(Q34568722)

English

A systematic analysis of disease-associated variants in the 3' regulatory regions of human protein-coding genes II: the importance of mRNA secondary structure in assessing the functionality of 3' UTR variants

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scholarly article

1 reference

Europe PubMed Central

3 August 2017

1 reference

Europe PubMed Central

A systematic analysis of disease-associated variants in the 3' regulatory regions of human protein-coding genes II: the importance of mRNA secondary structure in assessing the functionality of 3' UTR variants (English)

1 reference

Europe PubMed Central

3 August 2017

protein structure

0 references

David N. Cooper

3

1 reference

Europe PubMed Central

3 August 2017

author name string

Jian-Min Chen

1

1 reference

Europe PubMed Central

3 August 2017

Claude Férec

2

1 reference

Europe PubMed Central

3 August 2017

publication date

29 June 2006

1 reference

Europe PubMed Central

3 August 2017

1 reference

Europe PubMed Central

3 August 2017

120

1 reference

Europe PubMed Central

3 August 2017

3

1 reference

Europe PubMed Central

3 August 2017

301-333

1 reference

Europe PubMed Central

3 August 2017

https://scigraph.springernature.com/pub.10.1007/s00439-006-0218-x

0 references

Polymorphism at the 3'-UTR of the thymidylate synthase gene: a potential predictor for outcomes in Caucasian patients with esophageal adenocarcinoma treated with preoperative chemoradiation

1 reference

https://api.crossref.org/works/10.1007%2FS00439-006-0218-X

21 January 2018

Differential expression of the human insulin-like growth factor II gene. Characterization of the IGF-II mRNAs and an mRNA encoding a putative IGF-II-associated protein

1 reference

https://api.crossref.org/works/10.1007%2FS00439-006-0218-X

21 January 2018

A novel insertion mutation in the FOXL2 gene is detected in a big Chinese family with blepharophimosis-ptosis-epicanthus inversus

1 reference

https://api.crossref.org/works/10.1007%2FS00439-006-0218-X

21 January 2018

Characterization of a beta-actin mRNA zipcode-binding protein

1 reference

https://api.crossref.org/works/10.1007%2FS00439-006-0218-X

21 January 2018

Long-range RNA interaction of two sequence elements required for endonucleolytic cleavage of human insulin-like growth factor II mRNAs.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-006-0218-X

21 January 2018

An mRNA stability complex functions with poly(A)-binding protein to stabilize mRNA in vitro

1 reference

https://api.crossref.org/works/10.1007%2FS00439-006-0218-X

21 January 2018

Erythroid cell-specific determinants of alpha-globin mRNA stability

1 reference

https://api.crossref.org/works/10.1007%2FS00439-006-0218-X

21 January 2018

Erythroid cell-specific mRNA stability elements in the alpha 2-globin 3' nontranslated region

1 reference

https://api.crossref.org/works/10.1007%2FS00439-006-0218-X

21 January 2018

Association of interleukin-12 p40 gene 3'-untranslated region polymorphism and outcome of HCV infection

1 reference

https://api.crossref.org/works/10.1007%2FS00439-006-0218-X

21 January 2018

Dihydropyrimidinase-related protein 2 (DRP-2) gene and association to deficit and nondeficit schizophrenia

1 reference

https://api.crossref.org/works/10.1007%2FS00439-006-0218-X

21 January 2018

Possible Cis-acting signal that could be involved in the localization of different mRNAs in neuronal axons

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TIA-1 is a translational silencer that selectively regulates the expression of TNF-alpha

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 3'UTR mutation affects beta-globin expression without altering the stability of its fully processed mRNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

LBP-1c/CP2/LSF gene polymorphism and risk of sporadic Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of thymidylate synthase polymorphisms with gastric cancer susceptibility

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of a common polymorphism in the cyclooxygenase 2 gene with risk of non-small cell lung cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The AU-rich transcriptome: more than interferons and cytokines, and its role in disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Promoter and 3'-untranslated-region haplotypes in the vitamin d receptor gene predispose to osteoporotic fracture: the rotterdam study

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and identification of a protein binding to the localization element of Metallothionein-1 mRNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms in thyroid hormone pathway genes are associated with plasma TSH and iodothyronine levels in healthy subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of osteoporosis to chromosome 20p12 and association to BMP2

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A1166C polymorphism of angiotensin II type 1 receptor, blood pressure and arterial stiffness in hypertension

