Zobrazeno 1 - 10
of 156
pro vyhledávání: '"K G, Nair"'
Autor:
Mohammed Salahat, Muhammad Ahsan Raza, Zuha Khawar, Javaid Ahmad Malik, Hammad Raza, Harish K G Nair, Muath Jarrah
Publikováno v:
2023 International Conference on Business Analytics for Technology and Security (ICBATS).
Impact of IoT and Recource Based View on Digital Business: The Role of Strategic Thinking Leadership
Autor:
Naseem Abidi, Ramakrishna Yanamandra, Harish K. G. Nair, Mohammad Rustom Al Nasar, Osama Khassawneh
Publikováno v:
2023 International Conference on Business Analytics for Technology and Security (ICBATS).
Autor:
Syed Ali Raza, Asma Kanwal, Harish K G Nair, Atif Ishaq Khan, Iftikhar Naseer, Muhammad Amjad, Karamath Ateeq, Mahmoud Al Sakhnani
Publikováno v:
2023 International Conference on Business Analytics for Technology and Security (ICBATS).
Autor:
Muhamamd Saleem, Assma Khadim, Mayraj Fatima, Muhammad Asghar Khan, Harish K G Nair, Muhammad Asif
Publikováno v:
2022 International Conference on Cyber Resilience (ICCR).
Autor:
Mohammad Salahat, Harish K G Nair, Rasha Almajed, Naila Samar Naz, Aziz Ur Rehman, Muhammad Sheraz Javeid
Publikováno v:
2022 International Conference on Cyber Resilience (ICCR).
Autor:
Nidal A. Al-Dmour, Mohammad Salahat, Harish K G Nair, Nayab Kanwal, Muhammad Saleem, Nauman Aziz
Publikováno v:
2022 International Conference on Cyber Resilience (ICCR).
Autor:
K. G. Nair, Kavita K. Shalia, Seema P. Todur, Jamshed J. Dalal, Tester F. Ashavaid, C.K. Ponde, R.M. Rajani, Altaf A. Kondkar
Publikováno v:
Platelets. 22:85-91
Platelets play a critical role in normal blood hemostasis and thrombus formation in myocardial infarction (MI). Several polymorphisms of genes involved in platelet activation and fibrinolysis have been reported to be associated with MI. The aim of th
Genetic analysis of Indian subjects with clinical features of possible type IIa hypercholesterolemia
Publikováno v:
Journal of Clinical Laboratory Analysis. 21:375-381
We performed genetic analysis in 55 patients with clinical features of possible type IIa hypercholesterolemia and 76 normolipemic healthy subjects for mutations and polymorphisms in the low‐density lipoprotein (LDL) receptor (LDLR), apolipoprotein
Publikováno v:
Journal of Clinical Laboratory Analysis. 17:141-146
Gene encoding components of the renin angiotensin system (RAS) have been implicated with the increased risk of cardiovascular disease (CVD). Two variants of the angiotensinogen (AGT) gene, M235T and T174M, have been shown to be associated with increa
Publikováno v:
Indian Journal of Clinical Biochemistry. 15:11-19
Familial hypercholesterolemia (FH) is an autosomal dominant disease caused by a multitude of low-density lipoprotein (LDL) receptor gene mutations. The LDL receptor is a cell surface trans-membrane protein that mediates the uptake & lysosomal degrada