Chengjung Lai
Overview
Explore the profile of Chengjung Lai including associated specialties, affiliations and a list of published articles.
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Articles
6
Citations
175
Followers
0
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Recent Articles
1.
Forbes T, Brown B, Lai C
Br J Clin Pharmacol
. 2021 May;
88(6):2525-2538.
PMID: 34022071
RNA interference (RNAi) is a natural biological pathway that inhibits gene expression by targeted degradation or translational inhibition of cytoplasmic mRNA by the RNA induced silencing complex. RNAi has long...
2.
Lai C, Pursell N, Gierut J, Saxena U, Zhou W, Dills M, et al.
Mol Ther
. 2018 Jun;
26(8):1983-1995.
PMID: 29914758
Primary hyperoxalurias (PHs) are autosomal recessive disorders caused by the overproduction of oxalate leading to calcium oxalate precipitation in the kidney and eventually to end-stage renal disease. One promising strategy...
3.
Pursell N, Gierut J, Zhou W, Dills M, Diwanji R, Gjorgjieva M, et al.
Mol Ther
. 2018 May;
26(7):1771-1782.
PMID: 29784585
Glycogen storage diseases (GSDs) of the liver are devastating disorders presenting with fasting hypoglycemia as well as hepatic glycogen and lipid accumulation, which could lead to long-term liver damage. Diet...
4.
β-Catenin mRNA Silencing and MEK Inhibition Display Synergistic Efficacy in Preclinical Tumor Models
Ganesh S, Shui X, Craig K, Koser M, Chopda G, Cyr W, et al.
Mol Cancer Ther
. 2017 Dec;
17(2):544-553.
PMID: 29282298
Colorectal carcinomas harbor well-defined genetic abnormalities, including aberrant activation of Wnt/β-catenin and MAPK pathways, often simultaneously. Although the MAPK pathway can be targeted using potent small-molecule drugs, including BRAF and...
5.
Ganesh S, Koser M, Cyr W, Chopda G, Tao J, Shui X, et al.
Mol Cancer Ther
. 2016 Jul;
15(9):2143-54.
PMID: 27390343
The Wnt/β-catenin pathway is among the most frequently altered signaling networks in human cancers. Despite decades of preclinical and clinical research, efficient therapeutic targeting of Wnt/β-catenin has been elusive. RNA...
6.
Dutta C, Avitahl-Curtis N, Pursell N, Cohen M, Holmes B, Diwanji R, et al.
Mol Ther
. 2016 Jan;
24(4):770-8.
PMID: 26758691
Primary hyperoxaluria type 1 (PH1) is an autosomal recessive, metabolic disorder caused by mutations of alanine-glyoxylate aminotransferase (AGT), a key hepatic enzyme in the detoxification of glyoxylate arising from multiple...