Found 4 results
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Lu H, Galeano MCRondón, Ott E, Kaeslin G, P Kausalya J, Kramer C, Ortiz-Brüchle N, Hilger N, Metzis V, Hiersche M et al..  2017.  Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease.. Nat Genet. 49(7):1025-1034.
Wan X, Chen Z, Choi W-I, Gee HYung, Hildebrandt F, Zhou W.  2016.  Loss of Epithelial Membrane Protein 2 Aggravates Podocyte Injury via Upregulation of Caveolin-1.. J Am Soc Nephrol. 27(4):1066-75.
Ashraf S, Gee HYung, Woerner S, Xie LX, Vega-Warner V, Lovric S, Fang H, Song X, Cattran DC, Avila-Casado C et al..  2013.  ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption.. J Clin Invest. 123(12):5179-89.
Gee HYung, Saisawat P, Ashraf S, Hurd TW, Vega-Warner V, Fang H, Beck BB, Gribouval O, Zhou W, Diaz KA et al..  2013.  ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling.. J Clin Invest. 123(8):3243-53.