H. Steele-Stallard

Chemogenomic Profiling of Antileishmanial Efficacy and Resistance in the Related Kinetoplastid Parasite Trypanosoma brucei

D. Horn, S. Alsford, Clare F Collett, 2019, Antimicrobial Agents and Chemotherapy.

A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants

K. Steel, M. Bitner-Glindzicz, A. Coffey, 2015, European Journal of Human Genetics.

Comprehensive sequence analysis of nine Usher syndrome genes in the UK National Collaborative Usher Study

K. Steel, M. Bitner-Glindzicz, John C Ambrose, 2011, Journal of Medical Genetics.

Screening for duplications, deletions and a common intronic mutation detects 35% of second mutations in patients with USH2A monoallelic mutations on Sanger sequencing

M. Bitner-Glindzicz, M. Claustres, E. Lenassi, 2013, Orphanet Journal of Rare Diseases.

Pluripotent Stem Cells for Gene Therapy of Degenerative Muscle Diseases.

M. Loperfido, T. VandenDriessche, Francesco Saverio Tedesco, 2015, Current gene therapy.

Three-Dimensional Human iPSC-Derived Artificial Skeletal Muscles Model Muscular Dystrophies and Enable Multilineage Tissue Engineering

M. Duchen, O. Cappellari, D. Wells, 2018, Cell reports.

Modeling Skeletal Muscle Laminopathies Using Human Induced Pluripotent Stem Cells Carrying Pathogenic LMNA Mutations

Tanel Ozdemir, S. Sarcar, P. Zammit, 2018, Front. Physiol..