Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rani Akbar"'
Autor:
Asif Jan, Zakiullah, Sajid Ali, Basir Muhammad, Amina Arshad, Yasar Shah, Haji Bahadur, Hamayun Khan, Fazli Khuda, Rani Akbar, Kiran Ijaz
Publikováno v:
PLoS ONE, Vol 18, Iss 1, p e0281070 (2023)
Genome-wide association studies have greatly increased the number of T2DM associated risk variants but most of them have focused on populations of European origin. There is scarcity of such studies in developing countries including Pakistan. High pre
Externí odkaz:
https://doaj.org/article/42cd9d1a295947f7b9f7ef79a1c2bd57
Autor:
Asif Jan, Muhammad Saeed, Ramzi A. Mothana, Tahir Muhammad, Naveed Rahman, Abdullah R. Alanzi, Rani Akbar
Publikováno v:
Biomedicines, Vol 11, Iss 8, p 2282 (2023)
Polymorphism in cytochrome P450 (CYP) 2C9 enzyme is known to cause significant inter-individual differences in drug response and occurrence of adverse drug reactions. Different alleles of the CYP2C9 gene have been identified, but the notable alleles
Externí odkaz:
https://doaj.org/article/526dc2cf6b5041159c05e29ec3b2cd7f
Autor:
Waheed Ali Shah, Asif Jan, Muhammad Asghar Khan, Muhammad Saeed, Naveed Rahman, Zakiullah, Muhammad Sajjad Afridi, Fazli Khuda, Rani Akbar
Publikováno v:
Genes, Vol 14, Iss 6, p 1184 (2023)
Genome-wide association studies significantly increased the number of hypertension risk variants; however, most of them focused on European societies. There is lack of such studies in developing countries, including Pakistan. The lack of research stu
Externí odkaz:
https://doaj.org/article/88e877de1063467db3cde06ffde6950e
Autor:
Naveed Rahman, Zakiullah, Asif Jan, Muhammad Saeed, Muhammad Asghar Khan, Zahida Parveen, Javaid Iqbal, Sajid Ali, Waheed Ali Shah, Rani Akbar, Fazli Khuda
Publikováno v:
Genes, Vol 14, Iss 3, p 687 (2023)
Coronary Artery Diseases (CAD) remains the top among Non-communicable Diseases (NCDs). Variations in Apolipoprotein E (APOE) and Paroxonase 1 (PON1) have been associated with Myocardial Infarction (MI) in several populations. However, despite the hig
Externí odkaz:
https://doaj.org/article/9a76801925264e21ae39603d9063f0ef
Publikováno v:
Journal of the ASEAN Federation of Endocrine Societies, Vol 38, Iss S1 (2021)
Objective. To evaluate the Type 2 Diabetes (T2D) risk variants in the Pashtun ethnic population of Khyber Pakhtunkhwa using nascent whole-exome sequencing (WES) to better understand the pathogenesis of this complex polygenic disorder. Methodology.
Externí odkaz:
https://doaj.org/article/641bb4f5075b4e679b3d0237ec375877
Autor:
Asif Jan, Muhammad Saeed, Muhammad Hussain Afridi, Fazli Khuda, Muhammad Shabbir, Hamayun Khan, Sajid Ali, Muhammad Hassan, Samiullah, Rani Akbar, Zakiullah
Publikováno v:
Journal of Diabetes Research, Vol 2021 (2021)
Human leukocyte antigen (HLA) system is the most polymorphic and gene dense region of human DNA that has shown many disease associations. It has been further divided into HLA classes I, II, and III. Polymorphism in HLA class II genes has been reporte
Externí odkaz:
https://doaj.org/article/482479cfe9574edfa8520b946a8990dd
Autor:
Abdur Rahim, null Zakiullah, Asif Jan, Johar Ali, Fazli Khuda, Basir Muhammad, Hamayun Khan, Hussain Shah, Rani Akbar
Publikováno v:
African Health Sciences; Vol. 22 No. 3 (2022); 145-154
Background: Genetic studies play a significant role in understanding the underlying risk factors of breast cancer. Polymorphism in the tumor suppressor gene TP 53, CDH1 and ATM genes are found to increase susceptibility for breast cancer globally. Ob
Autor:
Samiullah, Asif Jan, Zakiullah, Muhammad Saeed, Muhammad Hussain Afridi, Muhammad Farooq Shabbir, Fazli Khuda, Muhammad Shahid Hassan, Hamayun Khan, Sajid Ali, Rani Akbar
Publikováno v:
Journal of Diabetes Research, Vol 2021 (2021)
Journal of Diabetes Research
Journal of Diabetes Research
Human leukocyte antigen (HLA) system is the most polymorphic and gene dense region of human DNA that has shown many disease associations. It has been further divided into HLA classes I, II, and III. Polymorphism in HLA class II genes has been reporte