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Sug Hyung Lee

Researcher at Catholic University of Korea

Publications -  463
Citations -  23933

Sug Hyung Lee is an academic researcher from Catholic University of Korea. The author has contributed to research in topics: Frameshift mutation & Germline mutation. The author has an hindex of 64, co-authored 454 publications receiving 21552 citations. Previous affiliations of Sug Hyung Lee include Chung-Ang University & The Catholic University of America.

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Expression of CARD6, an NF-κB activator, in gastric, colorectal and oesophageal cancers

TL;DR: The increased expression of CARD 6 in ESCC, GC and CRC tissues compared to their corresponding normal cells suggested that neoexpression of CARD6 might be related to activation of NF‐κB pathway in the cancers and might play a role in the development of most types of gastrointestinal cancers.
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Frameshift mutations of chromosome cohesion-related genes SGOL1 and PDS5B in gastric and colorectal cancers with high microsatellite instability.

TL;DR: The data indicate that frameshift mutations of SGOL1 and PDS5B and the loss of their expression may be a feature of gastric and colorectal cancers with high microsatellite instability and suggest that these alterations might contribute to cancer pathogenesis by deregulating cohesin-related functions.
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Immunohistochemical and mutational analysis of apoptosis-inducing factor (AIF) in colorectal carcinomas†

TL;DR: The increased expression of AIF in the malignant colorectal epithelial cells compared to the normal mucosal epithelium cells suggests that AIF expression may play a role in colOREctal tumorigenesis, and the data suggest that somatic mutation of Aif is a rare event in common human cancers.
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Frequent frameshift mutations in 2 mononucleotide repeats of RNF43 gene and its regional heterogeneity in gastric and colorectal cancers

TL;DR: The data indicate that RNF43 gene harbored not only exceedingly high mutations but also mutational ITH, which together might play a role in tumorigenesis of GC and CRC and suggest that regional analysis is required for a more comprehensive evaluation of the mutation status in these tumors.