Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Shazia Anwer Bukhari"'
Autor:
Muhammad Mustafa, Sehrish Murtaza, Rida Iqbal, Muhammad Ali, Muhammad Ehsan Safdar, Muhammad Sajjad, Tayyaba Huma, Shazia Anwer Bukhari
Publikováno v:
Molecular Biology Reports. 48:7703-7710
Numerous reports show that herbal medicines can be utilized in the treatment of different liver disorders. In this study, antioxidant, antibacterial, and anticancer activities of individual as well as combined 80% ethanolic extracts of Artemisia absi
Autor:
Muhammad Qasim, Saima Riazuddin, Muhammad Noman, Muhammad Ali, Sakina Rehman, Zubair M. Ahmed, Shazia Anwer Bukhari
Publikováno v:
Molecular Biology Reports. 47:9987-9993
Hearing loss (HL) is clinically and genetically heterogeneous disorder and is the most frequent occurring sensory deficit in humans. This study was conducted to decipher the genetic cause of HL occurring in two large consanguineous Pakistani families
Autor:
Muhammad Ali, Rida Iqbal, Muhammad Safdar, Sehrish Murtaza, Ghulam Mustafa, Muhammad Sajjad, Shazia Anwer Bukhari, Tayyaba Huma
Publikováno v:
Molecular Biology Reports. 49:3367-3367
Autor:
Mohammed Nasser Alyemeni, Nudrat Aisha Akram, Parvaiz Ahmad, Shahzad Bashir, Ghulam Mustafa, Bushra Sadia, Mahmood-ur Rahman, Shazia Anwer Bukhari
Publikováno v:
3 Biotech
In this study, the Sr22 gene was isolated and prepared for transformation in disease-susceptible commercial high-yielding wheat (Triticum aestivum L.) cultivar Lasani-2008. The Sr22 fragment was initially inserted in plasmid pUC57 for sequence confir
Autor:
Muhammad Qasim, Muhammad Asif, Irfan Ali, Shahid Mahmood Baig, Shazia Anwer Bukhari, Muhammad Imran Naseer, Mahmood Rasool, Neelam Sultan
Publikováno v:
Genes & Genomics. 40:553-559
Retinitis pigmentosa (RP) is the most frequent genetically and clinically heterogeneous inherited retinal degeneration. To date, more than 80 genes have been identified that cause autosomal dominant, autosomal recessive and X linked RP. However, locu