Abou-Seri, S. M., N. A. Farag, and G. S. Hassan,
"Novel Diphenylamine 2,4-Dicarboxamide Based Azoles as Potential Epidermal Growth Factor Receptor Inhibitors: Synthesis and Biological Activity",
Chem. Pharm. Bull. , vol. 59, issue 9, pp. 1124—1132, 2011.
Abou-Seri, S. M., N. A. Farag, and G. S. Hassan,
"Novel Diphenylamine 2,4′-Dicarboxamide Based Azoles as Potential Epidermal Growth Factor Receptor Inhibitors: Synthesis and Biological Activity",
Chem. Pharm. Bull.,, vol. 59, issue 9, pp. 1124-1132, 2011.
Mostafa, H., M. Anis, and M. Elmasry,
"A Novel Low Area Overhead Direct Adaptive Body Bias (D-ABB) Circuit for Die-to-Die and Within-Die Variations Compensation",
Very Large Scale Integration (VLSI) Systems, IEEE Transactions on, vol. 19, no. 10: IEEE, pp. 1848–1860, 2011.
Abstract
Kassem, N., A. A. Hamid, T. Attia, S. Baathallah, S. Mahmoud, Moemen, E, E. Safwat, Khala, f M, and O. r Shake,
"Novel mutations of the nucleophosmin (NPM-1) gene in Egyptian patients with acute myeloid leukemia: a pilot study.",
Egypt Natl Canc Inst., vol. 23, issue 2, pp. 73-8, 2011.
Abdel-Ghani, N. T., and A. M. Mansour,
"Novel Pd(II) and Pt(II) complexes of N,N-donor benzimidazole ligand: Synthesis, spectral, electrochemical, DFT studies and evaluation of biological activity",
Inorganica Chimica Acta, vol. 373, pp. 249-258, 2011.
Gaber, H. M., M. C. Bagley, S. M. Sherif, and M. A. Sayed,
"Novel phenylazo derivatives of condensed and uncondensed thiophene. Synthesis, characterization and antimicrobial studies",
Zeitschrift für Naturforschung B., vol. 66, issue b, pp. 585-596, 2011.
Shams, H. Z., R. M. Mohareb, M. H. Helal, and A. E. Mahmoud,
"Novel Synthesis and Antitumor Evaluation of Polyfunctionally Substituted Heterocyclic Compounds Derived from 2-Cyano-N-(3-cyano-4,5,6,7-tetrahydro-benzo[b]thiophen-2-yl)-acetamide ",
Molecules , vol. 16, pp. 52-73, 2011.
R. M. Mohareb, and A. A. El-Khair,
"Novel Synthesis of Hydrazide-Hydrazone and their uses for the synthesis of 1,3,4-oxadiazine, 1,2,4-triazine , pyrazole and pyridazine derivatives with antimicrobial and antifungal activities",
International Journal of Applied and Pharmaceutical Technology, vol. 2, pp. 435-446, 2011.
Mohareb, R. M., D. H. Fleita, and O. K. Sakka,
"Novel Synthesis of Hydrazide-Hydrazone Derivatives and TheirUtilization in the Synthesis of Coumarin, Pyridine, Thiazole and Thiophene Derivatives with Antitumor Activity",
Molecules, vol. 16, pp. 16-27, 2011.
Abdelrazek, F. M., A. A. Fadda, and A. N. Elsayed,
"A Novel Synthesis of Some New Pyridazine and Pyridazino[4,5-d]Pyridazine Derivatives.",
Synthetic Communications, vol. 41, issue ---, pp. 1119-1126, 2011.
Mostafa, H., M. Anis, and M. Elmasry,
"Novel timing yield improvement circuits for high-performance low-power wide fan-in dynamic OR gates",
Circuits and Systems I: Regular Papers, IEEE Transactions on, vol. 58, no. 8: IEEE, pp. 1785–1797, 2011.
Abstract
Abu-Ibrahim, B.,
"Nucleus-nucleus total reaction cross sections, and the nuclear interaction radius",
Physical Review C, vol. 83, pp. 044615, 2011.
AbstractWe study the nucleus-nucleus total reaction cross sections for stable nuclei, in the energy region from 30A MeV to about 1A GeV, and find them to be in proportion to (σ tot pp Z 2/3 1 +σ tot pn N 2/3 1 − − − − − − − − − − − − − − − √ +σ tot pp Z 2/3 2 +σ tot pn N 2/3 2 − − − − − − − − − − − − − − − √ ) 2 in the mass range 8 to 100. Also, we find a parameter-free relation that enables us to predict a total reaction cross section for any nucleus-nucleus within 10% uncertainty at most, using the experimental value of the total reaction cross section of a given nucleus-nucleus. The power of the relation is demonstrated by several examples. The energy dependence of the nuclear interaction radius is deduced; it is found to be almost constant in the energy range from about 200A MeV to about 1A GeV; in this energy range and for nuclei with N=Z , R I (A)=(1.14±0.02)A 1/3 fm.
]