A mouse model of AChR deficiency syndrome with a phenotype reflecting the human condition-Reference-Cited by-同舟云学术

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A mouse model of AChR deficiency syndrome with a phenotype reflecting the human condition

Published:2004-10-07 Issue:23 Volume:13 Page:2947-2957
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Cossins Judy,Webster Richard,Maxwell Susan,Burke Georgina,Vincent Angela,Beeson David

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/13/23/2947/1738254/ddh320.pdf

Reference35 articles.

1. Mishina, M., Takai, T., Imoto, K., Noda, M., Takahashi, T., Numa, S., Methfessel, C. and Sakmann, B. (1986) Molecular distinction between fetal and adult forms of muscle acetylcholine receptor. Nature, 321, 406–411.

2. Sanes, J.R. and Lichtman, J.W. (2001) Induction, assembly, maturation and maintenance of a postsynaptic apparatus. Nat. Rev. Neurosci., 2, 791–805.

3. Vincent, A., Cull-Candy, S., Newsom-Davis, J., Trautmann, A., Molenaar, P. and Polack, R. (1981) Congenital myasthenia: endplate acetylcholine receptors and electrophysiology in five cases. Muscle Nerve, 4, 306–318.

4. Engel, A.G., Ohno, K. and Sine, S.M. (2003) Neurological disease: Sleuthing molecular targets for neurological diseases at the neuromuscular junction. Nat. Rev. Neurosci., 4, 339–352.

5. Beeson, D. and Newsom-Davis, J. (2000) Mutations affecting muscle acetylcholine receptors and their role in congenital myasthenic syndromes. In Lehmann-Horn, F. and Jurkat-Rott, K. (eds), Channelopathies. Elsevier Science B.V, The Netherlands, pp. 85–114.

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