1.Application of PET in Breast Cancer.
Korean Journal of Nuclear Medicine 2002;36(1):34-38
No abstract available.
Breast Neoplasms*
;
Breast*
2.Application of PET in Breast Cancer.
Korean Journal of Nuclear Medicine 2002;36(1):34-38
No abstract available.
Breast Neoplasms*
;
Breast*
3.Right Breast Pain.
Journal of the Korean Medical Association 1997;40(1):110-113
No abstract available.
Breast*
;
Mastodynia*
4.Hormone Replacement Therapy and the Risk of Breast Cancer.
Journal of the Korean Medical Association 2000;43(5):438-447
No abstract available.
Breast Neoplasms*
;
Breast*
;
Hormone Replacement Therapy*
5.Management of matalgia.
Journal of the Korean Medical Association 1999;42(2):218-222
No abstract available.
7.Indication of Segmental Ostectomy by Bicoronal Approach in Reduction Maloplasty.
Young Hwan KIM ; Dong Ho HA ; Dong Il KIM
Journal of the Korean Society of Aesthetic Plastic Surgery 2001;7(1):63-68
No abstract available.
8.The metastatic features in the colorectal cancer.
Journal of the Korean Surgical Society 1992;42(5):643-649
No abstract available.
Colorectal Neoplasms*
9.Result of Patch Test in Kangwon Province.
Young Sik CHOI ; Dong Sik BANG
Korean Journal of Dermatology 1990;28(5):519-526
No abstract available.
Gangwon-do*
;
Patch Tests*
10.Overexpression of the E1193-283 find E2384-649 Proteins of Hepatitis C Virus in GST Fusion Forms in E. coli and Their Immunogenicity.
Young Rim SEONG ; Seeyoung CHOI ; Dong Soo IN
Journal of the Korean Society of Virology 1997;27(2):105-113
The truncated E1192-283 and E2384-649 genes of hepatitis C virus (HCV) linked to the gene for glutathione 5-transferase (GST) were constructed and their expressions were analyzed. The GST-E1192-283 fusion gene overexpressed the fusion protein in E. coli as a soluble form, while the GST-E1192-383 plasmid did not express expected fusion protein. The purified GST-E1192-283 fusion protein was efficiently cleaved by thrombin. More than 90% pure, HCV E1192-283 protein was obtained by GST-agarose chromatography. The truncated GST-E2384-649 fusion gene expressed the fusion protein mainly as an insoluble form, whereas the GST-E2384-740 did not express the fusion protein. The truncated GST-E1 182-283 and GST-E2384-649 fusion proteins reacted specifically with an HCV patient serum. In addition, mice immunized with either the purified E1192-283 or GST-E2384-649 proteins generated specific antibodies to each antigen. The results suggested that hydrophobic carboxyl portions of the E1 and E2 proteins might affect expression levels as well as the solubility of each fusion protein in bacteria. Also, the truncated E1 protein with Tyr-192 to Ser-283 contained antigenic epitope(s) which could be specifically recognized by an HCV patient serum.
Animals
;
Antibodies
;
Bacteria
;
Chromatography
;
Glutathione
;
Hepacivirus*
;
Hepatitis C*
;
Hepatitis*
;
Humans
;
Mice
;
Plasmids
;
Solubility
;
Thrombin
Result Analysis
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