G.A. Wells

Three rare diseases in one Sib pair: RAI1, PCK1, GRIN2B mutations associated with Smith–Magenis Syndrome, cytosolic PEPCK deficiency and NMDA receptor glutamate insensitivity

David R. Adams, Hongjie Yuan, Todd Holyoak et al. · Molecular Genetics and Metabolism · 2014 · 65 citations · Full text

Life Sciences, Molecular Genetics, Neuroscience +10

Micro–Computed Tomography Analysis of the Human Tuberculous Lung Reveals Remarkable Heterogeneity in Three-dimensional Granuloma Morphology

G.A. Wells, Joel N. Glasgow, Kievershen Nargan et al. · American Journal of Respiratory and Critical Care Medicine · 2021 · 65 citations · Full text

Medicine, Infectious Diseases, Pathology +17

Parasite-specific inserts in the bifunctional S-adenosylmethionine decarboxylase/ornithine decarboxylase of Plasmodium falciparum modulate catalytic activities and domain interactions

Lyn‐Marié Birkholtz, Carsten Wrenger, Fourie Joubert et al. · Biochemical Journal · 2004 · 45 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +17

Regulation of GluA1 α-Amino-3-Hydroxy-5-Methyl-4-Isoxazolepropionic Acid Receptor Function by Protein Kinase C at Serine-818 and Threonine-840

Meagan A. Jenkins, G.A. Wells, Julia L. Bachman et al. · Molecular Pharmacology · 2014 · 28 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17

Novel properties of malarial S-adenosylmethionine decarboxylase as revealed by structural modelling

G.A. Wells, Lyn‐Marié Birkholtz, Fourie Joubert et al. · Journal of Molecular Graphics and Modelling · 2005 · 25 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +16