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In this study the most stable isobar for some isobaric families (light and intermediate ) nuclei with mass number (A) equals to (15-30) & (101- 115) have been determined. This determination of stable nuclide can help to determine the suitable nuclide, which can be used in different fields. Most stable isobar can be determined by two means. First: plot mass parabolas (plotting the binding energy (B.E) as a function of the atomic number (Z)) for these isobaric families, in this method most stable isobars represent the lowest point in mass parabola (the nuclide with the highest value of binding energy). Second: calculated the atomic number for most stable isobar (ZA) value. Our results show that there is only one stable nuclide for isobars with odd mass number (A) (one mass parabolas), while for nuclides with an even mass number (A) there is more than one stable nuclide (two mass parabola). Also, our results show that nuclides representing the most stable isobars in the two methods, which used in this study practically, are the same nuclide.

A theoretical calculation of the binding and excitation energies have been used at low – lying energies based on shell model and quantum theory. In this model, we evaluated the energies under assume Ni 28 56 30 as inert core with two nucleon extra, nucleons in the 2P3/2 , 1f 5/2 and 2P1/2 configuration. Modified Surface Delta Interaction (MSDI) and Reid's Potential (RP) theory for two body matrix elements are evaluated by using a Matlab program to calculate the energies of experimental and Reid single particle energies. Our results of the theoretical calculation have been compared with the experimental results, which show no good agreement with the experiment but have a good agreement with the theoretical studies of Non Zero Pairing Shell Model (NZPSM) and Energy Spectra Method (ESM).

This research introduced the derivation of mathematical equations to calculate the Cartesian and geographical coordinates of a site situated at a far distance from the observer position by using GPS data. The geographical coordinates (ϕobs., λ obs., hobs.) for observer position were transformed to Cartesian coordinates (X obs., Y obs., Z obs.) of observer position itself. Then the Cartesian coordinates of unknown position mathematically were calculated from these calculated equations, and its transformed to geographical coordinates of (ϕunk., λunk.) position.

This study deals with the measurement of the specific activity radiation for beryllium -7 isotope in Baghdad city for samples of surface soils, by using gamma ray spectrometer technique. Twenty one samples were collected from surface soil of Baghdad city from Risafa and Karkh sides, (7) samples from Risafa side and(14) samples from Karkh side, where the axis for locations which are fixed by using (G.P.S.) . Gamma-ray spectrometry system (DSA 2000) with high purity germanium detector was used, which has (50%) efficiency and resolution of (2.2 keV) at gamma line (1332 keV) of 60Co source. The specific activity values for beryllium -7 isotope in surface soil of Risafa and Karkh sides, ranged between (B.D.L.- 32.827  6.636) Bq/kg for Risafa soil , and (B.D.L.-23.660  3.703) Bq/kg for Karkh soil. While the average of beryllium -7 isotope in surface soil of Baghdad city from Risafa and Karkh sides would be (32.827±6.636) Bq/kg & (23.660±3.703) respectively. The results showed that the most samples have a specific activity for beryllium -7 isotope which is higher than that for normal limits of international levels because of falls of atmosphere dust resulting from sun reactions.

Abstract Delivering genes to and across the brain vasculature efficiently and specifically across species remains a critical challenge for addressing neurological diseases. We have evolved adeno-associated virus (AAV9) capsids into vectors that transduce brain endothelial cells specifically and efficiently following systemic administration in wild-type mice with diverse genetic backgrounds, and in rats. These AAVs also exhibit superior transduction of the CNS across non-human primates (marmosets and rhesus macaques), and in ex vivo human brain slices, although the endothelial tropism is not conserved across species. The capsid modifications translate from AAV9 to other serotypes such as AAV1 and AAV-DJ, enabling serotype switching for sequential AAV administration in mice. We demonstrate that the endothelial-specific mouse capsids can be used to genetically engineer the blood-brain barrier by transforming the mouse brain vasculature into a functional biofactory. We apply this approach to Hevin knockout mice, where AAV-X1-mediated ectopic expression of the synaptogenic protein Sparcl1/Hevin in brain endothelial cells rescued synaptic deficits.