• 한국언론정보학보
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• 제34권
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• pp.132-160
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• 2006

본 논문은 1990년 2월부터 2005년 7월까지 호주제와 관련된 $\ulcorner$국민일보$\lrcorner$, $\ulcorner$조선일보$\lrcorner$, $\ulcorner$한겨레$\lrcorner$의 신문기사를 대상으로 기사 수, 기사유형별, 등장인물별, 프레이밍 방식, 보도기사 형식별 프레임을 기준으로 살펴보았다. 본 연구에서는 호주제와 관련된 논의를 5시기로 구분하여 각 시기별 두드러지는 프레임과 소외된 프레임에 대해 분석했다. 분석결과에 따르면 호주제 논의와 관련된 프레임은 총 3가지 차원의 6가지 속성으로 구분될 수 있었다. 시기별로 볼 때 호주제에 관한 논의는 호주제 자체에 대한 속성적 차원에서 정치적 법적논의에 대한 차원으로, 그리고 사회적 논의와 관련된 차원으로 이행함을 발견할 수 있었다. 전반적으로 호주제 관련 기사는 '사회변화 혹은 시대정신 반영' 프레임이 우세하나, 속성적 차원에서는 '남성중심 사회의 반영' 프레임이, 대선 및 총선에 가까운 시기에 가서는 '정치적 성향파악의 잣대' 및 '가족법 개정 및 절차' 프레임이 우세했다. 각 신문사별 특성은 조선일보의 경우 호주제를 남성중심 사회의 전통적으로 내려오는 관습으로 바라보면서 기존 전통유지를 강조하는 프레임을 보여주었다. 반면, 한겨레는 호주제를 여성 권익의 향상과 관련짓고 양성평등의 확대를 주장하고 있었다. 국민일보는 호주제 폐지는 여성의 존엄성을 인정하는 시작이며 이 같은 시대적 윤리의 변화를 수용하는 법개정이 중요하다고 보았다.

• Toxicological Research
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• 제21권2호
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• pp.135-140
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• 2005

Although the pathogenesis of cerebral cavernous malformation (CCM) is unknown, a familial predisposition has been recognized, with up to $55\%$ of patients having an affected relatives. Genetic linkage studies have recently mapped a gene causing CCM to a segment of the long arm of chromosome 7 (7q). We report herein a genetic linkage analysis conducted on a Korean three generation family with CCM. It's first report in Korean family. A Korean family in which one member had undergone surgery for ubtracerebrak hematoma (ICH) and confirmed the CCM, was evaluated. They were examined clinically (n=18) and by magnetic resonance (MR) imaging (n=10). Polymorphic markers (D7S1813, D7S1789) spanning the CCM1 locus on 7q were genotyped by the polymerase chain reaction and analysis of linkage was performed in this family (n=17). Six had multiple lesions on brain MR image, one of them being symptomatic, and five were asymptomatic. Seven remaining members were asymptomatic and refused MR image study. One had died of ICH from presumed CCM. Analysis of the pedigree was consistent with an autosomal dominant pattern of inheritance. All affected patients were linked to CCM1. Linkage to CCM1 can account for inheritance of CCM in this family. They had some striking features with a low clinical penetrance and the presence of multiple lesions. These findings have implications for genetic testing of this disorder and represent an important step toward identification of the gene responsible for the pathogenesis of this disease.

• Clinical and Experimental Pediatrics
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• 제49권10호
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• pp.1111-1115
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• 2006

유전성 췌장염은 비교적 젊은 연령에서 다른 이유 없이 반복적으로 급성 췌장염으로 나타나는데 나이가 들면서 만성 췌장염으로 이행된다. 동일 가계 내에 2세대 이상에 걸쳐서 3명 이상의 췌장염 환자가 있을 때 진단이 가능하며 이와 관련된 유전자로 trypsinogen을 만드는 PRSS1 유전자 변이(R122H, N29I)가 가장 대표적으로 알려져 있다. 저자들은 3세부터 반복적인 췌장염으로 입원 치료를 했던 15세 환아와 반복적 췌장염을 앓은 환아모, 환아 동생을 대상으로 CT 유전자의 exon 2, 3의 염기 서열을 분석하여 환아와 환아모에서 국내 처음으로 N29I 변이를 경험하였기에 보고하는 바이다.

