Variable-to-Fixed Length Homophonic Coding Suitable for Asymmetric Channel Coding

In communication through asymmetric channels the capacity-achieving input distribution is not uniform in general. Homophonic coding is a framework to invertibly convert a (usually uniform) message into a sequence with some target distribution, and is a promising candidate to generate codewords with the nonuniform target distribution for asymmetric channels. In particular, a Variable-to-Fixed length (VF) homophonic code can be used as a suitable component for channel codes to avoid decoding error propagation. However, the existing VF homophonic code requires the knowledge of the maximum relative gap of probabilities between two adjacent sequences beforehand, which is an unrealistic assumption for long block codes. In this paper we propose a new VF homophonic code without such a requirement by allowing one-symbol decoding delay. We evaluate this code theoretically and experimentally to verify its asymptotic optimality.Comment: Full version of the paper to appear in 2017 IEEE International Symposium on Information Theory (ISIT2017

High-temperature creep strength and room-temperature fracture toughness of MoSiBTiC alloy

Quite recently, the author and his coworkers have developed a new high-temperature material based on Mo-Si-B alloys with TiC addition for ultrahigh temperature applications. The alloys are produced not by powder sintering but by casting, and the constituent phases are of Mo solid solution, Mo5SiB2 (T2), (Ti, Mo)C and (Mo, Ti)2C. The density is reduced to less than 9.0 g/cm3, which is comparable to that of Ni-base superalloys. The high-temperature compressive strength is much stronger than that of commercial heat-resistant molybdenum alloys such as TZM and MHC in a wide high-temperature range. In this paper, the recent progress of our research and development of the MoSiBTiC alloys is reviewed focusing on high-temperature creep strength and room temperature fracture toughness. The alloy having a primary phase during solidification of (Ti, Mo)C and thus a higher (Ti, Mo)C volume fraction was examined for tensile creep properties, and it was found that the alloy showed typical tensile creep curves accompanying transient, steady-state and acceleration creep stages in all the test conditions. The creep strength was relatively good, for example, the rupture time at 1350 °C under 170 MPa was about 750 h. The stress exponents, n, in the temperature range of 1400 – 1600 °C and the stress range of 100 – 300 MPa were ≈ 3 while it was 5 – 6 at 1350 °C, suggesting that the rate-controlling process of creep deformation is different between at and below 1350 °C and at and above 1400 °C in the stress range. Room-temperature fracture toughness of the MoSiBTiC alloys was measured by three-point or four-point bending tests using Chevron-notched specimens. The alloy having the primary phase of (Ti, Mo)C showed the fracture toughness value of better than 15 MPa(m)1/2 at room temperature. The value was better than that of the alloy having a primary phase of Moss and thus a higher Moss volume fraction. The obtained results indicated that (Ti, Mo)C phase works for improving not only high-temperature strength but also room-temperature fracture toughness

Effects of spatially limited external magnetic fields on short sample tests of large-scale superconductors

For short sample tests of large-scale superconductor coil conductors, it is difficult to get sufficient spatial uniformity using external magnetic fields because of the size limitations of test facilities. The effects of spatially limited external magnetic fields on short sample tests are discussed by comparing the test results for narrow and broad external magnetic fields. The authors tested short samples of pool-cooled 10 kA class superconductors using two kinds of split coils which are different in bore size. The measured recovery currents for the narrow external field are more than twice those for the broad field. It shows that the insufficient spatial distribution of the external field biases the stability measurements of superconductor

Analysis of mineral apposition rates during alveolar bone regeneration over three weeks following transfer of BMP-2/7 gene via in vivo electroporation

Alveolar bone is not spontaneously regenerated following trauma or periodontitis. We previously proposed an animal model for new alveolar bone regeneration therapy based on the non-viral BMP-2/7 gene expression vector and in vivo electroporation, which induced the formation of new alveolar bone over the course of a week. Here, we analysed alveolar bone during a period of three weeks following gene transfer to periodontal tissue. Non-viral plasmid vector pCAGGS-BMP-2/7 or pCAGGS control was injected into palatal periodontal tissue of the first molar of the rat maxilla and immediately electroporated with 32 pulses of 50 V for 50 msec. Over the following three weeks, rats were double bone-stained by calcein and tetracycline every three days and mineral apposition rates (MAR) were measured. Double bone-staining revealed that MAR of alveolar bone was as similar level three days before BMP-2/7 gene transfer as three days after gene transfer. However, from 3 to 6 days, 6 to 9 days, 9 to 12 days, 12 to 15 days, 15 to 18 days, and 18 to 20 days after, MARs were significantly higher than prior to gene transfer. Our proposed gene therapy for alveolar bone regeneration combining non-viral BMP-2/7 gene expression vector and in vivo electroporation could increase alveolar bone regeneration potential in the targeted area for up to three weeks

A novel interplay between the Fanconi anemia core complex and ATR-ATRIP kinase during DNA cross-link repair.

When DNA replication is stalled at sites of DNA damage, a cascade of responses is activated in the cell to halt cell cycle progression and promote DNA repair. A pathway initiated by the kinase Ataxia teleangiectasia and Rad3 related (ATR) and its partner ATR interacting protein (ATRIP) plays an important role in this response. The Fanconi anemia (FA) pathway is also activated following genomic stress, and defects in this pathway cause a cancer-prone hematologic disorder in humans. Little is known about how these two pathways are coordinated. We report here that following cellular exposure to DNA cross-linking damage, the FA core complex enhances binding and localization of ATRIP within damaged chromatin. In cells lacking the core complex, ATR-mediated phosphorylation of two functional response targets, ATRIP and FANCI, is defective. We also provide evidence that the canonical ATR activation pathway involving RAD17 and TOPBP1 is largely dispensable for the FA pathway activation. Indeed DT40 mutant cells lacking both RAD17 and FANCD2 were synergistically more sensitive to cisplatin compared with either single mutant. Collectively, these data reveal new aspects of the interplay between regulation of ATR-ATRIP kinase and activation of the FA pathway