• Korean Journal of Microbiology
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• v.40 no.2
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• pp.73-80
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• 2004

Coenzyme Q is a quinone derivative that acts as a lipid electron carrier in the respiratory chain located at mito-chondrial inner membrane in eucaryotes or plasma membrane in procaryotes and also functions as antioxidant. A putative Neurospora crassa coq-4 gene was cloned and functionally expressed in Saccharomyces cerevisiae coq4 mutant. Complemented S. cerevisaie mutant strain was able to produce coenzyme $Q_{6}$ and showed a normal growth rate. They also showed less sensitivities to polyunsaturated fatty acids such as linoleic acid or linolenic acid. The predicted sequence of N. crassa COQ4 is consisted of 347 amino acids with a molecular mass of 39.7 kDa and showed 35% identity and 52% similarity with that of S. cerevisiae.

• Bulletin of the Korean Mathematical Society
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• v.60 no.3
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• pp.775-783
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• 2023

Van Hamme's (G.2) supercongruence modulo p⁴ for primes p ≡ 3 (mod 4) and p > 3 was first established by Swisher. A q-analogue of this supercognruence was implicitly given by the first author and Schlosser. In this paper, we present a new q-analogue of Van Hamme's (G.2) supercongruence for p ≡ 3 (mod 4).

• Honam Mathematical Journal
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• v.40 no.4
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• pp.621-659
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• 2018

Let us consider that ${\mathbb{K}}$ be a complete ultrametric algebraically closed field and A (${\mathbb{K}}$) be the ${\mathbb{K}}$-algebra of entire functions on ${\mathbb{K}}$. In this paper we introduce the notions of (p, q)-th relative order and (p, q)-th relative type of entire functions on ${\mathbb{K}}$ where p and q are any two positive integers and then study some basic properties of p-adic entire functions on the basis of their (p, q)-th relative order and (p, q)-th relative type.

• The Pure and Applied Mathematics
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• v.26 no.4
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• pp.315-353
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• 2019

Orders and types of entire and meromorphic functions have been actively investigated by many authors. In the present paper, we aim at investigating some basic properties in connection with sum and product of relative (p, q)-𝜑 order, relative (p, q)-𝜑 type, and relative (p, q)-𝜑 weak type of meromorphic functions with respect to entire functions where p, q are any two positive integers and 𝜑 : [0, +∞) → (0, +∞) is a non-decreasing unbounded function.

• Journal of the Institute of Electronics and Information Engineers
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• v.53 no.11
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• pp.66-70
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• 2016

This paper presents an 24 GHz I/Q LO generator for a heartbeat measurement radar system. In order to improve the mismatch performance between I and Q LO signals against process variation, a 24 GHz I/Q LO generator employing a low-pass phase shifter and a high-pass phase shifter composed of inductors and capacitors is proposed. The proposed 24 GHz I/Q LO generator consists of an LO buffer, a low-pass phase shifter and a high-pass phase shifter. It was designed using a 65 nm CMOS technology and draws 8 mA from a 1 V supply voltage. The proposed 24 GHz I/Q LO generator shows a gain of 7.5 dB, a noise figure of 2.3 dB, 0.1 dB gain mismatch and $4.3^{\circ}$ phase mismatch between I and Q-path against process and temperature variations for the operating frequencies from 24.05 GHz to 24.25 GHz.

• The Journal of Engineering Geology
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• v.28 no.1
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• pp.11-24
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• 2018

The purpose of slope stability analysis is to predict the location and occurrence time considering the rainfall, topographic and soil characteristics, etc. In this study, infinite slope stability analysis considering the time distribution characteristics of the daily maximum rainfall was conducted using a model that combines a digital terrain model and a groundwater flow model. As the results of slope stability analysis, 69.1~70.0% of Fs < 1 cells are in the range of slope angle $20{\sim}50^{\circ}$ and Fs < 1 starts to appear in 2 hours for $Q_1$ model, 5 hours for $Q_2$, 7 hours for $Q_3$ and 6 hours for $Q_4$. Furthermore, the maximum number of Fs < 1 cells appear in 6 hours for $Q_1$ model, 12 hours for $Q_2$, 16 hours for $Q_3$ and 20 hours for $Q_4$, and the area of Fs < 1 is 14.3% for $Q_1$ model, 15.0% for $Q_2$, 15.6% for $Q_3$, and 16.3% for $Q_4$.

