본 연구는 범국민 책 읽기 문화 확산과 독서진흥 활성화를 위해 개최 되는 대한민국 독서대전 개최지의 선정이유를 살펴보고, 해당 지역이 선 정되는데 영향을 미쳤던 지역의 특색있는 독서문화행사를 밝혀내어 지역 별 경쟁력 있는 독서문화행사의 우수사례를 발굴하는 것에 그 목표가 있 다. 독서대전은 2014년부터 개최된 이래 11년이 지났음에도 불구하고 관련 논의가 거의 이루어지지 않은 상황이라, 본 연구에서는 먼저 대한 민국 독서대전의 법적 근거, 운영 목적, 운영 과정 등을 포함한 독서대전 개요를 살펴보았다. 이에 더해 총 10개 개최지의 선정이유를 다룬 공식 보도자료, 지역신문기사, 관련 연구 등에서 언급된 독서문화행사를 분석 하여 선정이유를 파악하였다. 조사 결과, 10개 지역 중 6개 지역이 한 도시 한 책 읽기 운동을 하고 있었고, 해당 독서운동은 점점 지역과 밀 착된 모습으로 변모하고 있었다. 또 하나 눈에 띄는 특징은 지역 내 다 양한 기관의 관심과 협력을 기반으로 책과 독서와 관련한 지역 축제 및 행사가 운영 중이라는 점이었다. 본 연구를 계기로 지역 중심의 독서문 화행사의 성공사례가 공유되어 지역 독서 활성화에 긍정적 영향을 줄 수 있기를 기대한다.

This paper offers a diachronic examination of how the love story between Zhangsheng and Yingying in Yuanzhen‘s novel “Yingying zhuan” has evolved through different literary conventions. “Yingying Love Story” has remained a beloved narrative, enduring from the Song to the Jin-Yuan periods and continuing to be performed on stage today. The interplay between external factors such as societal and cultural backgrounds and internal changes in literary conventions allows for an understanding of the modified narrative of the “Yingying Love Story” and sheds light on the processes of literary creation, reception, and adaptation. Additionally, it provides a more nuanced understanding of the genre characteristics across different epochs. The transformation of the ending of the “Yingying Love Story” from a tragic conclusion where the woman is forsaken to a happy ending where their love prevails reflects the societal and cultural contexts of the time. In particular, the empathy shown by Ci writers of the Song dynasty towards Yingying and the non-defensive attitude towards Zhangsheng played a crucial role in shaping the evolution of the story's conclusion. Subsequent urban commercial development and the flourishing of private literature altered audience expectations of Yingying, naturally propelling the original tragic ending toward a happy resolution.

Functional magnetic resonance imaging (fMRI) is one of the best available devices that can record the activities of living human brain non-invasively. Its precision and high spatial resolution is matched by none other methodology. The entry barrier to fMRI research is exceptionally high. fMRI has widely been used in medical and scientific research, but its application to marketing research has been limited because of two important reasons. First, the cost problem. The MR scanning devices often cost multi-million dollars and using fMRI for marketing research can be costly. Second, analyzing data from fMRI study is another formidable task. fMRI measures the brain’s hemodynamic activities using voxel as a measuring unit; Voxels are often a cubic with 2 to 3 millimeters on one side. Since a typical adult brain represents over one million voxels in one scan volume, and each scan generally has 2 to 3 seconds of interval time, one experimental block of 40 seconds, for example, will create over 40 million data points. Compared to a typical marketing research data which in general have two dimensions (2d) of rows and columns, fMRI data is inherently 4d with added dimensions of voxel and time. Furthermore, the fMRI signal is sensitive to various sources of noises. In this talk, we offer support for marketing researchers who want to explore fMRI method for their research in the future. First, we discuss issues related to experimental design for fMRI experiments. We explain preprocessing steps that are recommended for fMRI data and show how to apply statistical methods to make inferences that can increase internal validity. Then, we will explicate how to apply big data analytics to fMRI data during this talk to find deep insights into customer’s brains. A real neuromarketing fMRI data will be used to break down the steps for fMRI research and data analytics. Finally, we will open a discussion to discover future research opportunities for marketing research using fMRI. The purpose of this talk is to lower the entry barrier of fMRI method in neuromarketing research so that more people in the marketing field can benefit from the most advanced scientific achievement of our time and discover deepest insights into our customers.

