Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Syed Qaiser Shah"'
Publikováno v:
Bangladesh Journal of Pharmacology, Vol 8, Iss 2 (2013)
The present study was undertaken to evaluate the anti microbial properties of Berberis jaeschkeana Schneid Var. jaeschkeana for the first time. The screening of B. jaeschkeana for its phytochemical constituents showed the presence of alkaloids, glyco
Externí odkaz:
https://doaj.org/article/427073f205514d00b96d2fda76164bfd
Autor:
Martha Sahylí Ortega, Pijeira, Alan Silva, de Menezes, Pierre Basílio Almeida, Fechine, Syed Qaiser, Shah, Derya, Ilem-Ozdemir, Elvis O, López, Juliana Terzi, Maricato, Daniela Santoro, Rosa, Eduardo, Ricci-Junior, Severino Alves, Junior, Luciana Magalhães Rebelo, Alencar, Ralph, Santos-Oliveira
Publikováno v:
European Journal of Pharmaceutics and Biopharmaceutics. 180:91-100
The use of graphene quantum dots as biomedical devices and drug delivery systems has been increasing. The nano-platform of pure carbon has shown unique properties and is approved to be safe for human use. In this study, we successfully produced and c
Autor:
Syed Qaiser Shah, Gul-e Raana
Publikováno v:
Radiochimica Acta. 109:905-913
The aim of this study was to investigate labeling of nimotuzumab (h-R3) with 111In using p-SCN-Bn-DTPA as bifunctional chelate, evaluate its targeting potential against SK-LU-1, H226, H650, H661, and HCC4006 non-small cell lung carcinoma (NSCLC) cell
Autor:
Muhammad Sadiq Aziz, Aziz-ul-Hasan Aamir, Ajab Khan, Zahid Khan, Syed Qaiser Shah, Sher Zaman Safi, Kalaivani Batumalaie, Hussah M. Alobaid, Abid Ali, Muhammad Imran
Publikováno v:
Genes; Volume 13; Issue 9; Pages: 1532
Objective: The objective was to study the association of Klotho gene G395A and C1818T single nucleotide polymorphisms with glycemia, serum, glycosylated hemoglobin (HbA1c) level and the risk of type 2 diabetes mellitus (T2DM) in the Pashtun populatio
Autor:
Syed Qaiser Shah, Bibi Faiza
Publikováno v:
Journal of Radioanalytical and Nuclear Chemistry. 325:147-154
In this study bevacizumab was labeled with 99mTc using p-SCN-Bzl-TCMC as a chelator for non invasive imaging of VEGF receptor in ovarian tumor Sprague Dawley rat and New Zealand rabbit models. High radiochemical purity and stability were observed usi
Autor:
Gul-e-Raana, Syed Qaiser Shah
Publikováno v:
Radiochimica Acta. 108:305-313
To assess the suitability of 99mTc labeled 5α-reductase (5α-Rds) inhibitors for non-invasive targeting of prostate cancer (PCa) using Male Sprague Dawely Rat (MSDR) model. In this work, dutasteride (Cpd-1) a 5α-Rds inhibitor was derivatized to its
Autor:
Syed Qaiser Shah, N. Ullah
Publikováno v:
Radiochemistry. 61:233-237
99mTc-ethambutol was preclinically evaluated as an alternative diagnostic tuberculosis agent. Its radiochemical purity, stability in saline and serum, in vitro Mycobacterium tuberculosis (MBT) binding, and biodistribution in mice were studied, and ta
Autor:
Gul-e-Raana, Syed Qaiser Shah
Publikováno v:
Molecular Biology Reports. 46:1675-1682
To assess the preclinical potential of technetium-99m labelled conjugated para-isothiocyanato-benzyl diethylene triamine penta-acetic acid cetuximab (99mTc-p-SCN-Bzl-DTPA cetuximab) for imaging EGFR in HNSCC mice and rabbits xenografts. Cetuximab, a
Autor:
Riti Thapar Kapoor, Mika Sillanpää, Mohd Rafatullah, R. M. Abdel Hameed, Ibrahim M. Maafa, Mariam M. Hassan, Ayman Yousef, Mathurin François, Kuen-Song Lin, Nova Rachmadona, Srinithya Ravinuthala, Dewansh, Saravanan Settu, Saprativ P. Das, Mahshid Zandjou, Fahimeh Hooriabad Saboor, Mehrdad Asgari, Swathy Satheesh, Tijo Cherian, Treesa Varghese, Shibin Eranhottu, Fahmeeda Parveen Panikkaveetil Shahulhameed, Nurul Alia Syufina Abu Bakar, Siti Suraya Munirah Normi, Siti Baidurah, Sidra Khan Orakzai, Fazle Subhan, Kifayatullah Khan, Syed Qaiser Shah, Muhammad Yaseen, Sidra Subhan, Sadiq Ur Rahman, Hieu Trung Nguyen, Ha Manh Bui, Thi-Huyen-Tran Ngo, Unnimaya Geetha, Poulomi Ghosh, Garima, Srishti Sharma, Deepak Pal, Arun Kumar, N. Sharmila Devi
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 61:550-556
This investigation aimed to modify finasteride (1) to finasteride dithiocarbamate (2) for subsequent synthesis of the rhenium analogue (3) and [99m Tc]tricarbonyl complexes (4), to assess its prostate cancer (PCa) targeting potential in a rat model.