98 research outputs found
What is the right form of the probability distribution of the conductance at the mobility edge?
The probability distribution of the conductance Pc(g) at the Anderson
critical point is calculated. It is find that Pc(g) has a dip at small g in
agreement with epsilon expansion results. The Pc(g) for the 3d system is quite
different from the 2d quantum critical point of the integer quantum Hall
effect. The universality or not of these distributions is of central importance
to the field of disordered systems.Comment: 1 page, 1 figure submitted to Phys. Rev. Lett. (Comment
Photosynthesis-assisted remodeling of three-dimensional printed structures
The mechanical properties of engineering structures continuously weaken during service life because of material fatigue or degradation. By contrast, living organisms are able to strengthen their mechanical properties by regenerating parts of their structures. For example, plants strengthen their cell structures by transforming photosynthesis-produced glucose into stiff polysaccharides. In this work, we realize hybrid materials that use photosynthesis of embedded chloroplasts to remodel their microstructures. These materials can be used to three-dimensionally (3D)-print functional structures, which are endowed with matrix-strengthening and crack healing when exposed to white light. The mechanism relies on a 3D-printable polymer that allows for an additional cross-linking reaction with photosynthesis-produced glucose in the material bulk or on the interface. The remodeling behavior can be suspended by freezing chloroplasts, regulated by mechanical preloads, and reversed by environmental cues. This work opens the door for the design of hybrid synthetic-living materials, for applications such as smart composites, lightweight structures, and soft robotics
Metal-insulator transitions in anisotropic 2d systems
Several phenomena related to the critical behaviour of non-interacting
electrons in a disordered 2d tight-binding system with a magnetic field are
studied. Localization lengths, critical exponents and density of states are
computed using transfer matrix techniques. Scaling functions of isotropic
systems are recovered once the dimension of the system in each direction is
chosen proportional to the localization length. It is also found that the
critical point is independent of the propagation direction, and that the
critical exponents for the localization length for both propagating directions
are equal to that of the isotropic system (approximately 7/3). We also
calculate the critical value of the scaling function for both the isotropic and
the anisotropic system. It is found that the isotropic value equals the
geometric mean of the two anisotropic values. Detailed numerical studies of the
density of states for the isotropic system reveals that for an appreciable
amount of disorder the critical energy is off the band center.Comment: 6 pages RevTeX, 6 figures included, submitted to Physical Review
Symmetry between absorption and amplification in disordered media
We address the issue of whether amplification, like absorption, suppresses
wave transmission at large gain, as has been claimed in previous studies of
wave propagation in active random media. A closer examination reveals that the
paradoxical symmetry between absorption and amplification is an artifact of
unphysical solutions from the time-independent wave equation. Solutions from
the time-dependent equation demonstrate clearly that when gain is above the
threshold, the amplitude of both the transmitted and the reflected wave
actually increases with time, apparently without bound. The implications of the
current finding is discusse
Scaling Properties of Conductance at Integer Quantum Hall Plateau Transitions
We investigate the scaling properties of zero temperature conductances at
integer quantum Hall plateau transitions in the lowest Landau band of a
two-dimensional tight-binding model. Scaling is obeyed for all energy and
system sizes with critical exponent nu =7/3 . The arithmetic average of the
conductance at the localization-delocalization critical point is found to be
_c = 0.506 e^2 / h, in agreement with the universal longitudinal conductance
predicted by an analytical theory. The probability distribution of the
conductance at the critical point is broad with a dip at small G.Comment: 4 pages, 3 postscript figures, Submitted to PR
Effect of Sustained Gene Delivery of Platelet‐Derived Growth Factor or Its Antagonist (PDGF‐1308) on Tissue‐Engineered Cementum
Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/141209/1/jper0429.pd
Estimation of Endocarpon pusillum Hedwig carbon budget in the Tengger Desert based on its photosynthetic rate
Identification of Genome-Wide Variations among Three Elite Restorer Lines for Hybrid-Rice
