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Muhammad Ajmal

Showing results (311-320 of 333) with videos related to

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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.
Frontiers in Endocrinology|June 24, 2024
Genetic and clinical characteristics of patients with lipoprotein lipase deficiency from Slovenia and Pakistan: case series and systematic literature reviewQuratul Ain, Matija Cevc, Tatiana Marusic, 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.
Molecules (Basel, Switzerland)|November 11, 2022
Uncovering the Anticancer Potential of Polydatin: A Mechanistic InsightMuhammad Ajmal Shah, Ayesha Hamid, Hafiza Ishmal Faheem, 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.
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.
Plos One|July 30, 2025
Whole exome sequencing reveals pathogenic variants in CNGA3, CACNA1F, and RPGRIP1 in consanguineous Pakistani families with diverse retinal phenotypesJahangir Khan Tareen, Hamid Khan, Shamsul Ghani, et al.
Pageof 34

Showing results (311-320 of 333) with videos related to

Sort By:
Pageof 34
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.
Frontiers in Endocrinology|June 24, 2024
Genetic and clinical characteristics of patients with lipoprotein lipase deficiency from Slovenia and Pakistan: case series and systematic literature reviewQuratul Ain, Matija Cevc, Tatiana Marusic, 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.
Molecules (Basel, Switzerland)|November 11, 2022
Uncovering the Anticancer Potential of Polydatin: A Mechanistic InsightMuhammad Ajmal Shah, Ayesha Hamid, Hafiza Ishmal Faheem, 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.
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.
Plos One|July 30, 2025
Whole exome sequencing reveals pathogenic variants in CNGA3, CACNA1F, and RPGRIP1 in consanguineous Pakistani families with diverse retinal phenotypesJahangir Khan Tareen, Hamid Khan, Shamsul Ghani, et al.
Pageof 34