Zobrazeno 1 - 10
of 37
pro vyhledávání: '"S. H. El Ashry"'
Publikováno v:
BMC Oral Health, Vol 20, Iss 1, Pp 1-12 (2020)
Abstract Background This study evaluated the marginal adaptation, solubility and biocompatibility of TheraCal LC compared with mineral trioxide aggregate (MTA-Angelus) and Biodentine when used as a furcation perforation repair material. Methods The m
Externí odkaz:
https://doaj.org/article/19cc7524d20e4caebfc18ec44b74f27b
Publikováno v:
BMC Oral Health, Vol 19, Iss 1, Pp 1-12 (2019)
Abstract Background This study evaluated the antibacterial efficiency and ability of propolis to promote regeneration of immature permanent non-vital dogs’ teeth. Methods Ninety six immature permanent premolars teeth in 6 mongrel dogs were divided
Externí odkaz:
https://doaj.org/article/a3d68fad1a794d9d8793d05136c252d4
Autor:
A. H. Shobier, E. S. H. El Ashry
Publikováno v:
Russian Journal of Marine Biology. 47:425-439
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e8a1ae64c699ae3746abab253885a24
https://doi.org/10.1134/s1063074021060122
https://doi.org/10.1134/s1063074021060122
Publikováno v:
ARKIVOC, Vol 2007, Iss 7, Pp 30-40 (2006)
Externí odkaz:
https://doaj.org/article/7db040f8f4ad43c8a59ad7ec4b6887c1
Autor:
Doaa A. Ghareeb, E. S. H. El Ashry, Nihad Abdel-Monem, Ahmed M. Abdel-Azeem, Asmaa Nabil-Adam
Publikováno v:
Open Journal of Medicinal Chemistry. :60-73
Marine derived fungi are considered as a promising source of novel drugs due to their biodiversity and consequent chemo-diversity. Although marine microorganisms especially fungi are not well defined taxonomically, making this a promising frontier fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb4a321720dadc118360b3d2f7832107
https://doi.org/10.4236/ojmc.2013.33009
https://doi.org/10.4236/ojmc.2013.33009
Autor:
Ibrahim M. Abdou, Hassan A. El-Sayed, Abd El‐Fattah Z. Haikal, Ahmed H. Moustafa, E. S. H. El‐Ashry
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 27:1061-1071
Reaction of ethyl 4-thioxo-3,4-dihydropyrimidine-5-carboxylate derivatives 1a,b and ethyl 4-oxo-3,4-dihydropyrimidine-5-carboxylate 1c with 2,3,4,6-tetra-O-acetyl-alpha-D-glucopyranosyl bromide in KOH or TEA afforded ethyl 2-aryl-4-(2',3',4',6'-tetra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f3c230ba25d3304c26fa55cb169ce20
https://doi.org/10.1080/15257770802271805
https://doi.org/10.1080/15257770802271805
Autor:
E. S. H. El-Ashry, M.E. El-Rafey, H.H. Abou-Elnaga, W.M.A. Bakry, M.H. El-Nagdi, Y.M. Boghdady
Publikováno v:
Lubrication Science. 18:109-118
Evaluation of a number of benzotriazole derivatives as antioxidants for turbine oils was carried out by formulating different blends of turbine oil with viscosity grade ISO 46 with different dosages of the synthesized compounds. Oxidation tests were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8707ee1cad1cc649936835c2eb5633c
https://doi.org/10.1002/ls.10
https://doi.org/10.1002/ls.10
Autor:
E. S. H. EL ASHRY, Y. EL KILANY
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6580a8523d358deb92e266267a740a29
https://doi.org/10.1002/chin.199720271
https://doi.org/10.1002/chin.199720271
Autor:
S. A. F. El Sayed, Adel Amer, E. S. H. El Ashry, M. M. Abdel‐Rahman, M. Badawi, A. M. El Massry
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::025c24bb601bb7736d90687716ef0c5e
https://doi.org/10.1002/chin.199721048
https://doi.org/10.1002/chin.199721048
Publikováno v:
ChemInform. 40
Reaction of 5,6-diphenylpyridazin-3(2H)-one 1a,b with 2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl bromide 2 in K(2)CO(3)/acetone gave 5,6-diphenyl-N(2)-(2',3',4',6'-tetra-O-acetyl-beta-D-glucopyranosyl)pyridazin-3-one 5a,b. The same nucleosides 5a,b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e59a4f5337c95c8e9587849d44c86a3d
https://doi.org/10.1002/chin.200940200
https://doi.org/10.1002/chin.200940200