Pluripotent stem cell–derived corneal endothelial cells as an alternative to donor corneal endothelium in keratoplasty

por Ali, Muhammad, Khan, Shahid Y., Gottsch, John D., Hutchinson, Eric K., Khan, Aisha, Riazuddin, S. Amer
Publicado 2021

Comparative transcriptome analysis of hESC- and iPSC-derived lentoid bodies

por Ali, Muhammad, Kabir, Firoz, Thomson, Jason J., Ma, Yinghong, Qiu, Caihong, Delannoy, Michael, Khan, Shahid Y., Riazuddin, S. Amer
Publicado 2019

Novel mutations in LTBP2 identified in familial cases of primary congenital glaucoma

por Rauf, Bushra, Irum, Bushra, Khan, Shahid Y., Kabir, Firoz, Naeem, Muhammad Asif, Riazuddin, Sheikh, Ayyagari, Radha, Riazuddin, S. Amer
Publicado 2020

Autosomal recessive congenital cataracts linked to HSF4 in a consanguineous Pakistani family

por Jiao, Xiaodong, Khan, Shahid Y., Kaul, Haiba, Butt, Tariq, Naeem, Muhammad Asif, Riazuddin, Sheikh, Hejtmancik, J. Fielding, Riazuddin, S. Amer
Publicado 2019

Proteome Profiling of Developing Murine Lens Through Mass Spectrometry

por Khan, Shahid Y., Ali, Muhammad, Kabir, Firoz, Renuse, Santosh, Na, Chan Hyun, Talbot, C. Conover, Hackett, Sean F., Riazuddin, S. Amer
Publicado 2018

Cigarette Smoke Triggers Loss of Corneal Endothelial Cells and Disruption of Descemet's Membrane Proteins in Mice

por Ali, Muhammad, Khan, Shahid Y., Jang, Yura, Na, Chan Hyun, Talbot, C. Conover, Gottsch, John D., Handa, James T., Riazuddin, S. Amer
Publicado 2021

Identification of novel transcripts and peptides in developing murine lens

por Khan, Shahid Y., Ali, Muhammad, Kabir, Firoz, Chen, Ruiqiang, Na, Chan Hyun, Lee, Mei-Chong W., Pourmand, Nader, Hackett, Sean F., Riazuddin, S. Amer
Publicado 2018

Whole genome sequencing data for two individuals of Pakistani descent

por Khan, Shahid Y., Kabir, Firoz, M’Hamdi, Oussama, Jiao, Xiaodong, Naeem, Muhammad Asif, Khan, Shaheen N., Riazuddin, Sheikh, Hejtmancik, J. Fielding, Riazuddin, S. Amer
Publicado 2018

A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts

por Irum, Bushra, Kabir, Firoz, Shoshany, Nadav, Khan, Shahid Y., Rauf, Bushra, Naeem, Muhammad Asif, Qaiser, Tanveer A., Riazuddin, Sheikh, Hejtmancik, J. Fielding, Riazuddin, S. Amer
Publicado 2022

Generation and Proteome Profiling of PBMC-Originated, iPSC-Derived Corneal Endothelial Cells

por Ali, Muhammad, Khan, Shahid Y., Vasanth, Shivakumar, Ahmed, Mariya R., Chen, Ruiqiang, Na, Chan Hyun, Thomson, Jason J., Qiu, Caihong, Gottsch, John D., Riazuddin, S. Amer
Publicado 2018

Examining the effects of cigarette smoke on mouse lens through a multi OMIC approach

por Khan, Shahid Y., Ali, Muhammad, Jang, Yura, Ryu, Taekyung, Schwab, Andrew J., Ingram, Brian O., Cable, Peter H., Na, Chan Hyun, Handa, James T., Riazuddin, S. Amer
Publicado 2021

Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts

por Jiaox, Xiaodong, Khan, Shahid Y., Irum, Bushra, Khan, Arif O., Wang, Qiwei, Kabir, Firoz, Khan, Asma A., Husnain, Tayyab, Akram, Javed, Riazuddin, Sheikh, Hejtmancik, J. Fielding, Riazuddin, S. Amer
Publicado 2015

Correction: Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts

por Jiao, Xiaodong, Khan, Shahid Y., Irum, Bushra, Khan, Arif O., Wang, Qiwei, Kabir, Firoz, Khan, Asma A., Husnain, Tayyab, Akram, Javed, Riazuddin, Sheikh, Hejtmancik, J. Fielding, Riazuddin, S. Amer
Publicado 2017

Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma

por Rauf, Bushra, Khan, Shahid Y., Jiao, Xiaodong, Irum, Bushra, Ashfaq, Ramla, Zehra, Mubashra, Khan, Asma A., Naeem, Muhammad Asif, Shahzad, Mohsin, Riazuddin, Sheikh, Hejtmancik, J. Fielding, Riazuddin, S. Amer
Publicado 2022

Mutations in FYCO1 identified in families with congenital cataracts

por Iqbal, Hira, Khan, Shahid Y., Zhou, Lin, Irum, Bushra, Ali, Muhammad, Ahmed, Mariya R., Shahzad, Mohsin, Ali, Muhammad Hassaan, Naeem, Muhammad Asif, Riazuddin, Sheikh, Hejtmancik, J. Fielding, Riazuddin, S. Amer
Publicado 2020

Splice-site mutations identified in PDE6A responsible for retinitis pigmentosa in consanguineous Pakistani families

por Khan, Shahid Y., Ali, Shahbaz, Naeem, Muhammad Asif, Khan, Shaheen N., Husnain, Tayyab, Butt, Nadeem H., Qazi, Zaheeruddin A., Akram, Javed, Riazuddin, Sheikh, Ayyagari, Radha, Hejtmancik, J. Fielding, Riazuddin, S. Amer
Publicado 2015

Whole genome sequencing data of multiple individuals of Pakistani descent

por Khan, Shahid Y., Ali, Muhammad, Lee, Mei-Chong W., Ma, Zhiwei, Biswas, Pooja, Khan, Asma A., Naeem, Muhammad Asif, Riazuddin, Saima, Riazuddin, Sheikh, Ayyagari, Radha, Hejtmancik, J. Fielding, Riazuddin, S. Amer
Publicado 2020

Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts

por Irum, Bushra, Khan, Shahid Y., Ali, Muhammad, Kaul, Haiba, Kabir, Firoz, Rauf, Bushra, Fatima, Fareeha, Nadeem, Raheela, Khan, Arif O., Al Obaisi, Saif, Naeem, Muhammad Asif, Nasir, Idrees A., Khan, Shaheen N., Husnain, Tayyab, Riazuddin, Sheikh, Akram, Javed, Eghrari, Allen O., Riazuddin, S. Amer
Publicado 2016

Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts

por Irum, Bushra, Khan, Shahid Y., Ali, Muhammad, Daud, Muhammad, Kabir, Firoz, Rauf, Bushra, Fatima, Fareeha, Iqbal, Hira, Khan, Arif O., Al Obaisi, Saif, Naeem, Muhammad Asif, Nasir, Idrees A., Khan, Shaheen N., Husnain, Tayyab, Riazuddin, Sheikh, Akram, Javed, Eghrari, Allen O., Riazuddin, S. Amer
Publicado 2016

Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts

por Irum, Bushra, Khan, Shahid Y., Ali, Muhammad, Daud, Muhammad, Kabir, Firoz, Rauf, Bushra, Fatima, Fareeha, Iqbal, Hira, Khan, Arif O., Obaisi, Saif Al, Naeem, Muhammad Asif, Nasir, Idrees A., Khan, Shaheen N., Husnain, Tayyab, Riazuddin, Sheikh, Akram, Javed, Eghrari, Allen O., Riazuddin, S. Amer
Publicado 2017