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Highlights • Among 100 hairs, mtDNA analysis was possible with 99 hairs and STR analysis was possible with 66 hairs. • 86 hairs (86.9%) out of 99 hairs were the victim's hair. (mtDNA). • 65 hairs (98.5%) out of the 66 hairs were the victim's hair. (STR). Abstract Hairs are often used for DNA analysis in criminal investigations. DNA analysis of hairs with root sheaths is easy in many cases, but analyses using only the shaft or tip of the hair are often difficult. Here we describe a suspected case of child abuse in which we were commissioned to perform DNA analysis. Among 100 hairs, PCR amplification was succeeded in 99 samples, and as a result of direct sequencing, mitochondrial DNA (mtDNA) of the 99 hairs were classified into 6 types. The most common type was the 8-base substitution type of 16,168T-16,172C-16,183C-16,189C-16,217C-16,249C-16,325C-16,390A, which was observed in 86 hairs. This corresponded to the type of the victim. Total 736 STRs (75.5%) in 975 loci of 65 hairs could be typed, and only an amelogenin locus was typed in another hair. All 15 loci were typed in 10 hairs. STR types of 65 (98.5%) in 66 hairs were consistent with that of the victim. From 10 naturally-shed hair of a person, only 37 STRs (30.8%) in 120 loci of 8 hairs were typed, and all 15 loci could not be typed in these hairs. This difference in success rates of STR analysis suggested strongly that the hairs in this case were not shed naturally but forcibly, and the relevance to child abuse was suspected. [ABSTRACT FROM AUTHOR]

A Delta-crossing tangle is a tangle of three arcs with three crossings, which appears in a Delta move (or Delta unknotting operation). A Delta-crossing diagram is a diagram which can be decomposed into Delta-crossing tangles joined by simple arcs. We prove that every knot has a Delta-crossing diagram, and then investigate the Delta-crossing number which is the minimum number of Delta-crossing tangles among all Delta-crossing diagrams of the given knot. We obtain upper and lower bounds on the number in terms of the ordinal crossing number and genus. We also determine the number for prime knots with nine crossings or less except six knots. [ABSTRACT FROM AUTHOR]

Iquius nipponicus Jordan was described on the basis of a single specimen from the Miocene of Iki Island, Nagasaki, Japan, and was tentatively assigned to the family Clupeidae. The holotype consists of the anterior portion of the body (lacking the anal and caudal fins and most of the caudal vertebrae), and is re-examined. The species is re-described based on additional specimens from the type locality. This species possesses an extremely stout third dorsal spine-like fin ray with a smooth posterior edge, an expanded anterior portion of the maxilla covering approximately half of the bone, 13 branched anal fin rays, and 22 abdominal and 16 caudal vertebrae. A phylogenetic study using the character matrix from a previous study suggests that the species forms a clade with xenocyprinins, but it differs from xenocyprinins in the form of the maxilla and the dentary and the numbers of branched anal fin rays and vertebrae. The present study concludes that the genus Iquius does not belong to the family Clupeidae. Iquius is a distinct and valid genus that is closely related to cultrins and xenocyprinins of the family Cyprinidae. [ABSTRACT FROM AUTHOR]

Abstract: 2-(p-amylcinnamoyl)amino-4-chlorobenzoic acid (PACA), pharmacological inhibitor of phospholipase A2 (PLA2), inhibits epinephrine-stimulated thromboxane production in human platelets. In this study, we investigated the effect of PACA on meiotic maturation individually in stages V and VI oocytes. PACA prevented the maturation in stage V but merely delayed the process in stage VI oocytes. This was associated with the strong inhibition of Mos synthesis at both stages. Besides, PACA-induced inhibition of MAPK activation was evident in stage V but not in stage VI oocytes. PACA also inhibited the activation of Cdc2 kinase (Cdc2) in stage V but merely delayed the process in stage VI oocytes. Furthermore, 5 μM and higher concentrations of PACA completely inhibited the activation of MAPK and Cdc2 only in stage V, not in stage VI, oocytes. Moreover, we propose PACA as a new tool for the study of Xenopus oocyte maturation, which can also play a unique role for the studies of the stage-specific activation of MAPK and Cdc2. [Copyright &y& Elsevier]

In various pathological events, particularly in oxygen radical-mediated cell injury, both apoptosis and necrosis play essential roles. Apoptosis and some types of necrosis are induced via increases in mitochondrial membrane permeability, called mitochondrial outer membrane permeabilization (MOMP) and permeability transition pore (PTP) opening, respectively. To search for small compounds that inhibit both MOMP-mediated apoptosis and PTP-mediated necrosis, we performed a mitochondria-based high-throughput screening of a chemical library. We identified TMD#7538, a small compound that inhibits both MOMP and PTP opening. Consistent with the fact that this compound inhibited both apoptosis and necrosis, it efficiently suppressed H 2 O 2 -induced cell death in mouse embryonic fibroblasts and rat neonatal cardiomyocytes. [ABSTRACT FROM AUTHOR]

Purpose: To investigate if early exercise can help prevent skeletal muscle loss and improve the clinical outcomes of esophageal cancer patients receiving preoperative neoadjuvant chemotherapy (NAC). Methods: This was a single-center, retrospective observational cohort study of 110 patients with advanced esophageal cancer. We analyzed the effect of early exercise on the risk of skeletal muscle loss (defined as > 2.98%) during NAC and the subsequent clinical outcomes. Patients in the early exercise group (n = 71) started exercise therapy 8 days earlier than those the late exercise group (n = 39). Results: The median age of the patients was 65.4 years, the mean BMI was 21.1 kg/m2, and 92 (84%) of the 110 patients were men. Skeletal muscle loss occurred in 34% and 67% of the early and late exercise groups, respectively (p < 0.001). There was a lower risk of surgical site infection in the early exercise group (1% vs 16%, p = 0.021). Multivariate analysis revealed that early exercise reduced the risk of skeletal muscle loss (OR = 0.25, 95% CI 0.09–0.65, p = 0.006). Conclusions: Our results suggest that early exercise reduces the risk of both skeletal muscle loss during NAC and subsequent surgical site infection in patients with esophageal cancer. [ABSTRACT FROM AUTHOR]

Nicotinamide phosphoribosyltransferase (Nampt) catalyzes the rate-limiting step in the salvage pathway for nicotinamide adenine dinucleotide (NAD+) biosynthesis, and thereby regulates the deacetylase activity of sirtuins. Here we show accommodative regulation of myocardial NAD+ by monocyte-derived extracellular Nampt (eNampt), which is essential for hemodynamic compensation to pressure overload. Although intracellular Nampt (iNampt) expression was decreased in pressure-overloaded hearts, myocardial NAD+ concentration and Sirt1 activity were preserved. In contrast, iNampt was up-regulated in spleen and monocytes, and circulating eNampt protein and nicotinamide mononucleotide (NMN), a key precursor of NAD+, were significantly increased. Pharmacological inhibition of Nampt by FK866 or depletion of monocytes/macrophages by clodronate liposomes disrupted the homeostatic mechanism of myocardial NAD+ levels and NAD+-dependent Sirt1 activity, leading to susceptibility to cardiomyocyte apoptosis and cardiac decompensation in pressure-overloaded mice. These biochemical and hemodynamic defects were prevented by systemic administration of NMN. Our studies uncover a crucial role of monocyte-derived eNampt in myocardial adaptation to pressure overload, and highlight a potential intervention controlling myocardial NAD+ against heart failure. [ABSTRACT FROM AUTHOR]