نتایج جستجو برای: genotyped individuals

تعداد نتایج: 340120  

Journal: :Clinical chemistry 2007
Arnab Gupta Mahua Maulik Poonam Nasipuri Ishita Chattopadhyay Shyamal K Das Prasanta K Gangopadhyay Kunal Ray

BACKGROUND Wilson disease (WD) is an autosomal recessive disorder caused by defects in the ATPase, Cu(2+) transporting, beta-polypeptide gene (ATP7B) resulting in accumulation of copper in liver and brain. WD can be thwarted if detected at a presymptomatic stage, but occasional recombination during carrier detection with dinucleotide repeat markers flanking the WD locus may lead to faulty diagn...

Journal: :Human molecular genetics 2016
Brian E Cade Daniel J Gottlieb Diane S Lauderdale David A Bennett Aron S Buchman Sarah G Buxbaum Philip L De Jager Daniel S Evans Tibor Fülöp Sina A Gharib W Craig Johnson Hyun Kim Emma K Larkin Seung Ku Lee Andrew S Lim Naresh M Punjabi Chol Shin Katie L Stone Gregory J Tranah Jia Weng Kristine Yaffe Phyllis C Zee Sanjay R Patel Xiaofeng Zhu Susan Redline Richa Saxena

Sleep duration is implicated in the etiologies of chronic diseases and premature mortality. However, the genetic basis for sleep duration is poorly defined. We sought to identify novel genetic components influencing sleep duration in a multi-ethnic sample. Meta-analyses were conducted of genetic associations with self-reported, habitual sleep duration from seven Candidate Gene Association Resou...

Journal: :BMC Proceedings 2007
Zhi Wei Mingyao Li

Rheumatoid arthritis (RA) is an autoimmune disease with a moderately strong genetic component. Previous linkage and candidate gene studies have identified several regions that predispose to RA, including the HLA-DRB1 and PTPN22. We conducted genome-wide linkage analysis with 128 affected individuals from 60 families in a Canadian cohort that were genotyped using the Illumina linkage panel and g...

Journal: :Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie 2009
H Simianer E C G Pimentel

In many farm animal populations, high-density single nucleotide polymorphism (SNP) genotypes are becoming available on a large scale, and routine estimation of breeding values is implemented for a multiplicity of traits. We propose to apply the basic principle of the quantitative transmission disequilibrium test (QTDT) to estimated Mendelian sampling terms. A two-step procedure is suggested, wh...

Journal: :Human molecular genetics 2010
Joseph P McElroy Bruce A C Cree Stacy J Caillier Peter K Gregersen Joseph Herbert Omar A Khan Jan Freudenberg Annette Lee S Louis Bridges Stephen L Hauser Jorge R Oksenberg Pierre-Antoine Gourraud

Multiple sclerosis (MS) is a common demyelinating disease of the central nervous system mediated by autoimmune and neurodegenerative pathogenic mechanisms. Multiple genes account for its moderate heritability, but the only genetic region shown to have a large replicable effect on MS susceptibility is the major histocompatibility complex (MHC). Strong linkage disequilibrium (LD) across the MHC h...

Journal: :Genetics and molecular research : GMR 2010
M C F Silva L W Zuccherato G B Soares-Souza Z M Vieira L Cabrera P Herrera J Balqui C Romero H Jahuira R H Gilman M L Martins E Tarazona-Santos

Admixture occurs when individuals from parental populations that have been isolated for hundreds of generations form a new hybrid population. Currently, interest in measuring biogeographic ancestry has spread from anthropology to forensic sciences, direct-to-consumers personal genomics, and civil rights issues of minorities, and it is critical for genetic epidemiology studies of admixed populat...

2012
Davidson Sodré Luis F.S. Rodrigues-Filho Rosália F.C. Souza Péricles S. Rêgo Horacio Schneider Iracilda Sampaio Marcelo Vallinoto

Carcharhinus limbatus has a cosmopolitan distribution and marked genetic structuring, mainly because of its philopatric behavior. However, analysis of this structuring has not previously included South American populations. In the present study, we analyzed a sample of adult individuals collected on the northern coast of Brazil and compared the sequences of the mitochondrial control region with...

Journal: :Human molecular genetics 2009
Elena Sánchez Rogelio J Palomino-Morales Norberto Ortego-Centeno Juan Jiménez-Alonso Miguel A González-Gay Miguel A López-Nevot Julio Sánchez-Román Enrique de Ramón M Francisca González-Escribano Bernardo A Pons-Estel Sandra D'Alfonso Gian Domenico Sebastiani Marta E Alarcón-Riquelme Javier Martín

Interleukin-18 (IL-18) is a proinflammatory cytokine that plays an important role in chronic inflammation and autoimmune disorders. In this study, we aimed to determine the potential role of the IL18 gene in SLE. To define the genetic association of the IL18 and SLE, we have genotyped nine SNPs in an independent set of Spanish cases and controls. The IL18 polymorphisms were genotyped by PCR, us...

Journal: :Immunobiology 2011
Julio Granados-Montiel Joaquin Zúñiga Jose Azocar Edmond J Feris Daniel Terreros Charles E Larsen Olga P Clavijo Alfredo Cruz-Lagunas Derek Middleton Chester A Alper Janardan P Pandey Edmond J Yunis

Genetic interactions between natural killer (NK) cells immunoglobulin-like receptor (KIR) genes and immunoglobulin allotypes have been previously reported in type 2 diabetes mellitus (DM) patients. Puerto Rican Americans with a history of intravenous drug use who developed DM following HCV infection (n=32) were compared to individuals infected with HCV without diabetes (n=121) and to DM non-inf...

Journal: :Physiological genomics 2013
Yi Fu Tim Cheetham David Bourn Eric Orwoll David M Cohen

The protein product of the AVPR2 gene, coding for the arginine vasopressin receptor type 2, is essential for vasopressin-dependent concentration of the urine. The arginine residue at position 137 in the protein product of this gene is uniquely pivotal for function. The R137H mutant inactivates the receptor conferring congenital nephrogenic diabetes insipidus, whereas activating mutations at thi...

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