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Human Fall Detection [+Cd]

Thesis Info

Author

Muaz, Muhammad

Department

University of Management and Technology

Institute

University of Management and Technology

Institute Type

Private

City

Lahore

Province

Punjab

Country

Pakistan

Thesis Completing Year

N.A.

Thesis Completion Status

Completed

Page

Various Pages CD

Language

English

Other

EN; Call No: TP 006.37 MUA-H

Added

2021-02-17 19:49:13

Modified

2023-01-06 19:20:37

ARI ID

1676713291232

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قاضی سلیمان منصور پوری

قاضی سلیمان صاحب منصور پوری
وہ مشرقی فاضل جس کی موت پر آج ہم کو ماتم کرنا ہے وہ قاضی محمد سلمان منصور پوری سابق جج پٹیالہ اور سیرت کی مشہور کتاب ’’رحمۃ للعالمین‘‘ کے مصنف ہیں، وہ علم و عمل، زہد و کمال اور فضل و ورع دونوں کے جامع تھے، روشن دل اور دماغ تھے، ان کے جدید و قدیم دونوں خیالات حداعتدال پر تھے، عربی زبان اور علوم دین کے مبصر عالم تھے، توراۃ و انجیل پر فاضلانہ و ناقدانہ نگاہ رکھتے تھے، غیرمسلموں سے مناظرہ کے شائق تھے، مگر ان کے مناظرہ کا طرز سنجیدگی، متانت اور عالمانہ وقار کے ساتھ تھا، مسلکاً اہل حدیث تھے، مگر اماموں اور مجتہدوں کی دل سے عزت اور ان کی محنتوں اور جانفشانیوں کی پوری قدر کرتے تھے۔
وہ ندوۃ العلماء کے دیرینہ رکن تھے اور اسی وساطت سے ان سے تعارف حاصل ہوا، اور تعارف نے باہم انس و مودّت کی صورت پیدا کی، جب مل جاتے دیر تک ہم ذوقی کا لطف قائم رہتا، سیرۃ، جدید مناظرات و کلام اور محاسن اسلام کے مختلف پہلوؤں پر گفتگو رہتی، اور اس لطف میں تھوڑی دیر کے لئے ہر چیز فراموش ہوجاتی، چند سال ہوئے کہ دارالمصنفین بھی ان کے فیض قدوم سے منور ہوا تھا، بلند قامت، خوش رو، خوش لباس، وجیہ، گھنی داڑھی، سپید صافہ باندھا کرتے تھے۔
ان کی مستقل تصنیفات میں رحمۃ للعالمین، الجمال والکمال (تفسیر سورۂ یوسف) اور سفرنامۂ حجاز، یادگار ہیں، ان کے علاوہ چھوٹے بڑے بیسوں رسائل ان کے قلم سے نکلے، مگر سب سے زیادہ ’’رحمۃ للعالمین‘‘ نے قبولیت حاصل کی، اسلامی مدرسوں میں داخل ہوئی، کورسوں میں شامل ہوئی، لوگوں نے ذوق و شوق سے پڑھا، خدا رحمۃ للعالمین کے مصنف کو اپنی رحمت عالم سے نوازے۔
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حوالہ کا فقہی تصور اور اس کی جدید صورتیں

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Identification and Modeling of Regulatory Networks and Development of Anti-Cancer Drug-Conjugated Nanoparticles for Breast Cancer Therapy

Breast cancer is the second leading cause of cancer-related mortalities among females worldwide. It is genetically heterogeneous disease caused by various environmental and genetic factors. Abnormal expression of various genes/proteins such as chemokine C-X-C motif (receptor 4), insulin like growth factor-1 receptor and estrogen growth factor receptor and their associated biological regulatory networks are linked with breast cancer. In this study, the crosstalk interaction between these genes/proteins and their associated signaling networks involved in breast cancer metastasis were studied by using both in-silico (qualitative modeling, hybrid PetriNet modeling, pharmacophore modeling and virtual screening) and in-vitro approaches (genotyping, cell viability assay, quantitative real time polymerase chain reaction and western blotting). The association of rs1801157 single nucleotide polymorphism, located within the C-X-C motif ligand 12 (CXCL12) gene, with the development of breast cancer was assessed. The results of genotyping showed the significant prevalence of genotype GG (p<0.05) with a number of variables including patient’s age, weight, lymph nodes status, hormonal imbalances (ER and PR) and family history using multivariable logistic regression among Pakistani breast cancer patients as compared to AA genotype. Our in-silico results suggested that rs1801157 single nucleotide polymorphism identified in CXCL12 gene has crosstalk link with insulin like growth factor-1 receptor (IGF-1R) and epidermal growth factor receptor (EGFR) signaling and is an important factor in predicting the outcomes of breast cancer therapy, which can also result in multidrug resistance due to induction of insulin like growth factor-1. Furthermore, to address the problem of multidrug resistance in breast cancer cells, an effective and non-toxic biologically synthesized silver nanoparticles (drug delivery vehicles) were conjugated with anti-cancer inhibitors such as fulvestrant and gefitinib to inhibit the activity of multiple genes and proteins such as estrogen growth factor receptor, C-X-C motif (ligand 12), phosphoinositide 3 kinase, insulin receptor substrate-1, insulin like growth factor-1 receptor, PDZ domain containing 1 and estrogen receptor-α to treat breast cancer cells. In conclusion, for a multifactorial disease like breast cancer, more than one therapeutic targets should be inhibited with an effective drug delivery vehicle to induce apoptosis in cancer cells.