• 식물병연구
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• 제21권4호
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• pp.326-329
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• 2015

후자린산은 Fusarium이 생성하는 독소로서 다른 Fusarium 독소와 함께 독성을 증진시킬 수 있다. 후자린산 독소를 특이적으로 검출하기 위해 후자린산의 생합성유전자 중 전사인자인 FUB10을 증폭하는 프라이머를 제작하였다. Fub10-f와 Fub10-r 프라이머쌍으로 PCR을 수행했을 때, F. oxysporum, F. proliferatum, F. verticillioides, F. anthophilum, F. bulbicola, F. circinatum, F. fujikuroi, F. redolens, F. sacchari, F. subglutinans, F. thapsinum에서 약 550 bp의 단일밴드가 증폭되었으며 이들은 모두 후자린산을 생성하는 것으로 알려졌다. 반면 트라이코쎄신을 생성하는 종에서는 FUB10 특이 밴드가 증폭되지 않았다. 후자린산은 푸모니신을 생성하는 종에서 함께 생성될 수 있기 때문에 FUB10 프라이머와 푸모니신 생합성유전자인 FUM1 프라이머를 이용한 multiplex PCR을 수행하였다. 그 결과 푸모니신 생성종인 F. proliferatum과 F. verticillioides에서 밴드가 모두 증폭되었으며 이는 두 가지 독소를 생성할 수 있는 종에서 동시 검출이 가능함을 시사하였다.

• 대한물리치료과학회지
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• 제8권2호
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• pp.997-1003
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• 2001

The purpose of this study is to know the average of pint range of motion and difference according to the aging for the elderly, This study consisted of elder male(n=75) and elder female(n=l09), The result of assessment and analysis in shoulder pint range of motion are as follows: 1) The average shoulder flexion pint range of motion in 60-69(from sixty to sixty-nine)years old are 163.04(Left-Male), 162.91(Right-Male), 158.74 (Left-Female), 158.74 (Right-Female). 70-79years old are 149.40(L-M), 152.38(R-M), 153,37(L-F), 153.37(R-F). 80-89 years old are 149.57(L-M), 147.93(R-M), 151.17(L-F), 150.33(R-F). There was no significant difference among group, 2) The average shoulder extension pint range of motion in 60-69years old are 48.15(L-M), 47.20(R-M), 45.16(L-F), 44.23(R-F), 70-79years old are 37.l1(L-M), 38.70(R-M), 35.17(L-F), 36.71(R-F), 80-89 years old are 34.46(L-M). 36.71(R-M), 33.90(L-F), 33.09(R-F). There was significant difference among group(p<.05). 3) The average shoulder abduction pint range of motion in 60-69years old are 164.22(L-M), 165.96(R-M), 159.34(L-F), 159.97(R-F), 70-79years old are 152.27(L-M), 155.05(R-M), 152.32(L-F), 53.66(R-F), 80-89 years old are 152.17(L-M), 153.76(R-M), 147.53(L-F), 147.37(R-F). There was significant difference in right shoulder abduction among group(p<05). 4) The average shoulder internal rotation pint range of motion in 60-69years old are 63.52(L-M), 65.70(R-M), 64.16(L-F), 64.61(R-F), 70-79years old are 64.50(L-M), 65.81(R-M) 61.10(L-F), 61.83(R-F). 80-89 years old are 61.60(L-M), 61.66(R-M), 57.53(L-F), 57.53(R-F). There was no significant difference among group. 5) The average shoulder external rotation pint range of motion in 60-69years old are 50.87(L-M), 50.22(R-M), 51.03(L-F), 50.42(R-F), 70-79years old are 50.91(L-M), 50.20(R-M) 48.37(L-F), 50.20(R-F). 80-89 years old are 46.83(L-M), 47.93(R-M), 43.43(L-F), 43.72(R-F).There was significant difference in left shoulder external rotation among group(p<.05).

