مولانا محمد اسحق جلیس
یہ محسوس کرکے بڑادکھ ہوتاہے کہ تین مہینے کے اندر اندر دارالعلوم ندوۃ العلماء اپنے تین نامور اور لائق وفائق کارکنوں سے محروم ہوگیا۔جون میں مولانا محمد الحسنی ایڈیٹر البعث الاسلامی کی جواں مرگی کاحادثہ پیش آیا تھا۔جولائی میں مولانامحمد اسحق جلیس ایڈیٹر’ تعمیر حیات‘، اچانک ۴۴برس کی عمر میں داغ مفارقت دے گئے۔ مرحوم گوناگوں علمی وعملی خصوصیات کے مالک تھے، ندوہ کے فارغ التحصیل، انگریزی میں گریجویٹ اوربی لب، ہندی،پشتو اورمرہٹی زبانوں کے عالم اور تحریر وتقریر دونوں میں فردتھے۔ ان خصوصیات کے باعث ’’پیامِ انسانیت‘‘ تحریک میں مولانا سید ابوالحسن علی میاں کے دستِ راست تھے اوراس کے بعد اگست میں یہ تیسراحادثہ پیش آگیا۔برہان ان حوادث ِپیہم میں مولانا علی میاں اور تمام ارباب ندوۃ العلماء کے ساتھ دلی ہمدردی اورشرکت غم والم کااظہار کرتا ہے۔ [ستمبر۱۹۷۹ء]
This article aims to present a concise overview regarding global economic ideas and its historical development with brief evaluation of capitalism and communism as well as question of laissez-faire and concept of ownership in relation to Islamic economic thought. What are the rudiments, fundamentals and historical sketch of these systems? Measuring them analytically vis-à-vis their comparative examination has been taken into account to visit the characteristics of prevailing as well as outdated and nonoperational economic systems. As capitalism emphasis on eagerness to find wealth where billionaires are about to getting more and more ignoring various other ethical perspectives and paying no attention to the poor classes of society. Communism claiming equality remained also not compatible to sustain around the globe as a balanced and stable system. At the end this article predicts that other than Islamic economic thought no system may fulfill the natural need of global economy and it also recommends that Islamic Scholars have to present an alternative full-fledged practical model for economics.
The sunshine vitamin is in the limelight for the last couple of years. Though Pakistan is located at favorable latitude and longitude yet vast majority of its people suffer from vitamin D deficiency. Calcium homeostasis, bone metabolism and many other functions of body are influenced by vitamin D. Nuclear vitamin D receptor and group specific vitamin D binding proteins are two important proteins play role in vitamin D metabolism and encoded by VDR and GC genes. There could be many reasons but in this study six single nucleotide polymorphisms in GC, VDR and CYP2R1 genes were looked into for their possible association with vitamin D deficiency. Blood samples of four hundred subjects were collected. Vitamin D and parathyroid harmone levels were calculated by chemiluminescence method. DNA extraction was carried out by phenolchloroform method. The qualitative and quantitative analysis of DNA was carried out on agarose gel electrophoresis. Tetra amplification refractory mutation system polymerase chain reaction was performed to genotype rs7041, rs4588, rs2060793, rs2282679, rs3847987, and rs7974353. Genotypic and allelic frequencies with relative risk was calculated. In Silico protein modelling, docking and analysis of rs7041 was done. Overall 77.5% subjects were found to be with vitamin D deficiency/insufficiency. There were 35% from newborn to 20 years age group, 88.8% from 21-40 years and 95.8% from to 41-60 years.Significant negative correlation was observed between vitamin D and parathyroid hormone levels. rs 7041 belonging to GC genes showed T>G polymorphism. Major allele was T and minor allele was G. Minor allele “G” with genotype GG could be a risk allele contributing in vitamin D deficiency. rs7974353 belonging to VDR gene showed T>A polymorphism. Though “TT’ was in high frequency in VDD subjects compared to control yet insignificant association with VDD was noted. RR for both alleles and genotypes TA and AA was not significant with reference to homozygous wild type TT (0.6 for AT, 0.7 for AA). Results might had been xxi sigificant if thenumber of subjects were more. Rest of the four SNPs showed equal frequency in control and cases and hence showed no association with vitamin D deficiency. In silico model of SNP rs 7041 showed variation in the 3D structure of protein because of replacement of asparctic acid by glutamic acid. This can explain the cause of VDD / VDI due to poor docking of vitamin D with its binding protein. Conclusion is that rs7041 and possibly rs7974353 are contributing to VDD / VDI in studied group. Results are supported by In silico analysis of rs 7041.