نتایج جستجو برای: nacl 25 gl

تعداد نتایج: 381385  

In this paper, we present new variants of global bi-conjugate gradient (Gl-BiCG) and global bi-conjugate residual (Gl-BiCR) methods for solving nonsymmetric linear systems with multiple right-hand sides. These methods are based on global oblique projections of the initial residual onto a matrix Krylov subspace. It is shown that these new algorithms converge faster and more smoothly than the Gl-...

2010
Onofrio Annunziata Donald G. Miller John G. Albright

Available online 23 May 2010

Journal: :The Journal of experimental biology 2005
H-W Kim E S Chang D L Mykles

Crustacean muscle has four calpain-like proteinase activities (CDP I, IIa, IIb and III) that are involved in molt-induced claw muscle atrophy, as they degrade myofibrillar proteins in vitro and in situ. Using PCR cloning techniques, three full-length calpain cDNAs (Gl-CalpB, Gl-CalpM and Gl-CalpT) were isolated from limb regenerates of the tropical land crab Gecarcinus lateralis. All three had ...

2001
T. R. Geballe D. Saumon S. K. Leggett G. R. Knapp M. S. Marley K. Lodders

We have obtained a good quality R∼400 0.8–2.5 µm spectrum and accurate photometry of Gl 570D, one of the coolest and least luminous brown dwarfs currently known. The spectrum shows that Gl 570D has deeper absorptions in the strong water and methane bands at 1. ′ than previously observed T dwarfs. Data analysis using model spectra coupled with knowledge of the well-understood primary implies tha...

Background and Objectives: Preparation and evaluation of nanocomposite films have become prevalent in recent years. Depending on the purpose of using the film, and considering the effects and interaction effects of nanomaterial and other modifiers on the film properties, the amounts of nanomaterials and modifiers should be optimized. The effects of montmorillonite (MMT), glycerol (GL), and thei...

Journal: :Journal of virology 2008
Brent J Ryckman Barb L Rainish Marie C Chase Jamie A Borton Jay A Nelson Michael A Jarvis David C Johnson

The entry of human cytomegalovirus (HCMV) into biologically relevant epithelial and endothelial cells involves endocytosis followed by low-pH-dependent fusion. This entry pathway is facilitated by the HCMV UL128, UL130, and UL131 proteins, which form one or more complexes with the virion envelope glycoprotein gH/gL. gH/gL/UL128-131 complexes appear to be distinct from the gH/gL/gO complex, whic...

1996
W. - S. Chung

Some Realization of gl q (n)-covariant Oscillator Algebra and gl q (n)-covariant q-Virasoro Algebra with q a root of unity. Abstract In this paper some realization of gl q (n)-covariant oscillators is obtained when q is a root of unity. And the gl q (n)-covariant q-Virasoro algebra is presented by using the gl q (n)-covariant oscillators.

1994
R. Chakrabarti R. Jagannathan

On the Hopf structure of U p,q (gl(1|1)) and the universal T-matrix of F un p,q (GL(1|1)) Abstract Using the technique developed by Fronsdal and Galindo (Lett. Math. Phys. 27 (1993) 57) for studying the Hopf duality between the quantum algebras F un p,q (GL(2)) and U p,q (gl(2)), the Hopf structure of U p,q (gl(1|1)), dual to F un p,q (GL(1|1)), is derived and the corresponding universal T-matr...

2003
Michael B. Jenkins

Rhizobial symbionts were isolated from the surface (0–0.5 M) and phreatic (3.9–5.0 M) root environments of a mature mesquite woodland in the Sonoran Desert of Southern California, and from variable depths (0–12 m) of non-phreatic mesquite ecosystems in the Chihuahuan Desert of New Mexico. They were tested for their ability to tolerate high salinity, and respire NO3 2 as mechanisms of free-livin...

2014
John R. Stembridge

as gl(V1)⊕ gl(V2)⊕ gl(V3)-modules. This yields a well-known reformulation of (2.1). Proposition A.1. If l(α) 6 dimV1 and l(β) 6 dimV2, then the Kronecker coefficient g(αβγ) is the multiplicity of V1(α)⊗ V2(β) in the gl(V1)⊕ gl(V2)-module (V1 ⊗ V2)(γ). If V is m-dimensional, then V (1) is the one-dimensional gl(V )-module carried by the trace map gl(V ) → C. It follows easily that V (n) ∼= V (1)...

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