Heather B. Stallard-Steele
London, ENG WC1E6DE, United Kingdom
Last Updated: 09/26/2026
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Found 8 publications
Advanced iPSC-based modelling of LMNA-related congenital muscular dystrophy enables development of genetic therapies for muscle laminopathies.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: December 16, 2025
Chemogenomic Profiling of Antileishmanial Efficacy and Resistance in the Related Kinetoplastid Parasite Trypanosoma brucei.
Journal: Antimicrobial agents and chemotherapy
Published: April 15, 2019
Three-Dimensional Human iPSC-Derived Artificial Skeletal Muscles Model Muscular Dystrophies and Enable Multilineage Tissue Engineering.
Journal: Cell reports
Published: November 15, 2016
Pluripotent Stem Cells for Gene Therapy of Degenerative Muscle Diseases.
Journal: Current gene therapy
Published: June 17, 2015
A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants.
Journal: European journal of human genetics : EJHG
Published: June 18, 2014
Screening for duplications, deletions and a common intronic mutation detects 35% of second mutations in patients with USH2A monoallelic mutations on Sanger sequencing.
Journal: Orphanet journal of rare diseases
Published: April 16, 2013
Comprehensive sequence analysis of nine Usher syndrome genes in the UK National Collaborative Usher Study.
Journal: Journal of medical genetics
Published: December 03, 2011
Showing 1-8 of 8
Last Updated: 09/26/2026