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19篇 您的检索式:作者名="Amany N"
    题名 作者 年代 出处 被引量
1Effect of blend levels on composite wheat doughs performance made from yam and cassava native starches and bread quality显示文摘Nindjin C Amani G N Sindic M 2011Carbohydrate Polymers2011,86,4:1
2Solvent-free and selective oxidation of hydroxy groups to their corre-sponding carbonyl functions with ferric nitrate activated by heteropoly acids显示文摘 Iranpoor N Amani K 2003Synthesis2003,,3:1
3Stability of yam starch gels during processing显示文摘AMANI N G KAMENAN A ROLLAND-SABATE A 2005African Journal of Biotechnology2005,4,1:1
4Effect of HEMADO on Level of CKMB and LDH Enzymes after Ischemia/Reperfusion In- jury in Isolated Rat Heart 显示文摘Amani M Jeddi S Ahmadiasl N 2013Bioimpacts2013,3,2:1
5Pleiotropic effects of miR-183 - 95 - 182 converge to regulate cell survival,proliferation and migration in medullo- blastoma 显示文摘Weeraratne SD Amani V Teider N Pierre-Francois J Winter D Kye M J 2012Acta Neuropathol2012,123,4:1
6Effect of HEMADO on level of CK-MB and LDH enzymes after ischemia/reperfusion injury in isolated rat heart显示文摘Amani M Jeddi S Ahmadiasi N 2013Bioimpacts2013,3,2:1
7Pleiotropic effects of miR-183-96-182 converge to regulate cell survival, proliferation and migration in medulloblastoma 显示文摘Weeraratne SD Amani V Teider N 2012Aeta Neuropathol2012,123,4:1
8Solvent-Free and Selective Oxidation of Hydroxy Groups to their Corresponding Carbonyl Functions with Ferric Nitrate Activated by Heteropoly Acids 显示文摘Firouzabadi H Iranpoor N Amani K 2003Synthesis2003,3,:1
9Effect of HEMADO onlevel of CKMB and LDH Enzymes after Ischemia/Reperfusion Inju-ry in Isolated Rat Heart 显示文摘Amani M Jeddi S Ahmadiasl N 2013Bioimpacts2013,3,2:1
10β-Tricalcium Phosphate Promotes Cell Proliferation,Osteogenesis and Bone Regeneration in Intrabony Defects in Dogs显示文摘Amany N Abeer G Amira M 2009Archives of Oral Biology2009,54,12:1
11Nutritional related eardiovascular risk factors in patients with coronary artery disease in lran: a ease-control study显示文摘Amani R Noorizadeh N Rahmanian S 2010Nutr J2010,9,1:1
12Agency costs, ownership structure, and corporate governance in preand post-ipo firms 显示文摘Wallance N D Amani K B Singh M 2006Corporate Ownership and Control2006,3,3:1
13Effect of oleozon on healing of exposed pulp tissues显示文摘Rania S M Amany N Ahmed E H - 2011Journal of American Science2011,7,5:1
14Polyoxygenated flavonoids from Eugenia edulis显示文摘SAHAR A M H AMANI N M H MOHAMMED A S 2003Phytochemistry2003,64,4:1
15Effect of HEMADO on level of CK-MB and LDH enzymes after ischemia/reperfusion injury in isolated rat heart显示文摘AMANI M JEDDI S AHMADIASL N 2013Bioimpacts2013,3,2:1
16Centrifugal osmotic dehydration and rehydration of carrot tissue pre-treated by pulsed electric field 显示文摘Amani E Fersi A Khezami L Kechaou N 2007Food Science and Technology2007,40,7:1
17Does vitamin D im- prove liver enzymes, oxidative stress, and inflammatory biomarkers in adults with non-alcoholic fatty liver disease? A randomized clinical trial 显示文摘Sharifi N Amani R Hajiani E 2014Endocrine2014,47,:1
18Effect of HEMADO on Level of CK-MB and LDH Enzymes after Ischemia/Reperfusion Injury in Isolated Rat Heart显示文摘Amani M Jeddi S Ahmadiasl N 2013Bioimpacts2013,3,2:1
19Effects of low intensity laser irradiation phototherapy on dental pulp constructs显示文摘AIM: To investigate low intensity laser irradiation phototherapy(LILIP) on the proliferation, mineralization and degradation of dental pulp constructs.METHODS: Stem cells from human exfoliated deciduous teeth(SHED) were grown to confluence and seeded on collagen scaffolds to create dental pulp constructs. LILIP was delivered to the dental pulp constructs using an 830 nm GaA IAs laser at an output power of 20 m W. The LILIP energy density was 0.4, 0.8, 1.2, and 2.4 J/cm2. After 8 d, the cell proliferation and degradation within the dental pulp constructs were measured using histologic criteria. After 28 d, the effect of LILIP on SHED mineralization was assessed by von Kossa staining.RESULTS: SHED proliferation within the dental pulp constructs varied after exposure to the 0.4, 0.8, 1.2,and 2.4 J/cm2 LILIP energy densities(P < 0.05). The maximum proliferation of SHED in nutrient deficient media was 218% after exposure to a 1.2 J/cm2 LILIP energy density. SHED grown in nutrient deficient media after exposure to a 0.4, 0.8, and 1.2 J/cm2 LILIP energy density, proliferated by 167-218% compared to the untreated(non-LILIP) control group(P < 0.05).SHED exposed to a 0.4, 0.8, and 1.2 J/cm2 LILIP energy density, and grown in optimal nutritional conditions and proliferated by 147%-164% compared to the untreated(non-LILIP) control group(P < 0.05). The exposure of SHED to the highest LILIP energy density(2.4 J/cm2) caused a reduction of the cell proliferation of up to 73% of the untreated(non-LILIP) control(P < 0.05). The amount of mineral produced by SHED increased over time up to 28 d(P < 0.05). The 0.8 and 1.2J/cm2 LILIP energy densities were the most effective at stimulating the increased the mineralization of the SHED from 150%-700% compared to untreated(nonLILIP) control over 28 d(P < 0.05). The degradation of dental pulp constructs was affected by LILIP(P <0.05). The dental pulp constructs grown in optimal nutritional conditions exposed to a 0.8 J/cm2 or 1.2 J/cm2 LILIP energy density had 13% to 16% more degradation than the untreated(non-LILIP) control groups(P < 0.05). The other LILIP energy densities caused a 1%degradation of dental pulp constructs in optimal nutritional conditions(P > 0.05).CONCLUSION: LILIP can enhance or reduce SHED proliferation, degradation and mineralization within dental pulp constructs. LILIP could promote the healing and regeneration of dental tissues.Amr M Elnaghy Peter E Murray Paul Bradley Melissa Marchesan Kenneth N Namerow Amany E Badr Youssry M El-Hawary Farid A Badria 2013World Journal of Stomatology2013,2,1:0
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