Burgess R - Search Results

1

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. Among authors: burgess r. 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.

2

An active dominant mutation of glycyl-tRNA synthetase causes neuropathy in a Charcot-Marie-Tooth 2D mouse model.

Seburn KL, Nangle LA, Cox GA, Schimmel P, Burgess RW. Seburn KL, et al. Neuron. 2006 Sep 21;51(6):715-26. doi: 10.1016/j.neuron.2006.08.027. Neuron. 2006. PMID: 16982418 Free article.

3

Age, experience and genetic background influence treadmill walking in mice.

Wooley CM, Xing S, Burgess RW, Cox GA, Seburn KL. Wooley CM, et al. Physiol Behav. 2009 Feb 16;96(2):350-61. doi: 10.1016/j.physbeh.2008.10.020. Epub 2008 Nov 6. Physiol Behav. 2009. PMID: 19027767 Free PMC article.

4

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

5

A novel null allele of mouse DSCAM survives to adulthood on an inbred C3H background with reduced phenotypic variability.

Fuerst PG, Harris BS, Johnson KR, Burgess RW. Fuerst PG, et al. Among authors: burgess rw. Genesis. 2010 Oct 1;48(10):578-84. doi: 10.1002/dvg.20662. Genesis. 2010. PMID: 20715164 Free PMC article.

6

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

Bogdanik LP, Burgess RW. Bogdanik LP, et al. 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.

7

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. PLoS One. 2012;7(1):e30217. doi: 10.1371/journal.pone.0030217. Epub 2012 Jan 17. PLoS One. 2012. PMID: 22272310 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. 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

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

10

Severity of Demyelinating and Axonal Neuropathy Mouse Models Is Modified by Genes Affecting Structure and Function of Peripheral Nodes.

Morelli KH, Seburn KL, Schroeder DG, Spaulding EL, Dionne LA, Cox GA, Burgess RW. Morelli KH, et al. Cell Rep. 2017 Mar 28;18(13):3178-3191. doi: 10.1016/j.celrep.2017.03.009. Cell Rep. 2017. PMID: 28355569 Free PMC article.

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