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Relationship between Myosin Isoforms and Meat Quality Traits in Pig Semitendinosus Neuromuscular Compartments

  • Graziotti, Guillermo H.;Menendez, Jose M. Rodriguez;Rios, Clara M.;Cossu, Maria E.;Bosco, Alexis;Affricano, Nestor O.;Ceschel, Alejandra Paltenghi;Moisa, Sonia;Basso, Lorenzo
    • Asian-Australasian Journal of Animal Sciences
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    • 제24권1호
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    • pp.125-129
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    • 2011
  • The aim was to determine the relationship between muscle structure and meat quality traits in neuromuscular compartments (NMCs: R1, R2, R3, R4) of pig semitendinosus muscle. Barrows from the INTA-MGC genetic line (Argentina) were slaughtered at 100 kg body weight. In each NMC the following parameters were determined: the fibre types I, IIA, IIX and IIB by immunohistochemistry, the fibre cross sectional area (FCSA), the pH of meat after 24 h post-mortem ($pH_{24}$), instrumental meat tenderness (WB) and colour ($L^*$, $a^*$, $b^*$). There were significant differences in the following: $L^*$ (R1 = R4$a^*$ (R1>R4>R2 = R3), $b^*$ (R1 = R4R1 = R3 = R4), $pH_{24}$ (R1 = R4>R2 = R3). The relative percentages of FCSA were as follows: I (R4>R1>R3>R2), IIA (R1>R4>R3>R2), IIX (R1 = R2 = R3 = R4) and IIB (R2>R3>R1>R4). The correlation values were statistically significant between IIB and WB (R1 and R4, $r_s$ = 0.66), (R2 and R3 $r_s$ = 0.74), IIB and $L^*$ (R1 and R4 $r_s$ = 0.84), IIX and $L^*$ without discriminating NMCs. Our data suggest that the NMC where the sampling takes place is important for determining meat quality traits because of the heterogeneity of the whole muscle.

THE STRUCTURE OF SEMIPERFECT RINGS

  • Han, Jun-Cheol
    • 대한수학회지
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    • 제45권2호
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    • pp.425-433
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    • 2008
  • Let R be a ring with identity $1_R$ and let U(R) denote the group of all units of R. A ring R is called locally finite if every finite subset in it generates a finite semi group multiplicatively. In this paper, some results are obtained as follows: (1) for any semilocal (hence semiperfect) ring R, U(R) is a finite (resp. locally finite) group if and only if R is a finite (resp. locally finite) ring; U(R) is a locally finite group if and only if U$(M_n(R))$ is a locally finite group where $M_n(R)$ is the full matrix ring of $n{\times}n$ matrices over R for any positive integer n; in addition, if $2=1_R+1_R$ is a unit in R, then U(R) is an abelian group if and only if R is a commutative ring; (2) for any semiperfect ring R, if E(R), the set of all idempotents in R, is commuting, then $R/J\cong\oplus_{i=1}^mD_i$ where each $D_i$ is a division ring for some positive integer m and |E(R)|=$2^m$; in addition, if 2=$1_R+1_R$ is a unit in R, then every idempotent is central.

Grignard Coupling Reaction of Bis(chloromethyl)diorganosilanes with Dichloro(diorgano)silanes: Syntheses of 1,3-Disilacyclobutanes

  • 조연석;유복렬;안삼영;정일남
    • Bulletin of the Korean Chemical Society
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    • 제20권4호
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    • pp.427-430
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    • 1999
  • The Grignard coupling reaction of bis(chloromethyl)diorganosilanes [(ClCH2)2SiR1R2: R1 = R2 = Me, la; R1 = Me, R2 = Ph, lb; R1 = R2 = Ph, lc] with diorganodichlorosilanes [(Cl2SiR3R4: R3 = R4 = Me, 2a; R3 = Me, R4 = Ph, 2b; R3 = R4 = Ph, 2c] at THE reflux temperature gave the intermolecular C-Si coupling product of 1,1,3,3-tetraorgano-1,3-disilacyclobutanes 3a-f in poor to moderate yields ranging from 7% to 50% along with polydiorganosilapropanes. The cyclization reaction of la-c with methyl-substituted dichlorosilanes 2a, b gave 1,3-disilacyclobutanes 3a-c, e, d in moderate yields (42-50%), while the same reaction with dichlorodiphenylsilane (2c) to 1,3-disilacyclobutanes 3d, f resulted in low yield (7-18%) probably due to the steric hindrance of two-phenyl groups on the silicon of 2c.

