5q-syndrome
|
0.080 |
Biomarker
|
disease |
BEFREE |
Moreover, combined loss of miR-145 and RPS14 cooperates to alter erythroid-megakaryocytic differentiation in a manner similar to the 5q- syndrome.
|
21873545 |
2011 |
5q-syndrome
|
0.080 |
Biomarker
|
disease |
BEFREE |
Identification of miR-145 and miR-146a as mediators of the 5q- syndrome phenotype.Nat.Med.16(1), 49-58 (2009).
|
20469997 |
2010 |
5q-syndrome
|
0.080 |
Biomarker
|
disease |
BEFREE |
Recent evidence suggests that haploinsufficiency of the microRNA genes miR-145 and miR-146a may contribute to the thrombocytosis seen in the 5q- syndrome.
|
22571696 |
2012 |
5q-syndrome
|
0.080 |
Biomarker
|
disease |
BEFREE |
Identification of miR-145 and miR-146a as mediators of the 5q- syndrome phenotype.
|
19898489 |
2010 |
5q-syndrome
|
0.080 |
Biomarker
|
disease |
BEFREE |
Macrophages, regulatory cells of erythropoiesis and the innate immune response, were significantly increased in Rps14/Csnk1a1/miR-145/146a deficient mice as well as in 5q- syndrome patient bone marrows and showed activation of the innate immune response, reflected by increased expression of S100A8, and decreased phagocytic function.
|
30651631 |
2019 |
5q-syndrome
|
0.080 |
GeneticVariation
|
disease |
BEFREE |
The megakaryocytic and platelet phenotype of the 5q-syndrome has been attributed to heterozygous deletion of miR145 and miR146a.
|
21943668 |
2011 |
5q-syndrome
|
0.080 |
Biomarker
|
disease |
BEFREE |
In 5q- syndrome haploinsufficiency of the ribosomal gene RPS14 appears to cooperate with loss of two micro-RNAs miR-145 and miR-146 to induce key features of the disease.
|
20211165 |
2010 |
5q-syndrome
|
0.080 |
Biomarker
|
disease |
BEFREE |
Other mouse modeling data suggest that haploinsufficiency of the microRNA genes miR-145 and miR-146a may contribute to the thrombocytosis seen in the 5q- syndrome.
|
20733155 |
2010 |
acute aortic dissection
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
miR-145 expression was downregulated in aortic dissection tissues and was associated with the survival of patients with AAD.
|
30900421 |
2019 |
Acute cerebral ischemia
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Results of further <i>in vivo</i> study revealed that anti-miR-145-5p administration brought about increasing expression of Nurr1 and reduction of infarct volume in acute cerebral ischemia.
|
29209166 |
2017 |
Acute Cerebrovascular Accidents
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
In the subchapter "miRNAs in acute stroke", we will provide insight into recent knowledge from animal and human studies concerning miRNA profiling in acute stroke and their expression dynamics in brain tissue and extracellular fluids (roles of, e.g. let-7 family, miR-21, miR-29 family, miR-124, miR-145, miR-181 family, miR-210 and miR-223).
|
26663183 |
2015 |
Acute Chest Syndrome
|
0.010 |
Biomarker
|
disease |
BEFREE |
In particular, miR-133a/b (5 studies), miR-208a/b (6 studies), and miR-499 (7 studies) were well studied and found to be significant diagnostic and/or prognostic markers across different cardiovascular disease progression stages. miR-1 and miR-145b are potential biomarkers of ACS; miR-1 with higher sensitivity for all acute myocardial infarction (AMI), and miR-145 for STEMI and worse outcome of AMI.
|
27357636 |
2016 |
Acute monocytic leukemia
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We found that miR-143 and miR-145 expression is significantly repressed in primary AML patient samples as compared to neutrophils of healthy donors.
