Robuta

https://www.mdpi.com/2077-0383/10/24/5892
The main aim of this work was to determine the impact of COMT and DRD2 gene polymorphisms together with temperament and character traits on alcohol craving...
initialstudycomtgenepolymorphisms
https://pubmed.ncbi.nlm.nih.gov/27965977/
genetic polymorphismslackassociationjakstat
https://pubmed.ncbi.nlm.nih.gov/26843965/
Genetics of autoimmune diseases represent a growing domain with surpassing biomarker results with rapid progress. The exact cause of Rheumatoid Arthritis (RA)...
rheumatoid arthritisidentificationbiomarkersbasedsingle
https://pubmed.ncbi.nlm.nih.gov/28226412/
Our findings indicate that both examined risk factors may be implicated in the occurrence of Hashimoto's thyroiditis, but this covers only a fraction of the...
oxidative stressragepolymorphismslevelshashimoto
https://pubmed.ncbi.nlm.nih.gov/34721291/
This study supported the finding that rs7756992 and rs7754840 are associated with susceptibility to GDM. However, further functional studies are warranted to...
regulatorysubunitassociatedproteinlike
https://pubmed.ncbi.nlm.nih.gov/17870204/
DNA mismatch repair (MMR) plays an important role in maintaining genome stability. Defects in MMR genes have been involved in several types of sporadic and...
lung cancerpolymorphismsriskearlyonset
https://www.omicsonline.org/peer-reviewed/polymorphisms-in-claudin-1-and-claudin-7-in-healthy-individuals-in-sweden-73225.html
Polymorphisms in Claudin 1 and Claudin 7 in Healthy Individuals in Sweden Abstract.
polymorphismsclaudinhealthyindividuals
https://pubmed.ncbi.nlm.nih.gov/21680027/
A haplotype in MAOA and two haplotypes in COMT are found to be associated with antidepressant treatment response in this sample. Stressors in early life may...
genetic polymorphismsneurotransmitter systemsinfluenceinteractioncatecholamine
https://pubmed.ncbi.nlm.nih.gov/29644956/
The aim of this study is to analyse the efficacy rate of folate for the treatment of hyperhomocysteinaemia (HHcy) and to explore how folate metabolism-related...
genetic polymorphismskeyenzymesfolatemetabolism
https://www.wikidata.org/wiki/Q35029517
in wildcaenorhabditis eleganssinglenucleotidepolymorphisms
https://pubmed.ncbi.nlm.nih.gov/25749274/
Genome-wide association studies (GWAS) in populations of European ancestry have identified nine single nuclear polymorphisms (SNP) on chromosome 11 related to...
joint effecton thepolymorphismsrisk
https://peerj.com/articles/2576/reviews/
View the review history for The impact of IL-6 and IL-28B gene polymorphisms on treatment outcome of chronic hepatitis C infection among intravenous drug users...
the impactreviewhistoryil
https://pubmed.ncbi.nlm.nih.gov/31440993/
The dopamine transporter is coded by the SLC6A3 gene and plays an important role in regulation of the neurotransmitter dopamine. To detect the association...
meta analysisthe associationgenepolymorphisms
https://pubmed.ncbi.nlm.nih.gov/22494359/
There is increasing interest in the role of striatal dopaminergic activity in social approach-avoidance motivation. The 9-repeat allele of the dopamine...
dopamine transporterpolymorphismsaffectsocialapproach
https://elifesciences.org/articles/89068
HLA-DRA intronic haplotype associates with opposite effects on type 1 diabetes and celiac disease, refining genetic risk prediction and implicating complement...
polymorphismsintronhladraassociate
https://pubmed.ncbi.nlm.nih.gov/24143106/
Bipolar disorder (BD) is a complex disorder with a number of susceptibility genes and environmental risk factors involved in its pathogenesis. In recent years,...
evidencesinglenucleotidepolymorphismsassociation
https://pubmed.ncbi.nlm.nih.gov/27521242/
These findings provide further evidence that variation in TPH2 is associated with antidepressant response and may also interact with childhood trauma to...
early lifetphpolymorphismsinteractstress
https://pubmed.ncbi.nlm.nih.gov/18694972/
A two-SNP screening test can identify the highest risk heterozygous genotype for type 1 diabetes in a time- and cost-effective manner.
the highesttwosinglenucleotidepolymorphisms
https://pubmed.ncbi.nlm.nih.gov/28119119/
Our results, for the first time, demonstrate that HLA-DPB1 gene rs9277535A allele has a major effect on the risk of persistent HBV infection. We suggest that...
chronic hepatitis bvirus infectionassociationhladp
https://www.mdpi.com/2077-0383/11/19/5645
Our aim was to assess the association between four inflammatory polymorphisms with the development of post-COVID pain and to associate these polymorphisms with...
post covidis notpainassociatedinflammatory
https://www.mdpi.com/2077-0383/12/8/2775
Atopy is an exaggerated IgE-mediated immune response to foreign antigens in which metabolic abnormalities of the leukotrienes (LTs) pathway play a crucial...
associationsexrelatedgenepolymorphisms
https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2020.00783/full
The furin cleavage site in the spike glycoprotein of the SARS-CoV-2 coronavirus is considered important for the virus to enter the host cells. By analyzing 4...
furin cleavage sitefrontiersnaturalpolymorphismspresent
https://pubmed.ncbi.nlm.nih.gov/31004399/
Genetic variations in opioid receptors may contribute to symptom severity and impulsivity in AUD patients.
