75 research outputs found
Crystalline structure of an ammonia borane-polyethylene oxide cocrystal: a material investigated for its hydrogen storage potential
The crystalline structure of a cocrystal comprising ammonia borane (AB) and a short-chain polyethylene oxide (PEO or PEG) has been determined by single-crystal X-ray diffraction. The components interact via hydrogen bonds between each of the hydrogen atoms at the NH3 end of the AB molecules and alternate oxygen atoms along the PEO backbone. The PEO chains in the structure exhibit an unusual conformation where their curvature reverses every 5 monomers, such that the polymer snakes through the crystal. This is the first time that an AB composite material has been determined to be a cocrystal, and no structure determination of a cocrystal to confine AB has been reported before
A novel ammonium pentaborate – poly(ethylene-glycol) templated polymer-inclusion compound
A new hydrogen-bonded supramolecular framework is reported, consisting of ammonium pentaborate, containing poly(ethylene-glycol) chains extending down tubular cavities in the structure. The crystal architecture is templated by the presence of the polyether chains, analogous to template synthesis of zeolites and metal organic frameworks. The ammonium pentaborate is formed by the thermolysis of ammonia borane, followed by hydrolysis of the dehydrogenation products by ambient water. This structure represents the first known example of a borate-based polymer inclusion compound
Mechanisms and Difference-Making
I argue that difference-making should be a crucial element for evaluating the
quality of evidence for mechanisms, especially with respect to the robustness of
mechanisms, and that it should take central stage when it comes to the general role
played by mechanisms in establishing causal claims in medicine. The difference-
making of mechanisms should provide additional compelling reasons to accept the gist
of Russo-Williamson thesis and include mechanisms in the protocols for Evidence-
Based Medicine (EBM), as the EBM+ research group has been advocatin
How can chiropractic become a respected mainstream profession? The example of podiatry
<p>Abstract</p> <p>Background</p> <p>The chiropractic profession has succeeded to remain in existence for over 110 years despite the fact that many other professions which had their start at around the same time as chiropractic have disappeared. Despite chiropractic's longevity, the profession has not succeeded in establishing cultural authority and respect within mainstream society, and its market share is dwindling. In the meantime, the podiatric medical profession, during approximately the same time period, has been far more successful in developing itself into a respected profession that is well integrated into mainstream health care and society.</p> <p>Objective</p> <p>To present a perspective on the current state of the chiropractic profession and to make recommendations as to how the profession can look to the podiatric medical profession as a model for how a non-allopathic healthcare profession can establish mainstream integration and cultural authority.</p> <p>Discussion</p> <p>There are several key areas in which the podiatric medical profession has succeeded and in which the chiropractic profession has not. The authors contend that it is in these key areas that changes must be made in order for our profession to overcome its shrinking market share and its present low status amongst healthcare professions. These areas include public health, education, identity and professionalism.</p> <p>Conclusion</p> <p>The chiropractic profession has great promise in terms of its potential contribution to society and the potential for its members to realize the benefits that come from being involved in a mainstream, respected and highly utilized professional group. However, there are several changes that must be made within the profession if it is going to fulfill this promise. Several lessons can be learned from the podiatric medical profession in this effort.</p
Experimental ‘Jet Lag’ Inhibits Adult Neurogenesis and Produces Long-Term Cognitive Deficits in Female Hamsters
Background: Circadian disruptions through frequent transmeridian travel, rotating shift work, and poor sleep hygiene are associated with an array of physical and mental health maladies, including marked deficits in human cognitive function. Despite anecdotal and correlational reports suggesting a negative impact of circadian disruptions on brain function, this possibility has not been experimentally examined. Methodology/Principal Findings: In the present study, we investigated whether experimental ‘jet lag ’ (i.e., phase advances of the light:dark cycle) negatively impacts learning and memory and whether any deficits observed are associated with reductions in hippocampal cell proliferation and neurogenesis. Because insults to circadian timing alter circulating glucocorticoid and sex steroid concentrations, both of which influence neurogenesis and learning/memory, we assessed the contribution of these endocrine factors to any observed alterations. Circadian disruption resulted in pronounced deficits in learning and memory paralleled by marked reductions in hippocampal cell proliferation and neurogenesis. Significantly, deficits in hippocampal-dependent learning and memory were not only seen during the period of the circadian disruption, but also persisted well after the cessation of jet lag, suggesting long-lasting negative consequences on brain function. Conclusions/Significance: Together, these findings support the view that circadian disruptions suppress hippocampal neurogenesis via a glucocorticoid-independent mechanism, imposing pronounced and persistent impairments on learnin
Functional impact and evolution of a novel human polymorphic inversion that disrupts a gene and creates a fusion transcript
Since the discovery of chromosomal inversions almost 100 years ago, how they are maintained in natural populations has been a highly debated issue. One of the hypotheses is that inversion breakpoints could affect genes and modify gene expression levels, although evidence of this came only from laboratory mutants. In humans, a few inversions have been shown to associate with expression differences, but in all cases the molecular causes have remained elusive. Here, we have carried out a complete characterization of a new human polymorphic inversion and determined that it is specific to East Asian populations. In addition, we demonstrate that it disrupts the ZNF257 gene and, through the translocation of the first exon and regulatory sequences, creates a previously nonexistent fusion transcript, which together are associated to expression changes in several other genes. Finally, we investigate the potential evolutionary and phenotypic consequences of the inversion, and suggest that it is probably deleterious. This is therefore the first example of a natural polymorphic inversion that has position effects and creates a new chimeric gene, contributing to answer an old question in evolutionary biology
Antimitotic drugs in the treatment of cancer
Cancer is a complex disease since it is adaptive
in such a way that it can promote proliferation and
invasion by means of an overactive cell cycle and in turn
cellular division which is targeted by antimitotic drugs
that are highly validated chemotherapy agents. However,
antimitotic drug cytotoxicity to non-tumorigenic cells and
multiple cancer resistance developed in response to drugs
such as taxanes and vinca alkaloids are obstacles faced in
both the clinical and basic research field to date. In this
review, the classes of antimitotic compounds, their mechanisms
of action and cancer cell resistance to chemotherapy
and other limitations of current antimitotic compounds are
highlighted, as well as the potential of novel 17-β estradiol
analogs as cancer treatment.Medical Research Council of South Africa, the Research Committee of the Faculty of Health Sciences of the University of Pretoria, the Cancer association of South Africa and the National Research Foundation.http://link.springer.com/journal/280hb201
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