• Kyungpook Mathematical Journal
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• 제56권3호
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• pp.939-949
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• 2016

In this paper, we give an algorithm to construct a space curve in Euclidean 3-space ${\mathbb{E}}^3$ from a plane curve which is called PDP-helix of order d. The notion of the PDP-helices is a generalization of a general helix and a slant helix in ${\mathbb{E}}^3$. It is naturally shown that the PDP-helix of order 1 and order 2 are the same as the general helix and the slant helix, respectively. We give a characterization of the PDP-helix of order d. Moreover, we study some geometric properties of that of order 3.

• 호남수학학술지
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• 제34권3호
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• pp.381-390
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• 2012

In this paper, we give some characterizations for a quaternionic general helix by means of curvatures of a curve in a 4-dimensional Euclidean space.

• 대한수학회보
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• 제50권3호
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• pp.885-899
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• 2013

In this paper, we study null helices, null slant helices and Cartan slant helices in $\mathb{E}^3_1$. Using some associated curves, we characterize the null helices and the Cartan slant helices and construct them. Also, we study a space-like curve with the principal normal vector field which is a degenerate plane curve.

• Bulletin of the Korean Chemical Society
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• 제17권2호
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• pp.131-138
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• 1996

The conformational transition of oligopeptide multimer,-(HPPHPPP)n-, is studied (H:hydrophobic amino acid, P:hydrophilic amino acid). The helix/coil transitions are detected in the multimer. The transition depends on the number of amino acid in the sequence, the concentration of the oligopeptide, and temperature which affects helix stability constant (${\xi}$) and hydrophobic interaction parameter (wj). In the thermodynamic equilibrium system jA${\rightarrow}$Aj (where A stands for oligopeptide monomer), Skolnick et al., explained helix/coil transition of dimer by the matrix method using Zimm-Bragg parameters ${\xi}$ and $\sigma$ (helix initiation constant). But the matrix method do not fully explain dangling H-bond effects which are important in oligopeptide systems. In this study we propose a general theory of conformational transitions of oligopeptides in which dimer, trimer, or higher multimer coexists. The partition of trimer is derived by using zipper model which account for dangling H-bond effects. The transitions of multimers which have cross-linked S-S bonds or long chains do not occur, because they keep always helical structures. The transitions due to the concentration of the oligopeptides are steeper than those due to the chain length or temperature.

• World Technopolis Review
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• 제6권2호
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• pp.90-101
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• 2017

This paper defines the role of the Science Park and makes policy recommendations for the "Era of $4^{th}$ Industrial Revolution" from a Triple Helix viewpoint. The role of traditional science parks, and theory of Triple Helix and the $4^{th}$ Industrial Revolution are reviewed, and strategies to cope with the $4^{th}$ Industrial Revolution in a few advanced countries are analyzed. This paper finishes by suggesting strategies such as acceleration of networking, education to foster creative and innovative manpower and initiating capacity building projects for the advancement of Science Parks in the $4^{th}$ Industrial Revolution.

• 대한수학회논문집
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• 제35권4호
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• pp.1269-1281
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• 2020

In this article, we show that a pseudo-Hermitian magnetic curve in a normal almost contact metric 3-manifold equipped with the canonical affine connection ${\hat{\nabla}}^t$ is a slant helix with pseudo-Hermitian curvature ${\hat{\kappa}}={\mid}q{\mid}\;sin\;{\theta}$ and pseudo-Hermitian torsion ${\hat{\tau}}=q\;cos\;{\theta}$. Moreover, we prove that every pseudo-Hermitian magnetic curve in normal almost contact metric 3-manifolds except quasi-Sasakian 3-manifolds is a slant helix as a Riemannian geometric sense. On the other hand we will show that a pseudo-Hermitian magnetic curve γ in a quasi-Sasakian 3-manifold M is a slant curve with curvature κ = |(t - α) cos θ + q| sin θ and torsion τ = α + {(t - α) cos θ + q} cos θ. These curves are not helices, in general. Note that if the ambient space M is an α-Sasakian 3-manifold, then γ is a slant helix.

