Randall C. Schatzman
Alder (United States)(US)
Publications by Year
Research Areas
Protein Kinase Regulation and GTPase Signaling, Marine Sponges and Natural Products, Iron Metabolism and Disorders, Hemoglobinopathies and Related Disorders, Trace Elements in Health
Most-Cited Works
- → A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis(1996)3,706 cited
- → The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding(1998)837 cited
- → HFE gene knockout produces mouse model of hereditary hemochromatosis(1998)528 cited
- → The Hemochromatosis Founder Mutation in HLA-H Disrupts β2-Microglobulin Interaction and Cell Surface Expression(1997)479 cited
- → Hereditary hemochromatosis: Effects of C282Y and H63D mutations on association with β 2 -microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells(1997)388 cited
- → Potentiation of epidermal growth factor receptor-mediated oncogenesis by c-Src: implications for the etiology of multiple human cancers.(1995)330 cited
- → A 52‐kb deletion in the SOST‐MEOX1 intergenic region on 17q12‐q21 is associated with van Buchem disease in the Dutch population(2002)300 cited
- → Phospholipid-sensitive Ca2+-dependent protein kinase from heart. II. Substrate specificity and inhibition by various agents.(1982)291 cited
- → Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastrointestinal tract(1997)259 cited
- → Phospholipid-sensitive calcium-dependent protein kinase: Inhibition by antipsychotic drugs(1981)243 cited