|
22093444 |
2012 |
Acute myocardial infarction
|
0.050 |
Biomarker
|
disease |
BEFREE |
Receiver Operating Characteristic (ROC) analysis indicated that miR-17-5p, miR-126-5p, and miR-145-3p showed considerable diagnostic efficiency for AMI.
|
30833907 |
2019 |
Acute myocardial infarction
|
0.050 |
AlteredExpression
|
disease |
BEFREE |
Chloroquine diphosphate (5 µM) inhibited the regulatory effect of miRNA‑145 upregulation on autophagy to adjust cell apoptosis, in the in vitro model of AMI.
|
29956747 |
2018 |
Acute myocardial infarction
|
0.050 |
GeneticVariation
|
disease |
BEFREE |
In a multivariable linear regression analysis, AMI and heart failure were independently associated with lower Ln_miRNA-145 (estimate -0.99, standard error [SE] 0.28; P= 0.001 and estimate -0.62, SE 0.21; P= 0.004).
|
28051023 |
2017 |
Acute myocardial infarction
|
0.050 |
Biomarker
|
disease |
BEFREE |
In particular, miR-133a/b (5 studies), miR-208a/b (6 studies), and miR-499 (7 studies) were well studied and found to be significant diagnostic and/or prognostic markers across different cardiovascular disease progression stages. miR-1 and miR-145b are potential biomarkers of ACS; miR-1 with higher sensitivity for all acute myocardial infarction (AMI), and miR-145 for STEMI and worse outcome of AMI.
|
27357636 |
2016 |
Acute myocardial infarction
|
0.050 |
AlteredExpression
|
disease |
BEFREE |
Noticeably, the expression levels of miR-24, miR-23a and miR-145 were significantly down-regulated in AMI<sup>+</sup>AKI<sup>+</sup> patients compared to those in AMI<sup>+</sup>AKI<sup>-</sup> patients.
|
31039814 |
2019 |
Adenocarcinoma
|
0.020 |
Biomarker
|
group |
BEFREE |
We successfully verified the expression of selected miRNAs using real-time reverse transcription-PCR assays for mature miRNAs, whereas in situ hybridization was used to detect the accumulation of miR-145 and miR-320 in normal epithelial cells and adenocarcinoma cells.
|
18676867 |
2008 |
Adenocarcinoma
|
0.020 |
Biomarker
|
group |
BEFREE |
An increased expression of miR-21 was found in the tumour-associated stroma with the most dramatic increase from adenoma to adenocarcinoma, while the number of positive miR-145 fibroblast-like cells in the normal lamina propria (stroma) decreased in a stepwise manner throughout the normal-adenoma-adenocarcinoma sequence.
|
26465597 |
2015 |
Adenocarcinoma of colon
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Furthermore, we found that LINC00491 positively regulates SERPINE1 expression through sponging miR-145 and promoting the proliferation, migration, and invasion of colon adenocarcinoma cells, thus playing an oncogenic role during colon adenocarcinoma pathogenesis.
|
31496744 |
2019 |
Adenocarcinoma Of Esophagus
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Finally, we demonstrate that expression of miR-145 in esophageal adenocarcinoma cell line (SK-GT-4) enhances tumor growth and metastasis in a NOD/SCID xenograft model.
|
29632636 |
2018 |
Adenocarcinoma Of Esophagus
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
MiR-145 expression accelerates esophageal adenocarcinoma progression by enhancing cell invasion and anoikis resistance.
|
25551563 |
2014 |
Adenocarcinoma of lung (disorder)
|
0.100 |
Biomarker
|
disease |
BEFREE |
And miR-145-5p tended to show better diagnostic performance in lung squamous cell carcinoma than in lung adenocarcinoma.
|
28347234 |
2017 |
Adenocarcinoma of lung (disorder)
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Most interestingly, an obvious inhibition of cell growth was observed in the EGFR mutant lung adenocarcinoma after transfection of hsa-pre-miR-145.
|
19493678 |
2009 |