Accepting PhD Students

PhD projects

PhD and MPhil projects are available. Current research interests include: -Neuropathophysiology of Duchenne muscular dystrophy -RNA processing of the dystrophin gene -Therapeutic targeting of dystrophin in the brain -Role of the DMD gene in cancer -RNA processing in neurodegeneration -RNA-based gene therapy/therapeutics Please get in touch by e-mail or telephone.

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20072019

Research output per year

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Research Output

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Article
2019

Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy

Naidoo, M. & Anthony, K., 13 Dec 2019, In : Molecular Neurobiology. p. 1-20 21 p.

Research output: Contribution to JournalArticle

Open Access
2018

A multicenter comparison of quantification methods for antisense oligonucleotide-induced DMD exon 51 skipping in Duchenne muscular dystrophy cell cultures

Hiller, M., Falzarano, M. S., Garcia-Jimenez, I., Sardone, V., Verheul, R. C., Popplewell, L., Anthony, K., Ruiz-Del-Yerro, E., Osman, H., Goeman, J. J., Mamchaoui, K., Dickson, G., Ferlini, A., Muntoni, F., Aartsma-Rus, A., Arechavala-Gomeza, V., Datson, N. A. & Spitali, P., 2 Oct 2018, In : PLoS ONE. 13, 10, p. 1-15 15 p.

Research output: Contribution to JournalArticle

Open Access
File
2017

A UV cross-linking method combined with infrared imaging to analyse RNA–protein interactions

Malmqvist, T., Spickett, C., Gallo, J-M. & Anthony, K., 5 Jun 2017, In : Biology Methods & Protocols. 2, 1, p. 1-4 4 p., 1.

Research output: Contribution to JournalArticle

Open Access
File
2014

Biochemical characterization of patients with in-frame or out-of-frame DMD deletions pertinent to Exon 44 or 45 skipping

Anthony, K., Arechavala-Gomeza, V., Ricotti, V., Torelli, S., Feng, L., Janghra, N., Tasca, G., Guglieri, M., Barresi, R., Armaroli, A., Ferlini, A., Bushby, K., Straub, V., Ricci, E., Sewry, C., Morgan, J. & Muntoni, F., 1 Jan 2014, In : JAMA Neurology. 71, 1, p. 32-40 9 p.

Research output: Contribution to JournalArticle

Open Access
File

Dystrophin quantification: biological and translational research implications

Anthony, K., Arechavala-Gomeza, V., Taylor, L. E., Vulin, A., Kaminoh, Y., Torelli, S., Feng, L., Janghra, N., Bonne, G., Beuvin, M., Barresi, R., Henderson, M., Laval, S., Lourbakos, A., Campion, G., Straub, V., Voit, T., Sewry, C. A., Morgan, J. E., Flanigan, K. M. & 1 others, Muntoni, F., 25 Nov 2014, In : Neurology. 83, 22

Research output: Contribution to JournalArticle

Open Access
File

Tau mRNA is present in axonal RNA granules and is associated with elongation factor 1A

Malmqvist, T., Anthony, K. & Gallo, J-M., 10 Oct 2014, In : Brain Research. 1584, p. 22-27 6 p.

Research output: Contribution to JournalArticle

File
2013

A Novel Morpholino Oligomer Targeting ISS-N1 Improves Rescue of Severe Spinal Muscular Atrophy Transgenic Mice

Zhou, H., Janghra, N., Mitrpant, C., Dickinson, R. L., Anthony, K., Price, L., Eperon, I. C., Wilton, S. D., Morgan, J. & Muntoni, F., Mar 2013, In : Human Gene Therapy. p. 331-342 12 p.

Research output: Contribution to JournalArticle

2012

Antisense Oligonucleotide-Mediated Exon Skipping for Duchenne Muscular Dystrophy: Progress and Challenges

Arechavala-Gomeza, V., Anthony, K., Morgan, J. & Muntoni, F., 1 Jun 2012, In : Current Gene Therapy. p. 152-160 9 p.

Research output: Contribution to JournalArticle

Exon Skipping Quantification by Quantitative Reverse-Transcription Polymerase Chain Reaction in Duchenne Muscular Dystrophy Patients Treated with the Antisense Oligomer Eteplirsen

Anthony, K., Feng, L., Arechavala-Gomeza, V., Guglieri, M., Straub, V., Bushby, K., Cirak, S., Morgan, J. & Muntoni, F., Oct 2012, In : Human Gene Therapy Methods. p. 336-345 10 p.

Research output: Contribution to JournalArticle

Restoration of the dystrophin-associated glycoprotein complex after exon skipping therapy in duchenne muscular dystrophy

Cirak, S., Feng, L., Anthony, K., Arechavala-Gomeza, V., Torelli, S., Sewry, C., Morgan, J. E. & Muntoni, F., 2012, In : Molecular Therapy. p. 462-467 6 p.

Research output: Contribution to JournalArticle

2011

Dystrophin quantification and clinical correlations in Becker muscular dystrophy: Implications for clinical trials

Anthony, K., Cirak, S., Torelli, S., Tasca, G., Feng, L., Arechavala-Gomeza, V., Armaroli, A., Guglieri, M., Straathof, C. S., Verschuuren, J. J., Aartsma-Rus, A., Helderman-Van Den Enden, P., Bushby, K., Straub, V., Sewry, C., Ferlini, A., Ricci, E., Morgan, J. E. & Muntoni, F., 2011, In : Brain. p. 3544-3556 13 p.

Research output: Contribution to JournalArticle

Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: An open-label, phase 2, dose-escalation study

Cirak, S., Arechavala-Gomeza, V., Guglieri, M., Feng, L., Torelli, S., Anthony, K., Abbs, S., Garralda, M. E., Bourke, J., Wells, D. J., Dickson, G., Wood, M. J., Wilton, S. D., Straub, V., Kole, R., Shrewsbury, S. B., Sewry, C., Morgan, J. E., Bushby, K. & Muntoni, F., 13 Aug 2011, In : The Lancet. p. 595-605 11 p.

Research output: Contribution to JournalArticle

2010

Aberrant RNA processing events in neurological disorders

Anthony, K. & Gallo, J. M., 18 Jun 2010, In : Brain Research. p. 67-77 11 p.

Research output: Contribution to JournalArticle

2009

Correction of tau mis-splicing caused by FTDP-17 MAPT mutations by spliceosome-mediated RNA trans-splicing

Rodriguez-Martin, T., Anthony, K., Garcia-Blanco, M. A., Mansfield, S. G., Anderton, B. H. & Gallo, J. M., 2009, In : Human Molecular Genetics. p. 3266-3273 8 p.

Research output: Contribution to JournalArticle

2007

Expression, localization and tau exon 10 splicing activity of the brain RNA-binding protein TNRC4

Chapple, P. J., Anthony, K., Martin, T. R., Dev, A., Cooper, T. A. & Gallo, J. M., 15 Nov 2007, In : Human Molecular Genetics. p. 2760-2769 10 p.

Research output: Contribution to JournalArticle