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Annexin A2 binds to the localization signal in the 3′ untranslated region of c-myc mRNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural and functional analysis of an mRNP complex that mediates the high stability of human beta-globin mRNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common variants in glutamine:fructose-6-phosphate amidotransferase 2 (GFPT2) gene are associated with type 2 diabetes, diabetic nephropathy, and increased GFPT2 mRNA levels

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 3' untranslated region of human vimentin mRNA interacts with protein complexes containing eEF-1gamma and HAX-1

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Four highly stable eukaryotic mRNAs assemble 3' untranslated region RNA-protein complexes sharing cis and trans components.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common variations in noncoding regions of the human natriuretic peptide receptor A gene have quantitative effects

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage disequilibrium of a type 1 diabetes susceptibility locus with a regulatory IL12B allele

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association study of candidate genes for the prevalence and progression of knee osteoarthritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms of the endothelin-A and -B receptor genes in relation to blood pressure and myocardial infarction: the Etude Cas-Témoins sur l'Infarctus du Myocarde (ECTIM) Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human dihydropyrimidinase-related protein 2 gene on chromosome 8p21 is associated with paranoid-type schizophrenia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of gene polymorphism in lipocalin-type prostaglandin D synthase and its association with carotid atherosclerosis in Japanese hypertensive patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

3'-UTR polymorphism in the human CYP2A6 gene affects mRNA stability and enzyme expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic association between an AACC insertion in the 3'UTR of the stratum corneum chymotryptic enzyme gene and atopic dermatitis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vitro phenotype of SDF1 gene mutant that delays the onset of human immunodeficiency virus disease in vivo.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 8818G allele of the agouti signaling protein (ASIP) gene is ancestral and is associated with darker skin color in African Americans.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single nucleotide polymorphisms in the human E-cadherin gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of a stromal cell-derived factor-1 chemokine gene variant in the clinical course of HIV-1 infection

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of Linkage Disequilibrium between Polymorphisms in the KCNJ9 Gene with Type 2 Diabetes Mellitus in Pima Indians

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Zipcodes and postage stamps: mRNA localisation signals and their trans-acting binding proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms of cardiac presynaptic alpha2C adrenergic receptors: Diverse intragenic variability with haplotype-specific functional effects

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Influence of interleukin 12B (IL12B) polymorphisms on spontaneous and treatment-induced recovery from hepatitis C virus infection

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for association between single nucleotide polymorphisms in T complex protein 1 gene and schizophrenia in the Chinese Han population

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mutation in the 3' untranslated region of the factor IX gene in four families with hemophilia B.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A frequent TG deletion near the polyadenylation signal of the human HEXB gene: occurrence of an irregular DNA structure and conserved nucleotide sequence motif in the 3' untranslated region

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel common single nucleotide polymorphism in the promoter region of the C-reactive protein gene associated with the plasma concentration of C-reactive protein.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 3'-UTR polymorphism in the oxidized LDL receptor 1 gene increases Abeta40 load as cerebral amyloid angiopathy in Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence variants of the gene encoding chemoattractant receptor expressed on Th2 cells (CRTH2) are associated with asthma and differentially influence mRNA stability

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a common nucleotide sequence in the 3'-untranslated region of mRNA molecules specifying inflammatory mediators

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure-expression relationships of the 15-kDa selenoprotein gene. Possible role of the protein in cancer etiology.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adaptive immune responses in acute and chronic hepatitis C virus infection

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification and functional outcome of mRNAs associated with RNA-binding protein TIA-1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cleavage/polyadenylation activity triggered by a U-rich motif sequence is differently required depending on the poly(A) site location at either the first or last 3'-terminal exon of the 2'-5' oligo(A) synthetase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence of multiple causal sites affecting weight in the IGF2-INS-TH region of human chromosome 11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human glucocorticoid receptor (hGR) beta isoform suppresses the transcriptional activity of hGRalpha by interfering with formation of active coactivator complexes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determination of the relative contribution of three genes-the cystic fibrosis transmembrane conductance regulator gene, the cationic trypsinogen gene, and the pancreatic secretory trypsin inhibitor gene-to the etiology of idiopathic chronic pancreat

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

eIF4E promotes nuclear export of cyclin D1 mRNAs via an element in the 3'UTR

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterisation of 34 patients with biotinidase deficiency ascertained by newborn screening and family investigation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A single nucleotide polymorphism in the 3?untranslated region of theCDKN2A gene is common in sporadic primary melanomas but mutations in theCDKN2B,CDKN2C,CDK4 andp53 genes are rare

