Literature DB >> 9789802

Development of the neuromuscular junction: genetic analysis in mice.

J R Sanes1, E D Apel, R W Burgess, R B Emerson, G Feng, M Gautam, D Glass, R M Grady, E Krejci, J W Lichtman, J T Lu, J Massoulié, J H Miner, L M Moscoso, Q Nguyen, M Nichol, P G Noakes, B L Patton, Y J Son, G D Yancopoulos, H Zhou.   

Abstract

Formation of the skeletal neuromuscular junction is a multi-step process that requires communication between the nerve and muscle. Studies in many laboratories have led to identification of factors that seem likely to mediate these interactions. 'Knock-out' mice have now been generated with mutations in several genes that encode candidate transsynaptic messengers and components of their effector mechanisms. Using these mice, it is possible to test hypotheses about the control of synaptogenesis. Here, we review our studies on neuromuscular development in mutant mice lacking agrin alpha CGRP, rapsyn, MuSK, dystrophin, dystrobrevin, utrophin, laminin alpha 5, laminin beta 2, collagen alpha 3 (IV), the acetylcholine receptor epsilon subunit, the collagenous tail of acetylcholinesterase, fibroblast growth factor-5, the neural cell adhesion molecule, and tenascin-C.

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Year:  1998        PMID: 9789802     DOI: 10.1016/s0928-4257(98)80004-1

Source DB:  PubMed          Journal:  J Physiol Paris        ISSN: 0928-4257


  15 in total

1.  The permissive cue laminin is essential for growth cone turning in vivo.

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2.  Motoneuron survival is enhanced in the absence of neuromuscular junction formation in embryos.

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Review 5.  Mechanisms controlling neuromuscular junction stability.

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