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| 1 | Protective role of aqueous turmeric extract against mutagenicity of direct-acting carcinogens as well as Benzo[a]pyrene-induced genotoxicity and carcinogenicity显示文摘 | M. A. Azuine J. J. Kayal S. V. Bhide | 1992 | Journal of Cancer Research and Clinical Oncology1992，，6： | 1 |
| 2 | Protective role of aqueous turmeric extract against mutagenicity of direct-acting carcinogens as well as benzo pyrene-induced genotoxicity and carcinogenicity显示文摘 | Kayal J J Bhide S V | 1992 | J Cancer Res Clin Oncol1992，118，6： | 1 |
| 3 | Chemopreventive effect of turmeric against stomach and skin tumors induced by chemical carcinogens in Swiss mice显示文摘 | AZUINE M A BHIDE S V | 1992 | Nutr Cancer1992，17，1： | 1 |
| 4 | Protective role of aqueous turmeric extract against mutagenicity of direct-acting carcinogens as well as Benzo[a]pyrene-induced genotoxicity and carcinogenicity显示文摘 | M. A. Azuine J. J. Kayal S. V. Bhide | 1992 | Journal of Cancer Research and Clinical Oncology1992，，6： | 1 |
| 5 | Protective role of aqueous turmeric extract against mutagenicity of directacting carcinogens as well as B (a) Pyrene2 induced geno toxicity and carcinogenicity显示文摘 | KAYAL J | 1992 | Cancer Res Clin Oncol1992，118，3： | 1 |
| 6 | Chemopre- vention of DMBA-induced UV-B promoted, NOR-l-lnduced TPA promoted skin carcinogenesis, and DEN-induced phenobarbital promoted liver tumors in mice by extract of beetroot 显示文摘 | KAPADIA G J AZUINE M A SRIDHAR R | 2003 | Phar- rnacol Res2003，47，2： | 1 |
| 7 | Chemo- preventive effect of resveratrol, sesamol, sesame oil and sunflower oil in the Epstein-Barr virus early antigen activation assay and the mouse skin two-stage car- cinogenesis 显示文摘 | Kapadia G J Azuine MA Tokuda H | 2002 | Pharmacol Res2002，45，6： | 1 |
| 8 | Chemopreventive effect of resveratrol,sesanol,sesame oil and sun llower oil in the Epstein-barr virus early antigen activation assay and the mouse skin two-stage carcinogenesis显示文摘 | Kapadia GJ Azuine MA Tokuda H | 2002 | Pharmacol Res2002，45，6： | 1 |
| 9 | Chemopreventive effect of resveratrol, sesamol, sesame oil and sunflower oil in the Epstein-Barr virus early antigen activation assay and the mouse skin two-stage carcinogenesis显示文摘 | Kapadia G J Azuine M A Tokuda H | 2002 | Pharmacol Res2002，45，6： | 1 |
| 10 | Aminonaphthoqainones-a novel class of compounds with potent antimalarial activity against plasmodium falciparum 显示文摘 | KAPADIA G J AZUINE M A BALASUBRAMANIAN V | 2001 | Pharmacological Research2001，43，4： | 1 |
| 11 | Chemopreventive effect of resvemtrol, sesamol, sesame oil and sunflower oil in the Epstein-Barr virus early antigen activation assay and the mouses kin two-stage carcinogenesis显示文摘 | KAPADIA GJ AZUINE MA TOKUDA H | 2002 | Pharmacol Res2002，45，6： | 1 |
| 12 | Protective role of aqueous turmeric extract against mutagenicity of direct-acting carcinogens as well as Benzo I-al py- rene-induced genotoxicity and carcinogenicity 显示文摘 | AZUINE M A KAYAL J J BHIDE S V | 1992 | Journal Cancer Res Clin Oncol1992，118，6： | 1 |
| 13 | Chemopreventive effect of resveratrol, sesamol, sesame oil and sunflower oil in the Epstein-Barr virus early antigen activation assay and the mouse skin two-stage carcinogenesis 显示文摘 | Kapadia GJ Azuine MA Tokuda H | 2002 | Pharmacol Res2002，45，6： | 1 |
| 14 | Chemoprevention of Dmba - Induced Uv - B Promoted, nor - 1 - Induced Tpa Promo- ted Skin Carcinogenesis, and Den - Induced Phenobarbital Promo- ted Liver Tumors in Mice by Extract of Beetroot显示文摘 | Kapadia G J Azuine M A Sridhar R | 2003 | Pharmacolog- ical Research2003，47，2： | 1 |
| 15 | 查看详情显示文摘 | azuin CGandEisenerg A | | 0，，： | 1 |
| 16 | Aminonaphthoquinones-A novel class of compounds with potent antimalarial activity against plasmodium falciparum显示文摘 | KAPADIA G J AZUINE M A BALASUBRAMANIAN V | | 0，，04： | 1 |
| 17 | Establishment of Human Neuroblastoma Cell-Line (SK-N-SH) as an In Vitro Model of Morphine Addiction显示文摘Morphine is a schedule II-controlled substance that used to allow the diminution of intra-operative, post-operative orchronic pain. However, its usage is limited due to addiction and overdose liabilities. Morphine was observed to cause tolerance,dependence and withdrawal in human. Justification: to date lack of scientific evidence of morphine addiction was carried out byusing specific single human neuroblastoma cell-line (SK-N-SH). Therefore, this study was performed to establish the morphineaddiction model in this cell line. The cells were exposed to morphine for 24 hrs before treatment with methadone, as ananti-withdrawal drug for subsequence 24 hours. The cytosolic fraction of the cell was used in different objectives including receptoraffinity, withdrawal properties, endocytic machinery, desensitisation or internalisation and cellular adaptation. The result shows thatmorphine and methadone bind to the μ-opioid receptor. The morphine-treated cells were observed to increase the expression ofaddiction markers, have a low rate of the endocytic machinery, cause desensitisation of receptor and reduce cellular adaptation.Those changes by morphine were normalised by the treatment of methadone. As a whole, it is postulated that neuroblastoma cell line,SK-N-SH, can be used as an in-vitro model to demonstrate morphine addiction before animal and human testing. | Noor Azuin Suliman Noor Azlina Abu Bakar Mohamad Aris Mohd Moklas Che Norma Mat Taib | 2021 | Journal of Pharmacy and Pharmacology2021，9，3： | 0 |
| 18 | Sedative, Cognitive Impairment and Anxiolytic Effects of Acute Mitragyna Speciosa in Rodents显示文摘 | Mohamad Aris Mohd Moklas Noor Azuin Suliman Che Norma Mat Taib Mohamad Taufik HidayatBaharuldin Sharida Fakurazi Fatin Nadzirah Zakaria Muhammad Khairulasraf Muhamamd Yusof Muhammad Farhan Adzhar Mohd Saifuddin Md Rasul Abdah Md Akim Zulkhairi Amom | 2013 | Journal of US-China Medical Science2013，10，1： | 0 |
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