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Molecular Vision|June 6, 2012
Identification of recurrent and novel mutations in TULP1 in Pakistani families with early-onset retinitis pigmentosaMuhammad Ajmal, Muhammad Imran Khan, Shazia Micheal, et al.
Molecular Vision|June 28, 2012
Novel mutations in RDH5 cause fundus albipunctatus in two consanguineous Pakistani familiesMuhammad Ajmal, Muhammad Imran Khan, Kornelia Neveling, et al.
Metabolic Brain Disease|November 27, 2022
The curative and mechanistic acumen of curcuminoids formulations against haloperidol induced Parkinson's disease animal modelUzma Saleem, Sundas Khalid, Zunera Chauhdary, et al.
Molecules (Basel, Switzerland)|November 11, 2022
Uncovering the Anticancer Potential of Polydatin: A Mechanistic InsightMuhammad Ajmal Shah, Ayesha Hamid, Hafiza Ishmal Faheem, et al.
Frontiers in Public Health|July 26, 2021
Factors Behind the Higher COVID-19 Risk in Diabetes: A Critical ReviewAmany Magdy Beshbishy, Victor B Oti, Diaa E Hussein, et al.
The Science of the Total Environment|May 30, 2020
Exploring the multimodal role of phytochemicals in the modulation of cellular signaling pathways to combat age-related neurodegenerationMd Sahab Uddin, Md Farhad Hossain, Abdullah Al Mamun, et al.
Plos One|June 21, 2014
Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani familiesSobia Shafique, Saima Siddiqi, Margit Schraders, et al.
Journal of Medical Genetics|April 17, 2014
A missense mutation in the splicing factor gene DHX38 is associated with early-onset retinitis pigmentosa with macular colobomaMuhammad Ajmal, Muhammad Imran Khan, Kornelia Neveling, et al.
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