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ترجمہ و تخریج تفسیر الکشف و البیان عن تفسیر القرآن

Thesis Info

Author

فتح محمد

Supervisor

حافظ عبد الرزاق

Program

Mphil

Institute

Riphah International University

Institute Type

Private

Campus Location

Faisalabad Campus

City

Faisalabad

Province

Punjab

Country

Pakistan

Thesis Completing Year

2016

Thesis Completion Status

Completed

Page

ii, 193 . ; 30 cm.

Subject

Islam

Language

Urdu

Other

Submitted in fulfillment of the requirements for the degree of Master of Philosophy (Isalmia) to the Faculty of Social Sciences and Humanities.; Includes bibliographical references; Thesis (M.Phil)--Riphah International University, 2016; Urdu; Call No: 297.12 FAT

Added

2021-02-17 19:49:13

Modified

2023-02-19 12:33:56

ARI ID

1676712150592

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حسن نگر کے سارے پنچھی مر جائیں گے

حسن نگر کے سارے پنچھی مر جائیں گے
عکس تمھارے حشر بپا سا کر جائیں گے

ہجر وصال کے جھگڑوں سے ہم دور بہت ہیں
رقص جنوں کی رسم تو پوری کر جائیں گے

تجھ پر مرنے والوں کی تو بات ہی کیا ہے
مرتے مرتے آخر اک دن مر جائیں گے

تیری تان پہ جھومیں گے یہ سب دیوانے
اور نچھاور اپنا سب کچھ کر جائیں گے

قیس میاں کے قصے بھی ہم جانتے ہیں سب
تم سمجھے ہم عشق میں شاید ڈر جائیں گے

پاگل لڑکی شعر جنوں کا قصہ ہے سن!
کون سنے گا جب کردار مکر جائیں گے

Incongruity in Contemporary and Shariah Compliant Current Accounts and Ijarah Operated by Islamic Banking

Current accounts and Ijarah has been foremost and important tools operated by the Islamic Financial Institutions. This study attempts to explore a few misgivings in the handling of current accounts by the Islamic banks in Pakistan. Financial management of Islamic banks is not under consideration which leads to the violation of Shariah’s fundamentals. Also in case of Ijarah, a bank’s client suffers from financial losses which must be borne in Islamic Banking system. Islamic Banks transfer the burden of some charges emerging form ownership of leased asset on their clientele which does not have any justification according to Shariah. This research has been carried out by taking unstructured interviews from some of the concerned staff of Islamic Banks. The results depict that current accounts and Ijarah is in operation and need to be revised and refined and must comply with Shariah.

Prevalence of Bacterial Pathogens Causing Nosocomial Infections With Reference to Identification of Resistant Genes Drug Designing

One of the most common places for the development and spread of bacterial resistance are hospitals. These bacteria are present on the inanimate objects and therefore can be a possible cause of cross infections. This cross infection can rise the disease and death rates, which results in increasing costs of healthcare, prolonged hospital stays and requires further expensive medications. Therefore, the current study was aimed at determining the prevalence of these resistant bacteria, their antibiogram pattern, presence of resistant gene(s) and molecular docking studies. In our study the most common bacteria among Gram-positive was Staphylococcus aureus (81%) while in Gram-negative Citro bacter (25%) showed the highest growth followed by Pseudomonas aeruginosa (23%), Provedencia spp (16%), Proteus spp and E.coli (10%), Klebsiella spp (6%), Shigella and Serratia spp (4%) and Salmonella spp (2%). The most potent antibiotic against S. aureus and Citrobacter was Vancomycin (80% sensitive) and Amikacin (63.04%), respectively. The β-lactamase TEM and Metallo- β-lactamase NDM were most common among the Extended-β-lactamase (ESBLs) and Metalo-β-lactamase (MBLs) genes. For β-lactamase TEM, Metallo-β-lactamase and other β-lactamase proteins, numerous classes of inhibitors have been reported in the literature. These proteins revealed to be involved in providing resistance to certain antibiotics, thus, the inhibition of these proteins is vital for achieving the optimum treatment. In the current work, In-silico methods were used for the discovery of novel and potent inhibitors for these proteins. On the basis of ligands attached in the three-dimensional proteins structures, Complex-based pharmacophore models were generated for screening the drug like ZINC database. Before screening, the generated pharmacophore models were validated on a test database of active and non-active compounds. From the result Abstract xxvi | P a g e of virtual-screening, 571 structurally varied compounds from Ethyl Boronic Acid, 866 from L-Captopril and 1020 from Nacubactam were saved. The initial retrieved hits were selected for cleaning via Lipinski’s rule of five to calculate the drug-like properties. The compounds which attained the standards of drug-like properties were additionally evaluated by the docking simulations. Final concluding 30 compounds (10 for each of the selected protein) producing varied structure and the modes of binding in the active pocket of the designated proteins were concluded as new and important inhibitors. Each identified inhibitor has diverse frameworks and possibility of novel and probable inhibitors for β-lactamase TEM, Metallo-β-lactamase and β lactamase.