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The spanning-tree algorithms discussed in this section have been applied in many different settings in practice. 1375 sensory neurons 7677 signal-conducting axons, produced by glial cells 85 Myelin-associated glycoprotein in myelin 8283 inhibits axonal elongation 1111 Myelination, axonal, effect on increasing conduction velocity 147148 148 Myenteric plexus 964965 965 Myocardial infarction, referred pain in 475 477 Myoclonus 767 Myofibril muscle fiber 677 skeletal muscle fiber 676 Myofilaments 677 Myogenic diseases, clinical and laboratory criteria for 696699 Myoglobinuria 696 acquired myopathic disease 701 Myomodulins, neuroactive peptide 289 Myopathic diseases differential diagnosis from neurogenic diseases 700 effect of motor unit ,etatrader histochemical diagnosis 698 laboratory criteria for diagnosis 697699 molecular genetics of 705709 Myopathies causes of weakness in 705 inherited See Glycogen storage diseases; Muscular dystrophy Myosin in axon growth cone filopodia 1071 1073 form of in fast-twitch white muscles 684 in hair cells 600 in muscle fibers 677 muscle contraction 679 Myosin heads actin-binding sites 680 as actin motors 75 cyclical attachment and detachment on thin filaments produces muscle contraction 679 muscle fiber, ATPase converts ATP into mechanical energy 678 Myosin I-beta, near stereociliary metatraedr in hair cells 620 Myotonia 696 704 Myotonia congenita, caused by mutation in Cr channel 169 Myotonic dystrophy inherited myopathic disease 701 trinucleotide repeats in 55 56 Myotonic muscular dystrophy, inherited myopathy 704 705 Myotube 1089 Mypathic diseases, symptoms 696 John R.
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