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Comparative Medicine|March 4, 2024
Erratum: AC-DC Electropenetrography as a Tool to Quantify Probing and Ingestion Behaviors of the Yellow Fever Mosquito (Aedes aegypti) on Mice in BiocontainmentLyndsi D Vaughan, Samuel B Jameson, Dawn M Wesson, et al.
Neurosci|June 27, 2023
Deficits in cerebellum-dependent learning and cerebellar morphology in male and female BTBR autism model miceElizabeth A Kiffmeyer, Jameson A Cosgrove, Jenna K Siganos, et al.
Endocrinology|January 6, 2007
Effects of loss of classical estrogen response element signaling on bone in male miceFarhan A Syed, Daniel G Fraser, Thomas C Spelsberg, et al.
Molecular Cancer Research : MCR|May 25, 2012
Alpha-melanocyte-stimulating hormone suppresses oxidative stress through a p53-mediated signaling pathway in human melanocytesAna Luisa Kadekaro, Juping Chen, Jennifer Yang, et al.
The Journal of Biological Chemistry|September 14, 2017
The metal chaperone Atox1 regulates the activity of the human copper transporter ATP7B by modulating domain dynamicsCorey H Yu, Nan Yang, Jameson Bothe, et al.
Frontiers in Pharmacology|June 26, 2026
Exploring early intervention in psychosis (EIP) perspectives towards pharmacogenomics (PGx) implementation to support antipsychotic prescribing: a multi-method qualitative explorationA Jameson, B Fylan, G S Sagoo, et al.
The Journal of General Virology|July 28, 1999
TT virus sequence heterogeneity in vivo: evidence for co-infection with multiple genetic typesJ K Ball, R Curran, S Berridge, et al.
The Journal of Bone and Joint Surgery. British Volume|July 20, 2011
Accelerating failure rate of the ASR total hip replacementD J Langton, S S Jameson, T J Joyce, et al.
Osteoarthritis and Cartilage|September 3, 2011
Association of vitamin D status with knee pain and radiographic knee osteoarthritisS Muraki, E Dennison, K Jameson, et al.
The Journal of Clinical Endocrinology and Metabolism|January 27, 1999
Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS geneP Kopp, O K Arseven, L Sabacan, et al.
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