نتایج جستجو برای: pakistani population

تعداد نتایج: 697482  

Journal: :Saudi Journal of Kidney Diseases and Transplantation 2015

Journal: :Stroke 2005
Danish Saleheen Shabbar Bukhari Shajjia Razi Haider Aisha Nazir Shaheen Khanum Saad Shafqat M Kashif Anis Philippe Frossard

BACKGROUND AND OBJECTIVES Identification of STRK1 locus by the deCODE group followed by the discovery of phosphodiesterase 4D (PDE4D) gene in strong association with ischemic stroke patients has provided useful insights toward understanding the genetic etiology of the disease. In this study, we aimed at investigating the association between 3 polymorphisms of the PDE4D gene and ischemic stroke ...

2016
Garima Arora Daniel F. Mackay David I. Conway Jill P. Pell

BACKGROUND Oral health impacts on general health and quality of life, and oral diseases are the most common non-communicable diseases worldwide. Non-White ethnic groups account for an increasing proportion of the UK population. This study explores whether there are ethnic differences in oral health and whether these are explained by differences in sociodemographic or lifestyle factors, or use o...

Journal: :Asian Pacific Journal of Cancer Prevention 2014

2012
Shazia Micheal Muhammad Imran Khan Farah Akhtar Mahmood Ali Asifa Ahmed Anneke I. den Hollander Raheel Qamar

PURPOSE Single nucleotide polymorphisms (SNPs) rs1048661 (p.R141L) and rs3825942 (p.G153D) in the lysyl oxidase-like 1 (LOXL1) gene have been previously reported to be associated with pseudoexfoliation glaucoma (PEXG) in various Asian and European populations, but these SNPs have not yet been studied in the Pakistani population. Therefore the aim of the present study was to investigate the asso...

2009
Maleeha Azam Rob W.J. Collin Muhammad Imran Khan Syed Tahir Abbas Shah Nadeem Qureshi Muhammad Ajmal Anneke I. den Hollander Raheel Qamar Frans P.M. Cremers

PURPOSE The purpose of this study was to identify the underlying molecular genetic defect in a large consanguineous Pakistani family with Oguchi disease who had been given a diagnosis of autosomal recessive retinitis pigmentosa. METHODS The family was genotyped with the Affymetrix 10K single nucleotide polymorphism array. Fine-mapping of a common homozygous region on chromosome 13q was perfor...

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