본 연구의 원예치료 프로그램 실시로 대상자들은 회기를 거듭할수록 작업에 흥미를 보이며 자신의 감정을 적극적으로 표현하거나 자신이 주체적으로 참여하려는 태도를 보였다. 이는 연구 결과에서 나타나듯이 부정적이고 낮은 자아개념를 가진 정신지체학생들에게 작업의 참여와 흥미를 유도하여, 자아존중감을 향상시키는 효과가 있음을 보여주는 것이다. 이러한 결과를 기초로 차후에 이들이 학교 졸업 후 사회생활과 연계되어 지속적으로 운영될 프로그램의 개발이 필요하다고 생각된다.

Human papillomavirus type 16(HPV16) has been known to the major factor for the development of uterine cervical carcinomas. We have extended these studies to investigate the in vivo activities of HPV-16 E6/E7 when expressed in squamous epithelia of transgenic mice. Grossly, hK14HPV16E6/E7 transgenic mice had multiple phenotypes, including wrinkled skin that was apparent prior to the appearance of hair on neonates, thickened ears, and loss of hair in adults. In the transgenic mice, the wrinkled skin phenotype on the body and legs died at the age of 3-4 weeks. Histological analysis of demonstrated that E6/E7 causes epidermal hyperplasia in multiple transgenic lineages with high penetrance. This epithelial hyperplasia was characterized by an expansion of the proliferating compartment and an expansion of the keratinocyte and was associated with hyperkeratosis. These transgenic mice expressed E6/E7 transgene mainly in skin, heart, pancreas and kidney. Hyperplasia was found at the skin. The enzyme activities of GR, GPx and CuZnSOD were measured from the transgene cause keratinocyte at the skin. The specific enzyme activities were significantly higher in transgenic mice skin compared to the normal mice skin. Thus these transgenic mice may be useful for the develpment of antioxidant enzymes or other therapies for HPV-associated hyperkeratosis.

In previous reports, pVPSV.IGR2.1 transgenic mouse were described that brain tumor and lymphoma by reason of Vasopressin-SV40 T antigen. In this study, we produced pVPSV.IGR3.6 transgenic mouse that used pVPSV.IGR3.6 vector. Expression of transgene was vary different in transgenic mouse. We obtained 6 transgenic mouse line, moreover they had died at the age of 2-6 weeks without transmitting the transgene to their offspring, and had tumorigenesis on same location with pVPSV.IGR2.1 transgenic mouse. Only a founder mouse was investigated for expression of fusion gene. Here we extended this transgenic approach to the study of tumor progression. From the mouse, we confirmed brain tumor cell, after then cultured for investigate characterization. In this report, we demonstrate that reduction of survival rate in transgenic mouse fused vasopressin gene length, acquisition of brain tumor cell, composition with astrocyte cells and neuronal cells. Finally, cells had no change with increase of passage.

As an effort to direct differentiation of human embryonic stem (hES, MB03) cells to dopamine-producing neuronal cells, Nurr1 was transfected using conventional transfection protocol into MB03 and examined the expression of tyrosine hydroylase (TH) after differentiation induced by retinoic acid (RA) and ascorbic acid (AA). Experimentally, cells were transfected with linearized Nurr1 cDNA in pcDNA3.1 (+)-hygovernight followed by selection in medium containing hygromycin-B (150 /ml). Expression of Nurr1 mRNA was confirmed by RT-PCR and protein by immunocytochemistry in the drug resistant clones. In order to study the effect of Nurr1 protein on the differentiation pattern of ES cells, one of the positive clones (MBNr24) was allowed to form embryoid body (EB) for 2 days and were induced to differentiate for another 4 days using RA (1 ) and AA (50 mM) (2-/4+ protocol) followed by selection in N2 medium for 10 or 20 days. After 10 days in N2 medium, cells immunoreactive to anti-GFAP, anti-TH, or anti-NF200 antibodies were 38.8%, 11%, and 20.5%, respectively. After 20 days in N2 medium, cells expressing GFAP, TH, or NF200 were 28%, 15% and 44.8%, respectively but approximately 9% of MB03 expressed TH protein when the cells were induced to differentiate using a similar prorocol, These results suggest that ectopic expression of Nurr1 enhances generation of TH+ cells as well as neuronal cells when hES cells were differentiated by 2-/4+ protocol.