Showing 1 - 7 results of 7 for search 'Asma A. Khan', query time: 0.04s Refine Results
  1. 1
    Endosomal TLR-8 Senses microRNA-1294 Resulting in the Production of NFḱB Dependent Cytokines

    Endosomal TLR-8 Senses microRNA-1294 Resulting in the Production of NFḱB Dependent Cytokines by Linda Pluta, Babak Yousefi, Blossom Damania, Asma A. Khan

    Published 2019-12-01
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  2. 2
    A Prospective Analysis of the Correlation Between Postoperative Pain and Vital Pulp Therapy

    A Prospective Analysis of the Correlation Between Postoperative Pain and Vital Pulp Therapy by Mark Shallal-Ayzin, Tam Trinh, William Yeung, Peter Z. Tawil, Carol L. Haggerty, Di Wu, Asma A. Khan

    Published 2021-03-01
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  3. 3
    A Common Ancestral Mutation in CRYBB3 Identified in Multiple Consanguineous Families with Congenital Cataracts.

    A Common Ancestral Mutation in CRYBB3 Identified in Multiple Consanguineous Families with Congenital Cataracts. by Xiaodong Jiao, Firoz Kabir, Bushra Irum, Arif O Khan, Qiwei Wang, David Li, Asma A Khan, Tayyab Husnain, Javed Akram, Sheikh Riazuddin, J Fielding Hejtmancik, S Amer Riazuddin

    Published 2016-01-01
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  4. 4
    Correction: Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts.

    Correction: Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts. by Xiaodong Jiao, Shahid Y Khan, Bushra Irum, Arif O Khan, Qiwei Wang, Firoz Kabir, Asma A Khan, Tayyab Husnain, Javed Akram, Sheikh Riazuddin, J Fielding Hejtmancik, S Amer Riazuddin

    Published 2017-01-01
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  5. 5
    Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts.

    Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts. by Xiaodong Jiao, Shahid Y Khan, Bushra Irum, Arif O Khan, Qiwei Wang, Firoz Kabir, Asma A Khan, Tayyab Husnain, Javed Akram, Sheikh Riazuddin, J Fielding Hejtmancik, S Amer Riazuddin

    Published 2015-01-01
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  6. 6
    Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma

    Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma by Bushra Rauf, Shahid Y. Khan, Xiaodong Jiao, Bushra Irum, Ramla Ashfaq, Mubashra Zehra, Asma A. Khan, Muhammad Asif Naeem, Mohsin Shahzad, Sheikh Riazuddin, J. Fielding Hejtmancik, S. Amer Riazuddin

    Published 2022-10-01
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  7. 7
    Variants of NAV3, a neuronal morphogenesis protein, cause intellectual disability, developmental delay, and microcephaly

    Variants of NAV3, a neuronal morphogenesis protein, cause intellectual disability, developmental delay, and microcephaly by Amama Ghaffar, Tehmeena Akhter, Petter Strømme, Doriana Misceo, Amjad Khan, Eirik Frengen, Muhammad Umair, Bertrand Isidor, Benjamin Cogné, Asma A. Khan, Ange-Line Bruel, Arthur Sorlin, Paul Kuentz, Christine Chiaverini, A. Micheil Innes, Michael Zech, Marek Baláž, Petra Havrankova, Robert Jech, Zubair M. Ahmed, Sheikh Riazuddin, Saima Riazuddin

    Published 2024-07-01
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