2020
DOI: 10.1007/s10143-020-01427-8
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Diagnostic and prognostic potential of circulating miRNAs for intracranial aneurysms

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Cited by 16 publications
(12 citation statements)
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“…miR-NAs can be detected in the cells, tissues, and body fluids such as serum, plasma, tears, urine, or cerebrospinal fluid (CSF) 23 . For this reason, these circulating miRNAs are a novel target for the diagnosis and prognosis of a SAH 24 . Understanding the complete miRNA pathway is important because every miRNA regulates the expression of hundreds of genes 25 .…”
Section: Micrornamentioning
confidence: 99%
“…miR-NAs can be detected in the cells, tissues, and body fluids such as serum, plasma, tears, urine, or cerebrospinal fluid (CSF) 23 . For this reason, these circulating miRNAs are a novel target for the diagnosis and prognosis of a SAH 24 . Understanding the complete miRNA pathway is important because every miRNA regulates the expression of hundreds of genes 25 .…”
Section: Micrornamentioning
confidence: 99%
“…As a result of this combination, they are resistant to RNAses. For this reason, circulating miRNAs could become potential biomarkers for IA and SAH [ 96 , 97 ].…”
Section: Micrornasmentioning
confidence: 99%
“…In particular, several protein markers, such as glial fibrillary acidic protein, neuro-specific enolase, and S100 calcium binding protein B, a protein involves in BBB dysfunction and brain lesion [88], are also present in stroke and traumatic brain injury [89,90]. Compared to protein and metabolite biomarkers, the advantages of using miRNAs as biomarkers for aSAH and DBI include tissue/cell type, pathophysiological specificity, and stability in biofluids [91], as well as ease of detection [35,[92][93][94].…”
Section: Current Limitation Of Using Mirnas As Biomarkers For Asah and Its Complicationsmentioning
confidence: 99%