Burgess RW - Search Results

1

A MusD retrotransposon insertion in the mouse Slc6a5 gene causes alterations in neuromuscular junction maturation and behavioral phenotypes.

Bogdanik LP, Chapman HD, Miers KE, Serreze DV, Burgess RW. Bogdanik LP, et al. Among authors: burgess rw. PLoS One. 2012;7(1):e30217. doi: 10.1371/journal.pone.0030217. Epub 2012 Jan 17. PLoS One. 2012. PMID: 22272310 Free PMC article.

2

Neuromuscular disease models and analysis.

Burgess RW, Cox GA, Seburn KL. Burgess RW, et al. Methods Mol Biol. 2010;602:347-93. doi: 10.1007/978-1-60761-058-8_20. Methods Mol Biol. 2010. PMID: 20012408

3

An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations.

Stum M, McLaughlin HM, Kleinbrink EL, Miers KE, Ackerman SL, Seburn KL, Antonellis A, Burgess RW. Stum M, et al. Among authors: burgess rw. Mol Cell Neurosci. 2011 Feb;46(2):432-43. doi: 10.1016/j.mcn.2010.11.006. Epub 2010 Nov 27. Mol Cell Neurosci. 2011. PMID: 21115117 Free PMC article.

4

A mouse model of heritable cerebrovascular disease.

Sproule TJ, Sled JG, Wentzell J, Wang B, Henkelman RM, Roopenian DC, Burgess RW. Sproule TJ, et al. Among authors: burgess rw. PLoS One. 2010 Dec 31;5(12):e15327. doi: 10.1371/journal.pone.0015327. PLoS One. 2010. PMID: 21217823 Free PMC article.

5

A valid mouse model of AGRIN-associated congenital myasthenic syndrome.

Bogdanik LP, Burgess RW. Bogdanik LP, et al. Among authors: burgess rw. Hum Mol Genet. 2011 Dec 1;20(23):4617-33. doi: 10.1093/hmg/ddr396. Epub 2011 Sep 1. Hum Mol Genet. 2011. PMID: 21890498 Free PMC article.

6

Charcot-Marie-Tooth-linked mutant GARS is toxic to peripheral neurons independent of wild-type GARS levels.

Motley WW, Seburn KL, Nawaz MH, Miers KE, Cheng J, Antonellis A, Green ED, Talbot K, Yang XL, Fischbeck KH, Burgess RW. Motley WW, et al. Among authors: burgess rw. PLoS Genet. 2011 Dec;7(12):e1002399. doi: 10.1371/journal.pgen.1002399. Epub 2011 Dec 1. PLoS Genet. 2011. PMID: 22144914 Free PMC article.

7

A spontaneous mutation in contactin 1 in the mouse.

Davisson MT, Bronson RT, Tadenev AL, Motley WW, Krishnaswamy A, Seburn KL, Burgess RW. Davisson MT, et al. Among authors: burgess rw. PLoS One. 2011;6(12):e29538. doi: 10.1371/journal.pone.0029538. Epub 2011 Dec 29. PLoS One. 2011. PMID: 22242131 Free PMC article.

8

Loss of the E3 ubiquitin ligase LRSAM1 sensitizes peripheral axons to degeneration in a mouse model of Charcot-Marie-Tooth disease.

Bogdanik LP, Sleigh JN, Tian C, Samuels ME, Bedard K, Seburn KL, Burgess RW. Bogdanik LP, et al. Among authors: burgess rw. Dis Model Mech. 2013 May;6(3):780-92. doi: 10.1242/dmm.010942. Epub 2013 Mar 8. Dis Model Mech. 2013. PMID: 23519028 Free PMC article.

9

Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders.

Fairfield H, Srivastava A, Ananda G, Liu R, Kircher M, Lakshminarayana A, Harris BS, Karst SY, Dionne LA, Kane CC, Curtain M, Berry ML, Ward-Bailey PF, Greenstein I, Byers C, Czechanski A, Sharp J, Palmer K, Gudis P, Martin W, Tadenev A, Bogdanik L, Pratt CH, Chang B, Schroeder DG, Cox GA, Cliften P, Milbrandt J, Murray S, Burgess R, Bergstrom DE, Donahue LR, Hamamy H, Masri A, Santoni FA, Makrythanasis P, Antonarakis SE, Shendure J, Reinholdt LG. Fairfield H, et al. Genome Res. 2015 Jul;25(7):948-57. doi: 10.1101/gr.186882.114. Epub 2015 Apr 27. Genome Res. 2015. PMID: 25917818 Free PMC article.

10

Neuromuscular Disease Models and Analysis.

Burgess RW, Cox GA, Seburn KL. Burgess RW, et al. Methods Mol Biol. 2016;1438:349-94. doi: 10.1007/978-1-4939-3661-8_19. Methods Mol Biol. 2016. PMID: 27150099

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