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Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 23, 2025
Basic Science and PathogenesisSusheel Varma, Laura M Heath, Jessica Malenfant, et al.
Scientific Reports|June 30, 2021
Constrained G4 structures unveil topology specificity of known and new G4 binding proteinsA Pipier, A Devaux, T Lavergne, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 18, 1997
Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastrointestinal tractS Parkkila, A Waheed, R S Britton, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 20, 2001
Naturally variant autosomal and sex-linked loci determine the severity of iron overload in beta 2-microglobulin-deficient miceT J Sproule, E C Jazwinska, R S Britton, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 16, 1997
Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosisS Parkkila, A Waheed, R S Britton, et al.
Development (Cambridge, England)|May 7, 2004
dMyc is required for larval growth and endoreplication in DrosophilaSarah B Pierce, Cynthia Yost, Jessica S Britton, et al.
The American Journal of Physiology|November 14, 1997
Fibronectin and cytokines increase JNK, ERK, AP-1 activity, and transin gene expression in rat hepatic stellate cellsJ E Poulos, J D Weber, J M Bellezzo, et al.
Human Genetics|November 18, 2005
Variants of the SFTPA1 and SFTPA2 genes and susceptibility to tuberculosis in EthiopiaS Malik, C M T Greenwood, T Eguale, et al.
Australian Veterinary Journal|September 29, 2023
Bluetongue disease in sheep in New South Wales - April 2023P D Kirkland, D S Finlaison, A Biddle, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 19, 2000
Transferrin receptor 2: continued expression in mouse liver in the face of iron overload and in hereditary hemochromatosisR E Fleming, M C Migas, C C Holden, et al.
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