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Items: 27

1.

Dramatic elevation in urinary amino terminal titin fragment excretion quantified by immunoassay in Duchenne muscular dystrophy patients and in dystrophin deficient rodents.

Robertson AS, Majchrzak MJ, Smith CM, Gagnon RC, Devidze N, Banks GB, Little SC, Nabbie F, Bounous DI, DiPiero J, Jacobsen LK, Bristow LJ, Ahlijanian MK, Stimpson SA.

Neuromuscul Disord. 2017 Jul;27(7):635-645. doi: 10.1016/j.nmd.2017.05.009. Epub 2017 May 12.

2.

Loss of niche-satellite cell interactions in syndecan-3 null mice alters muscle progenitor cell homeostasis improving muscle regeneration.

Pisconti A, Banks GB, Babaeijandaghi F, Betta ND, Rossi FM, Chamberlain JS, Olwin BB.

Skelet Muscle. 2016 Oct 4;6:34. eCollection 2016.

3.

Fnip1 regulates skeletal muscle fiber type specification, fatigue resistance, and susceptibility to muscular dystrophy.

Reyes NL, Banks GB, Tsang M, Margineantu D, Gu H, Djukovic D, Chan J, Torres M, Liggitt HD, Hirenallur-S DK, Hockenbery DM, Raftery D, Iritani BM.

Proc Natl Acad Sci U S A. 2015 Jan 13;112(2):424-9. doi: 10.1073/pnas.1413021112. Epub 2014 Dec 29.

4.

Muscle structure influences utrophin expression in mdx mice.

Banks GB, Combs AC, Odom GL, Bloch RJ, Chamberlain JS.

PLoS Genet. 2014 Jun 12;10(6):e1004431. doi: 10.1371/journal.pgen.1004431. eCollection 2014 Jun.

5.

Myofiber branching rather than myofiber hyperplasia contributes to muscle hypertrophy in mdx mice.

Faber RM, Hall JK, Chamberlain JS, Banks GB.

Skelet Muscle. 2014 May 23;4:10. doi: 10.1186/2044-5040-4-10. eCollection 2014.

6.

Microtubule binding distinguishes dystrophin from utrophin.

Belanto JJ, Mader TL, Eckhoff MD, Strandjord DM, Banks GB, Gardner MK, Lowe DA, Ervasti JM.

Proc Natl Acad Sci U S A. 2014 Apr 15;111(15):5723-8. doi: 10.1073/pnas.1323842111. Epub 2014 Mar 31.

7.

Successful regional delivery and long-term expression of a dystrophin gene in canine muscular dystrophy: a preclinical model for human therapies.

Wang Z, Storb R, Halbert CL, Banks GB, Butts TM, Finn EE, Allen JM, Miller AD, Chamberlain JS, Tapscott SJ.

Mol Ther. 2012 Aug;20(8):1501-7. doi: 10.1038/mt.2012.111. Epub 2012 Jun 12.

8.

Animal models of muscular dystrophy.

Ng R, Banks GB, Hall JK, Muir LA, Ramos JN, Wicki J, Odom GL, Konieczny P, Seto J, Chamberlain JR, Chamberlain JS.

Prog Mol Biol Transl Sci. 2012;105:83-111. doi: 10.1016/B978-0-12-394596-9.00004-4. Review.

9.

Expression of the dystrophin isoform Dp116 preserves functional muscle mass and extends lifespan without preventing dystrophy in severely dystrophic mice.

Judge LM, Arnett AL, Banks GB, Chamberlain JS.

Hum Mol Genet. 2011 Dec 15;20(24):4978-90. doi: 10.1093/hmg/ddr433. Epub 2011 Sep 23.

10.

Prevention of muscle aging by myofiber-associated satellite cell transplantation.

Hall JK, Banks GB, Chamberlain JS, Olwin BB.

Sci Transl Med. 2010 Nov 10;2(57):57ra83. doi: 10.1126/scitranslmed.3001081.

11.

Sequencing protocols to genotype mdx, mdx(4cv), and mdx(5cv) mice.

Banks GB, Combs AC, Chamberlain JS.

