Search or add a thesis

Advanced Search (Beta)
Home > Islamic banking system and investment financing

Islamic banking system and investment financing

Thesis Info

Author

Sehrish Bashir

Supervisor

Hameeda Akhtar

Department

Department of Accounting and Finance

Program

MBA

Institute

International Islamic University

Institute Type

Public

City

Islamabad

Province

Islamabad

Country

Pakistan

Thesis Completing Year

2012

Thesis Completion Status

Completed

Page

vi,42

Subject

Accounting & Finance

Language

English

Other

MA/MSc 658.152 SEI

Added

2021-02-17 19:49:13

Modified

2023-01-06 19:20:37

ARI ID

1676723694822

Asian Research Index Whatsapp Chanel
Asian Research Index Whatsapp Chanel

Join our Whatsapp Channel to get regular updates.

Similar


Loading...
Loading...

Similar Books

Loading...

Similar Chapters

Loading...

Similar News

Loading...

Similar Articles

Loading...

Similar Article Headings

Loading...

فقیروں کا بھٹو

فقیروں کابھٹو

1968ء یا 69کی بات ہے ذوالفقار علی بھٹو اندرونِ سندھ کے دورے سے اپنے گھر لاڑکانہ واپس جا رہے تھے اور سخت بخار کی حالت میںتھے ۔ان کی گاڑی ممتاز بھٹو چلا رہے تھے شہداد کوٹ اور قمبر کے نزدیک ایک مزار کے فقیروں ،ملنگوں اور درویشوں کو بھٹو کی آمد کا پتہ چلا تو انہوں نے بھٹو کی گاڑی کو وارہ پل کے مقام پر گھیر لیا ۔ممتاز بھٹو نے لاکھ سمجھانے کی کوشش کی کہ بھٹو صاحب کو بخار ہے مگر نہ مانے اور انہیں اپنے ساتھ آستانے پر لے جانے پر بضد رہے ۔ذوالفقار علی بھٹو ان کا مطالبہ مان کر ان کے ساتھ گئے ۔وہاں فقیروں ،ملنگوں اور درویشوں نے بھٹو کو اپنے ساتھ چرس اور بھنگ پینے کی پیشکش کی ۔بھٹو نے کہا آپ چائے پلا دیں ۔اسی وقت ان فقیروں نے گڑ کی چائے بنا کر پیش کی اسی دوران ایک ملنگ نے درباروں والا مخصوص ہار اپنے گلے سے اتار کر بھٹو کے گلے میں ڈال دیا ۔بھٹو تیز بخار کی صورت میں کچھ دیر وہاں فقیروں کے ساتھ بیٹھے اور پھر اجازت لے کر وہاں سے لاڑکانہ چلے گئے ۔

ان فقیروں ،ملنگوں اور درویشوں اوران جیسے کروڑوں لوگوں نے …جنہیں پیپلز پارٹی مدت ہوئی فراموش کر چکی ہے ،آج تک بھٹو کو اپنے دلوں میں بسایا ہوا ہے ۔

 

کاروباری تشہیر اور اخلاقیات: سیرت طیبہ کی روشنی میں

The History revealed the fact that merchants played a very prominent and vital role in spreading the religion of Islam. Prophet Muhammad (PBUH) remained one of the popular merchants of his time in the Arabian Peninsula. Similarly, the same profession was also adopted by the Prophet’s companions and they propagated the message of Islam almost in every corner of the world being a core mission of their lives. The number of Islamic countries on the world’s map witness their efforts in this regard. There are numerous sayings of the Prophet (PBUH) in which he praised the honest and truthful traders and cautioned with serious wrath for the otherwise. Keeping in view the contemporary scenario of corporate world, one can easily observe the lacking of professional and ethical values among the merchants more specifically concerned with commercialization and marketing. In fact, marketing is one of the sound sources to promote business but some companies try to exploit their consumers via fake commercialization and false advertising. Pakistan, being an Islamic country, has to devise such principles and regulations regarding commercial advertising which are in full conformity with Shariah standards that will definitely, secure the rights of all stakeholders along with fine attraction for foreign investment to put the economy on growing direction. The current paper deals with the morals and values of advertising in the light of Prophetic teaching.

