Showing 1 - 12 results of 12 for search 'Shahid Y. Khan', query time: 0.04s Refine Results
  1. 1
    Generation and proteome profiling of PBMC-originated, iPSC-derived lentoid bodies

    Generation and proteome profiling of PBMC-originated, iPSC-derived lentoid bodies by Muhammad Ali, Firoz Kabir, Snehal Raskar, Santosh Renuse, Chan Hyun Na, Michael Delannoy, Shahid Y. Khan, S. Amer Riazuddin

    Published 2020-07-01
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  2. 2
    Autosomal recessive congenital cataracts linked to HSF4 in a consanguineous Pakistani family.

    Autosomal recessive congenital cataracts linked to HSF4 in a consanguineous Pakistani family. by Xiaodong Jiao, Shahid Y Khan, Haiba Kaul, Tariq Butt, Muhammad Asif Naeem, Sheikh Riazuddin, J Fielding Hejtmancik, S Amer Riazuddin

    Published 2019-01-01
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  3. 3
    A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts

    A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts by Bushra Irum, Firoz Kabir, Nadav Shoshany, Shahid Y. Khan, Bushra Rauf, Muhammad Asif Naeem, Tanveer A. Qaiser, Sheikh Riazuddin, J. Fielding Hejtmancik, S. Amer Riazuddin

    Published 2022-09-01
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  4. 4
    Examining the effects of cigarette smoke on mouse lens through a multi OMIC approach

    Examining the effects of cigarette smoke on mouse lens through a multi OMIC approach by Shahid Y. Khan, Muhammad Ali, Yura Jang, Taekyung Ryu, Andrew J. Schwab, Brian O. Ingram, Peter H. Cable, Chan Hyun Na, James T. Handa, S. Amer Riazuddin

    Published 2021-09-01
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  5. 5
    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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  6. 6
    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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  7. 7
    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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  8. 8
    Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts.

    Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts. by Bushra Irum, Shahid Y Khan, Muhammad Ali, Haiba Kaul, Firoz Kabir, Bushra Rauf, Fareeha Fatima, Raheela Nadeem, Arif O Khan, Saif Al Obaisi, Muhammad Asif Naeem, Idrees A Nasir, Shaheen N Khan, Tayyab Husnain, Sheikh Riazuddin, Javed Akram, Allen O Eghrari, S Amer Riazuddin

    Published 2016-01-01
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  9. 9
    Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.

    Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts. by Bushra Irum, Shahid Y Khan, Muhammad Ali, Muhammad Daud, Firoz Kabir, Bushra Rauf, Fareeha Fatima, Hira Iqbal, Arif O Khan, Saif Al Obaisi, Muhammad Asif Naeem, Idrees A Nasir, Shaheen N Khan, Tayyab Husnain, Sheikh Riazuddin, Javed Akram, Allen O Eghrari, S Amer Riazuddin

    Published 2016-01-01
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  10. 10
    Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.

    Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts. by Bushra Irum, Shahid Y Khan, Muhammad Ali, Muhammad Daud, Firoz Kabir, Bushra Rauf, Fareeha Fatima, Hira Iqbal, Arif O Khan, Saif Al Obaisi, Muhammad Asif Naeem, Idrees A Nasir, Shaheen N Khan, Tayyab Husnain, Sheikh Riazuddin, Javed Akram, Allen O Eghrari, S Amer Riazuddin

    Published 2017-01-01
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  11. 11
    FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1

    FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1 by Shahid Y. Khan, Shivakumar Vasanth, Firoz Kabir, John D. Gottsch, Arif O. Khan, Raghothama Chaerkady, Mei-Chong W. Lee, Carmen C. Leitch, Zhiwei Ma, Julie Laux, Rafael Villasmil, Shaheen N. Khan, Sheikh Riazuddin, Javed Akram, Robert N. Cole, C. Conover Talbot, Nader Pourmand, Norann A. Zaghloul, J. Fielding Hejtmancik, S. Amer Riazuddin

    Published 2016-04-01
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  12. 12
    Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis.

    Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis. by Pooja Biswas, Adda L Villanueva, Angel Soto-Hermida, Jacque L Duncan, Hiroko Matsui, Shyamanga Borooah, Berzhan Kurmanov, Gabriele Richard, Shahid Y Khan, Kari Branham, Bonnie Huang, John Suk, Benjamin Bakall, Jeffrey L Goldberg, Luis Gabriel, Naheed W Khan, Pongali B Raghavendra, Jason Zhou, Sindhu Devalaraja, Andrew Huynh, Akhila Alapati, Qais Zawaydeh, Richard G Weleber, John R Heckenlively, J Fielding Hejtmancik, Sheikh Riazuddin, Paul A Sieving, S Amer Riazuddin, Kelly A Frazer, Radha Ayyagari

    Published 2021-10-01
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