Lauren Campbell

Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH

Joe Rainger, Hemant Bengani, Lauren Campbell et al. · Human Molecular Genetics · 2012 · 69 citations · Full text

Distinct Subgroup, Pyrimidine Biosynthesis, Genetics +21

Genetic Predictions of Prion Disease Susceptibility in Carnivore Species Based on Variability of the Prion Gene Coding Region

Paula Stewart, Lauren Campbell, Susan Skogtvedt et al. · PLoS ONE · 2012 · 45 citations · Full text

Prion Protein-Specific Antibodies that Detect Multiple TSE Agents with High Sensitivity

Sandra McCutcheon, Jan Langeveld, Boon Chin Tan et al. · PLoS ONE · 2014 · 25 citations · Full text

The PrPC C1 fragment derived from the ovine A136R154R171 PRNP allele is highly abundant in sheep brain and inhibits fibrillisation of full-length PrPC protein in vitro

Lauren Campbell, Andrew C. Gill, Gillian McGovern et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 2013 · 17 citations

Protein Function, Molecular Neuroscience, Signal Transduction +12