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Confer Susceptibility sentence examples within meta analysis proved



Associations of polymorphisms in interleukins with tuberculosis: evidence from a meta-analysis.



Associations between twelve common gene polymorphisms and susceptibility to hepatocellular carcinoma: evidence from a meta-analysis


Confer Susceptibility sentence examples within genome wide association



PRKCH polymorphism is associated with rheumatoid arthritis in a Chinese population.



Short AIP1 (ASK1-Interacting Protein-1) Isoform Localizes to the Mitochondria and Promotes Vascular Dysfunction.


Confer Susceptibility sentence examples within meta analysis demonstrated



Estimation of associations between 10 common gene polymorphisms and gastric cancer: evidence from a meta-analysis



Relationship of genetic polymorphisms in CTLA-4 and IL-18 with viral hepatitis: evidence from a meta-analysis




Confer Susceptibility sentence examples within May Confer Susceptibility



p53 p.Pro72Arg (rs1042522) and Mouse Double Minute 2 (MDM2) Single-Nucleotide Polymorphism (SNP) 309 Variants and Their Interaction in Chronic Lymphocytic Leukemia(CLL): A Survey in CLL Patients from Western Iran



Homozygosity of short VNTR lengths in the CEL gene may confer susceptibility to idiopathic chronic pancreatitis.


Confer Susceptibility sentence examples within Might Confer Susceptibility



The role of rs242941, rs1876828, rs242939 and rs110402 polymorphisms of CRHR1 gene and the depression: systematic review and meta-analysis.



An in-depth analysis reveals two new genetic variants on 22q11.2 associated with vitiligo in the Chinese Han population.


Confer Susceptibility sentence examples within Polymorphism Confer Susceptibility



Association of the rs17250932, rs4794067, and rs2240017 polymorphism in the TBX21 gene with autoimmune diseases: A meta-analysis.



Association of rs17250932, rs4794067, and rs2240017 polymorphisms in the TBX21 gene with autoimmune diseases: a meta-analysis.


Confer Susceptibility sentence examples within Variant Confer Susceptibility



Rare BAP1 variant of unknown significance (VUS) and analysis of BAP1 codon 146 genomics: Potential germline and therapeutic implications.



Significant association of DRD2 enhancer variant rs12364283 with heroin addiction in a Pakistani population


Confer Susceptibility sentence examples within Allele Confer Susceptibility



Polygenic impact of common genetic risk loci for Alzheimer’s disease on cerebral blood flow in young individuals



Abstract P1-08-13: A prospective evaluation of HLA expression in breast implant associated anaplastic large cell lymphoma to identify disease susceptibility


Confer Susceptibility sentence examples within Gene Confer Susceptibility



Socioemotional Mechanisms of Children’s Differential Response to the Effects of Maternal Sensitivity on Child Adjustment



Association of apoptosis genes in PDCD1 but not PDCD1LG2, FAS, and FASLG with pediatric idiopathic uveitis in Han Chinese


Confer Susceptibility sentence examples within Immunity Confer Susceptibility



Neuron-intrinsic immunity to viruses in mice and humans.



Disseminated Mycobacterial Disease in a Patient with 22q11.2 Deletion Syndrome: Case Report and Review of the Literature


Confer Susceptibility sentence examples within Factor Confer Susceptibility



Neuroprotection in Glaucoma: NAD+/NADH Redox State as a Potential Biomarker and Therapeutic Target



Clinical trials in the ALS syndrome: it is time for change


Confer Susceptibility sentence examples within Would Confer Susceptibility



Cancer as an infectious disease: A different treatment alternative using a combination of tigecycline and pyrvinium pamoate - An example of breast cancer.



Optimal human pathogenic TH2 cell effector function requires local epithelial cytokine signaling.


Confer Susceptibility sentence examples within Also Confer Susceptibility



1132-P: Genetic Relationships between Birth Weight and Type 2 Diabetes



Developmental Language Disorder and Psychopathology: Disentangling Shared Genetic and Environmental Influences.