• Journal of applied mathematics & informatics
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• 제25권1_2호
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• pp.17-33
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• 2007

Suppose F is an arbitrary field. Let ${\mid}F{\mid}$ be the number of the elements of F. Let $T_{n}(F)$ be the space of all $n{\times}n$ upper-triangular matrices over F. A map ${\Psi}\;:\;T_{n}(F)\;{\rightarrow}\;T_{n}(F)$ is said to preserve idempotence if $A-{\lambda}B$ is idempotent if and only if ${\Psi}(A)-{\lambda}{\Psi}(B)$ is idempotent for any $A,\;B\;{\in}\;T_{n}(F)$ and ${\lambda}\;{\in}\;F$. It is shown that: when the characteristic of F is not 2, ${\mid}F{\mid}\;>\;3$ and $n\;{\geq}\;3,\;{\Psi}\;:\;T_{n}(F)\;{\rightarrow}\;T_{n}(F)$ is a map preserving idempotence if and only if there exists an invertible matrix $P\;{\in}\;T_{n}(F)$ such that either ${\Phi}(A)\;=\;PAP^{-1}$ for every $A\;{\in}\;T_{n}(F)\;or\;{\Psi}(A)=PJA^{t}JP^{-1}$ for every $P\;{\in}\;T_{n}(F)$, where $J\;=\;{\sum}^{n}_{i-1}\;E_{i,n+1-i}\;and\;E_{ij}$ is the matrix with 1 in the (i,j)th entry and 0 elsewhere.

• Journal of applied mathematics & informatics
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• 제27권1_2호
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• pp.97-103
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• 2009

Suppose F is a field of characteristic not 2 and $F\;{\neq}\;Z_3$. Let $M_n(F)$ be the linear space of all $n{\times}n$ matrices over F, and let ${\Gamma}_n(F)$ be the subset of $M_n(F)$ consisting of all $n{\times}n$ involutory matrices. We denote by ${\Phi}_n(F)$ the set of all maps from $M_n(F)$ to itself satisfying A - ${\lambda}B{\in}{\Gamma}_n(F)$ if and only if ${\phi}(A)$ - ${\lambda}{\phi}(B){\in}{\Gamma}_n(F)$ for every A, $B{\in}M_n(F)$ and ${\lambda}{\in}F$. It was showed that ${\phi}{\in}{\Phi}_n(F)$ if and only if there exist an invertible matrix $P{\in}M_n(F)$ and an involutory element ${\varepsilon}$ such that either ${\phi}(A)={\varepsilon}PAP^{-1}$ for every $A{\in}M_n(F)$ or ${\phi}(A)={\varepsilon}PA^{T}P^{-1}$ for every $A{\in}M_n(F)$. As an application, the maps preserving inverses of matrces also are characterized.

• 대한수학회보
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• 제22권2호
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• pp.83-85
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• 1985

Let K be a real function field over a real closed field F. Then there exists an F-place .phi.:K.rarw.F.cup.{.inf.}. This is Lang's Existence of Rational Place Theorem (6). There is an equivalent version of Lang's Theorem in (4). That is, if K is a function field over a field F, then, for any ordering P$_{0}$ on F which extends to K, there exists an F-place .phi.: K.rarw.F'.cup.{.inf.} where F' is a real closure of (F, P$_{0}$). In [2], Knebusch pointed out the converse of the version of Lang's Theorem is also true. By a valuation theoretic approach to Lang's Theorem, we have found out the following generalization of Lang and Knebusch's Theorem. Let K be an arbitrary extension field of a field F. then an ordering P$_{0}$ on F can be extended to an ordering P on K if there exists an F-place of K into some real closed field R containing F. Of course R$^{2}$.cap.F=P$_{0}$. The restriction K being a function field of F is vanished, though the codomain of the F-place is slightly varied. Therefore our theorem is a generalization of Lang and Knebusch's theorem.

• Kyungpook Mathematical Journal
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• 제50권4호
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• pp.537-543
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• 2010

Let X be a regular $T_1$-space such that each single point set is a $G_{\delta}$ set. Denot 'hereditarily closure-preserving' by 'HCP'. To consider a question of closed maps of S. Lin in [6], we improve some results of Foged in [1], and prove the following propositions. Proposition 1. $D\;=\;\{x{\in}X\;:\;\mid\{F{\in}\cal{F}:x{\in}F\}\mid{\geq}{\aleph}_0\}$ is discrete and closed if $\cal{F}$ is a collection of HCP. Proposition 2. $\cal{H}\;=\;\{{\cup}\cal{F}'\;:\;F'$ is an fininte subcolletion of $\cal{F}_n\}$ is HCP if $\cal{F}$ is a collection of HCP. Proposition 3. Let (X,$\tau$) have a $\sigma$-HCP k-network. Then (X,$\tau$) has a $\sigma$-HCP k-network F = ${\cup}_n\cal{F}_n$ such that such tat: (i) $\cal{F}_n\;\subset\;\cal{F}_{n+1}$, (ii) $D_n\;=\;\{x{\in}X\;:\;\mid\{F{\in}\cal{F}_n\;:\;x{\in}F\}\mid\;{\geq}\;{\aleph}_0\}$ is a discrete closed set and (iii) each $\cal{F}_n$ is closed to finite intersections.

