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이문희 梨花女子大學校 社會科學大學 社會科學硏究所 2011 사회과학연구논총 Vol.25 No.-
상담자의 심리치료는 개인적 그리고 전문적인 성장을 위해 훈련과정에서 중요하게 강조되고 있는 상담자를 위한 심리상담 활동이다. 본 연구에서는 이러한 논쟁들을 인식하면서 ‘상담자의 심리치료가 상담자의 전문성을 향상시키는데 기여하는가?’ 그리고 ‘어떤 과정을 통해 상담자의 전문성을 향상시키는가?’에 대한 이해를 높이고자 선행연구들을 검토하였다. 결과, 상담자의 심리치료를 통한 상담자의 전문성 발달 과정으로는 ‘상담자의 정신적 기능 개선’, ‘상담자 문제로 인한 치료 방해 감소’, ‘모델링을 통한 상담실제 개선’, ‘상담자로서의 정체성 촉진’으로 요약할 수 있다. 논의에서는 선행연구를 기반으로 하여 향후 후속 연구를 제안하였다. Counselor’s psychotherapy is psychological counseling for personal and professional growth which is underlined as important tool in the counselor’s training process. This study aim to review about precedent studies about counselor’s psychotherapy recognizing this issues. We will focus on following problems; ‘Does counselor’s psychotherapy contribute on counselor’s expertise improvement?’ and ‘How dose it process to produce expertise development?’. The findings in the precedent studies show that counselor’s psychotherapy process on their expertise development is followed as ‘improving the emotional and mental functioning of the psychotherapist’, ‘alleviating interruption of therapist’s problems’, ‘improvement of counseling practice through modeling’, ‘promoting counselor’s identity’
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A Large-Scale Validation for QF-PCR Aneuploidy Testing in Korean
이문희,김도진,양재형,조율희,박소연,류현미 한국유전학회 2008 Genes & Genomics Vol.30 No.1
The quantitative fluorescent PCR (QF-PCR) assay for prenatal diagnosis of common chromosome aneuploidies introduced during the last few years. We report the first assessment of QF-PCR aneuploidy testing performed on a large Korean population. Blind prospective study was performed in 3700 amniotic fluid samples. All samples were analyzed by QF-PCR using with four STR markers located on chromosome 21 (D21S1435/D21S11/D21S1411/ D21S1412) and subsequently performed by conventional cytogenetic analysis. Trisomy 21 was identified in 35 samples. The informative rate for at least two STR markers was 97.3%. The uninformative rate by maternal cell contamination (MCC) and inconclusive results were 0.8%, 1.9% respectively. Rare polymorphic STR duplication and somatic microsatellite mutation were detected respectively. There were no false-positive or false-negative results. QF-PCR for the rapid identification of fetus with trisomy 21 is a reliable, accurate, and speedy technique. The quantitative fluorescent PCR (QF-PCR) assay for prenatal diagnosis of common chromosome aneuploidies introduced during the last few years. We report the first assessment of QF-PCR aneuploidy testing performed on a large Korean population. Blind prospective study was performed in 3700 amniotic fluid samples. All samples were analyzed by QF-PCR using with four STR markers located on chromosome 21 (D21S1435/D21S11/D21S1411/ D21S1412) and subsequently performed by conventional cytogenetic analysis. Trisomy 21 was identified in 35 samples. The informative rate for at least two STR markers was 97.3%. The uninformative rate by maternal cell contamination (MCC) and inconclusive results were 0.8%, 1.9% respectively. Rare polymorphic STR duplication and somatic microsatellite mutation were detected respectively. There were no false-positive or false-negative results. QF-PCR for the rapid identification of fetus with trisomy 21 is a reliable, accurate, and speedy technique.
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이문희 수원대학교 산업기술연구소 2005 산업기술연구소논문집 Vol.20 No.-
Opto-electroncic IR smoke detector was assembled with domestically produced IR-LED and eletronic parts and its possiblility for mass production was examined. The smoke detector was assembled by standard methods. Conditions for best smoke detecting such as distances and angles between IR emitting part and accepting part were investigated.
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