The shrinkage variation of Low Temperature Cofired Ceramics(LTCC) limits the size of the substrates that impose limitations on embedded passive components. This paper focuses on the method of minimizing or controlling planar shrinkage and reducing distortion during firing. The laminated sheets of alumina and glass were sintered at varying temperature, and depending on the amount of the glass ceramics. When the sintered of multi-layer structure with , the glass infiltrated entirely into layer at the temperature of about or higher.

정신분열병은 망상이나 환각과 같은 양성증상과 감정적 둔마와 같은 음성증상이 대표적인 사고장애로서 외부입력 정보를 통합하거나 체계적으로 처리하는 능력이 매우 부족하다. 즉, 정신분열병 환자는 시각, 청각, 촉각 등의 자극을 종합하고 통합하여 인지하지 못한다. 본 연구에서는 뇌 인지 통합 모델(Brain Multimodal Integration Model)에 기반하여 정신분열병 환자의 인지 능력을 측정하기 위한 가상현실시스템을 제안한다. 정신분열병 환자의 지각, 인지, 운동능력을 측정하기 위한 가상현실시스템은 환자에게 시각과 청각의 멀티모달 자극을 제시하여, 환자로 하여금 일정시간 동안 자극을 기억하고 처리하여 주어진 과제를 수행하도록 하였다. 수행 결과를 통해 환자의 멀티모달 자극 통합능력 및 작업기억 통합능력, 네비게이션 능력을 평가한다. 임상연구를 통해 개발된 가상현실시스템을 WCST과 같은 기존 검사방법들과 비교하여 검증하였는데, 가상현실로 측정한 파라미터와 WCST의 파라미터 및 SPM 점수 사이에 매우 유의미한 상관관계를 보여 가상현실시스템의 유용성을 확인할 수 있었다.

The seminiferous epithelium cycle and developmental stages of spermatids in Clethrionomys rufocanus were observed under a light microscope. The seminiferous epithelium cycle was divided into 8 stages. Type Ad spermatogonia appeared through all stages. Type Ap, In, and B spermatogonia appeared in stages Ⅰ, Ⅱ, Ⅲ, and Ⅳ. In the first meiosis prophase, the leptotene spermatocytes appeared from stage Ⅴ, the zygotene spermatocytes in stages Ⅰ, Ⅵ, Ⅶ, Ⅷ, the pachytene spermatocytes from stages Ⅱ to Ⅵ, the diplotene spermatocytes in stage Ⅶ. The meiotic figures and interkinesis spermatocytes were observed in stage Ⅷ. Developing spermatids were subdivided into 10 steps, based on the morphological characteristics such as the acrosome formation changes in spermatozoa, nucleus, cytoplasm, and spermiation changes. The C. rufocanus spermatocytogenesis and spermiogenesis results displayed similar results with Apodemus agrarius coreae and A. speciosus peninsulae. Considering all the results, the spermatogenesis may be useful information to analyze the differentiation of spermatogenic cells and the breeding season.

Thirty-two germplasms of Korean adlay landraces were examined to analyse the genetic relationship through the amplified fragment length polymorphism (AFLP) approach. Total number of AFLP products generated by 12 selective primer combinations was 882. The number of polymorphic fragments by each primer combination greatly varied from 4 to 51 with a mean of 20.3, bands visible on the polyacrylamide gel. A genetic similarity coefficient was used for cluster analysis following UPGMA (unweighted pair grouping method of averages) method. The resulting clusters were represented in the form of a dendrogram. The clustering was not tight in the dendrogram. There was generally no clear grouping of the adlay according to the geographic regions in which germplasms were collected. The present AFLP analysis imply that although Korean adlay displayed a larger amount of AFLP variation within germplasms, the variation was shown independently without reflecting a clinal variation. This study demonstrated that AFLP method can be used to examine the genetic relationships among different germplasms of adlay.

The effects of sonication and vacuum infiltration on transformation efficiency was investigated by using immature embryos of Korean wheat as explants. Two Agrobacterium tumefaciens strains, KYRT1 and EHA105, carrying pCAMBIA 1305.1 were used. Transformation efficiency was demonstrated by the detection of β-glucu-ronidase (GUS) activity. GUS expression showed clear difference among Korean wheat cultivars. Geurumil showed higher GUS expression efficiency 79.1~% compared with other cultivars. The effects of the duration of vacuum infiltration and sonication treatment showed a tendency high GUS expression efficiency by their combination. In comparison with other Agrobacterium strains, KYRT1 showed high efficiency in most Korean cultivars.

Immature and mature embryos of 18 Korean wheat genotypes were cultured in vitro to develop an efficient method of callus formation and plant regeneration, and to compare the responses of both embryo cultures. Immature and mature embryos were placed on a solid agar medium containing the MS salts and vitamins, 30g/l maltose, 2 mg/l 2,4-dichlorophenoxyacetic acid (2,4-D), and amino acids. The developed calli were maintained on regeneration medium containing MS salts and B5 vitamins, 20 g/l sucrose, and the combination of two plant growth regulators, 6-benzylaminopurine (BAP) and indole-3-acetic acid (IAA). Immature embryos in most genotypes showed high efficiency of callus induction except three genotypes; Eunpamil, Chunggemil, and Namhaemil, and significant differences among the genotypes. Plant regeneration of calli induced from immature embryos showed high efficiency in Geurumil (56.5%), Tapdongmil (50.5%), Gobunmil (45.5%), and Urimil(42.2%). The analysis of variance showed significant differences for regeneration frequency among the genotypes. Mature embryos showed low callus induction frequency compared with that in immature embryos, and significant differences among the genotypes. Plant regeneration of calli induced from mature embryos showed high efficiency in Keumkangmil (33.33%), Tapdongmil(28.13%), and Geurumil (27.78%). The analysis of variance showed significant differences for plant regeneration frequency among the genotypes.