Результаты поиска - Muhammad Ajmal
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Global Maximum Power Point Tracking of Photovoltaic Systems Using Artificial Intelligence по Rukhsar, Aidha Muhammad Ajmal, Yongheng Yang
Опубликовано 2025-06-01Recently, artificial intelligence (AI) has become a promising solution to the optimization of the energy harvesting and performance of photovoltaic (PV) systems. Traditional maximum power point tracking (MPPT) algorithms have several drawbacks on tracking the global maximum power point (GMPP) under...
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Targeted Drug Delivery of Anticancer Agents Using C<sub>5</sub>N<sub>2</sub> Substrate: Insights from Density Functional Theory по Syeda Huda Mehdi Zaidi, Muhammad Ajmal, Muhammad Ali Hashmi, Ahmed Lakhani
Опубликовано 2025-06-01Cancer has a threatening impact on human health, and it is one of the primary causes of fatalities worldwide. Different conventional treatments have been employed to treat cancer, but their non-specific nature reduces their therapeutic efficacy. This study employs a C<sub>5</sub>N<sub...
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Whole exome sequencing reveals pathogenic variants in CNGA3, CACNA1F, and RPGRIP1 in consanguineous Pakistani families with diverse retinal phenotypes по Jahangir Khan Tareen, Hamid Khan, Shamsul Ghani, Saeed Khan, Bakhtawar Khan, Yurong Wu, Muhammad Ajmal Khan, Syed Shahab Ud Din Shah, Abrar Hussain, Mubin Mustafa Kiyani, Shahid Bashir, Atta Ur Rehman, Muhammad Imran Shabbir, Hong-Tao Li
Опубликовано 2025-01-01Полный текст
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Whole exome sequencing reveals pathogenic variants in CNGA3, CACNA1F, and RPGRIP1 in consanguineous Pakistani families with diverse retinal phenotypes. по Jahangir Khan Tareen, Hamid Khan, Shamsul Ghani, Saeed Khan, Bakhtawar Khan, Yurong Wu, Muhammad Ajmal Khan, Syed Shahab Ud Din Shah, Abrar Hussain, Mubin Mustafa Kiyani, Shahid Bashir, Atta Ur Rehman, Muhammad Imran Shabbir, Hong-Tao Li
Опубликовано 2025-01-01This study investigates the genetic basis of retinal diseases in four consanguineous families from Pakistan, focusing on mutations in the CNGA3, CACNA1F, and RPGRIP1 genes that are implicated in retinal dysfunctions such as achromatopsia, congenital stationary night blindness, and retinal dystrophie...
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