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K. English, French, Korean, Simplified Chinese (Mandarin), Lithuanian, Italian, and European Portuguese. All of them reported validity, reliability, and translation method. Discussion and Conclusions High reliability and validity between various language versions of the SHI were identified. The current scoping review provides a useful summary and could be a helpful precursor to a systematic review on SHI in the future. Supplemental Material https//doi.org/10.23641/asha.14082704.Purpose Although tinnitus is highly prevalent among patients receiving audiology services, the extent to which most audiologists are trained in tinnitus management is not well documented. The extent and type of instruction in tinnitus clinical care provided by audiology graduate (AuD) programs is not clear, nor is it known whether training programs are consistent in their recommendations. It is certainly true that widely accepted standards do not exist to ensure that all tinnitus clinical services are supported by adequate scientific evidence, which may result in unsatisfactory outcomes and unnecessary expense for patients. The purpose of this clinical focus article is to describe the results of an informal survey of AuD programs to determine their level of training for tinnitus management. Method A short survey was sent to all 75 American Speech-Language-Hearing Association-accredited AuD programs to assess the extent and type of tinnitus training their students receive. Conclusions The 32 AuD programs that responded to our survey provide tinnitus training using a variety of settings and methods. Further research could explore in more detail the extent of training in specific methods provided by these programs, and aim to elicit responses from a greater number of programs and from the students themselves.Cationic surfactant mixed with fatty alcohol as cosurfactant in excess water can form stable emulsions, known as "lamellar gel networks," that contain extended and interconnected networks of swollen bilayers, including ones with in-plane liquidlike disorder (Lα phase) and solidlike order (Lβ phase). To study their structure and thermodynamics, molecular dynamics (MD) simulations with lateral pressure and temperature scans along reversible pathways were used to drive reversible phase changes, including formation at negative lateral pressure of the LβI phase with interdigitated tails of opposing leaflets. Thermodynamic integration, with extrapolations to infinitely slow scans, yielded a free energy difference between the interdigitated LβI and non-interdigitated Lβ phases of 2.4 ± 0.5 kJ/mol, which is consistent with the spontaneous formation of the Lβ phase under atmospheric pressure in simulation. Thermodynamic cycles involving temperature and lateral pressure for which the free energy difference is identically zero were constructed as negative controls to verify the method. Using lateral pressure, including negative lateral pressure, helps avoid kinetic bottlenecks that occur when temperature alone is used as the control variable. The method, using negative lateral pressure, should be widely applicable to other bilayers to identify molecular properties that control interdigitation and other bilayer properties.Colloidal nanoparticles with anisotropic interactions are promising building blocks for the fabrication of complex functional materials. A challenge in the self-assembly of colloidal particles is the rational design of geometry and chemistry to program the formation of a desired target structure. We report an inverse design procedure integrating Langevin dynamics simulations and evolutionary algorithms to engineer anisotropic patchy colloidal clusters to spontaneously assemble into a cubic diamond lattice possessing a complete photonic band gap. The combination of a tetrahedral cluster geometry and optimized placement of a single type of anisotropic interaction patch results in a colloidal building block predicted to assemble a cubic diamond lattice with more than 82% yield. This design represents an experimentally viable colloidal building block capable of high-fidelity assembly of a cubic diamond lattice.The ESKAPE pathogens (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter cloacae) represent clinically important bacterial species that are responsible for most hospital-acquired drug-resistant infections; hence, the need for rapid identification is of high importance. Previous work has demonstrated the suitability of liquid extraction surface analysis mass spectrometry (LESA MS) for the direct analysis of colonies of two of the ESKAPE pathogens (Staphylococcus aureus and Pseudomonas aeruginosa) growing on agar. Here, we apply LESA MS to the remaining four ESKAPE species (E. faecium E745, K. pneumoniae KP257, A. baumannii AYE, and E. cloacae S11) as well as E. faecalis V583 (a close relative of E. faecium) and a clinical isolate of A. baumannii AC02 using an optimized solvent sampling system. Metformin In each case, top-down LESA MS/MS was employed for protein identification. In total, 24 proteins were identified from 37 MS/MS spectra by searching against protein databases for the individual species. The MS/MS spectra for the identified proteins were subsequently searched against multiple databases from multiple species in an automated data analysis workflow with a view to determining the accuracy of identification of unknowns. Out of 24 proteins, 19 were correctly assigned at the protein and species level, corresponding to an identification success rate of 79%.Two monoclinic polymorphs of [Ag(NH3)2]MnO4 containing a unique coordination mode of permanganate ions were prepared, and the high-temperature polymorph was used as a precursor to synthesize pure AgMnO2. The hydrogen bonds between the permanganate ions and the hydrogen atoms of ammonia were detected by IR spectroscopy and single-crystal X-ray diffraction. Under thermal decomposition, these hydrogen bonds induced a solid-phase quasi-intramolecular redox reaction between the [Ag(NH3)2]+ cation and MnO4 - anion even before losing the ammonia ligand or permanganate oxygen atom. The polymorphs decomposed into finely dispersed elementary silver, amorphous MnO x compounds, and H2O, N2 and NO gases. Annealing the primary decomposition product at 573 K, the metallic silver reacted with the manganese oxides and resulted in the formation of amorphous silver manganese oxides, which started to crystallize only at 773 K and completely transformed into AgMnO2 at 873 K.