muscle fibre morphometry analysis. Neuromuscul. Disord. 20,
540-547.
Gaster, M., Staehr, P., Beck-Nielsen, H., Schroder, H.D., Handberg, A., 2001. GLUT4 is
reduced in slow muscle fibers of type 2 diabetic patients: is insulin resistance in type 2
diabetes a slow, type 1 fiber disease? Diabetes 50, 1324-1329.
Gauthier, G.F., Padykula, H.A., 1966. Cytological studies of fiber types in skeletal muscle.
A comparative study of the mammalian diaphragm. J. Cell Biol. 28, 333-354.
Gehrig, S.M., Koopman, R., Naim, T., Tjoakarfa, C., Lynch, G.S., 2010. Making fast-
twitch dystrophic muscles bigger protects them from contraction injury and attenuates
the dystrophic pathology. Am. J. Pathol. 176, 29-33.
Gelb, B.D., Tartaglia, M., 2011. RAS signaling pathway mutations and hypertrophic cardio-
myopathy: getting into and out of the thick of it. J. Clin. Invest. 121, 844-847.
Gentile, M.A., Nantermet, P.V., Vogel, R.L., Phillips, R., Holder, D., Hodor, P.,
Cheng, C., Dai, H., Freedman, L.P., Ray, W.J., 2010. Androgen-mediated improve-
ment of body composition and muscle function involves a novel early transcriptional
program including IGF1, mechano growth factor, and induction of {beta}-catenin.
J. Mol. Endocrinol. 44, 55-73.
George, J.C., Talesara, C.L., 1961. The succinic dehydrogenase levels of the pectoral muscles
of a few representative types of birds and a bat in relation to the fibre diameter, muscle
weight and body weight. Comp. Biochem. Physiol. 3, 267-273.
Giannoulis, M.G., Martin, F.C., Nair, K.S., Umpleby, A.M., Sonksen, P., 2012. Hormone
replacement therapy and physical function in healthy older men. Time to talk hormones?
Endocr. Rev. 33, 314-377.
Gigo-Benato, D., Russo, T.L., Geuna, S., Domingues, N.R., Salvini, T.F., Parizotto, N.A.,
2010. Electrical stimulation impairs early functional recovery and accentuates skeletal
muscle atrophy after sciatic nerve crush injury in rats. Muscle Nerve 41, 685-693.
Gilson, H., Schakman, O., Combaret, L., Lause, P., Grobet, L., Attaix, D.,
Ketelslegers, J.M., Thissen, J.P., 2007. Myostatin gene deletion prevents

glucocorticoid-induced muscle atrophy. Endocrinology 148, 452-460.
Glaser, B.W., You, G., Zhang, M., Medler, S., 2010. Relative proportions of hybrid fibres
are unaffected by 6 weeks of running exercise in mouse skeletal muscles. Exp. Physiol.
95, 211-221.