Xiao Zhou

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

Abdül Waheed, Seppo Parkkila, Xiao Zhou et al. · Proceedings of the National Academy of Sciences · 1997 · 389 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis

Seppo Parkkila, Abdül Waheed, Robert S. Britton et al. · Proceedings of the National Academy of Sciences · 1997 · 345 citations

Medicine, Genetics, Molecular Genetics +17

Association of HFE protein with transferrin receptor in crypt enterocytes of human duodenum

Abdül Waheed, Seppo Parkkila, Juha Saarnio et al. · Proceedings of the National Academy of Sciences · 1999 · 245 citations · Full text

Medicine, Cell Biology, Physiology +17

Immunohistochemistry of Carbonic Anhydrase Isozyme IX (MN/CA IX) in Human Gut Reveals Polarized Expression in the Epithelial Cells with the Highest Proliferative Capacity

Juha Saarnio, Seppo Parkkila, Anna‐Kaisa Parkkila et al. · Journal of Histochemistry & Cytochemistry · 1998 · 171 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +13

NF-κB pathway activation during endothelial-to-mesenchymal transition in a rat model of doxorubicin-induced cardiotoxicity

Anji Xu, Fei‐Yan Deng, Yongyi Chen et al. · Biomedicine & Pharmacotherapy · 2020 · 168 citations · Full text

Medicine, Cardiology, Pharmacology +16