Recent Publications

Yan MT, Yang SS, Tseng MH, Cheng CJ, Tsai JD, Sung CC, Hus YJ, Lin SH. (2021) Allele-specific RT=TCR for the rapid detection of recurrent SLC12A3 mutations for Gitelman syndrome. NPJ Genom Med 6:68.

Chen JC, Lin SH, Huang CL, Cheng CJ*. (2019) Reply to Farfel et al.: Is enhanced chloride reabsorption in proximal tubule a possible mechanism of metabolic acidosis in PHAII? Proc Natl Acad Sci U S A 16: 16175-16176. (corresponding)

Chen JC, Lo YF, Lin YW, Lin SH, Huang CL, Cheng CJ*. (2019) WNK4 kinase is a physiological intracellular chloride sensor. Proc Natl Acad Sci U S A doi: 10.1073/pnas.1817220116. (corresponding)

Lin CM, Cheng CJ, Yang SS, Tseng MH, Yen MT, Sung CC, and Lin SH. (2019) Generation and analysis of a mouse model of pseudohypoaldosteronism type II caused by KLHL3 mutation in BTB domain. FASEB J. 33: 1051-1061.

Tseng MH, Huang SM, Lo FS, Huang JL, Cheng CJ, Lee HJ, and Lin SH. (2017) Functional Analysis of VDR Gene Mutation R343H in A Child with Vitamin D-Resistant Rickets with Alopecia. Sci Rep. 7: 15337.