Muscle Nerve. 2010 Aug;42(2):268-70. doi: 10.1002/mus.21700.

12.

The polyproline site in hinge 2 influences the functional capacity of truncated dystrophins.

Banks GB, Judge LM, Allen JM, Chamberlain JS.

PLoS Genet. 2010 May 20;6(5):e1000958. doi: 10.1371/journal.pgen.1000958.

13.

Preclinical studies for gene therapy of Duchenne muscular dystrophy.

Odom GL, Banks GB, Schultz BR, Gregorevic P, Chamberlain JS.

J Child Neurol. 2010 Sep;25(9):1149-57. doi: 10.1177/0883073810371006. Epub 2010 May 24. Review.

PMID:
20498332
14.

The value of mammalian models for duchenne muscular dystrophy in developing therapeutic strategies.

Banks GB, Chamberlain JS.

Curr Top Dev Biol. 2008;84:431-53. doi: 10.1016/S0070-2153(08)00609-1. Review.

PMID:
19186250
15.

Truncated dystrophins can influence neuromuscular synapse structure.

Banks GB, Chamberlain JS, Froehner SC.

Mol Cell Neurosci. 2009 Apr;40(4):433-41. doi: 10.1016/j.mcn.2008.12.011. Epub 2009 Jan 8.

16.

Molecular and cellular adaptations to chronic myotendinous strain injury in mdx mice expressing a truncated dystrophin.

Banks GB, Combs AC, Chamberlain JR, Chamberlain JS.

Hum Mol Genet. 2008 Dec 15;17(24):3975-86. doi: 10.1093/hmg/ddn301. Epub 2008 Sep 16.

17.

rAAV6-microdystrophin rescues aberrant Golgi complex organization in mdx skeletal muscles.

Percival JM, Gregorevic P, Odom GL, Banks GB, Chamberlain JS, Froehner SC.

Traffic. 2007 Oct;8(10):1424-39. Epub 2007 Aug 20.

18.

Functional capacity of dystrophins carrying deletions in the N-terminal actin-binding domain.

Banks GB, Gregorevic P, Allen JM, Finn EE, Chamberlain JS.

Hum Mol Genet. 2007 Sep 1;16(17):2105-13. Epub 2007 Jun 22.

PMID:
17588958
19.

Relevance of motoneuron specification and programmed cell death in embryos to therapy of ALS.

Banks GB, Chamberlain JS.

Birth Defects Res C Embryo Today. 2005 Dec;75(4):294-304. Review.

PMID:
16425251
20.

Glycinergic and GABAergic synaptic activity differentially regulate motoneuron survival and skeletal muscle innervation.

Banks GB, Kanjhan R, Wiese S, Kneussel M, Wong LM, O'Sullivan G, Sendtner M, Bellingham MC, Betz H, Noakes PG.

J Neurosci. 2005 Feb 2;25(5):1249-59. Erratum in: J Neurosci. 2005 Mar 16;25(11):3018-21.

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23.

Genetic disruption of the growth hormone receptor does not influence motoneuron survival in the developing mouse.

Parsons SA, Banks GB, Rowland JA, Coschigano KT, Kopchick JJ, Waters MJ, Noakes PG.

Int J Dev Biol. 2003 Feb;47(1):41-9.

24.
25.

Alterations in ciliary neurotrophic factor signaling in rapsyn deficient mice.

Bartlett SE, Banks GB, Reynolds AJ, Waters MJ, Hendry IA, Noakes PG.

J Neurosci Res. 2001 Jun 15;64(6):575-81. Erratum in: J Neurosci Res 2001 Nov 15;66(4):731-2.

PMID:
11398180
26.

Promotion of motoneuron survival and branching in rapsyn-deficient mice.

Banks GB, Chau TN, Bartlett SE, Noakes PG.

J Comp Neurol. 2001 Jan 1;429(1):156-65.

PMID:
11086296
27.

Television pick-up tubes for x-ray screen intensification.

BANKS GB.

Br J Radiol. 1958 Nov;31(371):619-25. No abstract available.

PMID:
13596584

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