opioid receptorassociationgenepolymorphismsdrinking
https://pubmed.ncbi.nlm.nih.gov/29435279/
The present case-control study was conducted on 110 children with acute lymphoblastic leukemia (ALL) and 120 healthy children to determine the impact of...
non coding rnathe risklongpolymorphismsincrease
https://en.wikibooks.org/wiki/Structural_Biochemistry/Genome_Analysis/Single_Nucleotide_Polymorphisms_(SNPs)
genome analysisstructuralbiochemistrysinglenucleotide
https://pubmed.ncbi.nlm.nih.gov/29674985/
Variations in human infants' attachment behavior are associated with single nucleotide polymorphisms (SNPs) in the oxytocin receptor (OXTR) gene, suggesting a...
oxytocin receptordogownerattachmentassociated
https://www.mdpi.com/1660-4601/19/22/14687
Periodontitis is a chronic multifactorial inflammatory disease originating from microbial, environmental and genetic factors. The present study aimed to find...
associationilgenepolymorphismsstage
https://pubmed.ncbi.nlm.nih.gov/19729970/
The present association of dysbindin SNPs with negative symptoms and DAO SNPs with anxiety and depression is a replication of earlier findings and strengthens...
d amino aciddysbindinoxidasegenepolymorphisms
https://core.ac.uk/works/284148629/
funnelplotsstudiespolymorphismsrisk
https://www.nist.gov/publications/mitomorphy-alignment-and-annotation-tool-human-mitochondrial-dna-polymorphisms
MitoMorphy uses a number of publicly available human mitochondrial DNA sequences from different ethnic groups to compare and annotate the associated polymorphic
human mitochondrial dnaalignmentannotationtool
https://pubmed.ncbi.nlm.nih.gov/17630229/
Several studies have suggested that the norepinephrine transporter (NET) may play an important role in the pathogenesis of alcohol dependence. Additional...
norepinephrine transporterpolymorphismsassociated
https://www.cambridge.org/core/journals/twin-research-and-human-genetics/article/polymorphisms-in-nevusassociated-genes-mtap-pla2g6-and-irf4-and-the-risk-of-invasive-cutaneous-melanoma/E35C7CD54BF1E7689500841F84240B27
Polymorphisms in Nevus-Associated Genes MTAP, PLA2G6, and IRF4 and the Risk of Invasive Cutaneous Melanoma - Volume 14 Issue 5
polymorphismsnevusassociatedgenesmtap
https://www.mdpi.com/2072-6643/14/15/3094
This study attempted to learn the association between maternal betaine-homocysteine methyltransferase (BHMT) gene polymorphisms, maternal dietary habits, and...
interaction effectassociationbhmtgenepolymorphisms
https://ojp.gov/ncjrs/virtual-library/abstracts/ldr-pcr-approach-multiplex-polymorphisms-genotyping-severely
ldrpcrapproachmultiplexpolymorphisms
https://pubmed.ncbi.nlm.nih.gov/26125837/
Infertility affects 1 in 6 couples and approximately 1 in 25 men. Male factor infertility is a major cause of spermatogenic anomalies, the causes of which are...
associationsinglenucleotidepolymorphisms
https://pubmed.ncbi.nlm.nih.gov/28451394/
to begenepolymorphismsidentifiedassociated
https://www.mdpi.com/2309-608X/9/6/629
The species complexes Cryptococcus neoformans and Cryptococcus gattii are the causative agents of cryptococcosis. Virulence and susceptibility to antifungals...
group imitochondrial genesdistributionpolymorphismsintrons
https://pubmed.ncbi.nlm.nih.gov/19223990/
Our data suggest that none of the investigated PEDF polymorphisms is likely a major risk factor for exudative AMD in a white European population.
pigment epitheliumanalysisthreederivedfactor
https://pubmed.ncbi.nlm.nih.gov/29016630/
After adjustment for clinical factors, kidney function was associated with BRAP rs3782886 and SPATA5L1 rs2467853 and the GRS for CKD that we developed was...
kidney functiongenetic polymorphismsassociationatherosclerotic
https://www.cea.fr/drf/ifrancoisjacob/english/Lists/Publications%20CNRGH/StructuredDisplayForm.aspx?ID=65769
dna repair genesgenetic polymorphismsbladder cancer
https://www.jci.org/articles/view/32377/pdf
class ijcihlapolymorphismsassociated
https://pubmed.ncbi.nlm.nih.gov/30104900/
Our data show that HLA gene polymorphisms are associated with SI in patients with HBV-related HCC, and the absence of minor allele A (rs7453920) promotes SI...
human leukocyte antigensystemic inflammationgenepolymorphismsassociated
https://www.cea.fr/drf/ifrancoisjacob/Lists/Publications%20CNRGH/StructuredDisplayForm.aspx?ID=50874
mass spectrometrygenotypingsinglenucleotidepolymorphisms
https://publications.gmi.tirol/abstract/pubmed33454797/
Brainblood ratios of methadone and ABCB1 polymorphisms in methadone-related deaths
brainbloodratiosmethadonepolymorphisms
https://pubmed.ncbi.nlm.nih.gov/30501958/
The aim of this study was to evaluate the association of rs1805193, rs5361, and rs5355 E-selectin gene single nucleotide polymorphisms (SNPs) with the risk of...
singlenucleotidepolymorphisms
https://pubmed.ncbi.nlm.nih.gov/33969140/
This study suggest that VDR gene polymorphism may not contribute to the progression of CHB infection.
vitamin d receptorgenotypedistributionpolymorphismsamong