• 한국사회복지학
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• 제64권2호
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• pp.31-54
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• 2012

본 연구는 생활시간조사자료를 활용하여 가구 내에서 배분되는 일-가족시간에 대한 실증분석을 수행하였다. 부부의 유급노동시간과 가족시간에서 차지하는 남성의 비중을 근거로 일-가족 시간 배분을 4개의 모형(전통적 남성생계부양, 이중노동부담, 협조적 적응, 가족친화적 남성생계부양)으로 유형화하였으며, 퍼지셋이상형분석을 통해 각 유형에 소속되어 있는 정도를 점수화한 후, 각 모형의 소속점수에 대한 중다회귀분석을 수행하였다. 연구결과, 지난 10년간 이중노동부담의 비중이 감소하고 협조적 적응 유형이 증가한 것으로 나타나고 있으나, 여전히 전체적인 모형별 분포를 보면 전통적인 성분업에 고착된 구조를 보여주고 있었다. 4개의 시간배분 모형에 대한 회귀분석 결과 역시 각 모형별 분석의 유용성을 보여주었으며, 무엇보다 성분업 의식의 역할은 제한적인 것으로 나타났다. 이를 바탕으로 향후 가족정책의 논의에 있어 가구내의 미시적 성분업 구조와 일-가족시간의 배분과 관련된 역동성을 좀 더 면밀히 파악할 필요가 있다는 점과, 방법론적 함의로 미시자료를 이용한 양적연구에서도 퍼지셋 활용이 방법론적 다양성을 제공해 줄 수 있다는 점을 논의하였다.

• 가정과삶의질연구
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• 제24권1호
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• pp.1-9
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• 2006

The purpose of this research is to identify stereotypes toward the mother-in-law held by female students. Stereotypes toward the mother-in-law were examined at two levels: to assess female students' beliefs about the traits of mother-in-law and to categorize the traits into stereotypes. The main results of this study were as follows: 1) Students reported 91 traits associated with the mother-in-law. 2) Hierarchical cluster analysis of the trait groupings revealed two high-level clusters: a cluster of 42 positive traits and a cluster of 49 negative traits. Within the positive and negative clusters, 14 middle-level categories, 6 positive categories(tough, leisurely, traditional image of prudent elders, image of the eldest in the family, intimate, tolerant), and 8 negative categories(dominant, self-assertive, cold, discriminating, fearful, mean, sadistic, authoritative, nervous) were identified. This results suggested that female students believed negative stereotypes are more typical than positive ones.

• Annals of Clinical Neurophysiology
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• 제7권2호
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• pp.138-140
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• 2005

Strumpell, in 1880, was the first to describe familial case of spastic paraplegia characterized by progressive weakness and spasticity of the lower limbs with little or no involvement of the upper extremities. This syndrome is heterogeneous in inheritance, age of onset, severity and associated signs. We present one family with autosomal dominant hereditary spastic paraplegia (HSP) due to SPG4 (spastin) gene mutation which is confirmed by genomic DNA isolated from peripheral blood.

• Clinical and Experimental Pediatrics
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• 제53권12호
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• pp.1018-1021
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• 2010

Townes-Brocks syndrome (TBS) is a rare autosomal dominant congenital disorder caused by mutations in the $SALL1$ gene. Its signs and symptoms overlap with other genetic syndromes, including VACTERL association, Pendred syndrome, Baller-Gerold syndrome, and cat eye syndrome. Structural vertebral abnormalities, hypoplasia of the thumb, and radial bone abnormalities, which are not usually associated with TBS, help in the differential diagnosis of these syndromes. We report the case of a family whose members were diagnosed with TBS with congenital hypothyroidism and had a novel $SALL1$ gene mutation.

• Journal of Genetic Medicine
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• 제13권1호
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• pp.55-58
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• 2016

Pseudomyxoma peritonei (PMP) is a rare tumor that usually originates in the appendix, but a small number of cases originate in the ovary. Lynch syndrome (LS) is an autosomal dominant hereditary condition that increases the risk of cancer, particularly in the colon and endometrium. Mutations in the mismatch repair genes (MSH2, MLH1, MSH6, and PMS2) increase the risk of LS. Reported PMP cases with hereditary gene mutations of unknown significance are also rare. Here, we investigated a PMP patient and her family members, who have an MSH2 variant of unknown significance. Physicians have an important role in counseling, management, and surveillance based on genetics and pathogenicity.

• 가정과삶의질연구
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• 제14권2호
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• pp.51-60
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• 1996

The purpose of this study is to identify the objective picture of developmental pattern of marital satisfaction of couples based on family life cycle length of marriage marriage cohort birth cohort and age of couples using data from 317 couples in urban cities. The result indicate that the U-curve of marital satisfaction is the special pattern of family life cycle while W-curve is more dominant pattern when data are analysed with length of marriage birth cohort and marriage cohort. The couples differ in their assessment of marital satisfaction through entire their life span which seems for wives to become more dissatisfied over time. The similarity of developmental pattern the spouses appears only in their birth cohort. Discussion and recommendations for future research of the marital satisfaction are suggested.

• East Asian mathematical journal
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• 제27권3호
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• pp.299-308
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• 2011

The purpose of the present paper is to obtain some subordination and superordination preserving properties involving a certain family of multiplier transformations for meromorphic functions in the open unit disk. The sandwich-type theorems for these linear operators are also considered.