University research records

Shaheed Zulfiqar Ali Bhutto Medical University, Islamabad

16 imported, source-linked research records. Open-access records.

Open-access records

16 matching research records

Only records linked to Shaheed Zulfiqar Ali Bhutto Medical University, Islamabad are included. Historical ingestion is still running; these are imported records, not a count of all research worldwide.

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Showing 1–16 of 16 matching records. Counts update as records arrive.

  1. Integrating Epigenetic Clocks in Aesthetic Dermatology: A New Paradigm for Personalized Skin Rejuvenation

    May 8, 2026 · 0 citations · Open access

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  2. Evaluation of Essential Newborn Care Practices among Mothers in Community and Health Facility Settings in Tehsil Kharian District Gujrat, Pakistan

    March 30, 2026 · 0 citations · Open access

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  3. A Randomized Trial of Collagen Peptides Combined with Resistance Training for Pain and Cartilage Turnover in Knee Osteoarthritis

    December 15, 2025 · 0 citations · Open access

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  4. Novel Insights into T-Cell Exhaustion and Cancer Biomarkers in PDAC Using ScRNA-Seq

    August 7, 2025 · 4 citations · Open access

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  5. Vitamin C as a Serum Uric Acid Lowering Agent in Hyperuricaemia

    June 1, 2025 · 0 citations · Open access

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  6. Efficacy of Sodium-Glucose Cotransporter-2 (SGLT2) Inhibitors in Heart Failure Management: A Narrative Review

    September 29, 2024 · 0 citations · Open access

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  7. PHARMACOTHERAPEUTIC PURSUANCE AND REHILIBATION OF THE PATIENTS ADMITTED IN THE INTERNAL MEDICINE SERVICE OF THE KING EDWARD MEDICAL UNIVERSITY HOSPITAL

    December 30, 2023 · 0 citations · Open access

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  8. Tracing down the updates on Ebola virus surges: An update on anti-ebola therapeutic strategies

    September 1, 2023 · 7 citations · Open access

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  9. Depression and Sleep Issues in Aging: A Prospective Study

    September 30, 2022 · 2 citations · Open access

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  10. Effectiveness of Balance Training and Postural Stability in Post Stroke Patients; Randomized Control Trial

    April 30, 2022 · 0 citations · Open access

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  11. THUMPD1 bi-allelic variants cause loss of tRNA acetylation and a syndromic neurodevelopmental disorder

    February 22, 2022 · 52 citations · Open access

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  12. Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness

    September 24, 2020 · 20 citations · Open access

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  13. Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouse

    March 28, 2018 · 48 citations · Open access

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  14. Modifier variant of METTL13 suppresses human GAB1–associated profound deafness

    February 6, 2018 · 44 citations · Open access

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  15. Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts

    December 9, 2016 · 12 citations · Open access

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  16. Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial cases.

    January 1, 2016 · 16 citations · Open access

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