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apal polymorphism in insulin-like growth factor II (IGF2) gene and weight in middle-aged males

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphism in the 3'-untranslated region of the thymidylate synthase gene and sensitivity of stomach cancer to fluoropyrimidine-based chemotherapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association testing of the protein tyrosine phosphatase 1B gene (PTPN1) with type 2 diabetes in 7,883 people

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms in the thrombopoietin gene are associated with risk of myocardial infarction at a young age

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variants of angiotensin II receptors and cardiovascular risk in hypertension.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Iron regulation of transferrin receptor mRNA levels requires iron-responsive elements and a rapid turnover determinant in the 3' untranslated region of the mRNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AU binding proteins recruit the exosome to degrade ARE-containing mRNAs

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Statistical evidence for conserved, local secondary structure in the coding regions of eukaryotic mRNAs and pre-mRNAs

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence that the pathway of transferrin receptor mRNA degradation involves an endonucleolytic cleavage within the 3' UTR and does not involve poly(A) tail shortening.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

mRNA stability in mammalian cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Binge eating as a major phenotype of melanocortin 4 receptor gene mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a target RNA motif for RNA-binding protein HuR.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distinct RNA structural domains cooperate to maintain a specific cleavage site in the 3'-UTR of IGF-II mRNAs

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A conserved AU sequence from the 3' untranslated region of GM-CSF mRNA mediates selective mRNA degradation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Control of Na+-K+-ATPase beta 1-subunit expression: role of 3'-untranslated region

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genealogy of the CCR5 locus and chemokine system gene variants associated with altered rates of HIV-1 disease progression

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An AU-rich stem-loop structure is a critical feature of the perinuclear localization signal of c-myc mRNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cytosolic protein binds to structural elements within the iron regulatory region of the transferrin receptor mRNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of single nucleotide polymorphisms in the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion in a (T)8 microsatellite abrogates expression regulation by 3'-UTR.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human CRP Gene Polymorphism Influences CRP Levels

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tumor suppression by the prohibitin gene 3'untranslated region RNA in human breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Facilitation of mRNA deadenylation and decay by the exosome-bound, DExH protein RHAU

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RNA-protein interactions within the 3 ' untranslated region of vimentin mRNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distribution and functional consequences of nucleotide polymorphisms in the 3'-untranslated region of the human Sep15 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rare variant of the leptin gene has large effects on blood pressure and carotid intima-medial thickness: a study of 1428 individuals in 248 families.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of N-acetyl transferase 1 and 2 polymorphisms on bladder cancer risk in Caucasians

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Definition of candidate low risk APC alleles in a Swedish population

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

E-cadherin gene 3'-UTR C/T polymorphism is associated with prostate cancer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transport and localization elements in myelin basic protein mRNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth inhibition and induction of apoptosis in mesothelioma cells by selenium and dependence on selenoprotein SEP15 genotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional polymorphisms in the vascular endothelial growth factor gene are associated with development of end-stage renal disease in males

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RNA destabilization by the granulocyte colony-stimulating factor stem-loop destabilizing element involves a single stem-loop that promotes deadenylation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AU-rich transient response transcripts in the human genome: expressed sequence tag clustering and gene discovery approach.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Give me A5 for lipoprotein hydrolysis!

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in PITX2 may contribute to cases of omphalocele and VATER-like syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Constitutive Decay Element Promotes Tumor Necrosis Factor Alpha mRNA Degradation via an AU-Rich Element-Independent Pathway

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of the AUUUUA hexamer for the posttranscriptional regulation of the AT1 receptor mRNA stability.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A TaqI polymorphism in the 3'UTR of the IL-12 p40 gene correlates with increased IL-12 secretion

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

VEGF gene polymorphisms and susceptibility to rheumatoid arthritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vivo and in vitro studies support that a new splicing isoform of OLR1 gene is protective against acute myocardial infarction

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Taq-I polymorphism in 3′UTR of the IL-12B and association with IL-12p40 production from human PBMC

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A C----G mutation at nt position 6 3' to the terminating codon may be the cause of a silent beta-thalassemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new human selenium-containing protein. Purification, characterization, and cDNA sequence

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AU-rich elements and associated factors: are there unifying principles?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A polymorphism in type I deiodinase is associated with circulating free insulin-like growth factor I levels and body composition in humans.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 6 bp polymorphism in the thymidylate synthase gene causes message instability and is associated with decreased intratumoral TS mRNA levels

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variants in the interleukin 6 receptor gene are associated with obesity in Pima Indians

