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A 3' untranslated region polymorphism rs2304277 in the DNA repair pathway gene OGG1 is a novel risk modulator for urothelial bladder carcinoma.

artículo científico publicado en 2017

A missense mutation in the splicing factor gene DHX38 is associated with early-onset retinitis pigmentosa with macular coloboma.

artículo científico publicado en 2014

Association of IGF1 and VEGFA polymorphisms with diabetic retinopathy in Pakistani population

scientific article published on 31 August 2019

Association of rs10490924 in ARMS2/HTRA1 with age-related macular degeneration in the Pakistani population

scientific article published on 20 March 2019

CBS mutations and MTFHR SNPs causative of hyperhomocysteinemia in Pakistani children.

artículo científico publicado en 2018

CLRN1 Mutations Cause Nonsyndromic Retinitis Pigmentosa ⬇️

artículo científico publicado el 18 de febrero de 2011

Compound heterozygous mutations p.Q1530X and 6103delG in COL7A1 causing recessive dystrophic epidermolysis bullosa in a Pakistani family ⬇️

artículo científico publicado el 4 de octubre de 2011

Cystathione gamma lyase/Hydrogen Sulphide Pathway Up Regulation Enhances the Responsiveness of α1A and α1B-Adrenoreceptors in the Kidney of Rats with Left Ventricular Hypertrophy

artículo científico publicado en 2016

Exome sequencing identifies three novel candidate genes implicated in intellectual disability

artículo científico publicado en 2014

Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum

scientific article published on 06 October 2016

Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families.

artículo científico publicado en 2014

Identification of novel potential genetic predictors of urothelial bladder carcinoma susceptibility in Pakistani population.

artículo científico publicado en 2017

Implementation of public health genomics in Pakistan

artículo científico publicado en 2019

Interaction between nitric oxide and renal α1-adrenoreceptors mediated vasoconstriction in rats with left ventricular hypertrophyin Wistar Kyoto rats.

artículo científico publicado en 2018

Molecular Mechanisms of Complement System Proteins and Matrix Metalloproteinases in the Pathogenesis of Age-Related Macular Degeneration

scientific article published on 01 January 2019

Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cells

artículo científico publicado en 2016

Role of Nitric Oxide in the Cardiovascular and Renal Systems

artículo científico publicado en 2018

TNF-α Genetic Predisposition and Higher Expression of Inflammatory Pathway Components in Keratoconus.

artículo científico publicado en 2017

The molecular basis of retinal dystrophies in pakistan.

artículo científico publicado en 2014

Up Regulation of cystathione γ lyase and Hydrogen Sulphide in the Myocardium Inhibits the Progression of Isoproterenol-Caffeine Induced Left Ventricular Hypertrophy in Wistar Kyoto Rats

artículo científico publicado en 2016

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