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Unity3D와 ProudNet을 이용한 네트워크게임 개발
남영준(Yeong-Jun Nam),성귀중(Gwi-Jung Seong),고용위(Yong-Wi Ko),백철(Cheol Baek),김번영(Beon-Yeong Kim),박광후(Gwang-Hu Park),김훈수(Hun-Su Kim),방경섭(Gyeong-Seop Bang),강명주(Myung-Ju Kang),박찬일(Chan-Il Park),오현주(Hyoun-Ju Oh) 한국컴퓨터정보학회 2014 한국컴퓨터정보학회 학술발표논문집 Vol.22 No.2
본 논문은 Unity3D와 게임서버엔진인 ProudNet을 이용해 네트워크 게임을 개발한 방법을 설명하였다. ProudNet 서버를 Unity3D 클라이언트와 연결하여 네트워크 기능을 구현할 때 ProudNet의 어떤 기능을 쓰며 또 서버가 보낸 메시지를 클라이언트가 어떠한 방식을 이용하여 메시지를 처리하게 구현하였는지를 설명하였다.
대인관계 증진 집단모래놀이치료가 중학생의 우울, 불안에 미치는 영향
박혜영(Hye-Yeong Park),강귀임(Gwi-Im Kang),김미향(Mi-Hyang Kim) (사)한국학교공공모래놀이학회 2020 학교상담 및 모래놀이 Vol.2 No.2
본 연구에서는 대인관계 증진 집단모래놀이치료가 중학생의 우울과 불안에 미치는 영향에 대해 알아보고자 하였다. 천안시에 위치한 A, B, C 중학교에 재학 중인 학생 48명을 대상으로 박혜영과 조성근(2020)이 개발한 대인관계 증진 집단모래놀이치료를 회기당 45분씩 주 2회, 총 8회기 실시했다. 프로그램의 효과를 검증하기 위해 Beck이 개발한 우울척도(BDI)와 불안척도(BAI)를 측정도구로 사용했고, 수집한 자료는 SPSS 18.0을 이용하여 paired t-test를 실시했다. 연구결과, 대인관계 증진 집단모래놀이치료는 중학생의 우울, 불안 감소에 긍정적인 영향을 미치는 것으로 나타났다. 이러한 결과는 대인관계 증진 집단모래놀이치료가 중학생의 우울, 불안 감소에 효과적인 치료기법이 될 수 있음을 시사한다. The purpose of this study was to examine the effects of group sandplay therapy programs on depression and anxiety in middle school students. For 48 students attending middle schools A, B, and C located in Cheonan, a group sandplay therapy program developed by Park (2020) was conducted twice a week, 45 minutes per session, eight times a week, and its effects were verified. The program effectiveness verification used the depression scale (BDI) and anxiety scale (BAI) developed by Beck as measurement tools, and the collected data was conducted using SPSS 18.0. These results suggest that group sand play therapy that promotes interpersonal relations can be an effective treatment technique to reduce depression and anxiety in middle school students.
Park, Chan Hum,Lee, Ah Young,Kim, Ji Hyun,Seong, Su Hui,Jang, Gwi Yeong,Cho, Eun Ju,Choi, Jae Sue,Kwon, Jungkee,Kim, Young Ock,Lee, Sang Won AMERICAN JOURNAL OF CHINESE MEDICINE INC 2018 The American journal of Chinese medicine Vol.46 No.1
<P>Cisplatin, a platinum chelate with potent antitumor activity against cancers of the testis, ovary, urinary bladder, prostate, and head and neck, has adverse effects on the kidney, bone marrow, and digestive organs, and its use is particularly limited by nephropathy as a side effect. In the present study, safflower seed extract was administered to a mouse model of cisplatin-induced acute renal failure to investigate its activity. Cisplatin (20 mg/kg body weight) was administered by intraperitoneal injection to mice that had received oral safflower seed extract (100 or 200 mg/kg body weight per day) for the preceding 2 days. Three days after the cisplatin injection, serum and renal biochemical factors; oxidative stress, inflammation, and apoptosis-related protein expression; and histological findings were evaluated. Cisplatin-treated control mice showed body-weight, food intake and water intake loss, and increased kidney weight, whereas the administration of safflower seed extract attenuated these effects (p < 0: 05, p < 0: 01). Moreover, safflower seed extract significantly decreased the renal functional parameters urea nitrogen and creatinine in the serum (p < 0: 05 and p < 0: 01, respectively). Safflower seed extract also significantly reduced the enhanced levels of reactive oxygen species in the kidney observed following cisplatin treatment, with significance. The expression of proteins related to the anti-oxidant defense system in the kidney was down-regulated following cisplatin treatment, but safflower seed extract significantly up-regulated the expression of the anti-oxidant enzyme catalase. Furthermore, safflower seed extract reduced the overexpression of phosphor (p)-p38, nuclear factor-kappa B p65, cyclooxygenase-2, inducible nitric oxide synthase, ATR, p-p53, Bax, and caspase 3 proteins, and mice treated with safflower seed extract exhibited less renal histological damage. These results provide important evidence that safflower seed extract exerts a pleiotropic effect on several oxidative stress-and apoptosis-related parameters and has a renoprotective effect in cisplatin-treated mice.</P>