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Potential Structure (potential + structure)
Selected AbstractsPotential Structures That Could Be Confused With a Nonrecurrent Inferior Laryngeal Nerve: An Anatomic Study,THE LARYNGOSCOPE, Issue 1 2008Eva Maranillo MD Abstract Objectives: Study and detailed description of the large connections between the normally recurrent inferior laryngeal nerve (RILN) and the sympathetic trunk (ST) because these may be mistaken for a nonrecurrent inferior laryngeal nerve (NRILN). Study Design: Morphologic study of adult human necks. Methods: The necks of 144 human, adult, embalmed cadavers were examined (68 males, 76 females). They had been partially dissected by Cambridge preclinical medical students and then further dissected by the authors using magnification. The RILN, the ST, and their branches were identified and dissected. A total of 277 RILNs and STs (137 rights, 140 lefts) were observed. Results: A communicating branch (CB) with a similar diameter to the RILN occurred between the ST and the RILN in 48 of the 277 (17.3%) dissections, 24 from the 137 (17.5%) right dissections, and 24 from the 140 (17%) left dissections. In 12 cases, the CB was bilateral. The CB arose from the superior cervical sympathetic ganglion in 3 of the 48 (6.25%) cases, from the middle ganglion in 10 (21%) cases, from the stellate ganglion in 3 (6.25%) cases, and from the ST in 32 (66.6%) cases. One (0.36%) NRILN associated with a right retro-esophageal subclavian artery (arteria lusoria) was found. Conclusions: 1) The CB between the RILN and the ST may have a diameter and course similar to an NRILN and may be confused with it. 2) The occurrence of the CB is greater than the occurrence referred to in previous studies. 3) The occurrence of the CB is similar by side and sex. 4) The CB may arise at different levels from the cervical ST and ganglia and end in the thyroid area. 5) Other neural elements may also be confused with an RILN, such as the cardiac nerves and the collateral branches from an NRILN to the trachea and esophagus. [source] Exactly solvable effective mass Schrödinger equation with coulomb-like potentialINTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, Issue 15 2010C. Pacheco-García Abstract Exactly solvable Schrödinger equation (SE) with a position-dependent mass distribution allowing Morse-like eigenvalues is presented. For this, the position-dependent mass Schrödinger equation is transformed into a standard SE, with constant mass, by means of the point canonical transformation scheme. In that method, the choice of potential for the position-dependent mass Schrödinger equation allows us to obtain the transformation that should be used to find the exactly solvable SE. As a useful application of the proposal, the equivalent of the Witten superpotential is chosen to be constant to find the position-dependent mass distribution and the exactly solvable potential V(m(x)) allowing Morse-type energy spectra. This V(m(x)) is shown to have a Coulomb potential structure and can be useful in the study of the electronic properties of materials in which the carrier effective mass depends on the position. Moreover, the worked example, the approach is general and can be applied in the search of new potentials suitable on the study of quantum chemical systems. © 2010 Wiley Periodicals, Inc. Int J Quantum Chem, 2010 [source] In vivo evaluation of hydroxyapatite foamsJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 4 2002P. Sepulveda Abstract Hydroxyapatite (HA) is widely applied as bone graft material due to its osteoconductive potential and well-established biocompatibility. In this work, macroporous hydroxyapatite structures made through foaming of aqueous suspensions and gelcasting were tested for in vivo osteointegration. These foams are composed of a three-dimensional array of spherical pores with diameters of approximately 100,500 ,m, interconnected by windows of smaller size in the range of 30,120 ,m. The HA foams were implanted in the tibia of albino New Zealand rabbits and removed after a period of 8 weeks. Histological analysis revealed that the pores in the foams were partially or completely filled progressively with mature new bone tissue and osteoid after the implanted period. No immune or inflammatory reactions were detected. The high osteoconductive potential of the HA foams provides a potential structure for use as bone substitute in orthopedic, oral, and cranio-maxillofacial reconstructive surgery, and as dento-alveolar implants. © 2002 Wiley Periodicals, Inc. J Biomed Mater Res 62: 587,592, 2002 [source] Determining the topology of virus assembly intermediates using ion mobility spectrometry,mass spectrometryRAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 20 2010Tom W. Knapman We have combined ion mobility spectrometry,mass spectrometry with tandem mass spectrometry to characterise large, non-covalently bound macromolecular complexes in terms of mass, shape (cross-sectional area) and stability (dissociation) in a single experiment. The results indicate that the quaternary architecture of a complex influences its residual shape following removal of a single subunit by collision-induced dissociation tandem mass spectrometry. Complexes whose subunits are bound to several neighbouring subunits to create a ring-like three-dimensional (3D) architecture undergo significant collapse upon dissociation. In contrast, subunits which have only a single neighbouring subunit within a complex retain much of their original shape upon complex dissociation. Specifically, we have determined the architecture of two transient, on-pathway intermediates observed during in vitro viral capsid assembly. Knowledge of the mass, stoichiometry and cross-sectional area of each viral assembly intermediate allowed us to model a range of potential structures based on the known X-ray structure of the coat protein building blocks. Comparing the cross-sectional areas of these potential architectures before and after dissociation provided tangible evidence for the assignment of the topologies of the complexes, which have been found to encompass both the 3-fold and the 5-fold symmetry axes of the final icosahedral viral shell. Such insights provide unique information about virus assembly pathways that could allow the design of anti-viral therapeutics directed at the assembly step. This methodology can be readily applied to the structural characterisation of many other non-covalently bound macromolecular complexes and their assembly pathways. Copyright © 2010 John Wiley & Sons, Ltd. [source] | ||||||||||