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Cell Calcium|January 7, 2004
A role for hTRPC1 and lipid raft domains in store-mediated calcium entry in human plateletsSharon L Brownlow, Alan G S Harper, Matthew T Harper, et al.American Journal of Human Genetics|October 1, 1991
Covariate-dependent age-at-onset distributions for Huntington diseaseM Krawczak, B Bockel, L Sandkuijl, et al.Clinical Genetics|April 1, 1985
Carrier detection in Becker muscular dystrophy using creatine kinase estimation and DNA analysisH M Kingston, M Sarfarazi, R G Newcombe, et al.Diabetologia|October 25, 2017
Correction to: Islet-intrinsic effects of CFTR mutationFiona N Manderson Koivula, Neville H McClenaghan, Alan G S Harper, et al.Journal of the Neurological Sciences|December 1, 1988
Evidence against location of the gene for facioscapulohumeral muscular dystrophy on the distal long arm of chromosome 14P W Lunt, J G Noades, M Upadhyaya, et al.Clinical Genetics|March 1, 1988
Population studies of Huntington's disease in WalesO W Quarrell, A Tyler, M P Jones, et al.Nano Research|January 21, 2021
Controlling human platelet activation with calcium-binding nanoparticlesDavid Cabrera, Karen Walker, Sandhya Moise, et al.Journal of the American Chemical Society|May 13, 2004
Electrochemistry and optical absorbance and luminescence of molecule-like Au38 nanoparticlesDongil Lee, Robert L Donkers, Gangli Wang, et al.Muscle & Nerve. Supplement|January 1, 1995
Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, J Maynard, M Osborn, et al.The Journal of Comparative Neurology|June 15, 1994
Localization of nerve growth factor (NGF) and low-affinity NGF receptors in touch domes and quantification of NGF mRNA in keratinocytes of adult ratsK B English, S Harper, N Stayner, et al.Pageof 105