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A human glucocorticoid receptor gene variant that increases the stability of the glucocorticoid receptor beta-isoform mRNA is associated with rheumatoid arthritis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of resistin gene 3'-untranslated region +62G-->A polymorphism with type 2 diabetes and hypertension in a Chinese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic polymorphisms of osteopontin in association with multiple sclerosis in Japanese patients.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two variants of the CIP1/WAF1 gene occur together and are associated with human cancer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A P387L variant in protein tyrosine phosphatase-1B (PTP-1B) is associated with type 2 diabetes and impaired serine phosphorylation of PTP-1B in vitro

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein tyrosine phosphatase-1B gene PTPN1: selection of tagging single nucleotide polymorphisms and association with body fat, insulin sensitivity, and the metabolic syndrome in a normal female population

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular, haematological and clinical studies of a silent beta-gene C-->G mutation at 6 bp 3' to the termination codon (+1480 C-->G) in twelve Greek families

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Translation and the stability of mRNAs encoding the transferrin receptor and c-fos

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The beta-globin C-->G mutation at 6 bp 3' to the termination codon causes beta-thalassaemia by decreasing the mRNA level

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A single homozygous point mutation in a 3'untranslated region motif of selenoprotein N mRNA causes SEPN1-related myopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effects of CCR5-Delta32, CCR2-64I, and SDF-1 3'A alleles on HIV-1 disease progression: An international meta-analysis of individual-patient data.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AUUUA motifs in the 3'UTR of human glucocorticoid receptor alpha and beta mRNA destabilize mRNA and decrease receptor protein expression.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An apolipoprotein CIII haplotype protective against hypertriglyceridemia is specified by promoter and 3' untranslated region polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mammalian selenoprotein in which selenocysteine (Sec) incorporation is supported by a new form of Sec insertion sequence element

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A hairpin-like structure within an AU-rich mRNA-destabilizing element regulates trans-factor binding selectivity and mRNA decay kinetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Perinuclear localization of slow troponin C m RNA in muscle cells is controlled by a cis-element located at its 3' untranslated region

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of phenylketonuria in South Brazil

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic association of an LBP-1c/CP2/LSF gene polymorphism with late onset Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pro-opiomelanocortin gene is associated with serum leptin levels in lean but not in obese individuals

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational analysis of a heterogeneous nuclear ribonucleoprotein A2 response element for RNA trafficking

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apa I and Sst I RFLPs at the insulin-like growth factor II (IGF2) locus on chromosome 11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Translational blockade imposed by cytokine-derived UA-rich sequences.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human histamine N-methyltransferase pharmacogenetics: common genetic polymorphisms that alter activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A (G->C) transversion in the 3' UTR of the human ECP (eosinophil cationic protein) gene correlates to the cellular content of ECP

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms in prostaglandin synthase 2/cyclooxygenase 2 (PTGS2/COX2) and risk of colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parameters for reliable results in genetic association studies in common disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prohibitin 3′ untranslated region polymorphism and breast cancer risk in Australian women

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic modulation of plasma protein S levels by two frequent dimorphisms in the PROS1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The upstream sequence element of the C2 complement poly(A) signal activates mRNA 3' end formation by two distinct mechanisms.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Specific endonucleolytic cleavage of IGF-II mRNAs

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence variants in SLITRK1 are associated with Tourette's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution of polymorphisms in the endothelial protein C receptor gene to soluble endothelial protein C receptor and circulating activated protein C levels, and thrombotic risk.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human glucocorticoid receptor beta isoform. Expression, biochemical properties, and putative function

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The prohibitin 3′ untranslated region polymorphism is not associated with risk of ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two cis-acting elements in the 3' untranslated region of alpha-CaMKII regulate its dendritic targeting

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymerase chain reaction (PCR) for detection of APal polymorphism at the insulin like growth factor II gene (IGF2)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

T cells and viral persistence: lessons from diverse infections

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A polymorphism in a conserved posttranscriptional regulatory motif alters bone morphogenetic protein 2 (BMP2) RNA:protein interactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms of thymidylate synthase in the 5'- and 3'-untranslated regions associated with risk of gastric cancer in South China: a case-control analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical course of bladder neoplasms and single nucleotide polymorphisms in theCDKN2Agene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nontruncating APC germ-line mutations and mismatch repair deficiency play a minor role in APC mutation-negative polyposis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Searching expressed sequence tag databases: discovery and confirmation of a common polymorphism in the thymidylate synthase gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MicroRNAs: genomics, biogenesis, mechanism, and function

