• The Korean Journal of Ecology
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• 제14권3호
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• pp.231-241
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• 1991

The analyses of correlation, enviromental gradient, continuum and polar ordination methods were used for studing on relationships between forest vegetation and their habitats in Mt. changan, chagsu-gun, korea. influencing correlation of moisture index to the main 41species from the study area they were composed of several groups by leading species of quercus mongoulica, that of carpinus tschonoskii and that of fraxinus mandshurica. On the other hand, it was found three communities in different habitats by environmental gradient i.e. each community of f. mandshurica, mangnolia sieboldii and hydrangea serrata for. acuminata have occurred in moist place, that of c. teschonoskii and q. serrata, in mesic and that of q. mongolica, q.variabilis, rhododendron schlippenbachii, in dry. in addition an occupied distribution area was investigated according to continuum index e.g. cornus controversa,betula costata,q. variabilis, q. serrata and q. mongolica over altitudinal 800m were distributed to a habitat were forming climax by q. mongolica, and/or c. controversa, f. mandshurica, q. serrata and c. tschonoskii under altitudinal 800m were done, by g. tschonoskii. while the forest vegetation of the area was classified into 6 communities such as q. mongolica community, q. variabilis community,q. serrata community, g. tschonoskii community,c. controversa community and f. mandshurica community by means of polar ordination analysis and these have come under the influence of environmental factors.

• 조명전기설비학회논문지
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• 제14권1호
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• pp.67-74
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• 2000

본 논문에서는 GIS내 파티클에 의해 발생할 수 있는 절연사고를 미연에 방지하고 또한 파티클의 상태를 파 악하기 위하여 GIS 41 파티클 상태에 따른 부분방전 신호를 측정하고 분석하였다. 본 논문에서는 GIS내 파티콜 의 상태를 4가지(전극부착시, 외함부착시, 스페이서 부착시, 자유운동시)로 모의하였으며, 이때 발생하는 부분방전 신호의 $\Phi$-Q-N 분포를 형태적으로 분석하였다 또한, $\Phi$-Q 분포에 대하여 통계적 연산자를 도입하여 파티 클 상태에 따른 부분방전 신호를 정량적으로 분석하였다. 그 결과 파티클 상태에 따른 $\Phi$-Q-N 분포의 형태적인 분석과 $\Phi$-Q 분포의 정량적인 분석으로 파티콜의 상태 구별이 가능하였다.

• Clinical and Experimental Pediatrics
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• 제59권2호
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• pp.91-95
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• 2016

We report the case of a 22-month-old boy with a new mosaic partial unbalanced translocation of 1q and 18q. The patient was referred to our Pediatric Department for developmental delay. He showed mild facial dysmorphism, physical growth retardation, a hearing disability, and had a history of patent ductus arteriosus. White matter abnormality on brain magnetic resonance images was also noted. His initial routine chromosomal analysis revealed a normal 46,XY karyotype. In a microarray-based comparative genomic hybridization (aCGH) analysis, subtle copy number changes in 1q32.1-q44 (copy gain) and 18q21.33-18q23 (copy loss) suggested an unbalanced translocation of t(1;18). Repeated chromosomal analysis revealed a low-level mosaic translocation karyotype of 46,XY,der(18)t(1;18) (q32.1;q21.3)[12]/46,XY[152]. Because his parents had normal karyotypes, his translocation was considered to be de novo. The abnormalities observed in aCGH were confirmed by metaphase fluorescent in situ hybridization. We report this patient as a new karyotype presenting developmental delay, facial dysmorphism, cerebral dysmyelination, and other abnormalities.

• 대한두경부종양학회지
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• 제24권1호
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• pp.33-42
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• 2008

Head and neck squamous cell carcinoma(HNSCC) is notorious for its poor outcome and increasing incidence. But, the studies of cytogenetic analysis in HNSCC are relatively rare, because of difficulties in culturing solid tumor cells and complexity in chromosomal DNA abberations associated with the lesions. The purpose of this study is to evaluate the location of chromosomal aberrations in Korean HNSCC cell lines (SNU-1041, 1066, and 1076) with comparative genomic hybridization(CGH) and array based CGH(array-CGH). Chromosomal gains of 3q23-q27, 5p13-p15.3, 7p21-pter, 8q11.2-q12, 8q21.1-qter, 9q22-q34, 16q22-q24, and 20q11.2-qter, as well as chromosomal losses on 3p10-p14 were found in all 3 SNU cell lines. Losses on 3p15- p23, 4q22-q27, 4q31.3-qter, 6q14-q15, 7q31-q34, 8p12-pter, 18q21-q23, and 21q11.2-q12 were observed in 2 of 3 cell lines. In array-CGH, many genes were altered including gains of PIK3CA, MYC, EVI1, MAD1L1 genes and losses of SERPIN genes. These aberrations of gene and chromosome coincide with other results of study, generally. These data about the patterns of chromosomal aberrations could be a basic step for understanding more detailed genetic events in the carcinogenesis and also provide information for diagosis and treatment in HNSCC.

