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Traumatic brain injury (TBI) causes death and disability in the United States and around the world. The traumatic insult causes the mechanical injury of the brain and primary cellular death. While a comprehensive pathological mechanism of TBI is still lacking, the focus of the TBI research is concentrated on understanding the pathophysiology and developing suitable therapeutic approaches. Given the complexities in pathophysiology involving interconnected immunologic, inflammatory, and neurological cascades occurring after TBI, the therapies directed to a single mechanism fail in the clinical trials. This has led to the development of the paradigm of a combination therapeutic approach against TBI. While there are no drugs available for the treatment of TBI, stem cell therapy has shown promising results in preclinical studies. But, the success of the therapy depends on the survival of the stem cells, which are limited by several factors including route of administration, health of the administered cells, and inflammatory microenvironment of the injured brain. Reducing the inflammation prior to cell administration may provide a better outcome of cell therapy following TBI. This review is focused on different therapeutic approaches of TBI and the present status of the clinical trials. © 2020 The Authors. CNS Neuroscience & Therapeutics Published by John Wiley & Sons Ltd.OBJECTIVE The aim of this study was to investigate the differences in six anthropometric measurements of people born during and immediately after the 1959 to 1961 Great Chinese Famine using a regression discontinuity approach. METHODS Data were drawn from the baseline of the China Kadoorie Biobank study, and a subset of data from 76,912 participants was analyzed. Linsitinib We performed regression discontinuity among participants who were born during the famine (October 1959 to October 1962) and immediately after the famine period (November 1962 to October 1964) by using local linear and parametric regressions. All analyses were conducted by sex and study area. RESULTS Significantly, there were increases of 0.30 kg/m2 (P = 0.007) in BMI, 0.81 kg (P = 0.028) in weight, 8.57 mm (P = 0.004) in waist circumference, and 5.07 mm (P = 0.004) in hip circumference for rural women who were exposed to famine during their fetal period compared with those who were not exposed to famine in utero. However, such statistically significant increases in anthropometric values were not observed in local linear regression and most parametric models among rural men or in the urban population. CONCLUSIONS Rural Chinese women who were exposed to famine during the fetal period were observed to have higher levels of BMI, weight, waist circumference, and hip circumference in adulthood. © 2020 The Obesity Society.Binary transition metal selenides have been more promising than single transition metal selenides as anode materials for sodium-ion batteries (SIBs). However, the controlled synthesis of transition metal selenides, especially those derived from metal-organic-frameworks with well-controlled structure and morphology is still challenging. In this paper, highly porous NiCoSe4 @NC composite microspheres were synthesized by simultaneous carbonization and selenization of a Ni-Co-based metal-organic framework (NiCo-MOF) and characterized by scanning electron microscopy, transition electron microscopy, X-Ray diffraction, X-Ray photoelectron spectroscopy and electrochemical techniques. The rationally engineered NiCoSe4 @NC composite exhibits a capacity of 325 mAh g-1 at a current density of 1 A g-1 , and 277.8 mAh g-1 at 10 A g-1 . Most importantly, the NiCoSe4 @NC retains a capacity of 293 mAh g-1 at 1 A g-1 after 1500 cycles, with a capacity decay rate of 0.025 % per cycle. © 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.Interactions between gut microbiota not only regulate physical health, but also form a vital bridge between the environment and the host, thus helping the host to better adapt to the environment. The improvement of modern molecular sequencing techniques enables in-depth investigations of the gut microbiota of vertebrate herbivores without harming them. By sequencing the 16S rRNA V4-V5 region of the gut microbiota of both the captive and wild kiang in winter and summer, the diversity and function of the microbiota could be compared. The reasons for observed differences were discussed. The results showed that the dominant phyla of the kiang were Bacteroidetes and Firmicutes, and the structure and abundance of the gut microbiota differed significantly between seasons and environments. However, the relatively stable function of the gut microbiota supplies the host with increased adaptability to the environment. The diversity of the intestinal flora of the kiang is relatively low in captivity, which increases their risk to catch diseases to some extent. Therefore, importance should be attached to the impact of captivity on wildlife. © 2020 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd.The two most fundamental processes describing change in biology, development, and evolution, occur over drastically different timescales. Development involves temporal sequences of cell states controlled by hierarchies of regulatory structures. It occurs over the lifetime of a single individual and is associated with gene expression level change of a given genotype. Evolution, by contrast, entails genotypic change through mutation, the acquisition/loss of genes and changes in the network topology of interactions among genes. It involves the emergence of new, environmentally selected phenotypes over the lifetimes of many individuals. We start by reviewing the most limiting aspects of the theoretical modeling of gene regulatory networks (GRNs) which prevent the study of both timescales in a common, mathematical language. We then consider the simple framework of Boolean network models of GRNs and point out its inadequacy to include evolutionary processes. As opposed to one-to-one maps to specific attractors, we adopt a many-to-one map which makes each phenotype correspond to multiple attractors. This definition no longer requires a fixed size for the genotype and opens the possibility for modeling the phenotypic change of a genotype, which is itself changing over evolutionary timescales. At the same time, we show that this generalized framework does not interfere with established numerical techniques for the identification of the kernel of controlling nodes responsible for cell differentiation through external signals. © 2020 Wiley Periodicals, Inc.

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