Results 41 to 50 of about 3,153,117 (306)

The extensive polymorphism of KIR genes [PDF]

open access: yesImmunology, 2009
SummaryThe functions of human natural killer (NK) cells are controlled by diverse families of antigen receptors. Prominent among these are the killer cell immunoglobulin‐like receptors (KIR), a family of genes clustered in one of the most variable regions of the human genome.
Derek, Middleton, Faviel, Gonzelez
openaire   +2 more sources

Association of the AFF3 gene and IL2/IL21 gene region with juvenile idiopathic arthritis [PDF]

open access: yes, 2010
Recent genetic studies have led to identification of numerous loci that are associated with susceptibility to autoimmune diseases. The strategy of using information from these studies has facilitated the identification of novel juvenile idiopathic ...
S Eyre   +21 more
core   +2 more sources

Association of Rho-kinase Gene Polymorphisms with Respiratory Distress Syndrome in Preterm Neonates

open access: yesPediatrics and Neonatology, 2017
Respiratory distress syndrome (RDS) of the newborn is one of the most common causes of morbidity and mortality in preterm infants. Our objective was to determine the association between Rho-kinase (ROCK1 and ROCK2) gene polymorphisms and RDS in preterm ...
Gül Kaya   +6 more
doaj   +1 more source

Born to fight? Genetics and combat sports

open access: yesRevista de Artes Marciales Asiáticas, 2014
Recently, the influence of genetics on sports performance has received increased attention from many researchers. In combat sports, some investigations have also been conducted.
Emerson Franchini
doaj   +5 more sources

Fibromyalgia: A Review of Related Polymorphisms and Clinical Relevance

open access: yesAnais da Academia Brasileira de Ciências, 2021
Fibromyalgia (FM) is a chronic pain syndrome that affects the central nervous system and generates disability, which is characterized by generalized pain, fatigue, and functional decline.
LUÍSA P. JANSSEN   +3 more
doaj   +1 more source

Association between oxytocin receptor gene polymorphisms and self-rated 'empathic concern' in schizophrenia [PDF]

open access: yes, 2012
The nonapeptide oxytocin (OXT) and its receptor (OXTR) have been implicated in social cognition, empathy, emotion and stress regulation in humans. Previous studies reported associations between OXT and OXTR genetic polymorphisms and risk for disorders ...
Müller, Daniel J.   +23 more
core   +2 more sources

A preliminary study: MUC5B promoter polymorphism and its association with IPF

open access: yesThe Egyptian Journal of Bronchology, 2020
Background The (T) allele of MUC5B gene is strongly correlated with idiopathic pulmonary fibrosis (IPF) and interstitial lung diseases (ILD) related to autoimmune conditions in Caucasians, but no data is available regarding this polymorphism in the ...
Hoda Ali Abu Yusuf   +5 more
doaj   +1 more source

The rpl23 gene and pseudogene are hotspots of illegitimate recombination in barley chloroplast mutator seedlings

open access: yesScientific Reports, 2019
Previously, through a TILLING (Targeting Induced Local Lesions in Genomes) approach applied on barley chloroplast mutator (cpm) seedlings a high frequency of polymorphisms in the rpl23 gene was detected.
F. Lencina   +5 more
doaj   +1 more source

Associations between IL-1RN variable number of tandem repeat, IL-1β (−511) and IL-1β (+3954) gene polymorphisms and urolithiasis in Uighur children of China

open access: yesAsian Journal of Urology, 2022
Objective: Interleukin-1 (IL-1) is a pro-inflammatory cytokine which may be related to urolithiasis. Genetic polymorphisms of the interleukin-1beta (IL-1β) have been proposed as markers for urolithiasis in some areas.
Jiefeng Xiao   +3 more
doaj   +1 more source

GENE POLYMORPHISM;

open access: yesThe Professional Medical Journal, 2019
Introduction: Reduced bone density in postmenopausal women is a complex disease with a strong genetic association. Causative factors are both acquired and genetic. Single nucleotide polymorphisms may be associated with genetic predisposition of this condition. Objectives: The purpose of this study is to find out an association between single nucleotide
Amal Shoukat   +5 more
openaire   +2 more sources

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