Projects per year
Personal profile
Biography
Karen studied biochemistry at the University of Leeds spending one year as a sandwich student at GlaxoSmithKline (GSK), Essex. At GSK Karen experienced the drug discovery process through performing large-scale purifications of protein drug targets. Developing a strong interest in neurodegeneration Karen joined the lab of Dr Jean-Marc Gallo at the Institute of Psychiatry, King’s College London. Her PhD “tau RNA processing in neurodegeneration: trans-acting factors regulating alternative splicing and mRNA localisation” was awarded in 2009. As a post-doc in Dr Gallo’s lab Karen established proof-of-concept for RNA reprogramming strategies including RNA trans-splicing therapies for spinocerebellar ataxia type 1 and the tauopathies. In 2010 Karen successfully translated her RNA expertise to the neuromuscular field and moved to the Dubowitz Neuromuscular Centre, Institute of Child Health, University College London (UCL). Working with Professor Francesco Muntoni, Karen played a key role in developing antisense oligonucleotide-mediated exon skipping as a therapeutic strategy for Duchenne muscular dystrophy (DMD). Her pre-clinical and clinical work in this area culminated in the first FDA-approved drug for DMD. In 2015 Karen attained a lectureship at the University of Northampton where she founded and leads the Molecular Biosciences Research Group. Her laboratory investigates the molecular mechanisms of neurological disorders with a focus on the neuropathophysiology of DMD. Karen also consults for international pharmaceutical and biotechnology companies on methodology for clinical trial biochemical outcome measures and the development of exon skipping and trans-splicing therapies. She is currently leading the the proof-of-concept and pre-clinical development of innovative trans-splicing applications for rare diseases.
Research Interests
Karen’s research is focused on RNA processing and the pre-clinical development of RNA therapeutics (exon skipping and trans-splicing) for rare neurological diseases. Current research projects and interests include:
-Neuropathophysiology of Duchenne muscular dystrophy
-The role of the DMD gene in cancer
-RNA processing of the dystrophin gene
-Therapeutic targeting of dystrophin in the brain
-RNA processing in neurodegeneration
-RNA-based gene therapy/therapeutics
-Spinocerebellar ataxia
-Trans-splicing
Teaching Interests
Undergraduate teaching:
Karen teaches across the BSc (Hons) in Biological Science, Biochemistry, Pharmacology and Biomedical Science programmes:
Module Leader:
- SLS3010: Molecular and Cellular Neuroscience
Teaching on other modules:
- SLS2001: Genes and Genomics
- SLS2013: Bioscience Research Methods
Postgraduate teaching (taught programmes)
- MSc in Molecular Medicine
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
Education/Academic qualification
Master, PGCert in Research Degree Supervision, University of Northampton
2016 → 2017
PhD, PhD “tau RNA processing in neurodegeneration: trans-acting factors regulating alternative splicing and mRNA localisation” , King's College London
2005 → 2009
Bachelor, BSc (Hons) Biochemistry with medical biochemistry, University of Leeds
2001 → 2005
City & Guilds licentiateship award in applied biochemistry, GlaxoSmithKline
2003 → 2004
Keywords
- RM Therapeutics. Pharmacology
- RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry
- RC0254 Neoplasms. Tumors. Oncology (including Cancer)
- QP Physiology
- QM Human anatomy
- QH301 Biology
- QH426 Genetics
Fingerprint
- 1 Similar Profiles
Projects
- 5 Finished
-
The Northampton Advanced Imaging Facility
Anthony, K. (PI) & Machado, L. (CoPI)
31/01/24 → 31/03/24
Project: Capital Funding
-
Evaluation of RNA trans-splicing as a therapeutic strategy for spinocerebellar ataxia, type 1
Anthony, K. (PI)
17/10/22 → 17/10/23
Project: Research › Charitable Funding
-
Investigating a role for dystrophin protein Dp71 in cell migration
Anthony, K. (PI)
27/06/22 → 8/08/22
Project: Research › Charitable Funding
File -
RNA processing of the brain dystrophin isoform Dp71
Anthony, K. (PI) & Wood, C. (CoI)
4/08/20 → 4/02/22
Project: Research › Charitable Funding
-
The role of Dp71 in cell migration and the neuropathophysiology of Duchenne muscular dystrophy
Anthony, K. (PI)
3/06/19 → 27/07/19
Project: Research › Charitable Funding
-
A systematic literature review and meta-analysis of the effectiveness of vitamin D supplementation for patients with Duchenne muscular dystrophy
Guo, J. & Anthony, K., 15 Oct 2023, In: Neuromuscular Disorders. 33, 11, p. 835-844 10 p.Research output: Contribution to Journal › Article › peer-review
Open AccessFile -
