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■ Search Result - Abbreviation : 3'-UTR

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Abbreviation: 3'-UTR
Appearance Frequency: 1516 time(s)
Long forms: 8

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
3'-untranslated region
(1492 times)
(332 times)
miRNAs (260 times)
miRNA (80 times)
EMT (57 times)
1987 Posttranscriptional gene regulation and specific binding of the nonhistone protein HMG-I by the 3' untranslated region of bovine interleukin 2 cDNA.
(16 times)
Molecular Biology
(5 times)
miRNAs (7 times)
NSCLC (2 times)
5'-UTR (1 time)
1998 Homozygous deletions of methylthioadenosine phosphorylase (MTAP) are more frequent than p16INK4A (CDKN2) homozygous deletions in primary non-small cell lung cancers (NSCLC).
3'-untranslated region of the gene
(3 times)
(3 times)
ADHD (3 times)
DAT (3 times)
VNTR (2 times)
2006 A promoter polymorphism (-839 C > T) at the dopamine transporter gene is associated with attention deficit/hyperactivity disorder in Brazilian children.
3'-untranslated binding region
(1 time)
Cell Biology
(1 time)
CRC (1 time)
CRCSCs (1 time)
CSCs (1 time)
2019 Regulatory mechanisms of microRNAs in colorectal cancer and colorectal cancer stem cells.
3'-untranslated region polymorphism
(1 time)
Allergy and Immunology
(1 time)
AICU (1 time)
HNMT (1 time)
RBCs (1 time)
2009 Histamine N-methyltransferase 939A>G polymorphism affects mRNA stability in patients with acetylsalicylic acid-intolerant chronic urticaria.
(1 time)
(1 time)
CIs (1 time)
ORs (1 time)
SCLC (1 time)
2015 A Regulatory MDM4 Genetic Variant Locating in the Binding Sequence of Multiple MicroRNAs Contributes to Susceptibility of Small Cell Lung Cancer.
un-translation reagon
(1 time)
(1 time)
HSC-T6 cells (1 time)
MMP (1 time)
NAC (1 time)
2015 BCL2 promotor methylation and miR-15a/16-1 upregulation is associated with sanguinarine-induced apoptotic death in rat HSC-T6 cells.
untranslated region of the 3' mRNA
(1 time)
(1 time)
CNS (1 time)
MS (1 time)
NRG1 (1 time)
2022 Significant Association of rs77493513 Polymorphism in 3'-UTR of the NRG1 Gene with the Risk of Multiple Sclerosis Disease.