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MEG3 gene

Known as: MATERNALLY EXPRESSED GENE 3, NCRNA00023, onco-lncRNA-83 
National Institutes of Health

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Related topics

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MEG8 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2018
Highly Cited
2018
Knockdown of lncRNA MEG3 inhibits viability, migration, and invasion and promotes apoptosis by sponging miR‐127 in osteosarcoma cell
Osteosarcoma (OS) is one of the most common bone malignancies and occurs almost exclusively in children and adolescents. This… 
2018
2018
Long noncoding RNA maternally expressed gene 3 knockdown alleviates lipopolysaccharide-induced inflammatory injury by up-regulation of miR-203 in ATDC5 cells.
2018
2018
LncRNA MEG3 participates in neuronal cell injury induced by subarachnoid hemorrhage via inhibiting the Pi3k/Akt pathway.
OBJECTIVE To explore the effect of LncRNA MEG3 in the subarachnoid hemorrhage (SAH) and its underlying mechanism. PATIENTS AND… 
Highly Cited
2016
Highly Cited
2016
Fenofibrate inhibited pancreatic cancer cells proliferation via activation of p53 mediated by upregulation of LncRNA MEG3.
Review
2016
Review
2016
Long Non-coding RNAs in Urologic Malignancies: Functional Roles and Clinical Translation
Early diagnosis and surveillance for metastasis and recurrences are critical issues of urologic cancer. Deregulation of long non… 
Highly Cited
2006
Highly Cited
2006
Imprinted DLK1 is a putative tumor suppressor gene and inactivated by epimutation at the region upstream of GTL2 in human renal cell carcinoma.
A common deletion at chromosomal arm 14q32 in human renal cell carcinoma (RCC) prompted us to explore a tumor suppressor gene… 
2005
2005
Increased plasticity of genomic imprinting of Dlk1 in brain is due to genetic and epigenetic factors
The expression of six imprinted genes (Dlk1, Gtl2, Igf2r, Kcnq1, Nnat, and Peg1) was examined in brains of 21 mice derived from… 
Highly Cited
2002
Highly Cited
2002
Paternal UPD14 is responsible for a distinctive malformation complex.
We present a boy and two girls with paternal uniparental disomy of chromosome 14q (patUPD14). One girl had a Robertsonian… 
2000
2000
Novel Imprinted DLK 1 / GTL 2 Domain on Human Chromosome 14 Contains Motifs that Mimic Those Implicated in IGF 2 / H 19 Regulation
The evolution of genomic imprinting in mammals occurred more than 100 million years ago, and resulted in the formation of genes… 
1994
1994
A protein-specific monoclonal antibody to rat liver beta 1-->4 galactosyltransferase and its application to immunohistochemistry.
We have produced a new protein-specific monoclonal antibody (MAb) to rat liver beta 1-->4 galactosyltransferase. This MAb, GTL2… 
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