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Home > قصہ یونسہ : معارف القرآن و تفہیم القرآن کی روشنی میں تقابلی جائزہ

قصہ یونسہ : معارف القرآن و تفہیم القرآن کی روشنی میں تقابلی جائزہ

Thesis Info

Author

شمائل اقبال

Supervisor

فرخندہ اکرام

Department

شعبہ علوم اسلامیہ وتقابل ادیان

Program

MA

Institute

The Women University

Institute Type

Public

City

Multan

Province

Punjab

Country

Pakistan

Degree Starting Year

2015

Degree End Year

2017

Language

Urdu

Keywords

انبیاء، دعوت، تذکرہ
Prophets, Dawah

Added

2021-02-17 19:49:13

Modified

2023-01-06 19:20:37

ARI ID

1676709265647

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اردو کے اہم مدونین (ڈاکٹر عطش درانی)

اردو کے اہم مدونین (ڈاکٹرعطش درانی)
ڈاکٹر عطش درانی پاکستان کے ایک ماہر لسانیات، محقق، تنقید نگار، مصنف، ماہر تعلیم اور ماہر علم جوہریات تھے۔ انہوں نے 275 کتابیں لکھیں اور متعدد اطلاقیے بنائے۔ نیز اردو اور انگریزی میں 500 مقالے لکھے۔ عطش درانی کی ان علمی و تحقیقی خدمات پر انہیں تمغہ امتیاز اور ستار? امتیاز سے نوازا گیا۔وہ ماہر لسانیات، علم کمپیوٹر کے پاکستان میں اہم ترین ماہر،اصطلاحات ساز، ماہرتعلیم، ماہر جواہرات، صحافی، تنقید نگار، محقق، اور سب سے بڑھ کر ایک مخلص دوست
پیدائش :
عطاء اللہ عطش درانی 22 جنوری1952ء کو ساہی وال میں پیدا ہوئے۔
تعلیم:
پنجاب یونیورسٹی سے ایم اے ایجوکیشن، ایم اے اردو اور پی ایچ ڈی کی اسناد حاصل کیں۔ مختلف جرائد کے عملۂ ادارت میں شریک رہے۔ جس ادارے میں بھی گئے وہاں اپنے کام کی دھاک بٹھا دی۔ ہمیشہ قائداعظم کے فرمان ’’کام ،کام … اور… کام‘‘ کی تعبیر نظر آئے۔
تصانیف:
عطش کی آخری تصنیف کتاب الجواہر جو البیرونی کی تصنیف کتاب الجماہر فی معرفۃ الجواہر کے اْس حصے کا ترجمہ ہے جو جواہرات سے متعلق ہے، نیشنل بک فاؤنڈیشن اسلام آباد نے جولائی2018 ء میں شائع کی۔آپ کی دیگر تصانیف میں اسلامی فکر و ثقافت ،مغربی ممالک میں ترجمے کے قومی اور عالمی مراکز ، "لسانی و ادبی تحقیق وتدوین کے اصول" کتابیات قانون، پاکستانی اردو کے خد و خال ،لغات و اصطلاحات میں مقتدرہ کی خدمات ، اردو اصطلاحات نگاری (کتابیاتی جائزہ) ،اردو اصطلاحات نگاری (تحقیقی و تنقیدی جائزہ) ، اصناف ادب کی مختصر تاریخ ، اماں سین اور دیگر شخصے ودیگر شامل ہیں۔
ملازمت اور خدمات
مکتبہ شاہکار:
1976 میں سید قاسم محمود کی سربراہی میں مکتبہ شاہکار میں اسلامی انسائیکلوپیڈیا اور متعدد کتابوں پر کام کیا۔
رسائل سے وابستگی:
سیارہ ڈائجسٹ کی ادارت اڑھائی تین برس کی۔ مجلس زبان دفتری کے...

The Gray area Beyond Raised Objections (Sharia’h Perspective) Regarding In-practice Islamic Banking System

Shari‘ah’s teachings are perfect and forever. They leave everlasting impacts on society towards its spiritual as well as material purification (Tazkia) if implemented properly according to Qur’an and Sunnah. Interest (Sood/Rib┐) has been forbidden by Almighty Allah whereas Trade (Ba‘a) has been legitimated. To bring the Muslims of today out of Interest-based Banking System, religious scholars have outlined and introduced Islamic Banking System which, although, has got fast growth in market but still, a number of objections are being raised by different scholars leading to an impression that this system is not working in accordance with Shari‘ah. This not only discourages the entry of new ones to Islamic Banking Sector but also create confusions in the minds of the enlisted customers. Keeping in view the above scenario, need is felt to assess, evaluate and analyze the Objections raised with special emphasis on Islamic Concept of Bank, Charity Fund (Iltez┐m be tasaduq) and Mur┐ba╒a being the major points of objections of the critics. The present study investigates different aspects and dimensions of these objections in the context of Shariah and ground realities in order to know the extent of validity of these objections, highlight the gray areas giving rise to objections and give real picture to the public in general and enhance the satisfactory level of the enlisted Islamic Banking customers in particular.

