1.
Yonsei Medical Journal
;
: 20-29, 2020.
Article
in English
| WPRIM
| ID: wpr-782127
ABSTRACT
Subject(s)
Humans , Apoptosis , B-Lymphocytes , Blotting, Western , Carcinogenesis , Caspase 3 , Cell Line , Cell Proliferation , Curcumin , Immunoprecipitation , In Situ Hybridization , Lymphoma , Lymphoma, B-Cell , MicroRNAs , Real-Time Polymerase Chain Reaction , RNA , RNA, Messenger
2.
Kosin Medical Journal
;
: 446-453, 2018.
Article
in English
| WPRIM
| ID: wpr-739004
ABSTRACT
Pheochromocytomas might be sporadic or genetic. Genetic pheochromocytoma is associated with multiple endocrine neoplasia (MEN) type 2A, MEN type 2B, and von Hippel-Lindau (VHL) disease. RET mutations are identified in more than 90% of index cases of MEN2 and familial medullary thyroid cancer and in about 4–12% of apparent sporadic cases. Here, we report a 54-year-old man presenting with pheochromocytoma and renal cell carcinoma, who was identified as having a novel missense RET mutation.