Molecular Genetics of Autosomal Recessive Retinitis Pigmentosa in Consanguineous Pakistani Families

It is an established fact that genetic disorders are one of the most important threats to human health. Several genetic disorders have been described clinically but their etiology is still unidentified and mysterious. The molecular basis for most of them is also unknown. With the advancement in the field of molecular biology different powerful techniques have been developed to understand the molecular basis of hereditary disorders. This would help in the subsequent identification of causative genes and mutations. Blindness and visual impairment due to genetic disorders are more common in developing countries like Pakistan than in developed countries. Retinitis pigmentosa (RP) is a major form of incurable blindness affecting one out of 4000 people worldwide. This highly heterogeneous disease has numerous inheritance patterns with the end result of partial to complete irreversible blindness. Another ocular disorder called fundus albipunctatus (FAP) also has some symptoms similar to RP like night blindness. In FAP this night blindness occurs in childhood but it remains stationary and day vision is not affected as in the case of RP where constriction of day vision occurs gradually. The present study was aimed to analyze families with ocular disorder. Families with autosomal recessive hereditary retinitis pigmentosa were used for mapping the disease genes and mutations. Seven consanguineous unrelated families (RP8, RP9, RP11, RP12, RP13, RP14 and RP16) with inherited RP were ascertained from different regions of Pakistan. The mode of inheritance in all families was inferred as autosomal recessive. The strategy used for this study was candidate gene approach. Linkage analysis was performed by PCR using STR (short tandem repeats) microsatellite markers for the known loci/genes. Direct sequencing (next generation sequencing) of the PCR products was carried out for identification of pathogenic mutations. In the present study linkage to crumbs homolog 1 (CRB1) gene on chromosome 1q31.3 was confirmed in family RP12. A novel missense mutation in human CRB1 gene has been found after sequence analysis of exon 6 of the CRB1 gene at nucleotide position xx 1459 (c.1459T>C). At protein level this mutation resulted in a substitution of proline for serine at amino acid 487 (p.Ser487Pro). It was inferred that mutation in this gene is strong enough to cause autosomal recessive retinitis pigmentosa. After the initial screening of autosomal recessive retinitis pigmentosa loci for family RP13, it was evident that there was no involvement of retinitis pigmentosal loci in the disease phenotype and it was a rare case of fundus albipunctatus, with RDH5 gene defect as the underlying cause. The family RP13 showed linkage to retinol dehydrogenase 5 (11-cis/9-cis) RDH5 gene after homozygosity mapping. A novel missense mutation at nucleotide position 602 (c.602 C>T) was identified after next generation sequencing of exon 4 of the RDH5 gene .This mutation resulted in substitution of phenylealanine for serine at amino acid 201 (p.Ser201Phe) of the RDH5 gene. The mutations in RDH5 gene are related to fundus albipunctatus (FAP). This is an exceptional form of stationary night blindness, it was deduced that mutation in this gene was responsible for autosomal recessive FAP in this family. The family RP14 showed exclusion to all the known genes and loci of RP. It was inferred that a novel locus/gene is responsible for causing RP in this family. The strongest candidate gene was RY2R which was earlier involved in cardiac disorder. Fine mapping in future would confirm the involvement of this gene in RP. Four families (RP8, RP9, RP11 and RP16) with some of the common selected loci/gene showed heterozygosity for the different combinations of the parental alleles in both affected and normal individuals after the linitial linkage. This heterozygosity confirmed exclusion to five selected known loci or genes on different chromosomes associated with autosomal recessive RP. Since many genes and loci are involved in this disease and genotyping using vertical polyacrylamide gel electrophoresis (PAGE) is a time taking and laborious method so commonly found genes in RP were initially selected which showed exclusion.On the basis of these exclusions it was inferred that a novel locus/gene or mutation is involved in these families which could be identified by SNP affymetrix array technique and sequencing. Many loci/genes/mutations are yet to be identified for this phenotype. It would be helpful in future to understand the disease prognosis. This research will also provide a smooth way for carrier screening, genetic counseling and prenatal diagnosis. This study may help gaining insight into the genetic causes underlying these disorders, to improve the clinical management and prevention.