L
Luqman Khan
Researcher at University of California, San Francisco
Publications - 23
Citations - 85
Luqman Khan is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Cytidine deaminase & Population. The author has an hindex of 5, co-authored 21 publications receiving 53 citations. Previous affiliations of Luqman Khan include Government College University, Faisalabad & Tohoku University.
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Tick burden and tick species prevalence in small ruminants of different agencies of the Federally Administered Tribal Areas (FATA), Pakistan
Adil Khan,Nasreen Nasreen,Sadaf Niaz,Said Sajjad Ali Shah,Robert D. Mitchell,Sultan Ayaz,Huma Naeem,Luqman Khan,Adalberto A. Pérez de León +8 more
TL;DR: T ticks collected from goats and sheep of the FATA region of Pakistan found that Rhipicephalus sanguineus and Haemaphysalis sulcata were the two most abundant species on small ruminants in the region.
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Exploring the utility of extracellular vesicles in ameliorating viral infection-associated inflammation, cytokine storm and tissue damage.
TL;DR: Extracellular vesicles (EVs) have emerged as potential mediators of intercellular communication as discussed by the authors and hold great promise for therapeutic treatments, particularly in treating a potentially fatal autoimmune response and attenuate inflammation.
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Hearing impairments, presbycusis and the possible therapeutic interventions
TL;DR: Hearing loss can be congenital or acquired, syndromic; HL associated with other abnormalities or non-syndromic, HL is not associated with any other anomalies, and genetic of presbycusis is not well-known.
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Molecular basis of glaucoma and its therapeutical analysis in Pakistan: an overview
TL;DR: This review will focus on Glaucoma which comprises a predictable visual illnesses concerning optic nerve deterioration and if remains without any cure can result in failure in eyesight.
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Genetics of congenital cataract, its diagnosis and therapeutics
TL;DR: Discovering the mutations and the genes responsible for cataractogenesis are important in achieving a response to the molecular deficiencies and pathophysiologic features of inherited congenital cataracts.