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Post-transcriptional control of gene expression: a genome-wide perspective.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of metazoan replication-dependent histone genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of E-Cadherin Gene 3’-UTR C/T Polymorphism with Calcium Oxalate Stone Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An eleven nucleotide section of the 3'-untranslated region is required for perinuclear localization of rat metallothionein-1 mRNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel 13 Bp deletion in the 3'UTR of the beta-globin gene causes beta-thalassemia in a Turkish patient

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angiotensin II type 1 receptor gene polymorphisms in human essential hypertension

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Positive associations between single nucleotide polymorphisms in the IGF2 gene region and body mass index in adult males

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Seven novel point mutations in the uroporphyrinogen decarboxylase (UROD) gene in patients with familial porphyria cutanea tarda (f-PCT).

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A polymorphism in the 3' untranslated region of the gene for tumor necrosis factor receptor 2 modulates reporter gene expression.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An essential non-Watson-Crick base pair motif in 3'UTR to mediate selenoprotein translation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of the muscarinic cholinergic 2 receptor (CHRM2) gene with major depression in women

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic variants of natriuretic peptide receptor genes are associated with family history of hypertension and cardiovascular phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determination of the functionality of common APOA5 polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Iron-responsive elements: regulatory RNA sequences that control mRNA levels and translation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Site-specific cleavage of IGF-II mRNAs requires sequence elements from two distinct regions of the IGF-II gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common variant in PPP1R3 associated with insulin resistance and type 2 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two candidate genes for low platelet count identified in an Asian Indian kindred by genome-wide linkage analysis: glycoprotein IX and thrombopoietin

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allele-specific transcript quantification detects haplotypic variation in the levels of the SDF-1 transcripts

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Influence of the 4600A/G and 4678G/C polymorphisms in the endothelial protein C receptor (EPCR) gene on the risk of venous thromboembolism in carriers of factor V Leiden

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Endotoxin-responsive sequences control cachectin/tumor necrosis factor biosynthesis at the translational level

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphism at 3′ UTR +28 of the prion-like protein gene is associated with sporadic Creutzfeldt–Jakob disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A single-nucleotide polymorphism in C-type natriuretic peptide gene may be associated with hypertension

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single nucleotide polymorphism in prohibitin 3' untranslated region and breast-cancer susceptibility

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IL-12 and IL-10 polymorphisms and their effects on cytokine production

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphism at the C-reactive protein locus influences gene expression and predisposes to systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum response factor regulates a muscle-specific microRNA that targets Hand2 during cardiogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recruitment of a basal polyadenylation factor by the upstream sequence element of the human lamin B2 polyadenylation signal.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AU-rich elements: characterization and importance in mRNA degradation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of the 2 adenine (g.11293_11294insAA) insertion polymorphism in the 3' untranslated region of the factor VII (FVII) gene: molecular characterization of a patient with severe FVII deficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A polymorphic site in the 3' untranslated region of the cholesteryl ester transfer protein (CETP) gene is associated with low CETP activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Removal of a 3' non-coding sequence is an initial step in degradation of gro alpha mRNA and is regulated by interleukin-1

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative association between a newly identified molecular variant in the endothelin-2 gene and human essential hypertension.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of cyclooxygenase-2 expression by the translational silencer TIA-1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alleles of the IL12B 3'UTR associate with late onset of type 1 diabetes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interplay between hnRNP A1 and a cis-acting element in the 3' UTR of CYP2A5 mRNA is central for high expression of the gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of the 3' UTR transcription factor LBP-1c/CP2/LSF polymorphism with late-onset Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Upstream sequence elements enhance poly(A) site efficiency of the C2 complement gene and are phylogenetically conserved.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between birth weight, body mass index and IGF2/ApaI polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of mammalian selenoproteomes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of E-cadherin gene 3'-UTR C/T polymorphism with primary open angle glaucoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 3' untranslated region of prohibitin and cellular immortalization

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel single nucleotide polymorphism in the 3' untranslated region of human glutathione peroxidase 4 influences lipoxygenase metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic polymorphisms in the angiotensin II receptor gene and their association with open-angle glaucoma in a Japanese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Untranslated regions of mRNAs

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of alpha-globin mRNA stability.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of hundreds of conserved and nonconserved human microRNAs

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of EDNRA, but not WNK4 or FKBP1B, polymorphisms with essential hypertension

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of angiotensin II type 1 receptor gene polymorphism with essential hypertension

