Search or add a thesis

Advanced Search (Beta)
Home > ديوان الشنفرى دراسة مقطعية احصائية

ديوان الشنفرى دراسة مقطعية احصائية

Thesis Info

Author

ناصر محمود

Supervisor

انعام الحق غازى

Department

Department of Arabic Language

Program

Mphil

Institute

International Islamic University

Institute Type

Public

City

Islamabad

Country

Pakistan

Thesis Completing Year

2009

Thesis Completion Status

Completed

Page

253ص

Subject

Arabic Language

Language

Arabic

Other

Available at Dr Hamidullah Library,Islamic Research Institute, International Islamic University, Pakistan on T/1331

Added

2021-02-17 19:49:13

Modified

2023-02-19 12:33:56

ARI ID

1676721405127

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...

ٹیلی ویژن کی اہمیت

ٹیلی ویژن کی اہمیت
نحمدہ ونصلی علی رسولہ الکریم امّا بعد فاعوذ بااللہ من الشیطن الرجیم
بسم اللہ الرحمن الرحیم
معزز سامعین اور میرے ہم مکتب شاہینو!
آج مجھے جس موضوع پر اظہار خیال کرنا ہے وہ ہے:’’ٹیلی ویژن کی اہمیت‘‘
جنابِ صدر!
ترقی انسان کا مقدر ہے، یہ انسان ہمیشہ سے آگے بڑھتا آیا ہے مختلف قسم کی ایجادیں ہوئیں، مختلف حوالوں سے ترقی ہوئی ،مختلف شعبوں میں انسان نے ترقی کیلئے سرتوڑ کوشش کی اور پھر اس میں کامیابی حاصل ہوئی، انسان کو وہی کچھ ملتا ہے جس کے لیے جتنی کوشش کرتا ہے ،جتنی کدوکاوش کرتا ہے، اس کو اس کی محنت کا پھل اللہ تعالیٰ ضرور عطا فرماتا ہے۔
صدرِذی وقار!
کچھ عرصہ قبل کی بات ہے کہ ریڈ یوکی ایجاد نے دنیا کو ورطۂ حیرت میں ڈال دیا، اس میں ترقی ہوئی تو ٹیلی ویژن ایجاد ہو گیا، ٹیلی ویژن کی ایجاد ایک اہم ایجاد ہے ، ریڈیو نے کائنات کی وسعتیں اور فاصلے سمیٹے اور انسانی آوازوں کو ہزاروں میلوں تک پہنچایا توٹیلی ویژن نے اس سے بڑھ کر کام کیا ، اس نے ایک قدم اور آگے بڑھایا۔ آپ ٹیلی ویژن میں انسانوں کو گفتگو کرتے اورمتحرک دیکھ سکتے ہیں۔
صدرِ محترم!
ہم ٹیلی ویژن میں انسانوں کو اپنی آواز میں ، ان کی اپنی شکل وصورت میں، ان کے اپنے رنگ ڈھنگ میں، ان کے اپنے طور طریقوں میں دیکھ سکتے ہیں، ٹیلی ویژن کی ایجاداس جدید دور میں ایک نعمت سے کم نہیں ہے۔ مختلف پروگرام پیش کرتا ہے۔ مختلف علاقوں کی ثقافت سے متعارف کرواتا ہے، مختلف علاقوں کے خوبصورت مناظر سے قاری کی قوت بصارت کوتقویت دینے کا سبب بنتا ہے،تفریح کے مواقع پیش کرتا ہے۔
معزز سامعین!
پاکستان میں ٹیلی ویژن کی ابتدا1964ء میں ہوئی ، ٹیلی ویژن کے...

اسلامی فوجداریت کا ضابطۂ قرائن

Qara’in - usually translated as circumstantial evidence - is a derived form of Arabic word " " قر ن which literally means a fact associated or accompanied with an event or circumstances. But when an event or circumstances discloses such associated or accompanied fact then such a fact becomes circumstantial evidence. Both proto-juristic and modern legal terms held circumstantial evidence for an evidence which is offered to prove certain attendant circumstances from which the existence of the fact at issue may be inferred. In Islamic Law, majority of jurists do not endorse Qara’in as an authoritative evidence, particularly, in offences leading to corporal punishments. On the other side, Ibn Farhun from Malikites and Ibn Qayyem from Hanbalites terms it equal to the direct evidence of Iqrar and Shahadah. It is not very strange that Dr. Anwarullah, a prominent Muslim scholar and Prof. Robert Preach are of the opinion that circumstantial evidence is, after all, more authentic even than the aforesaid two evidences. Herbert Broom- a western legal expert- also says that certain hidden facts can be deducted from the mode of a relevant act or to some extent it is modus operandi which gives birth to a circumstantial evidence. In this shortened article the juristic opinion of some early and contemporary legal experts has been discussed as to judge the legal mode and authenticity of circumstantial evidence.

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.