Rice restorer lines play an important role in three-line hybrid rice production. Previous research based on molecular tagging has suggested that the restorer lines used widely today have narrow genetic backgrounds. However, patterns of genetic variation at a genome-wide scale in these restorer lines remain largely unknown. The present study performed re-sequencing and genome-wide variation analysis of three important representative restorer lines, namely, IR24, MH63, and SH527, using the Solexa sequencing technology. With the genomic sequence of the Indica cultivar 9311 as the reference, the following genetic features were identified: 267,383 single-nucleotide polymorphisms (SNPs), 52,847 insertion/deletion polymorphisms (InDels), and 3,286 structural variations (SVs) in the genome of IR24; 288,764 SNPs, 59,658 InDels, and 3,226 SVs in MH63; and 259,862 SNPs, 55,500 InDels, and 3,127 SVs in SH527. Variations between samples were also determined by comparative analysis of authentic collections of SNPs, InDels, and SVs, and were functionally annotated. Furthermore, variations in several important genes were also surveyed by alignment analysis in these lines. Our results suggest that genetic variations among these lines, although far lower than those reported in the landrace population, are greater than expected, indicating a complicated genetic basis for the phenotypic diversity of the restorer lines. Identification of genome-wide variation and pattern analysis among the restorer lines will facilitate future genetic studies and the molecular improvement of hybrid rice
Nanofibrous Scaffolds Incorporating PDGF-BB Microspheres Induce Chemokine Expression and Tissue Neogenesis In Vivo
Platelet-derived growth factor (PDGF) exerts multiple cellular effects that stimulate wound repair in multiple tissues. However, a major obstacle for its successful clinical application is the delivery system, which ultimately controls the in vivo release rate of PDGF. Polylactic-co-glycolic acid (PLGA) microspheres (MS) in nanofibrous scaffolds (NFS) have been shown to control the release of rhPDGF-BB in vitro. In order to investigate the effects of rhPDGF-BB release from MS in NFS on gene expression and enhancement of soft tissue engineering, rhPDGF-BB was incorporated into differing molecular weight (MW) polymeric MS. By controlling the MW of the MS over a range of 6.5 KDa–64 KDa, release rates of PDGF can be regulated over periods of weeks to months in vitro. The NFS-MS scaffolds were divided into multiple groups based on MS release characteristics and PDGF concentration ranging from 2.5–25.0 µg and evaluated in vivo in a soft tissue wound repair model in the dorsa of rats. At 3, 7, 14 and 21 days post-implantation, the scaffold implants were harvested followed by assessments of cell penetration, vasculogenesis and tissue neogenesis. Gene expression profiles using cDNA microarrays were performed on the PDGF-releasing NFS. The percentage of tissue invasion into MS-containing NFS at 7 days was higher in the PDGF groups when compared to controls. Blood vessel number in the HMW groups containing either 2.5 or 25 µg PDGF was increased above those of other groups at 7d (p<0.01). Results from cDNA array showed that PDGF strongly enhanced in vivo gene expression of the CXC chemokine family members such as CXCL1, CXCL2 and CXCL5. Thus, sustained release of rhPDGF-BB, controlled by slow-releasing MS associated with the NFS delivery system, enhanced cell migration and angiogenesis in vivo, and may be related to an induced expression of chemokine-related genes. This approach offers a technology to accurately control growth factor release to promote soft tissue engineering in vivo
Mouse Sphingosine Kinase 1a Is Negatively Regulated through Conventional PKC-Dependent Phosphorylation at S373 Residue
Sphingosine kinase is a lipid kinase that converts sphingosine into sphingosine-1-phosphate, an important signaling molecule with intracellular and extracellular functions. Although diverse extracellular stimuli influence cellular sphingosine kinase activity, the molecular mechanisms underlying its regulation remain to be clarified. In this study, we investigated the phosphorylation-dependent regulation of mouse sphingosine kinase (mSK) isoforms 1 and 2. mSK1a was robustly phosphorylated in response to extracellular stimuli such as phorbol ester, whereas mSK2 exhibited a high basal level of phosphorylation in quiescent cells regardless of agonist stimulation. Interestingly, phorbol ester-induced phosphorylation of mSK1a correlated with suppression of its activity. Chemical inhibition of conventional PKCs (cPKCs) abolished mSK1a phosphorylation, while overexpression of PKC alpha, a cPKC isoform, potentiated the phosphorylation, in response to phorbol ester. Furthermore, an in vitro kinase assay showed that PKC alpha directly phosphorylated mSK1a. In addition, phosphopeptide mapping analysis determined that the S373 residue of mSK1a was the only site phosphorylated by cPKC. Interestingly, alanine substitution of S373 made mSK1a refractory to the inhibitory effect of phorbol esters, whereas glutamate substitution of the same residue resulted in a significant reduction in mSK1a activity, suggesting the significant role of this phosphorylation event. Taken together, we propose that mSK1a is negatively regulated through cPKC-dependent phosphorylation at S373 residueopen
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