Brydson M - Search Results

1

Primary structure of the human muscle acetylcholine receptor. cDNA cloning of the gamma and epsilon subunits.

Beeson D, Brydson M, Betty M, Jeremiah S, Povey S, Vincent A, Newsom-Davis J. Beeson D, et al. Among authors: brydson m. Eur J Biochem. 1993 Jul 15;215(2):229-38. doi: 10.1111/j.1432-1033.1993.tb18027.x. Eur J Biochem. 1993. PMID: 7688301 Free article.

2

Nucleotide sequence of human muscle acetylcholine receptor beta-subunit.

Beeson D, Brydson M, Newsom-Davis J. Beeson D, et al. Among authors: brydson m. Nucleic Acids Res. 1989 Jun 12;17(11):4391. doi: 10.1093/nar/17.11.4391. Nucleic Acids Res. 1989. PMID: 2740233 Free PMC article. No abstract available.

3

cDNA and genomic clones encoding the human muscle acetylcholine receptor.

Beeson D, Vincent A, Morris A, Brydson M, Jacobson L, Baggi F, Jeremiah S, Povey S, Newsom-Davis J. Beeson D, et al. Among authors: brydson m. Ann N Y Acad Sci. 1993 Jun 21;681:165-7. doi: 10.1111/j.1749-6632.1993.tb22882.x. Ann N Y Acad Sci. 1993. PMID: 8357162 No abstract available.

4

Structural abnormalities of the AChR caused by mutations underlying congenital myasthenic syndromes.

Beeson D, Webster R, Ealing J, Croxen R, Brownlow S, Brydson M, Newsom-Davis J, Slater C, Hatton C, Shelley C, Colquhoun D, Vincent A. Beeson D, et al. Among authors: brydson m. Ann N Y Acad Sci. 2003 Sep;998:114-24. doi: 10.1196/annals.1254.013. Ann N Y Acad Sci. 2003. PMID: 14592868

5

End-plate gamma- and epsilon-subunit mRNA levels in AChR deficiency syndrome due to epsilon-subunit null mutations.

Croxen R, Young C, Slater C, Haslam S, Brydson M, Vincent A, Beeson D. Croxen R, et al. Among authors: brydson m. Brain. 2001 Jul;124(Pt 7):1362-72. doi: 10.1093/brain/124.7.1362. Brain. 2001. PMID: 11408331

6

Acetylcholine receptor delta subunit mutations underlie a fast-channel myasthenic syndrome and arthrogryposis multiplex congenita.

Brownlow S, Webster R, Croxen R, Brydson M, Neville B, Lin JP, Vincent A, Newsom-Davis J, Beeson D. Brownlow S, et al. Among authors: brydson m. J Clin Invest. 2001 Jul;108(1):125-30. doi: 10.1172/JCI12935. J Clin Invest. 2001. PMID: 11435464 Free PMC article.

7

Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes.

Croxen R, Hatton C, Shelley C, Brydson M, Chauplannaz G, Oosterhuis H, Vincent A, Newsom-Davis J, Colquhoun D, Beeson D. Croxen R, et al. Among authors: brydson m. Neurology. 2002 Jul 23;59(2):162-8. doi: 10.1212/wnl.59.2.162. Neurology. 2002. PMID: 12141316

8

Mutation in the AChR ion channel gate underlies a fast channel congenital myasthenic syndrome.

Webster R, Brydson M, Croxen R, Newsom-Davis J, Vincent A, Beeson D. Webster R, et al. Among authors: brydson m. Neurology. 2004 Apr 13;62(7):1090-6. doi: 10.1212/01.wnl.0000118205.99701.41. Neurology. 2004. PMID: 15079006

9

Voluntary partial retraction of: Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes.

Croxen R, Hatton C, Shelley C, Brydson M, Chauplannaz G, Oosterhuis H, Vincent A, Newsom-Davis J, Colquhoun D, Beeson D. Croxen R, et al. Among authors: brydson m. Neurology. 2009 Jan 20;72(3):294. doi: 10.1212/01.wnl.0000344248.36823.b5. Neurology. 2009. PMID: 19153382 No abstract available.

10

Properties of the human muscle nicotinic receptor, and of the slow-channel myasthenic syndrome mutant epsilonL221F, inferred from maximum likelihood fits.

Hatton CJ, Shelley C, Brydson M, Beeson D, Colquhoun D. Hatton CJ, et al. Among authors: brydson m. J Physiol. 2003 Mar 15;547(Pt 3):729-60. doi: 10.1113/jphysiol.2002.034173. Epub 2003 Jan 24. J Physiol. 2003. PMID: 12562900 Free PMC article.

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