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노인성 우울증 환자에서 지역사회 기반 ‘목표달성 프로그램’의 효용성
강규하(Gyu Ha Kang),장기중(Ki Jung Chang),임현국(Hyun Kook Lim),한진주(Jin joo Han),이은희(Eun Hee Lee),노현웅(Hyun Woong Roh),노재성(Jai Sung Noh),정영기(Young Ki Chung),임기영(Ki Young Lim),홍창형(Chang Hyung Hong),손상준(Sang Joon 대한노인정신의학회 2017 노인정신의학 Vol.21 No.1
Objective:This study aimed to investigate the effect of community-based Goal-Achieving program in geriatric depressive symptoms preliminarily. Methods:We obtained data from elderly Korean subjects with major depressive disorder (n=51) aged 60 years or older at baseline, taking case management from community mental health center. Subjects were randomly assigned to intervention group (n=24) and control group (n=27). We investigated depressive symptoms through Short Form Geriatric Depression Scale-Korean version (SGDS-K) at baseline and every month for 3 months to all subjects. We tested interaction between group and time in SGDSK score to evaluate the effect of program. And post hoc test examined between group differences of SGDS-K at each time points. Results:In quadratic linear mixed effects model analysis, interaction between group and time was statistically significant (Total SGDS-K score : coefficient=0.29, p<0.001 ; SGDS-K dysphoria subscale : 0.18, p<0.001 ; SGDS-K hopelessness subscale : 0.05, p=0.089 ; SGDS-K cognitive impairment subscale : 0.06, p=0.003). And significant between group difference was shown in post hoc test at time points of third month (SGDS-K score of control group : SGDS-K score of intervention group=10.74±3.482 : 7.25±4.475, p=0.0184). Conclusion:These results may suggest that ‘Community-based the Goal-Achieving program’ has efficacy in reducing geriatric depressive symptoms.
용이한 Subcloning 을 위한 pCAT�3-Basic vector의 변형
국중기,한진주,김명수,박주철,김흥중 朝鮮大學校 口腔生物學硏究所 2001 Oral Biology Research (Oral Biol Res) Vol.25 No.2
To increase convenience and facilitate subcloning in construction of chloramphenicol acetyl transferase (CAT) plasmids for transient expression assay, modification of the pCAT^(R)3-Basic vector were performed. The procedures of this study were as follows : ⑴ The pCAT^(R)3-Basic vector was digested with bamH I and Sal I and then the 5'-end overhanging were filled with Klwnow Fragment and dNTPs. ⑵ The resulting blunt-end DNA fragment was self-ligated using T4 DNA ligase. ⑶ The ligation mixture was transformed into E. Coli DH5α. ⑷ The modified pCAT^(R)3-Basic vector was named pCAT^(R)3△B/S-Basic vector. ⑸ The pCAT^(R)3△B/S-Basic vector was digested with Xba I and then the 5'-end overhanging were filled with Klenow Fragment and dNTPs. ⑹ The result modified pCAT^(R)3△B/S-Basic vector was named pCAT^(R)3b-Basic vector. ⑺ The multiple cloning site (from Kpn I to Xho I sites) of pCR2.1-TOPO cloned into the pCAT^(R)3b-Basic vector. The resulting plasmid was named pCAT^(R)3b-CR-Basic vector. As the result, the new vector. pCAT^(R)3b-CR-Basic vector. As the result, the new vector. pCAT^(R)3b-CR-Basic vector has more five single cloning stites-BamH I, Spe I, BstX I, EcoR V, and EcoR I- than the pCAT^(R)3-Basic vector. This data indicate that the pCAT^(R)3b-CR-Basic vector can be useful for constructioin of CAT plasmids in conventience and facility.