Clinicla and Molecular Characterization of Human Hereditary Skin Disorders in Consanguineous Families

A study, presented in the dissertation, described clinical and genetic characterization of nineteen consanguineous families (A-S) featuring various forms of inherited skin disorders. Fifteen of these families (A-I, K-P) showed various forms of isolated skin anomalies, while the remaining four families (J, Q-S) exhibited distinct forms of syndromic conditions. Isolated X-linked ichthyosis (XLI) was identified in four families (A-D). Initial marker analysis revealed two distinct interstitial deletions at chromosome Xp22.3. SNP array fine mapped the underlying deletions to ~ 1.67 Mb (family A, B, C) and ~ 1.62 Mb (family D). Different forms of isolated scaling skin phenotype, with autosomal recessive inheritance, was identified in five consanguineous families (E-I). Genotyping using microsatellite markers and haplotype analysis established linkage in the family E, segregating ichthyosis vulgaris, to a previously known gene FLG at chromosome 1q21.3. Subsequently, Sanger sequencing identified a novel homozygous nonsense variant (c.10459A>T; p.Arg3487*) in the third exon of the FLG gene in affected individuals. In family F, with ichthyosiform erythroderma, genetic delineation by exome sequencing revealed a previously reported nonsense variant (c.1630C>T; p.Gln544*) in the ALOXE3 gene. In the third family, segregating scaling phenotype, SNP genotyping and exome sequencing identified a novel gene CLUH carrying a homozygous missense variant (c.2852G>A; p.Arg951His) in affected members. Two other families (H and I), segregating autosomal recessive form of ichthyosis, failed to show linkage to the known genes. Abstract Clinical and Molecular Characterization of Human Hereditary Skin Disorders in Consanguineous Families XXVIII Pure hair and nail ectodermal dysplasia, with autosomal recessive transmission, was observed in an inbred family J. Genotyping established linkage in the family at chromosome 12p11.1-q21.1. Sanger sequencing identified a novel homozygous nonsense variant (c.404C>A; p.Ser135*) in the HOXC13 gene. Clinically various forms of isolated hypotrichosis was observed in six consanguineous families (K-P). Sequencing of a panel of genes failed to reveal potential pathogenic variants in two families (K, L), segregating autosomal dominant form of hair loss disorders. Direct sequencing of the gene LPAR6 in the family M identified a previously defined missense variant (c.562A>T; P.Ile188Phe) causing hypotrichosis with wooly hair. The in-silico studies of mutated LPAR6 protein verified aberrant receptor activity and downstream phospholipid signaling resulting in hair disorder, with curly phenotype. The conventional homozygosity mapping using microsatellites failed to identify linkage to known genes/loci in two other families (N, O). Exome sequencing in the family P wasn’t successful in identifying a homozygous pathogenic sequence variant causing hair loss. The study, described in the dissertation, elaborated genetic characterization of three consanguineous families segregating syndromic forms of hair loss disorders. In the family Q, with hypotrichosis and Juvenile Macular Dystrophy, haplotype analysis established linkage to gene CDH3 on chromosome 16q. Sequence analysis identified a novel homozygous in-frame deletion variant (c.764_766delACT; p.255delTyr) in the CDH3 gene. In family R and S clinical investigation found the condition Woodhouse Sakati syndrome (WSS) and Nonphotosensitive trichothiodystrophy (TTDN), respectively. Exome sequencing identified a novel truncating homozygous variant Abstract Clinical and Molecular Characterization of Human Hereditary Skin Disorders in Consanguineous Families XXIX (c.270delA; p.Lys90Asnfs8*) in the gene DCAF17 and splice site variant c.339+1G>A in the gene MPLKIP in the family S. Structural investigation of mutated CDH3 p.255delTyr and DCAF17 p.Lys90Asnfs8* predicted atypical interactions with associated proteins. cDNA analysis of mutated MPLKIP c.339+1G>A verified unusual splicing event resulting in intron retention and setting up syndromic attributes in the family S.