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Regenerative Therapy|February 8, 2023
Priming with caffeic acid enhances the potential and survival ability of human adipose-derived stem cells to counteract hypoxiaH M Shifa Ul Haq, Ramla Ashfaq, Azra Mehmood, et al.
Advances in Experimental Medicine and Biology|May 4, 2018
Whole-Exome Sequencing Identifies Novel Variants that Co-segregates with Autosomal Recessive Retinal Degeneration in a Pakistani PedigreePooja Biswas, Muhammad Asif Naeem, Muhammad Hassaan Ali, et al.
Molecular Vision|December 2, 2005
A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 geneQingjiong Zhang, Fareeha Zulfiqar, S Amer Riazuddin, et al.
The Journal of Clinical Investigation|February 7, 2018
Modifier variant of METTL13 suppresses human GAB1-associated profound deafnessRizwan Yousaf, Zubair M Ahmed, Arnaud Pj Giese, et al.
Molecular Vision|June 10, 2011
Mutations in the β-subunit of rod phosphodiesterase identified in consanguineous Pakistani families with autosomal recessive retinitis pigmentosaShahbaz Ali, S Amer Riazuddin, Amber Shahzadi, et al.
World Journal of Gastroenterology|October 28, 2009
Hepatitis C virus genotype 3a infection and hepatocellular carcinoma: Pakistan experienceMuhammad Idrees, Shazia Rafique, Irshadur Rehman, et al.
Molecular Vision|July 24, 2013
Novel mutations in RPE65 identified in consanguineous Pakistani families with retinal dystrophyFiroz Kabir, Shagufta Naz, S Amer Riazuddin, et al.
Investigative Ophthalmology & Visual Science|June 28, 2005
Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani familiesS Amer Riazuddin, Fareeha Zulfiqar, Qingjiong Zhang, et al.
Human Genome Variation|September 8, 2022
A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataractsBushra Irum, Firoz Kabir, Nadav Shoshany, et al.
Human Genome Variation|December 6, 2016
Mutations in phosphodiesterase 6 identified in familial cases of retinitis pigmentosaInayat Ullah, Firoz Kabir, Clare Brooks S Gottsch, et al.
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