• Clinical and Experimental Pediatrics
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• v.45 no.2
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• pp.273-277
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• 2002

Syndrome of 4q deletion is characterized by an abnormal shape of the skull, craniofacial dysmorphism, cardiovascular malformations, genitourinary defects, limb and digital anomalies, and developmental delay. We experienced a case of 4q interstitial deletion in a 2 day-old female neonate who showed short extremities, partial agenesis of corpus callosum and congenital heart defects. We report the case with a brief review of the literature.

• Journal of applied mathematics & informatics
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• v.31 no.3_4
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• pp.523-531
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• 2013

In this paper we construct a new type of $q$-Bernstein polynomials related to $q$-Euler numbers and polynomials with weak weight ${\alpha}$ ; $E^{(\alpha)}_{n,q}$, $E^{(\alpha)}_{n,q}(x)$ respectively. Some interesting results and relationships are obtained.

• Honam Mathematical Journal
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• v.39 no.4
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• pp.527-559
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• 2017

The main motivation of this article is to generalized the concept of fuzzy ideals, (${\alpha},{\beta}$)-fuzzy ideals, (${\in},{\in}{\vee}q_k$)-fuzzy ideals of semigroups. By using the concept of $q^{\delta}_K$-quasi-coincident of a fuzzy point with a fuzzy set, we introduce the notions of (${\in},{\in}{\vee}q^{\delta}_k$)-fuzzy left ideal, (${\in},{\in}{\vee}q^{\delta}_k$)-fuzzy right ideal of a semigroup. Special sets, so called $Q^{\delta}_k$-set and $[{\lambda}^{\delta}_k]_t$-set, condition for the $Q^{\delta}_k$-set and $[{\lambda}^{\delta}_k]_t$-set-set to be left (resp. right) ideals are considered. We finally characterize different classes of semigroups (regular, left weakly regular, right weakly regular) in term of (${\in},{\in}{\vee}q^{\delta}_k$)-fuzzy left ideal, (${\in},{\in}{\vee}q^{\delta}_k$)-fuzzy right ideal and (${\in},{\in}{\vee}q^{\delta}_k$)-fuzzy ideal of semigroup S.

• Journal of Nutrition and Health
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• v.24 no.4
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• pp.299-307
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• 1991

The present study was designed to evaluate the effects of dietary coenzyme $Q_{10}$ on mitochondrial coenzyme $Q_{10}$ and fatty acid composition in adriamycin (ADR)-treated rats. Two experiments were conducted in rats. Experiment 1 was undertaken under the condition of simultaneous administration of ADR and coenzyme $Q_{10}$ for 4 weeks. Experiment 2 was undertaken under the same condition as experiment 1 after feeding the experimental diets alone without administration of ADR for 4 weeks. Heart mitochondrial coenzyme $Q_{10}$ level of rats was greatly decreased by ADR treatment. but higher level of dietary coenzyme $Q_{10}$ elevated this decrease to control ranges. Pretreatment with dietary supplementation of coenzyme $Q_{10}$ showed a significant increase in myocardial coenzyme $Q_{10}$ level. With ADR treatment. polyunsaturated fatty acids such as arachidonic acid (20 : 4) and docosahexaenoic acid (22 : 6) were decreased. However, dietary supplementation of coenzyme $Q_{10}$ modified this decrement to some extent. In both experiment 1 and 2. the polyunsaturated fatty acids/saturated and polyunsaturated fatty acids (P/S+ M) ratio of ADR-treated rats tended to be lower than that of control rats.