A Survey of Machine Learning Approaches Applied to Gene Expression Analysis for Cancer Prediction
Khalsan, M., Machado, L., SALIH AL-SHAMERY, E., Ajit, S., Anthony, K., Mu, M. & Opoku Agyeman, M., 18 Mar 2022, In: IEEE Access.Research output: Contribution to Journal › Article › peer-review
Open AccessFile -
Duchenne muscular dystrophy gene expression is an independent prognostic marker for IDH mutant low-grade glioma
Naidoo, M., Jones, L., Conboy, B., Hamarneh, W., D'Souza, D., Anthony, K. & Machado, L., 5 Sept 2022. 1 p.Research output: Contribution to Conference › Poster › peer-review
Open AccessFile -
Duchenne muscular dystrophy gene expression is an independent prognostic marker for IDH mutant low-grade glioma
Naidoo, M., Jones, L., Conboy, B., Hamarneh, W., D'Souza, D., Anthony, K. & Machado, L., 25 Feb 2022, In: Scientific Reports. 12, 1, 3200.Research output: Contribution to Journal › Article › peer-review
Open AccessFile -
Evaluation of RNA trans-splicing as a therapeutic strategy for spinocerebellar ataxia type 1
Buijsen, R., Green, E., Avale, E., Gallo, J.-M. & Anthony, K., 1 Nov 2022.Research output: Contribution to Conference › Poster › peer-review
Open AccessFile -
RNA-based therapeutics for neurological diseases
Anthony, K., 22 Jan 2022, In: RNA Biology. 19, 1, p. 176-190 15 p.Research output: Contribution to Journal › Review Article › peer-review
Open AccessFile -
T Cell Responses to Dystrophin in a Natural History Study of Duchenne Muscular Dystrophy
Anthony, K., Ala, P., Catapano, F., Meng, J., Domingos, J., Perry, M., Ricotti, V., Maresh, K., Phillips, L., Servais, L., Seferian, A., De Lucia, S., de Groot, I., D Krom, Y., Verschuuren, J., Niks, E., Straub, V., Guglieri, M., Voit, T. & Morgan, J. & 1 others, , 1 Dec 2022, (E-pub ahead of print) In: Human Gene Therapy.Research output: Contribution to Journal › Article › peer-review
Open AccessFile -
Outcomes of treatment of synovial sarcoma
Robertson-Smith, B., McCulloch, T., Campbell, J., Anthony, K. & Ashford, R., 8 Oct 2021.Research output: Contribution to Conference › Abstract › peer-review
Open AccessFile
Datasets
-
Dataset for - 'Duchenne muscular dystrophy gene expression is an independent prognostic marker for low-grade glioma'
Anthony, K. (Creator) & Machado, L. (Creator), University of Northampton, Jul 2021
DOI: 10.24339/ae20690c-1bdf-48b0-8c5d-c88fbc40ad4a
Dataset
File
Activities
-
A population-based survey to ascertain the risk and incidence of cancer in DMD
Anthony, K. (Author)
22 Jul 2022Activity: Academic Talks or Presentations › Invited talk › Research
-
From concept to therapy: adventures in RNA therapeutics and the importance of basic science
Anthony, K. (Author)
15 Mar 2022Activity: Academic Talks or Presentations › Keynote › Research
-
The major brain dystrophin protein, Dp71, is a potential independent prognostic marker for low grade glioma
Anthony, K. (Author)
2 Feb 2021Activity: Academic Talks or Presentations › Invited talk › Research
-
The limitless world of RNA therapeutics
Anthony, K. (Author)
23 Sept 2021Activity: Academic Talks or Presentations › Invited talk › Research
File -
The brain and Duchenne muscular dystrophy: exploring the role of dystrophin proteins in the brain.
Anthony, K. (Author)
5 Nov 2021Activity: Academic Talks or Presentations › Invited talk › Research
File -
External PhD examiner
Anthony, K. (Examiner)
21 Jul 2020Activity: Examinations › Examination › Research
-
Understanding the brain in Duchenne muscular dystrophy
Anthony, K. (Author)
8 Jun 2020Activity: Academic Talks or Presentations › Oral presentation › Research
-
25th International Annual Congress of theWorld Muscle Society
Anthony, K. (Participant)
28 Sept 2020 → 2 Oct 2020Activity: Organising a conference or workshop › Participating in a conference or workshop › Research
Press/Media
-
Professor revisits research to develop a treatment for a rare type of ataxia
24/09/22
1 item of Media coverage
Press/Media
-
Significant contribution recognised for new Associate Professors
Maunder, R., Anthony, K., Devecchi, C., Opoku Agyeman, M., Rothery, M., Jackson, P., Caldwell, H., Nasir, J., Lumsden, E., Farini, F., Hill, K., Redwood, T., Smith, C., Pryce, A., Callender, M. & Paterson-Young, C.
3/09/20
1 item of Media coverage
Press/Media
-
-
-
Mentoring event helps Bioscience students speed toward career success
30/10/17
1 Media contribution
Press/Media
-
-
Delight and controversy over new drug to treat Duchenne muscular dystrophy
23/09/16
1 Media contribution
Press/Media
Impacts
-
FDA approves first drug to treat Duchenne muscular dystrophy (DMD)
Anthony, K. (Co-Investigator)
Impact: Public policy impacts, Health and Well-Being impacts, Quality of life impacts, 03: Good Health and Well-Being (UN SDG)