• 한국응용곤충학회지
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• 제16권2호
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• pp.115-119
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• 1977

Fusarium spp가 1976년 포장에서 채집한 벼밀 보리에서 분리되었다. 병원성이 있는 것은 Fuarium(Calonectria) nivale, F.(Gibberella) moniliforme와 F.(Gibberella) roseum 'Graminearum'과 'Avenaceum'이었다. 부생균가운데 F.(Nectria) episphaeria가 분리되었다. F. nivale와 F. episphaeria의 완전시대인 Calonectria Nectria가 발견되었고 이것들은 한국에서 보고되지 않은 것으로 보인다. 분리된 Fusaria는 벼에서 $66.3\%$가 F. moniliforme 이고 보리, 밀에서$68.2\%$가 F. roseum 'Graminearum 이었다. 자낭각은 실험실 조건하에서 형성되었고 F. moniliforme는 밀이삭, 보리씨에 접종한 결과 병원성이 나타났다.

• 한국균학회지
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• 제18권3호
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• pp.132-136
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• 1990

Fusarium속의 10균주를 PDA 배지에서 배양하고 HCI-Giemsa 염색법을 이용하여 균사내에서의 영양핵의 핵분열을 관찰하였다. 관찰한 결과는 F. moniliforme 1750과 7219는 n=8개였다. F. subglutinans 1082는 n=8개, F subglutinans 1083은 n=7개로 균주에 따라 염색체수에 차이가 있었다. F. nygamai 5668과 F. nygamai 7132는 각각 n=7, n=5개로 달랐다. F. beomiforme 9758과 9760은 두 균주 모두 n=7개였고, F. coccidicola ATCC 24138과 F. acuminatum ATCC 16560은 n=6개였다. 본 실험의 재료에서는 n=5-8개의 염색체수를 나타내고 있으나 다른 여러 종들에 대한 보고 등을 고려할 때 본 속의 기본 염색체수는 n=4개로 추정하였다.

• The Plant Pathology Journal
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• 제35권4호
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• pp.301-312
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• 2019

Sorghum is the fifth most important cereal worldwide, spreading from Africa throughout the world. It is particularly important in the semi-arid tropics due to its drought tolerance, and when cultivated in Southeast Asia commonly occurs as a second crop during the dry season. We recovered Fusarium from sorghum in Thailand and found F. proliferatum, F. thapsinum and F. verticillioides most frequently, and intermittent isolates of F. sacchari and F. beomiforme. The relatively high frequencies of F. proliferatum and F. verticillioides, suggest mycotoxin contamination, particularly fumonisins and moniliformin, should be evaluated. Genetic variation within the three commonly recovered species was characterized with vegetative compatibility, mating type, Amplified Fragment Length Polymorphisms (AFLPs), and female fertility. Effective population number ($N_e$) was highest for F. verticillioides and lowest for F. thapsinum with values based on mating type allele frequencies higher than those based on female fertility. Based on AFLP genetic variation, the F. thapsinum populations were the most closely related, the F. verticillioides populations were the most distantly related, and the F. proliferatum populations were in an intermediate position. The genetic variation observed could result if F. thapsinum is introduced primarily with seed, while F. proliferatum and F. verticillioides could arrive with seed or be carried over from previous crops, e.g., rice or maize, which sorghum is following. Confirmation of species transmission patterns is needed to understand the agricultural systems in which sorghum is grown in Southeast Asia, which are quite different from the systems found in Africa, Australia, India and the Americas.

• 충청수학회지
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• 제20권4호
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• pp.387-399
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• 2007

In this paper, we prove the generalized Hyers-Ulam stability of the following linear functional equations f(x + iy) + f(x - iy) + f(y + ix) + f(y - ix) = 2f(x) + 2f(y) and f((1 + i)x) = (1 + i)f(x), and of the following quadratic functional equations f(x + iy) + f(x - iy) + f(y + ix) + f(y - ix) = 0 and f((1 + i)x) = 2if(x) in complex Banach spaces.