Bronson R - Search Results

1

Dysferlin overexpression in skeletal muscle produces a progressive myopathy.

Glover LE, Newton K, Krishnan G, Bronson R, Boyle A, Krivickas LS, Brown RH Jr. Glover LE, et al. Among authors: bronson r. Ann Neurol. 2010 Mar;67(3):384-93. doi: 10.1002/ana.21926. Ann Neurol. 2010. PMID: 20373350 Free PMC article.

2

Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency.

Ho M, Post CM, Donahue LR, Lidov HG, Bronson RT, Goolsby H, Watkins SC, Cox GA, Brown RH Jr. Ho M, et al. Among authors: bronson rt. Hum Mol Genet. 2004 Sep 15;13(18):1999-2010. doi: 10.1093/hmg/ddh212. Epub 2004 Jul 14. Hum Mol Genet. 2004. PMID: 15254015

3

IGF-1:tetanus toxin fragment C fusion protein improves delivery of IGF-1 to spinal cord but fails to prolong survival of ALS mice.

Chian RJ, Li J, Ay I, Celia SA, Kashi BB, Tamrazian E, Matthews JC, Bronson RT, Rossomando A, Pepinsky RB, Fishman PS, Brown RH Jr, Francis JW. Chian RJ, et al. Among authors: bronson rt. Brain Res. 2009 Sep 1;1287:1-19. doi: 10.1016/j.brainres.2009.06.066. Epub 2009 Jun 27. Brain Res. 2009. PMID: 19563785

4

Genetic ablation of NMDA receptor subunit NR3B in mouse reveals motoneuronal and nonmotoneuronal phenotypes.

Niemann S, Kanki H, Fukui Y, Takao K, Fukaya M, Hynynen MN, Churchill MJ, Shefner JM, Bronson RT, Brown RH Jr, Watanabe M, Miyakawa T, Itohara S, Hayashi Y. Niemann S, et al. Eur J Neurosci. 2007 Sep;26(6):1407-20. doi: 10.1111/j.1460-9568.2007.05774.x. Eur J Neurosci. 2007. PMID: 17880385

5

Activation of paternally expressed genes and perinatal death caused by deletion of the Gtl2 gene.

Zhou Y, Cheunsuchon P, Nakayama Y, Lawlor MW, Zhong Y, Rice KA, Zhang L, Zhang X, Gordon FE, Lidov HG, Bronson RT, Klibanski A. Zhou Y, et al. Development. 2010 Aug;137(16):2643-52. doi: 10.1242/dev.045724. Epub 2010 Jul 7. Development. 2010. PMID: 20610486 Free PMC article.

6

Reversible neural stem cell niche dysfunction in a model of multiple sclerosis.

Rasmussen S, Imitola J, Ayuso-Sacido A, Wang Y, Starossom SC, Kivisäkk P, Zhu B, Meyer M, Bronson RT, Garcia-Verdugo JM, Khoury SJ. Rasmussen S, et al. Ann Neurol. 2011 May;69(5):878-91. doi: 10.1002/ana.22299. Epub 2011 Mar 9. Ann Neurol. 2011. PMID: 21391234 Free PMC article.

7

Transgenic mice with a mutated collagen promoter display normal response during bleomycin-induced fibrosis and possess neurological abnormalities.

Stoddart JH Jr, Ladd D, Bronson RT, Harmon M, Jaworski J, Pritzker C, Lausen N, Smith BD. Stoddart JH Jr, et al. Among authors: bronson rt. J Cell Biochem. 2000 Feb;77(1):135-48. doi: 10.1002/(sici)1097-4644(20000401)77:1<135::aid-jcb14>3.0.co;2-x. J Cell Biochem. 2000. PMID: 10679824

8

Mutant p53 gain of function in two mouse models of Li-Fraumeni syndrome.

Olive KP, Tuveson DA, Ruhe ZC, Yin B, Willis NA, Bronson RT, Crowley D, Jacks T. Olive KP, et al. Cell. 2004 Dec 17;119(6):847-60. doi: 10.1016/j.cell.2004.11.004. Cell. 2004. PMID: 15607980 Free article.

9

Cln3(Deltaex7/8) knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth.

Cotman SL, Vrbanac V, Lebel LA, Lee RL, Johnson KA, Donahue LR, Teed AM, Antonellis K, Bronson RT, Lerner TJ, MacDonald ME. Cotman SL, et al. Hum Mol Genet. 2002 Oct 15;11(22):2709-21. doi: 10.1093/hmg/11.22.2709. Hum Mol Genet. 2002. PMID: 12374761

10

Gastric hyperplasia in mice lacking the putative Cdc42 effector IQGAP1.

Li S, Wang Q, Chakladar A, Bronson RT, Bernards A. Li S, et al. Among authors: bronson rt. Mol Cell Biol. 2000 Jan;20(2):697-701. doi: 10.1128/MCB.20.2.697-701.2000. Mol Cell Biol. 2000. PMID: 10611248 Free PMC article.

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