A NOTE ON GENERALIZED DERIVATIONS AS A JORDAN HOMOMORPHISMS

  • Chandrasekhar, Arusha;Tiwari, Shailesh Kumar
    • 대한수학회보
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    • 제57권3호
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    • pp.709-737
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    • 2020
  • Let R be a prime ring of characteristic different from 2. Suppose that F, G, H and T are generalized derivations of R. Let U be the Utumi quotient ring of R and C be the center of U, called the extended centroid of R and let f(x1, …, xn) be a non central multilinear polynomial over C. If F(f(r1, …, rn))G(f(r1, …, rn)) - f(r1, …, rn)T(f(r1, …, rn)) = H(f(r1, …, rn)2) for all r1, …, rn ∈ R, then we describe all possible forms of F, G, H and T.

THE FINITE DIMENSIONAL PRIME RINGS

  • Koh, Kwangil
    • 대한수학회보
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    • 제20권1호
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    • pp.45-49
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    • 1983
  • If R is ring and M is a right (or left) R-module, then M is called a faithful R-module if, for some a in R, x.a=0 for all x.mem.M then a=0. In [4], R.E. Johnson defines that M is a prime module if every non-zero submodule of M is faithful. Let us define that M is of prime type provided that M is faithful if and only if every non-zero submodule is faithful. We call a right (left) ideal I of R is of prime type if R/I is of prime type as a R-module. This is equivalent to the condition that if xRy.subeq.I then either x.mem.I ro y.mem.I (see [5:3:1]). It is easy to see that in case R is a commutative ring then a right or left ideal of a prime type is just a prime ideal. We have defined in [5], that a chain of right ideals of prime type in a ring R is a finite strictly increasing sequence I$_{0}$.contnd.I$_{1}$.contnd....contnd.I$_{n}$; the length of the chain is n. By the right dimension of a ring R, which is denoted by dim, R, we mean the supremum of the length of all chains of right ideals of prime type in R. It is an integer .geq.0 or .inf.. The left dimension of R, which is denoted by dim$_{l}$ R is similarly defined. It was shown in [5], that dim$_{r}$R=0 if and only if dim$_{l}$ R=0 if and only if R modulo the prime radical is a strongly regular ring. By "a strongly regular ring", we mean that for every a in R there is x in R such that axa=a=a$^{2}$x. It was also shown that R is a simple ring if and only if every right ideal is of prime type if and only if every left ideal is of prime type. In case, R is a (right or left) primitive ring then dim$_{r}$R=n if and only if dim$_{l}$ R=n if and only if R.iden.D$_{n+1}$ , n+1 by n+1 matrix ring on a division ring D. in this paper, we establish the following results: (1) If R is prime ring and dim$_{r}$R=n then either R is a righe Ore domain such that every non-zero right ideal of a prime type contains a non-zero minimal prime ideal or the classical ring of ritght quotients is isomorphic to m*m matrix ring over a division ring where m.leq.n+1. (b) If R is prime ring and dim$_{r}$R=n then dim$_{l}$ R=n if dim$_{l}$ R=n if dim$_{l}$ R<.inf. (c) Let R be a principal right and left ideal domain. If dim$_{r}$R=1 then R is an unique factorization domain.TEX>R=1 then R is an unique factorization domain.

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Syntheses and Structures of 1,2,3-Substituted Cyclopentadienyl Titanium(IV) Complexes

  • Joe, Dae-June;Lee, Bun-Yeoul;Shin, Dong-Mok
    • Bulletin of the Korean Chemical Society
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    • 제26권2호
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    • pp.233-237
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    • 2005
  • Cyclopentadiene compounds, 2-[CR'R(OMe)]-1,3-Me$_2C_5H_3$ (R, R' = 2,2'-biphenyl, 2) and 2-[CR'R(OSiMe$_3$)]-1,3-Me$_2C_5H_3$ (R, R' = 2,2'-biphenyl, 3; R = ph, R' = ph, 4; R = 2-naphthyl, R' = H, 5) are readily synthesized from 2-bromo-3-methoxy-1,3-dimethylcyclopentene (1). Reaction of the cyclopentadienes with Ti(NMe$_2$)$_4$ in toluene results in clean formation of the cyclopentadienyl tris(dimethylamido)titanium complexes, which are transformed to the trichloride complexes, 2-[CR'R(OMe)]-1,3-Me$_2C_5H_2$}TiCl$_3$ (R, R' = 2,2'-biphenyl, 6) and {2-[CR'R(OSiMe$_3$)]-1,3-Me$_2C_5H_2$}TiCl$_3$ (R, R' = 2,2'-biphenyl, 7; R = ph, R' = ph, 8; R = 2-naphthyl, R' = H, 9). Attempts to form C1-bridged Cp/oxido complexes by elimination of MeCl or Me$_3$SiCl were not successful. X-ray structures of 6, 7 and an intermediate complex {2-[Ph$_2$C(OSiMe$_3$)]-1,3-Me$_2C_5H_2$}TiCl$_2$(NMe$_2$) (10) were determined.

