Wood MJA - Search Results

1

Dysregulation of Tweak and Fn14 in skeletal muscle of spinal muscular atrophy mice.

Meijboom KE, Sutton ER, McCallion E, McFall E, Anthony D, Edwards B, Kubinski S, Tapken I, Bünermann I, Hazell G, Ahlskog N, Claus P, Davies KE, Kothary R, Wood MJA, Bowerman M. Meijboom KE, et al. Among authors: wood mja. Skelet Muscle. 2022 Jul 28;12(1):18. doi: 10.1186/s13395-022-00301-z. Skelet Muscle. 2022. PMID: 35902978 Free PMC article.

2

Survival of motor neuron gene downregulation by RNAi: towards a cell culture model of spinal muscular atrophy.

Trülzsch B, Davies K, Wood M. Trülzsch B, et al. Brain Res Mol Brain Res. 2004 Jan 5;120(2):145-50. doi: 10.1016/j.molbrainres.2003.10.015. Brain Res Mol Brain Res. 2004. PMID: 14741404

3

Knockdown of SMN by RNA interference induces apoptosis in differentiated P19 neural stem cells.

Trülzsch B, Garnett C, Davies K, Wood M. Trülzsch B, et al. Brain Res. 2007 Dec 5;1183:1-9. doi: 10.1016/j.brainres.2007.09.025. Epub 2007 Sep 21. Brain Res. 2007. PMID: 17976539

4

The acute inflammatory response to intranigral α-synuclein differs significantly from intranigral lipopolysaccharide and is exacerbated by peripheral inflammation.

Couch Y, Alvarez-Erviti L, Sibson NR, Wood MJ, Anthony DC. Couch Y, et al. J Neuroinflammation. 2011 Nov 28;8:166. doi: 10.1186/1742-2094-8-166. J Neuroinflammation. 2011. PMID: 22122884 Free PMC article.

5

Therapy for Duchenne muscular dystrophy: renewed optimism from genetic approaches.

Fairclough RJ, Wood MJ, Davies KE. Fairclough RJ, et al. Nat Rev Genet. 2013 Jun;14(6):373-8. doi: 10.1038/nrg3460. Epub 2013 Apr 23. Nat Rev Genet. 2013. PMID: 23609411 Review.

6

Functional correction in mouse models of muscular dystrophy using exon-skipping tricyclo-DNA oligomers.

Goyenvalle A, Griffith G, Babbs A, El Andaloussi S, Ezzat K, Avril A, Dugovic B, Chaussenot R, Ferry A, Voit T, Amthor H, Bühr C, Schürch S, Wood MJ, Davies KE, Vaillend C, Leumann C, Garcia L. Goyenvalle A, et al. Nat Med. 2015 Mar;21(3):270-5. doi: 10.1038/nm.3765. Epub 2015 Feb 2. Nat Med. 2015. PMID: 25642938

7

Systemic peptide-mediated oligonucleotide therapy improves long-term survival in spinal muscular atrophy.

Hammond SM, Hazell G, Shabanpoor F, Saleh AF, Bowerman M, Sleigh JN, Meijboom KE, Zhou H, Muntoni F, Talbot K, Gait MJ, Wood MJ. Hammond SM, et al. Proc Natl Acad Sci U S A. 2016 Sep 27;113(39):10962-7. doi: 10.1073/pnas.1605731113. Epub 2016 Sep 12. Proc Natl Acad Sci U S A. 2016. PMID: 27621445 Free PMC article.

8

Identification of a Peptide for Systemic Brain Delivery of a Morpholino Oligonucleotide in Mouse Models of Spinal Muscular Atrophy.

Shabanpoor F, Hammond SM, Abendroth F, Hazell G, Wood MJA, Gait MJ. Shabanpoor F, et al. Among authors: wood mja. Nucleic Acid Ther. 2017 Jun;27(3):130-143. doi: 10.1089/nat.2016.0652. Epub 2017 Jan 24. Nucleic Acid Ther. 2017. PMID: 28118087 Free PMC article.

9

Splice-Switching Therapy for Spinal Muscular Atrophy.

Meijboom KE, Wood MJA, McClorey G. Meijboom KE, et al. Among authors: wood mja. Genes (Basel). 2017 Jun 12;8(6):161. doi: 10.3390/genes8060161. Genes (Basel). 2017. PMID: 28604635 Free PMC article. Review.

10

Therapeutic strategies for spinal muscular atrophy: SMN and beyond.

Bowerman M, Becker CG, Yáñez-Muñoz RJ, Ning K, Wood MJA, Gillingwater TH, Talbot K; UK SMA Research Consortium. Bowerman M, et al. Among authors: wood mja. Dis Model Mech. 2017 Aug 1;10(8):943-954. doi: 10.1242/dmm.030148. Dis Model Mech. 2017. PMID: 28768735 Free PMC article. Review.

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