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Vascular Endothelial Growth Factor Gene Polymorphisms in Japanese Patients With Sarcoidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The relationship between the prothrombin upstream sequence element and the G20210A polymorphism: the influence of a competitive environment for mRNA 3'-end formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IGF2 genotype and obesity in men and women across the adult age span

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prohibitin 3' untranslated region polymorphism and breast cancer risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A variation in 3' UTR of hPTP1B increases specific gene expression and associates with insulin resistance

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RNA-dependent integrin alpha3 protein localization regulated by the Muscleblind-like protein MLP1

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Formation of mRNA 3' ends in eukaryotes: mechanism, regulation, and interrelationships with other steps in mRNA synthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ARED: human AU-rich element-containing mRNA database reveals an unexpectedly diverse functional repertoire of encoded proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic restriction of AIDS pathogenesis by an SDF-1 chemokine gene variant. ALIVE Study, Hemophilia Growth and Development Study (HGDS), Multicenter AIDS Cohort Study (MACS), Multicenter Hemophilia Cohort Study (MHCS), San Francisco City Cohort (SF

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of RNA sequences and structures involved in site-specific cleavage of IGF-II mRNAs

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further evidence for LBP-1c/CP2/LSF association in Alzheimer's disease families

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A type 2 diabetes-associated polymorphic ARE motif affecting expression of PPP1R3 is involved in RNA-protein interactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Translation initiation of ornithine decarboxylase and nucleocytoplasmic transport of cyclin D1 mRNA are increased in cells overexpressing eukaryotic initiation factor 4E.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The hairpin loop but not the bulged C of the iron responsive element is essential for high affinity binding to iron regulatory protein-1

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcription and polyadenylation in a short human intergenic region.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of four gene variants associated with myocardial infarction

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human Gene Mutation Database (HGMD): 2003 update.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of the AU-rich elements of mRNAs in controlling translation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A systematic analysis of disease-associated variants in the 3' regulatory regions of human protein-coding genes I: general principles and overview

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Control of translation and mRNA degradation by miRNAs and siRNAs

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two independent apolipoprotein A5 haplotypes influence human plasma triglyceride levels

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence determinants in human polyadenylation site selection

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An apolipoprotein influencing triglycerides in humans and mice revealed by comparative sequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of two KH domain proteins in the alpha-globin mRNP stability complex

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RNA localization

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms in the IL-12B gene and outcome of HCV infection

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The SDF1-G801A polymorphism is not associated with SDF1 gene expression in Epstein-Barr virus-transformed lymphoblastoid cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel intronic polymorphisms in theRET proto-oncogene and their association with Hirschsprung disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interaction of heterogeneous nuclear ribonucleoprotein A1 with cytochrome P450 2A6 mRNA: implications for post-transcriptional regulation of the CYP2A6 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alternative polyadenylation of cyclooxygenase-2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incorporating structure to predict microRNA targets

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angiotensin II type 2 receptors and cardiac hypertrophy in women with hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of an erythroid-enriched endoribonuclease activity involved in specific mRNA cleavage

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human Fip1 is a subunit of CPSF that binds to U-rich RNA elements and stimulates poly(A) polymerase

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DHPLC-based germline mutation screening in the analysis of the VHL tumor suppressor gene: usefulness and limitations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the association of the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction or coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MicroRNA function: multiple mechanisms for a tiny RNA?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mfold web server for nucleic acid folding and hybridization prediction

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A polymorphism in the agouti signaling protein gene is associated with human pigmentation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No association of reported functional protein tyrosine phosphatase 1B 3' UTR gene polymorphism with features of the metabolic syndrome in a Swedish population

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common 936 C/T gene polymorphism of vascular endothelial growth factor is associated with decreased breast cancer risk.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Insights into the hierarchy of selenium incorporation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Insulin-like growth factor-2 genotype, fat-free mass, and muscle performance across the adult life span

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oligogenic combinations associated with breast cancer risk in women under 53 years of age.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bioinformatic identification of candidate cis-regulatory elements involved in human mRNA polyadenylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Upstream elements present in the 3'-untranslated region of collagen genes influence the processing efficiency of overlapping polyadenylation signals

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel RNA structural motif in the selenocysteine insertion element of eukaryotic selenoprotein mRNAs

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cytokine mRNA-destabilizing element that is structurally and functionally distinct from A+U-rich elements.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16807757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-006-0218-X

1 reference

Europe PubMed Central

3 August 2017

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

3 August 2017

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