• 한국자기공명학회논문지
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• 제25권2호
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• pp.17-23
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• 2021

High mobility group protein B1 (HMGB1) is a highly conserved, non-histone, chromatin associated nuclear protein encoded by HMGB1 gene. HMGB1 proteins may be general co-factors in Hox-mediated transcriptional activation that facilitate the access of Hox proteins to specific DNA targets. It is unclear that the exact binding interface of Hoxc9DBD and HMGB1. To identify the interface and binding affinity of Hoxc9DBD and HMGB1 A-box, the paramagnetic probe, MTSL was used in NMR titration experiment. It is attached to the N-terminal end of HMGB1 A-box by reaction with thiol groups. The backbone assignment of HMGB1 A-box was achieved with 3D NMR techinques. The ¹⁵N-labeled HMGB1 A-box was titrated with MTSL-labeled Hoxc9DBD respectively. Based on the chemical shift changes we can identify the interacting residues and further map out the binding sites on the protein structure. The NMR titration result showed that the binding interface of HMGB1 A-box is around loop-1 between helix-1 and helix-2. In addition, the additional contacts were found in N- and C-terminus. The N-terminal arm region of Hoxc9DBD is the major binding region and the loop between helix1 and helix2 is the minor binding region.

• 설비공학논문집
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• 제19권7호
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• pp.500-511
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• 2007

The Optimal solutions of the design variables in internally finned tubes have been obtained for three-dimensional periodically fully developed turbulent flow and heat transfer. For a trapezoidal fin profile, performances of the heat exchanger are determined by considering the heat transfer rate and pressure drop, simultaneously, that are interdependent quantities. Therefore, Pareto frontier sets of a heat exchanger can be acquired by integrating CFD and a multi-objective optimization technique. The optimal values of fin widths $(d_1,\;d_2)$, fin height(h) and helix angle$(\gamma)$ are numerical1y obtained by minimizing the pressure loss and maximizing the heat transfer rate within ranges of $d_1=0.5\sim1.5mm$, $d_2=0.5\sim1.5mm$, $h=0.5\sim1.5mm$, and $\gamma=0\sim20^{\circ}$. For this, a general CFD code and a global genetic algorithm(GA) are used. The Pareto sets of the optimal solutions can be acquired after $30^{th}$ generation.

• Kyungpook Mathematical Journal
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• 제63권2호
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• pp.263-285
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• 2023

In this paper, we investigate the spherical indicatrices of a new relationship between Bertrand pair curves in Euclidean 3-space. We obtain necessary and sufficient conditions for this type of Bertrand pair curves to be slant helix, and provide an example.

• 정보보호학회논문지
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• 제15권1호
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• pp.29-40
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• 2005

본 논문에서는 최근 제안된 소프트웨어 구현에 적합한 (블록 단위) 스트림 암호는 HELIX, SCREAM, MUGI, PANAMA 알고리즘들의 대수적 공격에 대한 안전성을 분석한다. 대수적 공격은 알려진 입출력 쌍을 가지고 내부 알고리즘의 기본 대수 방정식을 이용하는 방법으로, 과포화된 다변수 연립 방정식을 통하여 변수의 값을 얻고 이를 이용하여 키를 복구해내는 방업이다. 이 분석법은 초기 대수적 특성을 지닌 블록 암호의 분석에 적용되었으나. 이후 블록 암호보다는 스트림 암호의 분석에 보다 용이하게 적용되었다. 그러나 일반적인 알고리즘을 이 분석법을 그대로 적용하기에는 많은 어려움이 존재한다. 따라서 본 논문에서는 최근 제안된 워드 단위의 소프트웨어 구현에 적합한 스트림 암호의 각 알고리즘에 대해 대수적 방정식과 변수의 수를 비교 및 분석함으로써 각 알고리즘의 대수적 공격에 대한 내성을 살펴본다. 또한 이러한 분석을 통해 대수적 공격에 안전한 소프트웨어 구현에 적합한 스트림 암호의 설계 시 고려해야 할 세 가지 설계 고려사항을 제시한다.