Two More Radicals for Right Near-Rings: The Right Jacobson Radicals of Type-1 and 2

  • Rao, Ravi Srinivasa;Prasad, K. Siva
    • Kyungpook Mathematical Journal
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    • 제46권4호
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    • pp.603-613
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    • 2006
  • Near-rings considered are right near-rings and R is a near-ring. $J_0^r(R)$, the right Jacobson radical of R of type-0, was introduced and studied by the present authors. In this paper $J_1^r(R)$ and $J_2^r(R)$, the right Jacobson radicals of R of type-1 and type-2 are introduced. It is proved that both $J_1^r$ and $J_2^r$ are radicals for near-rings and $J_0^r(R){\subseteq}J_1^r(R){\subseteq}J_2^r(R)$. Unlike the left Jacobson radical classes, the right Jacobson radical class of type-2 contains $M_0(G)$ for many of the finite groups G. Depending on the structure of G, $M_0(G)$ belongs to different right Jacobson radical classes of near-rings. Also unlike left Jacobson-type radicals, the constant part of R is contained in every right 1-modular (2-modular) right ideal of R. For any family of near-rings $R_i$, $i{\in}I$, $J_{\nu}^r({\oplus}_{i{\in}I}R_i)={\oplus}_{i{\in}I}J_{\nu}^r(R_i)$, ${\nu}{\in}\{1,2\}$. Moreover, under certain conditions, for an invariant subnear-ring S of a d.g. near-ring R it is shown that $J_2^r(S)=S{\cap}J_2^r(R)$.

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THE GENERAL LINEAR GROUP OVER A RING

  • Han, Jun-Cheol
    • 대한수학회보
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    • 제43권3호
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    • pp.619-626
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    • 2006
  • Let m be any positive integer, R be a ring with identity, $M_m(R)$ be the matrix ring of all m by m matrices eve. R and $G_m(R)$ be the multiplicative group of all n by n nonsingular matrices in $M_m(R)$. In this pape., the following are investigated: (1) for any pairwise coprime ideals ${I_1,\;I_2,\;...,\;I_n}$ in a ring R, $M_m(R/(I_1{\cap}I_2{\cap}...{\cap}I_n))$ is isomorphic to $M_m(R/I_1){\times}M_m(R/I_2){\times}...{\times}M_m(R/I_n);$ and $G_m(R/I_1){\cap}I_2{\cap}...{\cap}I_n))$ is isomorphic to $G_m(R/I_1){\times}G_m(R/I_2){\times}...{\times}G_m(R/I_n);$ (2) In particular, if R is a finite ring with identity, then the order of $G_m(R)$ can be computed.

AN EXTREMAL PROBLEM ON POTENTIALLY $K_{r,r}$-ke-GRAPHIC SEQUENCES

  • Chen, Gang;Yin, Jian-Hua
    • Journal of applied mathematics & informatics
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    • 제27권1_2호
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    • pp.49-58
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    • 2009
  • For $1{\leq}k{\leq}r$, let ${\sigma}$($K_{r,r}$ - ke, n) be the smallest even integer such that every n-term graphic sequence ${\pi}$ = ($d_1$, $d_2$, ..., $d_n$) with term sum ${\sigma}({\pi})$ = $d_1$ + $d_2$ + ${\cdots}$ + $d_n\;{\geq}\;{\sigma}$($K_{r,r}$ - ke, n) has a realization G containing $K_{r,r}$ - ke as a subgraph, where $K_{r,r}$ - ke is the graph obtained from the $r\;{\times}\;r$ complete bipartite graph $K_{r,r}$ by deleting k edges which form a matching. In this paper, we determine ${\sigma}$($K_{r,r}$ - ke, n) for even $r\;({\geq}4)$ and $n{\geq}7r^2+{\frac{1}{2}}r-22$ and for odd r (${\geq}5$) and $n{\geq}7r^2+9r-26$.

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