Oberflächenspannung und Schallgeschwindigkeit

Summary The preceding empirical relation was found between the surface tension of liquids, the specific weight of liquids, and the velocity of sound:=6.3 · 10^{–4 3/2}. In place of the vèocity of sound can be used, with suitable changes in the equation, the compressibility or, in the case of solid substances, the elasticity of the material in question. The range of validity of this relation is so large that it is possible by means of it to calculate the surface tension of solid substances and of gases.     

Reaction mechanism determines NMDA receptor response to repetitive stimulation

At central excitatory synapses, N-methyl-D-aspartate (NMDA) receptors, which have a high affinity for glutamate, produce a slowly rising synaptic current in response to a single transmitter pulse and an additional current after a second, closely timed stimulus. Here we show, by examining the kinetics of transmitter binding and channel gating in single-channel currents from recombinant NR1/NR2A receptors, that the synaptic response to trains of impulses is determined by the molecular reaction mechanism of the receptor. The rate constants estimated for the activation reaction predict that, after binding neurotransmitter, receptors hesitate for approximately 4 ms in a closed high-affinity conformation before they either proceed towards opening or release neurotransmitter, with about equal probabilities. Because only about half of the initially fully occupied receptors become active, repetitive stimulation elicits currents with distinct waveforms depending on pulse frequency. This high-affinity/low-efficiency activation mechanism might serve as a link between stimulation frequency and the directionality of the ensuing synaptic plasticity.     

Recommendations of the 2006 Human Variome Project meeting

Lists of variations in genomic DNA and their effects have been kept for some time and have been used in diagnostics and research. Although these lists have been carefully gathered and curated, there has been little standardization and coordination, complicating their use. Given the myriad possible variations in the estimated 24,000 genes in the human genome, it would be useful to have standard criteria for databases of variation. Incomplete collection and ascertainment of variants demonstrates a need for a universally accessible system. These and other problems led to the World Heath Organization-cosponsored meeting on June 20-23, 2006 in Melbourne, Australia, which launched the Human Variome Project. This meeting addressed all areas of human genetics relevant to collection of information on variation and its effects. Members of each of eight sessions (the clinic and phenotype, the diagnostic laboratory, the research laboratory, curation and collection, informatics, relevance to the emerging world, integration and federation and funding and sustainability) developed a number of recommendations that were then organized into a total of 96 recommendations to act as a foundation for future work worldwide. Here we summarize the background of the project, the meeting and its recommendations.     

Spontaneous macroscopic magnetization at the superconducting transition temperature of YBa2Cu3O(7-delta)

A noteworthy feature of the high-temperature superconductors is the unconventional symmetry of the superconducting order parameter. Several experiments have established that the order parameter has a four-fold d(x2 - y2) symmetry under rotation of the lattice (the order parameter of conventional superconductors is, in contrast, isotropic). An intriguing and much debated possibility is that, in certain cases, an additional imaginary component might be present, having an isotropic s-wave or d(xy) symmetry. A consequence of a complex order parameter of the form d(x2 - y2) + id(xy) is that it would break both reflection (parity, P) symmetry and time-reversal (T) symmetry, a clear signature of which would be the spontaneous appearance of a macroscopic magnetization at the superconducting transition temperature. Broken T symmetry has been reported, but searches for the effects of combined P and T symmetry breaking have so far yielded null results. Here we report the observation of a weak (approximately 10(-5) gauss) magnetic field that appears spontaneously at the superconducting transition temperature of epitaxial thin films of YBa2Cu3O(7-delta). The magnetic signal originates near the edges of the samples. One interpretation for this observation is that the order parameter carries an intrinsic angular momentum, related to the breaking of P and T symmetries, but other possibilities cannot yet be excluded.     

Genetical effects of radiation and chemicals

Zusammenfassung Die populären Auffassungen der durch Bestrahlung erzeugten genetischen Schädigungen irren gewöhnlich weit vom Ziele, und zwar in entgegengesetzten Richtungen. Oft hört man die Behauptung, dass bestrahlte Eltern die Gefahr laufen, Missgeburten oder sonstwie anormale Nachkommen zu haben. Noch öfter werden die genetischen Gefahren ionisierender Strahlen als unbeträchtlich und nicht beachtenswert hingestellt. In Wirklichkeit sind diese Gefahren sehr ernst zu nehmen. Sie betreffen aber nicht Individuen, sondern die menschliche Rasse als Ganzes. Über ihre Natur sind wir gut unterrichtet, über ihr Ausmass können wir uns gegenwärtig nur sehr ungenaue Vorstellungen machen. Genetisch unterschwellige Strahlungsdosen gibt es nicht; die gesetzlich festgesetzte Toleranzdosis muss daher einen Kompromiss darstellen zwischen gegenwärtigem Nutzen und zukünftigen Gefahren.     

Dopamine neurons derived from embryonic stem cells function in an animal model of Parkinson's disease

Parkinson's disease is a widespread condition caused by the loss of midbrain neurons that synthesize the neurotransmitter dopamine. Cells derived from the fetal midbrain can modify the course of the disease, but they are an inadequate source of dopamine-synthesizing neurons because their ability to generate these neurons is unstable. In contrast, embryonic stem (ES) cells proliferate extensively and can generate dopamine neurons. If ES cells are to become the basis for cell therapies, we must develop methods of enriching for the cell of interest and demonstrate that these cells show functions that will assist in treating the disease. Here we show that a highly enriched population of midbrain neural stem cells can be derived from mouse ES cells. The dopamine neurons generated by these stem cells show electrophysiological and behavioural properties expected of neurons from the midbrain. Our results encourage the use of ES cells in cell-replacement therapy for Parkinson's disease.