• 식물분류학회지
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• 제35권1호
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• pp.57-80
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• 2005

본 연구에서는 한국산 참나무속 참나무아속(Quercus subgen. Quercus) 6종 및 종간 잡종으로 추정되는 개체들을 대상으로 잎, 동아, 소지, 견과, 각두 및 포린의 형태 및 크기에 관한 40개의 형질들을 측정, 수리분류학적 분석(주성분분석)을 수행하여 주요 형태 형질의 변이 양상을 파악하고, 한국산 참나무아속 분류군들의 실체를 이해하고자 하였다. 그 결과, 본 아속 한국산 개체들은 크게, 1) Q. acutissima-Q. variabilis, 2) Q. dentata, 3) Q. aliena, 4) Q. mongolica, 그리고 5) Q. serrata 개체들로 구성된 5개의 집단으로 구분되었고, 종간 잡종으로 추정되는 개체들은 대부분 추정 부모종의 중간적 특징을 갖는 것으로 밝혀졌다. 주성분분석에서 하나의 집단을 형성하면서 약하게 구분되는 Q. acutissima와 Q. variabilis는 잎 하면 털의 종류 및 분포 양상에 의해 뚜렷이 식별되는 것으로 나타났다. 또한, 외부형태 형질의 경우, 잎의 형태, 엽신의 길이와 폭, 거치의 크기와 형태, 소지의 직경, 견과의 길이와 폭의 비, 포린의 길이와 폭 등이 참나무아속 한국산 분류군들을 구분하고 잡종 형성을 이해하는데 매우 유용한 것으로 밝혀졌다.

• 한국엔터테인먼트산업학회논문지
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• 제15권8호
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• pp.411-421
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• 2021

논문의 목적은 Q방법론을 사용하여 COVID-19 시대의 의료 언택트 서비스 캠페인 인식을 확인하고 그 의미를 논의하는 것이었다. 이 연구에서는 위와 같은 연구주제와 목적을 위하여 주관성 연구분석을 사용하였다. 또한 이 분석은 연구문제로서, 1) 언택트 의료서비스 캠페인 인식의 유형들은 어떠하며, 2) 논의된 유형들 간의 유사한(일치하는) 특성과 함의점(시사점)들은 무엇인지에 관하여 점검(진단)하였다. Q진술문들은 사전 조사에 참여한 대학생들(설문조사 응답자)과의 인터뷰를 통한 Q모집단으로 최종 구성되었다. 그리고 사용처리된 Q-과정체제는 PC QUANL 프로그램의 Q요인분석을 통하여 분석되었다. 본 논의에서 사용된 Q방법론은 COVID-19 시대의 의료 언택트 서비스 캠페인 인식에 관한 주관적인 성향을 알아보기 위하여 사용되었다. 연구분석의 결과, 총 4개의 유형이 확인되었으며, 1유형(N=7)은 '신뢰 및 공지 유형', 2유형(N=4)은 '정부적 차원의 공지 유형', 3유형(N=3)은 '의학적 정보의 공지 유형', 4유형(N=2)은 '공감적 정보 유형' 등으로 분류되었다. 이와 같은 통찰력있는 논의분석은 COVID-19 시대의 의료 언택트 서비스와 관련된 응답자들의 주관성 유형요인들을 확인하고 진단하는 데 도움을 주었다.

• Geomechanics and Engineering
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• 제29권5호
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• pp.487-496
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• 2022

Most of the pile's vertical static load tests in construction sites are the proof load tests, which is difficult to accurately estimate the ultimate bearing capacity and analyze the reliability of piles. Therefore, a reliability analysis method based on the proof load-settlement (Q-s) data is proposed in this study. In this proposed method, a simple ultimate limit state function based on the hyperbolic model is established, where the random variables of reliability analysis include the model factor of the ultimate bearing capacity and the fitting parameters of the hyperbolic model. The model factor M = R_uR / R_uP is calculated based on the available destructive Q-s data, where the real value of the ultimate bearing capacity (R_uR) is obtained by the complete destructive Q-s data; the predicted value of the ultimate bearing capacity (R_uP) is obtained by the proof Q-s data, a part of the available destructive Q-s data, that before the predetermined load determined by the pile test report. The results demonstrate that the proposed method can easy and effectively perform the reliability analysis based on the proof Q-s data.

