Subcell

A. Harten, ENO Schemes with Subcell Resolution, J. Comput. Phys. 83 (1989). 

A further improvement can be seen for the situation depicted in Eigure lb. Let ( )i, (r) denote the potential due to the charges in the cell about point b, evaluated at the point r. Let a be the center of the subcell containing q. Then (j), (r) can be approximated by a second-order Taylor expansion about a ... 

Harter C, Reinhard C (2000) The secretory pathway from history to the state ofthe art. Subcell Biochem 34 1-38... 

Nickel atoms in BajNi B form distorted, puckered 3.6.3.6-kagome nets stacked in six layers perpendicular to the c axis. The densely packed framework of trigonal-Ni prisms again result in boron-pair formation, although Ba atoms are too large to be sandwiched between two Ni layers, and only four Ba can be accommodated within six Ni layers. Superconductivity is found for ( a, Sr, Ba)2pt9Bg borides with a structure related to Ba2Ni9Bfi and e o,B2 however, with respect to crystal chemistry and boron coordination, only the subcell is derived so far. 

Gund P. Three-dimensional pharmacophoric pattern searching. Prog Mol Subcell Biol 1977 5 117-43. 

Crystalline phases pack into two distinct classes of subcells depending on chemical structure and environmental factors. The first class is characterized by specific chain-chain... 

Avruch, J., Belham, C., Weng, Q., Hara, K., and Yonezawa, K. (2001). The p70 S6 kinase integrates nutrient and growth signals to control translational capacity. Prog. Mol. Subcell. Biol. 26, 115-154. 

Taken together, the field is now well placed to design new biosensors, examine protein-protein and protein-lipid interactions, and sensitively determine protein conformation in living tissues at submicron resolution. These interactions are either impossible or extraordinarily difficult to examine in other ways, and the subcel-lular resolution of FRET-FLIM that allows detection of interactions in specific subcellular compartments may provide insight that... 

The unit cell of cellulose from Chaetomorpha melagonium is monoclinic, with a = 16.43 A (1.643 nm), b(fiber axis) = 10.33 A (1.033 nm), c = 15.70 A (1.570 nm), and /3 = 96.97°. In base-plane projection, each of the Meyer-Misch subcells that make up the super-lattice are identical. All equatorial reflections can be indexed by using a one-chain unit-cell, meaning that every single chain has... 

Figure 4.10 Schematic representation of ordered structures in the Pb1 xZrt K2+2x system (a) Pb3ZrF10 and (b) Pb5ZrF14. Pairs of square antiprisms, at two levels, are represented by the small square motifs. Spheres represent cations at two levels anions are omitted for clarity. The fluorite subcell is indicated in the top left of each figure. [Adapted from J. P. Laval, C. Depierrefixe, B. Frit, and G. Roult, J. Solid State Chem., 54, 260-276 (1984).]...

Inouye, H., and Kirschner, D. A. (2005). Alzheimer s //-amyloid Insights into fibril formation and structure from Congo red binding. Subcell. Biochem. 38, 203-224. 

Moch H, Kononen J, Kallioniemi OP, Sauter G (2001) Tissue microarrays what will they bring to molecular and anatomic pathology Adv Anat Pathol 8 14 20 Moll R (1998) Cytokeratins as markers of differentiation in the diagnosis of epithelial tumors. Subcell Biochem 31 205 262... 

Other representations may be obtained by subdividing the unit cell into a number of similar subcells. In the cubic system the subdivision is made along the three axes by the same factor which is used as a subscript in the new lattice complex... 

The tI10-MoNi4 type is another superstructure based on face-centred cubic pseudo-cells. In the projection shown in Fig. 3.36, inside the true cell, the pseudo-cubic subcell (aps = 362 pm, cps = 356.4 pm) has been evidenced by dotted lines. Close-packed layers can be identified in this structure they are stacked in a 15 close-packed repeat sequence. 

The cell can be described as formed by two superimposed slightly distorted body-centred cubic subcells of the metal atoms. The O atom is surrounded by a slightly compressed Ta atom octahedron. 

Figure 3.42. Schematic representation of a double layer composite structure. Two substructures (1 and 2) are sketched. The composite structure (1 + 2) resulting from the mutual intermingling of the two substructures has a period corresponding to six subcells 1 commensurate to seven subcells 2.

The TiAl3-type structure is a superstructure of AuCu3 and may be described in terms of two, distorted, AuCu3-type subcells stacked one above the other. 

The metabolism of C-DEHP by rainbow trout liver subcell-ular fractions and serum was studied by Melancon and Lech (14). The data in Table VI show that without added NADPH, the major metabolite produced was mono-2-ethylhexyl phthalate. When NADPH was added to liver homogenates or the mitochondrial or microsomal fractions, two unidentified metabolites more polar than the monoester were produced. Additional studies showed that the metabolism of DEHP by the mitochondrial and the microsomal fractions were very similar (Figure 1). Both fractions show an increased production of metabolites of DEHP resulting from addition of NADPH and the shift from production of monoester to that of more polar metabolites. The reduced accumulation of monoester which accompanied this NADPH mediated production of more polar metabolites may help in interpreting the pathway of DEHP metabolism in trout liver. This decreased accumulation of monoester could be explained either by metabolism of the monoester to more polar metabolites or the shift of DEHP from the hydrolytic route to a different, oxidative pathway. The latter explanation is unlikely because in these experiments less than 20% of the DEHP was metabolized. 

Veldhuizen R, Possmayer F (2004) Phospholipid metabolism in lung surfactant. Subcell Biochem 37 359-388... 

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