PMID- 35099787 OWN - NLM STAT- MEDLINE DCOM- 20220331 LR - 20220401 IS - 1940-6029 (Electronic) IS - 1064-3745 (Linking) VI - 2417 DP - 2022 TI - Real-Time Quantitative PCR and Fluorescence In Situ Hybridization for Subcellular Localization of miRNAs in Neurons. PG - 1-17 LID - 10.1007/978-1-0716-1916-2_1 [doi] AB - Neuronal miRNAs play major roles in regulation of synaptic development and plasticity. The small size of miRNAs and, in some cases, their low level of expression make their quantification and detection challenging. Here, we outline methods to quantify steady state levels of miRNAs in neurons and the brain by using real-time quantitative PCR (RT-qPCR) and to determine miRNA subcellular localization in primary neurons by a sensitive fluorescence in situ hybridization (FISH) method. CI - (c) 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature. FAU - Tatarakis, Antonis AU - Tatarakis A AD - Department of Cell Biology, and Howard Hughes Medical Institute, Harvard Medical School, Boston, MA, USA. antonis_tatarakis@hms.harvard.edu. FAU - Moazed, Danesh AU - Moazed D AD - Department of Cell Biology, and Howard Hughes Medical Institute, Harvard Medical School, Boston, MA, USA. danesh@hms.harvard.edu. LA - eng PT - Journal Article PL - United States TA - Methods Mol Biol JT - Methods in molecular biology (Clifton, N.J.) JID - 9214969 RN - 0 (MicroRNAs) SB - IM MH - In Situ Hybridization, Fluorescence MH - *MicroRNAs/metabolism MH - Neurons/metabolism MH - Real-Time Polymerase Chain Reaction/methods OTO - NOTNLM OT - Brain OT - Expression profile OT - Isolation OT - Neurons OT - miRNA RT-qPCR assays OT - miRNA fluorescence in situ hybridization OT - miRNAs EDAT- 2022/02/01 06:00 MHDA- 2022/04/01 06:00 CRDT- 2022/01/31 12:18 PHST- 2022/01/31 12:18 [entrez] PHST- 2022/02/01 06:00 [pubmed] PHST- 2022/04/01 06:00 [medline] AID - 10.1007/978-1-0716-1916-2_1 [doi] PST - ppublish SO - Methods Mol Biol. 2022;2417:1-17. doi: 10.1007/978-1-0716-1916-2_1.