• 한국전자통신학회논문지
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• 제8권2호
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• pp.329-337
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• 2013

본 논문에서는 자율 주행 자동차의 연구 방향을 결정하기 위한 기관별 개인별 논문 분석을 통한 계량정보 분석을 검토한다. 기관별 개인별 논문 수 분석, 수준 분석, 국제협력연구 네트워크 분석, 핵심 기관과 개인의 Q-L분포를 이용하여 자율 주행 자동차의 연구 동향을 확인한다.

• Clinical and Experimental Pediatrics
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• 제54권6호
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• pp.267-271
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• 2011

Distal duplication, or trisomy 15q, is an extremely rare chromosomal disorder characterized by prenatal and postnatal overgrowth, mental retardation, and craniofacial malformations. Additional abnormalities typically include an unusually short neck, malformations of the fingers and toes, scoliosis and skeletal malformations, genital abnormalities, particularly in affected males, and, in some cases, cardiac defects. The range and severity of symptoms and physical findings may vary from case to case, depending upon the length and location of the duplicated portion of chromosome 15q. Most reported cases of duplication of the long arm of chromosome 15 frequently have more than one segmental imbalance resulting from unbalanced translocations involving chromosome 15 and deletions in another chromosome, as well as other structural chromosomal abnormalities. We report a female newborn with a de novo duplication, 15q24- q26.3, showing intrauterine overgrowth, a narrow asymmetric face with down-slanting palpebral fissures, a large, prominent nose, and micrognathia, arachnodactyly, camptodactyly, congenital heart disease, hydronephrosis, and hydroureter. Chromosomal analysis showed a 46,XX,inv(9)(p12q13),dup(15)(q24q26.3). Array comparative genomic hybridization analysis revealed a gain of 42 clones on 15q24-q26.3. This case represents the only reported patient with a de novo 15q24-q26.3 duplication that did not result from an unbalanced translocation and did not have a concomitant monosomic component in Korea.

• Nonlinear Functional Analysis and Applications
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• 제26권2호
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• pp.331-345
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• 2021

Let p(z)be a polynomial of degree n. Then Bernstein's inequality [12,18] is $${\max\limits_{{\mid}z{\mid}=1}}\;{\mid}p^{\prime}(z){\mid}\;{\leq}\;n\;{\max_{{\mid}z{\mid}=1}{\mid}(z){\mid}}$$. For q > 0, we denote $${\parallel}p{\parallel}_q=\{{\frac{1}{2{\pi}}}{\normalsize\displaystyle\smashmargin{2}{\int\nolimits_{0}}^{2{\pi}}}\;{\mid}p(e^{i{\theta}}){\mid}^qd{\theta}\}^{\frac{1}{q}}$$, and a well-known fact from analysis [17] gives $${{\lim_{q{\rightarrow}{{\infty}}}}\{{\frac{1}{2{\pi}}}{\normalsize\displaystyle\smashmargin{2}{\int\nolimits_{0}}^{2{\pi}}}\;{\mid}p(e^{i{\theta}}){\mid}^qd{\theta}\}^{\frac{1}{q}}={\max\limits_{{\mid}z{\mid}=1}}\;{\mid}p(z){\mid}$$. Above Bernstein's inequality was extended by Zygmund [19] into L^q norm by proving ║p'║_q ≤ n║p║_q, q ≥ 1. Let p(z) = a₀ + ∑ⁿ_𝜈=𝜇 a_𝜈z^𝜈, 1 ≤ 𝜇 ≤ n, be a polynomial of degree n having no zero in |z| < k, k ≥ 1. Then for 0 < r ≤ R ≤ k, Aziz and Zargar [4] proved $${\max\limits_{{\mid}z{\mid}=R}}\;{\mid}p^{\prime}(z){\mid}\;{\leq}\;{\frac{nR^{{\mu}-1}(R^{\mu}+k^{\mu})^{{\frac{n}{\mu}}-1}}{(r^{\mu}+k^{\mu})^{\frac{n}{\mu}}}\;{\max\limits_{{\mid}z{\mid}=r}}\;{\mid}p(z){\mid}}$$. In this paper, we obtain the L^q version of the above inequality for q > 0. Further, we extend a result of Aziz and Shah [3] into L^q analogue for q > 0. Our results not only extend some known polynomial inequalities, but also reduce to some interesting results as particular cases.