Search Results - "Arshad, Muhammad Waqar"

Linking the willingness of smallholder dairy farmers to adopt minimum food safety and quality standards to the country's export potential by Arshad, Muhammad Waqar, Moazzam, Muhammad, Raziq, Muhammad Mustafa, Ahmed, Waqas

“…Summary Food safety is a crucial aspect of human well‐being, covered under the second sustainable development goal (SDG). Sustainable food supply chains must…”
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Designing a multi-epitope vaccine against Shigella dysenteriae using immuno-informatics approach by Qureshi, Hurria, Basheer, Amina, Faheem, Muhammad, Arshad, Muhammad Waqar, Rai, Sunil Kumar, Jamal, Syed Babar

“…has been recognized as the second most prevalent pathogen associated with diarrhea that contains blood, contributing to 12.9% of reported cases, and it is…”
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FRMD7 Gene Alterations in a Pakistani Family Associated with Congenital Idiopathic Nystagmus by Arshad, Muhammad Waqar, Shabbir, Muhammad Imran, Asif, Saaim, Shahzad, Mohsin, Leydier, Larissa, Rai, Sunil Kumar

“…Congenital idiopathic nystagmus (CIN) is an oculomotor disorder characterized by repetitive and rapid involuntary movement of the eye that usually develops in…”
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Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families by Khan, Jahangir, Asif, Saaim, Ghani, Shamsul, Khan, Hamid, Arshad, Muhammad Waqar, Khan, Shujaat Ali, Lin, Siying, Baple, Emma L, Salter, Claire, Crosby, Andrew H, Rawlins, Lettie, Shabbir, Muhammad Imran

“…Oculocutaneous albinism (OCA) is a genetically heterogeneous condition that is associated with reduced or absent melanin pigment in the skin, hair, and eyes,…”
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PCR Optimization for Beginners: A Step by Step Guide by Asif, Saaim, Khan, Maaz, Waqar Arshad, Muhammad, Shabbir, Muhammad Imran

“…Background: The invention of Polymerase Chain Reaction (PCR) marked a breakthrough in biomedical research. Its invention divided the timeline into an era…”
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IFRMD7/I Gene Alterations in a Pakistani Family Associated with Congenital Idiopathic Nystagmus by Arshad, Muhammad Waqar, Shabbir, Muhammad Imran, Asif, Saaim, Shahzad, Mohsin, Leydier, Larissa, Rai, Sunil Kumar

“…Congenital idiopathic nystagmus (CIN) is an oculomotor disorder characterized by repetitive and rapid involuntary movement of the eye that usually develops in…”
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Identification of Novel Mutation in CNGA3 gene by Whole-Exome Sequencing and In-Silico Analyses for Genotype-Phenotype Assessment with Autosomal Recessive Achromatopsia in Pakistani families by Arshad, Muhammad Waqar, Lee, Yujin, Malik, Muhammad Arshad, Khan, Jahangir, Khan, Aslam, Kareem, Abdul, Kang, Changsoo, Shabbir, Muhammad Imran

“…To identify the underlying genetic anomalies in two consanguineous Pakistani families with autosomal recessive achromatopsia. The exploratory study was…”
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Junctional Epidermolysis Bullosa (Non-Herlitz Type) by Bhinder, Munir Ahmad, Arshad, Muhammad Waqar, Zahoor, Muhammad Yasir, Shehzad, Wasim, Tariq, Muhammad, Shabbir, Muhammad Imran

“…Junctional epidermolysis bullosa (JEB) is a recessively inherited skin blistering disease and is caused due to abnormalities in proteins that hold layers of…”
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Mutations in TYR and OCA2 associated with oculocutaneous albinism in Pakistani families by Arshad, Muhammad Waqar, Harlalka, Gaurav V., Lin, Siying, D'Atri, Ilaria, Mehmood, Sarmad, Shakil, Muhammad, Hassan, Muhammad Jawad, Chioza, Barry A., Self, Jay E., Ennis, Sarah, O'Gorman, Luke, Norman, Chelsea, Aman, Tahir, Ali, Shaheer Sabz, Kaul, Haiba, Baple, Emma L., Crosby, Andrew H., Ullah, Muhammad Ikram, Shabbir, Muhammad Imran

“…Oculocutaneous albinism (OCA) is a genetically heterogeneous disorder of abnormal melanin synthesis, resulting in decreased or absent pigmentation of eyes,…”
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