1,622 research outputs found
Internal noise driven generalized Langevin equation from a nonlocal continuum model
Starting with a micropolar formulation, known to account for nonlocal
microstructural effects at the continuum level, a generalized Langevin equation
(GLE) for a particle, describing the predominant motion of a localized region
through a single displacement degree-of-freedom (DOF), is derived. The GLE
features a memory dependent multiplicative or internal noise, which appears
upon recognising that the micro-rotation variables possess randomness owing to
an uncertainty principle. Unlike its classical version, the new GLE
qualitatively reproduces the experimentally measured fluctuations in the
steady-state mean square displacement of scattering centers in a polyvinyl
alcohol slab. The origin of the fluctuations is traced to nonlocal spatial
interactions within the continuum. A constraint equation, similar to a
fluctuation dissipation theorem (FDT), is shown to statistically relate the
internal noise to the other parameters in the GLE
Ultra-narrow and widely tunable Mn^(2+) Emission from Single Nanocrystals of ZnS-CdS alloy
Extensively studied Mn-doped semiconductor nanocrystals have invariably
exhibited photoluminescence (PL) over a narrow energy window of width <= 149
meV in the orange-red region and a surprisingly large spectral width (>= 180
meV), contrary to its presumed atomic-like origin. Carrying out emission
measurements on individual single nanocrystals and supported by ab initio
calculations, we show that Mn PL emission, in fact, can (i) vary over a much
wider range (~ 370 meV) covering the deep green-deep red region and (ii)
exhibit widths substantially lower (~ 60-75 meV) than reported so far, opening
newer application possibilities and requiring a fundamental shift in our
perception of the emission from Mn-doped semiconductor nanocrystals.Comment: 5 pages, 5 figure
Transcriptional profiling and consensus molecular subtype (CMS) assignment to understand response and resistance to anti-EGFR therapy in colorectal cancer
View full abstracthttps://openworks.mdanderson.org/leading-edge/1057/thumbnail.jp
Asymmetric rotations and dimerization driven by normal to modulated phase transition in 4-biphenylcarboxy coupled L-phenylalaninate
Amongst the derivatives of 4-biphenylcarboxylic acid and amino acid esters,
the crystal structure of 4-biphenylcarboxy-(L)-phenylalaninate is unusual owing
to its monoclinic symmetry within a pseudo-orthorhombic lattice. The distortion
is described by disparate rotational property around the chiral centers
( -129 degrees and 58 degrees) of the two
molecules in the asymmetric unit. Each of these molecules comprise of planar
biphenyl moieties ( = 0 degrees). Using
temperature dependent single crystal X-ray diffraction experiments we show that
the compound undergoes a phase transition below 124 K that is
characterized by a commensurate modulation wave vector, =
, = . The (3+1) dimensional modulated
structure at = 100 K suggests that the phase transition drives the biphenyl
moieties towards non coplanar conformations with significant variation of
internal torsion (
degrees). These intramolecular rotations lead to dimerization of the molecular
stacks that are described predominantly by intermolecular tilts and small
variations in intermolecular distances. Atypical of modulated structures and
superstructures of biphenyl and other polyphenyls, the rotations of individual
molecules are asymmetric ( 5
degrees) while of one independent molecule is two
to four times larger than the other. Crystal-chemical analysis and phase
relations in superspace suggest multiple competing factors involving
intramolecular steric factors, intermolecular H--CC--H
contacts and weak C--HO hydrogen bonds that govern the
distinctively unequal torsional property of the molecules
Appendiceal Adenocarcinoma PDX Models Have Improved Tumor Growth in an Orthotopic Tumor Environment
https://openworks.mdanderson.org/sumexp23/1085/thumbnail.jp
Insulin secretory actions of polyphenols of <i>Momordica charantia</i> regulate glucose homeostasis in alloxan-induced type 2 diabetic rats
Objective Momordica charantia, commonly known as bitter gourd, is traditionally used as remedies for various diseases including diabetes. The main objective of this study is to investigate the in vitro and in vivo insulinotropic and anti-diabetic effects of an 80% ethanolic extract of Momordica charantia (EEMC) fruit, as well as the underlying molecular mechanism involved and preliminary phytochemical screening. Methods The insulin secretion was measured using clonal pancreatic BRIN-BD11 β-cells and isolated mouse islets. The ability of EEMC to inhibit carbohydrate digestive enzymes and glucose absorption and, scavenge free radicals were assessed via starch digestion, glucose diffusion and DPPH assay methods. The effects of EEMC on a variety of metabolic parameters were evaluated in alloxan-induced type 2 diabetic rats, including lipid profile. Finally, a preliminary phytochemical screening was conducted to identify the active phytoconstituents. Key findings EEMC increased insulin release through the KATP-dependent/cAMP pathway, which depolarizes the β-cell membrane and elevates intracellular calcium. It also inhibited glucose absorption and free radicals, suggesting its potential to delay gastric emptying, attenuate oxidative stress, and reduce inflammatory cytokines. In vivo studies showed that EEMC improves oral glucose tolerance, food intake, fasting blood glucose, plasma insulin, lipids, and promotes intestinal motility. The active phytoconstituents in EEMC, such as flavonoids, alkaloids, tannins, saponins, steroids, and glycosides, are likely responsible for these effects. Conclusion The antihyperglycemic properties of EEMC indicate that it might be a promising candidate for diabetes management. However, additional study into the application of Momordica charantia in type 2 diabetes is essential
Goblet Cell Tumors of the Appendix: Clinical & Molecular Features
View full abstracthttps://openworks.mdanderson.org/leading-edge/1047/thumbnail.jp
Utility of plasma tumor marker levels in management of patients with appendiceal adenocarcinoma
View full abstracthttps://openworks.mdanderson.org/leading-edge/1049/thumbnail.jp
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