Ong Nam Phuong Nguyen

Human lysozyme gene mutations cause hereditary systemic amyloidosis

Mark B. Pepys, Philip N. Hawkins, David R. Booth et al. · Nature · 1993 · 660 citations

Life Sciences, Genetics, Molecular Biology +12

Agonist-mediated switching of ion selectivity in TPC2 differentially promotes lysosomal function

Susanne Gerndt, Cheng‐Chang Chen, Yu‐Kai Chao et al. · eLife · 2020 · 154 citations · Full text

Life Sciences, Biochemistry, Cell Biology +17

Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis.

Anne K. Soutar, Philip N. Hawkins, David M. Vigushin et al. · Proceedings of the National Academy of Sciences · 1992 · 144 citations

Life Sciences, Genetics, Molecular Genetics +14

Two-Pore Channel Function Is Crucial for the Migration of Invasive Cancer Cells

Ong Nam Phuong Nguyen, Christian Grimm, Lina S. Schneider et al. · Cancer Research · 2017 · 129 citations

Medicine, Cell Biology, Oncology +14

A new apolipoprotein Al variant, Trp50Arg, causes hereditary amyloidosis

David R. Booth, Shouyong Tan, S E Booth et al. · QJM · 1995 · 76 citations

Life Sciences, Genetics, Molecular Genetics +17