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3' Untranslated Region SNP

Known as: 3' UTR SNP, UTR, 3' SNP 
A 3' Untranslated Region SNP consists of a variation at an appreciable frequency between individuals of a single interbreeding population of a single… 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Admixture mapping and fine-mapping of birth weight loci in the Black Women’s Health Study
Several genome-wide association studies (GWAS) have identified genetic variants associated with birth weight. To date, however… 
2015
2015
A 1.6-Mb Microdeletion in Chromosome 17q22 Leads to NOG-Related Symphalangism Spectrum Disorder without Intellectual Disability
Microdeletions in chromosome 17q22, where the NOG gene resides, have been reported leading to the NOG-related symphalangism… 
2014
2014
Positional cloning and next-generation sequencing identified a TGM6 mutation in a large Chinese pedigree with acute myeloid leukaemia
An inherited predisposition to acute myeloid leukaemia (AML) is exceedingly rare, but the investigation of these families will… 
Review
2014
Review
2014
Haplotype analysis of PPARγ C681G and intron CT variants
BackgroundThere is strong evidence suggesting an association between the peroxisome-activated receptor γ (PPARγ) gene and… 
2014
2014
Lack of association between single nucleotide polymorphism rs10818488 in TRAF1/C5 region and rheumatoid arthritis in iranian population.
The association of rs10818488 SNP located in TRAF1/C5 region with Rheumatoid Arthritis (RA), has been picked up by genome-wide… 
2013
2013
Typing early Australian healthcare-associated MRSA: confirmation of major clones and emergence of ST1-MRSA-IV and novel ST2249-MRSA-III
Aims: To investigate the evolutionary origins of Australian healthcare-associated (HCA) methicillin-resistant Staphylococcus… 
2012
2012
Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2
Fibrochondrogenesis is a severe, recessively inherited skeletal dysplasia shown to result from mutations in the gene encoding the… 
2012
2012
Alteration in RGS2 expression level is associated with changes in haloperidol induced extrapyramidal features in a mutant mouse model
2011
2011
Polymorphisms of Mir-34b/c, Mir-146a and Mir-196a-2 and Predisposition to Chronic Lymphocytic Leukemia and Monoclonal B-Cell Lymphocytosis
Abstract 4585 Since microRNAs control expression of protein-coding oncogenes and tumor suppressor genes, functional microRNAs… 
2009
2009
Manganese superoxide dismutase and chemokine genes polymorphisms in chinese patients with anterior uveitis.
PURPOSE To investigate the association of single-nucleotide polymorphisms (SNPs) in the manganese superoxide dismutase (MnSOD… 
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