141 research outputs found
Hybrid laser metal deposition of a Fe–Cr–Mo–V–Mn tool steel for hot stamping applications
In this investigation, a novel Fe–Cr–Mo–V–Mn hot work tool steel powder was specifcally developed for laser-based additive manufacturing, targeting the possibility to create conformal cooling channels in hot stamping tools for improved cooling efciency during the forming of steel sheets for the automotive industry. Specimens of the proposed tool steel were printed via laser metal deposition and characterized to demonstrate its compatibility with hot work tool steels that are commonly used in the tooling industry. The applicability of the developed material was proved by fabricating cooling channels in a simple geometry demonstrator using a hybrid process combining milling and laser metal deposition. Finally, a hybridmanufactured hot stamping tool segment was tested in a pilot plant to evaluate the efect of the investigated material on the
cooling performance when compared to a conventional tool machined from H13 hot work tool steel. The results showed that the Fe–Cr–Mo–V–Mn tool steel features thermophysical properties similar to the most popular H13 steel and it can be efficiently used to produce tools containing conformal cooling channels by hybrid laser metal deposition, without the need of intermediate structures to improve the compatibility between the substrate and the deposited volumes
Comparing the Epidermal Growth Factor Interaction with Four Different Cell Lines: Intriguing Effects Imply Strong Dependency of Cellular Context
The interaction of the epidermal growth factor (EGF) with its receptor (EGFR) is known to be complex, and the common over-expression of EGF receptor family members in a multitude of tumors makes it important to decipher this interaction and the following signaling pathways. We have investigated the affinity and kinetics of 125I-EGF binding to EGFR in four human tumor cell lines, each using four culturing conditions, in real time by use of LigandTracer®
Towards a landscape ecosophy. Interpreting how the Villarrica-Pucón urban system inhabitants in the AraucanÃa region of Chile perceive and relate with the dynamics of Landscape
Gefitinib Induces Epidermal Growth Factor Receptor Dimers Which Alters the Interaction Characteristics with 125I-EGF
The tyrosine kinase inhibitor gefitinib inhibits growth in some tumor types by targeting the epidermal growth factor receptor (EGFR). Previous studies show that the affinity of the EGF-EGFR interaction varies between hosting cell line, and that gefitinib increases the affinity for some cell lines. In this paper, we investigate possible mechanisms behind these observations. Real-time interaction analysis in LigandTracer® Grey revealed that the HER2 dimerization preventing antibody pertuzumab clearly modified the binding of 125I-EGF to EGFR on HER2 overexpressing SKOV3 cells in the presence of gefitinib. Pertuzumab did not affect the binding on A431 cells, which express low levels of HER2. Cross-linking measurements showed that gefitinib increased the amount of EGFR dimers 3.0–3.8 times in A431 cells in the absence of EGF. In EGF stimulated SKOV3 cells the amount of EGFR dimers increased 1.8–2.2 times by gefitinib, but this effect was cancelled by pertuzumab. Gefitinib treatment did not alter the number of EGFR or HER2 expressed in tumor cell lines A431, U343, SKOV3 and SKBR3. Real-time binding traces were further analyzed in a novel tool, Interaction Map, which deciphered the different components of the measured interaction and supports EGF binding to multiple binding sites. EGFR and HER2 expression affect the levels of EGFR monomers, homodimers and heterodimers and EGF binds to the various monomeric/dimeric forms of EGFR with unique binding properties. Taken together, we conclude that dimerization explains the varying affinity of EGF – EGFR in different cells, and we propose that gefitinib induces EGFR dimmers, which alters the interaction characteristics with 125I-EGF
Genetic aspects of dental disorders
The document attached has been archived with permission from the Australian Dental Association. An external link to the publisher’s copy is included.This paper reviews past and present applications of quantitative and molecular genetics to dental disorders. Examples are given relating to craniofacial development (including malocclusion), oral supporting tissues (including periodontal diseases) and dental hard tissues (including defects of enamel and dentine as well as dental caries). Future developments and applications to clinical dentistry are discussed. Early investigations confirmed genetic bases to dental caries, periodontal diseases and malocclusion, but research findings have had little impact on clinical practice. The complex multifactorial aetiologies of these conditions, together with methodological problems, have limited progress until recently. Present studies are clarifying previously unrecognized genetic and phenotypic heterogeneities and attempting to unravel the complex interactions between genes and environment by applying new statistical modelling approaches to twin and family data. linkage studies using highly polymorphic DNA markers are providing a means of locating candidate genes, including quantitative trait loci (QTL). In future, as knowledge increases: it should be possible to implement preventive strategies for those genetically-predisposed individuals who are identified-predisposed individuals who are identified to be at risk.Grant C. Townsend, Michael J. Aldred and P. Mark Bartol
Principles of Hand Fracture Management
The hand is essential in humans for physical manipulation of their surrounding environment. Allowing the ability to grasp, and differentiated from other animals by an opposing thumb, the main functions include both fine and gross motor skills as well as being a key tool for sensing and understanding the immediate surroundings of their owner
Perinatal mortality among twins and singletons in a city in southeastern Brazil, 1984-1996
122 Acid and Bile Acids Modulate the Esophageal Squamous Barrier Function By Modulating the Localization of Claudins
1061 Acid Modulates the Squamous Epithelial Barrier Function by Modulating the Localization of Claudins
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