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Kruger, M, J Wright, and K Wang 1991 Nebulin as a length regulator of thin laments of vertebrate skeletal muscles: Correlation of thin lament length, nebulin size, and epitope pro le Journal of Cell Biology 115:97 Kurzban, G P, and K Wang 1987 Titin subunit molecular-weight by hydrodynamic characterization in guanidine-hydrochloride Biophysical Journal 51:A323 A323 Kurzban, G P, and K Wang 1988 Giant polypeptides of skeletal-muscle titin sedimentation equilibrium in guanidine-hydrochloride Biochemical and Biophysical Research Communications 150:1155 1161 Lametsch, R, S Lonergan, and E Huff-Lonergan 2008 Disul de bond within -calpain active site inhibits activity and autolysis Biochimica et Biophysica Acta (BBA) Proteins & Proteomics In press, corrected proof Lehman, W, M Rosol, L S Tobacman, and R Craig 2001 Troponin organization on relaxed and activated thin laments revealed by electron microscopy and three-dimensional reconstruction Journal of Molecular Biology 307:739 Levine, R L, J.

A Williams, E R Stadtman, and E Shacter 1994 Carbonyl assays for determination of oxidatively modi ed proteins Methods in Enzymology 233:346 357 Lonergan, S M, E Huff-Lonergan, B R Wiegand, and L A Kriese-Anderson 2001 Postmortem proteolysis and tenderization of top loin steaks from brangus cattle Journal of Muscle Foods 12:121 136 Loo, D T, S B Kanner, and A Aruffo 1998 Filamin binds to the cytoplasmic domain of the beta1-integrin Journal of Biological Chemistry 273:23304 Lukoyanova, N, M S VanLoock, A Orlova, V E Galkin, K Wang, and E H Egelman 2002 Each actin subunit has three nebulin binding sites Current Biology 12:383 Lusby, M L, J F Ridpath, F C Parrish, and R M Robson 1983 Effect of postmortem storage on degradation of the myo brillar protein titin in bovine longissimus muscle Journal of Food Science 48:1787 1790 Ma, K, J G.

these until a change is made. At any point in time a PNC can make a change to a CTA. However, if a DEV needs to make a change to a CTA, it uses a stream modi cation procedure. 8.3.5 Guard Times

Forbes, G Gutierrez-Cruz, and K Wang 2006 Titin as a giant scaffold for integrating stress and src homology domain 3-mediated signaling pathways the clustering of novel overlap ligand motifs in the elastic pevk segment Journal of Biological Chemistry 281:27539 27556 MacBride, M A, and F C Parrish 1977 30,000-dalton component of tender bovine longissimus muscle Journal of Food Science 42:1627 1629 Maddock, K R, E Huff-Lonergan, L J Rowe, and S M Lonergan 2006 Effect of oxidation, ph, and ionic strength on calpastatin inhibition of - and m-calpain Journal of Animal Science 84:925 937 Malhotra, A 1994 Role of regulatory proteins (troponin-tropomyosin) in pathological states Molecular and Cellular Biochemistry 135:43 50 Martinaud, A, Y Mercier, P Marinova, C Tassy, P Gatellier, and M Renerre 1997 Comparison of oxi-.

rate have emerged (Figure 2.1). Most estimates of natural recharge rates range between about 5% and 25% of rainfall. In certain types of terrain, values as high as 75% have been recorded: for instance, this is the rate at which recharge occurs in the highly permeable lavas of Mount Etna (Guest et al. 2003, p. 178). However, such exceptionally high rates of conversion from rainfall to recharge are relatively uncommon in practice, and it is normally wise to carefully scrutinize any recharge estimates which exceed about 30% of the total rainfall in the study area.

Serial sequence: [137] [Velocity high byte] [Velocity low byte] [Radius high byte] [Radius low byte] Drive data bytes 1 and 2: Velocity (-500 500 mm/s) Drive data bytes 3 and 4: Radius (-2000 2000 mm) Special cases: Straight = 32768 = hex 8000 Turn in place clockwise = -1 Turn in place counter-clockwise = 1 Example: To drive in reverse at a velocity of -200 mm/s while turning at a radius of 500mm, you would send the serial byte sequence [137] [255] [56] [1] [244]. Velocity = -200 = hex FF38 = [hex FF] [hex 38] = [255] [56]