Gene Panel Sequencing in a Chinese High-risk Breast Cancer Cohort



Structure of the trypanosome transferrin receptor reveals mechanisms of ligand recognition and immune evasion



Structure of the trypanosome transferrin receptor reveals mechanisms of ligand recognition and immune evasion.



Polymorphisms of Ionotropic Glutamate Receptor-Related Genes and the Risk of Autism Spectrum Disorder in a Chinese Population


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10.1136/bjophthalmol-2019-314483

Association of toll-like receptor 10 polymorphisms with paediatric idiopathic uveitis in Han Chinese


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10.1016/j.ebiom.2019.05.052

Composition of the gut microbiota transcends genetic determinants of malaria infection severity and influences pregnancy outcome



Genome-wide association study of right-sided colonic diverticulosis in a Korean population


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10.1136/annrheumdis-2019-eular.8299

AB0267 ROLE OF FCGAMMA RECEPTORS IIA, IIIA, AND IIIB POLYMORPHISMS IN RHEUMATOID ARTHRITIS SEVERITY



[T-786C endothelial nitric oxide gene polymorphism and type 1 diabetic retinopathy in the Algerian population].



Interaction between DNA damage response, translation and apoptosome determines cancer susceptibility to TOP2 poisons


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10.1136/annrheumdis-2019-eular.1501

AB0007 IL12B POLYMORPHISMS ARE ASSOCIATED WITH ELEVATED SERUM LEVELS OF IL-12P40, IL-23 AND GENETIC PREDISPOSITION TO RHEUMATOID ARTHRITIS


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10.1016/J.JTCMS.2019.02.002

Serum protein profile of yang-deficiency constitution in traditional Chinese medicine revealed by protein microarray analyses



The long and winding road: from genetic risk factors to the understanding of disease-pathogenesis in Crohn’s disease


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10.1080/13803395.2019.1652728

Cognitive impairments in HCV infection: From pathogenesis to neuroimaging



Reduced DNA Methylation of the Oxytocin Receptor Gene Is Associated With Anhedonia-Asociality in Women With Recent-Onset Schizophrenia and Ultra-high Risk for Psychosis.


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10.1016/J.ARCMED.2019.05.014

Association of CCL2 Gene Variants with Osteoarthritis.



Genetic architecture of hippocampal subfields on standard resolution MRI: How the parts relate to the whole



Ethanol-induced changes in synaptic amino acid neurotransmitter levels in the nucleus accumbens of differentially sensitized mice



The activating p.Ser466Arg change in STAT1 causes a peculiar phenotype with features of interferonopathies


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10.1016/j.envres.2019.01.023

Ambient air pollution is associated with cardiac repolarization abnormalities in healthy adults



PPARG rs3856806 C>T Polymorphism Increased the Risk of Colorectal Cancer: A Case-Control Study in Eastern Chinese Han Population



Identification of 12 novel loci that confer susceptibility to early-onset dyslipidemia



The ORMDL3 Asthma Gene Regulates ICAM1 and Has Multiple Effects on Cellular Inflammation


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10.1161/STROKEAHA.118.020379

Genetics of Vascular Cognitive Impairment


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10.2174/1566524019666191024104930

Immunogenetics of Celiac Disease: A focus on Arab countries.



Identification of Chromosomal Regions Linked to Diabetic Nephropathy: A Meta-Analysis of Genome-Wide Linkage Scans.



A polymorphism in the IL1B gene (rs16944 T/C) is associated with cutaneous leishmaniasis caused by Leishmania guyanensis and plasma cytokine interleukin receptor antagonist.



Can verapamil be effective in controlling vertigo and headache attacks in vestibular migraine accompanied with Meniere’s disease? A preliminary study



The Cancer Microbiota: EMT and Inflammation as Shared Molecular Mechanisms Associated with Plasticity and Progression


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10.1016/j.diabres.2019.03.037

Genetic polymorphisms associated with type 2 diabetes in the Arab world: A systematic review and meta-analysis.


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