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European Journal of Human Genetics : EJHG|April 13, 2019
A genome-wide analysis in consanguineous families reveals new chromosomal loci in specific language impairment (SLI)Erin M Andres, Huma Hafeez, Adnan Yousaf, et al.Growth Factors (Chur, Switzerland)|November 8, 2017
Serum from CCl4-induced acute rat injury model induces differentiation of ADSCs towards hepatic cells and reduces liver fibrosisMaria Tayyab Baig, Gibran Ali, Sana Javaid Awan, et al.Life Sciences|July 8, 2017
Protective role of vitamin E preconditioning of human dermal fibroblasts against thermal stress in vitroHira Butt, Azra Mehmood, Muhammad Ali, et al.Journal of Translational Medicine|November 2, 2011
Huh-7 cell line as an alternative cultural model for the production of human like erythropoietin (EPO)Humera Kausar, Sana Gull, Bushra Ijaz, et al.American Journal of Ophthalmology|March 16, 2010
A novel locus for autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family maps to chromosome 2pShagufta Naz, S Amer Riazuddin, Lin Li, et al.Investigative Ophthalmology & Visual Science|January 27, 2005
A new locus for autosomal recessive nuclear cataract mapped to chromosome 19q13 in a Pakistani familyS Amer Riazuddin, Afshan Yasmeen, Qingjiong Zhang, et al.Molecular Vision|March 14, 2020
Novel mutations in LTBP2 identified in familial cases of primary congenital glaucomaBushra Rauf, Bushra Irum, Shahid Y Khan, et al.Plos Genetics|March 29, 2018
Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouseRizwan Yousaf, Chunfang Gu, Zubair M Ahmed, et al.Life Sciences|July 16, 2020
Curcumin preconditioned human adipose derived stem cells co-transplanted with platelet rich plasma improve wound healing in diabetic ratsHafiz Ghufran, Azra Mehmood, Maryam Azam, et al.Plos One|December 10, 2019
Autosomal recessive congenital cataracts linked to HSF4 in a consanguineous Pakistani familyXiaodong Jiao, Shahid Y Khan, Haiba Kaul, et al.Pageof 22