Proposed explanations of galactic rotation curves (RC = tangential velocity vs.equatorial radius, determined from Doppler measurements) involve dramatically different assumptions.A dominant, original camp invoked huge amounts of unknown, non-baryonic dark matter (NBDM) in surrounding haloes to reconcile RC simulated using their Newtonian orbital mo
Design of dispatching management system of mine-used locomotives
In view of problems of low efficiency of material transportation, safety hazards of potential safety of personnel and locomotive coexistence in incline roadway, and not fused linkage control system of winch existed in dispatching management system of vehicle, a novel dispatching management system of mine-used locomotives was designed.The dispatchin
Epigenetic signatures associated with different levels of differentiation potential in human stem cells.
BackgroundThe therapeutic use of multipotent stem cells depends on their differentiation potential, which has been shown to be variable for different populations.These differences are likely to be the result of key changes in their epigenetic profiles.Methodology/principal findingsto address this issue, we have investigated the levels of epigenetic
Conduction band offset-dependent induced threshold voltage shifts in a-InGaZnO TFTs under positive bias illumination stress
In this paper, the dependence of threshold voltage (Vth) changes to amorphous-indium gallium zinc oxide (a-IGZO) thin film transistors (TFTs) under positive bias light illumination (PBIS) on the height of the conduction band offset was studied.Using SiO2, HfO2, and Al2O3 as gate dielectrics, three different types of a-IGZO TFTs were used in the exp
Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsia
Abstract Background Autosomal recessive non-syndromic hearing loss (NSHL) and cone dystrophies (CODs) are highly genetically and phenotypically heterogeneous disorders.In this study, we applied the whole exome sequencing (WES) to find the cause of HL and COD in an Iranian consanguineous family with three affected individuals.Methods Three members f