University of California, Davis

About: University of California, Davis is a education organization based out in Davis, California, United States. It is known for research contribution in the topics: Population & Gene. The organization has 78770 authors who have published 180033 publications receiving 8064158 citations. The organization is also known as: UC Davis & UCD.

Synthesis and Characterization of Nanometer-Size Fe3O4 and γ-Fe2O3 Particles

Abstract: Synthesis of suspensions of nanosize particles of Fe3O4 was carried out in bulk aqueous solutions without the presence of surfactants. The Fe3O4 nanoparticles were oxidized to γ-Fe2O3 by direct aeration of the suspension at 100 °C. The shape and size distribution and crystallinity of the Fe3O4 nanoparticles were assessed by transmission electron microscopy and selected area electron diffraction. Very uniform and stable colloidal suspensions of the Fe3O4 nanoparticles in water could be synthesized. Oxidation of the colloidal system leads to γ-Fe2O3 nanoparticles of much larger size than Fe3O4.

Human tissue-engineered blood vessels for adult arterial revascularization

Abstract: There is a crucial need for alternatives to native vein or artery for vascular surgery. The clinical efficacy of synthetic, allogeneic or xenogeneic vessels has been limited by thrombosis, rejection, chronic inflammation and poor mechanical properties. Using adult human fibroblasts extracted from skin biopsies harvested from individuals with advanced cardiovascular disease, we constructed tissue-engineered blood vessels (TEBVs) that serve as arterial bypass grafts in long-term animal models. These TEBVs have mechanical properties similar to human blood vessels, without relying upon synthetic or exogenous scaffolding. The TEBVs are antithrombogenic and mechanically stable for 8 months in vivo. Histological analysis showed complete tissue integration and formation of vasa vasorum. The endothelium was confluent and positive for von Willebrand factor. A smooth muscle-specific alpha-actin-positive cell population developed within the TEBV, suggesting regeneration of a vascular media. Electron microscopy showed an endothelial basement membrane, elastogenesis and a complex collagen network. These results indicate that a completely biological and clinically relevant TEBV can be assembled exclusively from an individual's own cells.

DECKARD: Scalable and Accurate Tree-Based Detection of Code Clones

Abstract: Detecting code clones has many software engineering applications. Existing approaches either do not scale to large code bases or are not robust against minor code modifications. In this paper, we present an efficient algorithm for identifying similar subtrees and apply it to tree representations of source code. Our algorithm is based on a novel characterization of subtrees with numerical vectors in the Euclidean space \mathbb{R}^n and an efficient algorithm to cluster these vectors w.r.t. the Euclidean distance metric. Subtrees with vectors in one cluster are considered similar. We have implemented our tree similarity algorithm as a clone detection tool called DECKARD and evaluated it on large code bases written in C and Java including the Linux kernel and JDK. Our experiments show that DECKARD is both scalable and accurate. It is also language independent, applicable to any language with a formally specified grammar.

STAT4 and the Risk of Rheumatoid Arthritis and Systemic Lupus Erythematosus

Abstract: A SNP haplotype in the third intron of STAT4 was associated with susceptibility to both rheumatoid arthritis and systemic lupus erythematosus. The minor alleles of the haplotype-defining SNPs were present in 27% of chromosomes of patients with established rheumatoid arthritis, as compared with 22% of those of controls (for the SNP rs7574865, P = 2.81×10 −7 ; odds ratio for having the risk allele in chromosomes of patients vs. those of controls, 1.32). The association was replicated in Swedish patients with recent-onset rheumatoid arthritis (P = 0.02) and matched controls. The haplotype marked by rs7574865 was strongly associated with lupus, being present on 31% of chromosomes of case patients and 22% of those of controls (P = 1.87×10 −9 ; odds ratio for having the risk allele in chromosomes of patients vs. those of controls, 1.55). Homozygosity of the risk allele, as compared with absence of the allele, was associated with a more than doubled risk for lupus and a 60% increased risk for rheumatoid arthritis. CONCLUSIONS

Modern Tests of Lorentz Invariance

Abstract: Motivated by ideas about quantum gravity, a tremendous amount of effort over the past decade has gone into testing Lorentz invariance in various regimes. This review summarizes both the theoretical frameworks for tests of Lorentz invariance and experimental advances that have made new high precision tests possible. The current constraints on Lorentz violating effects from both terrestrial experiments and astrophysical observations are presented.