Below are the most recent publications written about "In Situ Hybridization, Fluorescence" by people in Profiles.
-
Afzal Z, Krumlauf R. Optimized smFISH Pipeline for Studying Nascent Transcription in Mouse Embryonic Tissue Samples. Methods Mol Biol. 2025; 2889:53-66.
-
Vrinceanu D, Dumitru M, Bratiloveanu M, Marinescu A, Serboiu C, Manole F, Palade DO, Costache A, Costache M, Patrascu O. Parotid Gland Tumors: Molecular Diagnostic Approaches. Int J Mol Sci. 2024 Jul 04; 25(13).
-
Frusone V, Maurer K, Emanuel BS, McDonald-McGinn D, Sullivan KE. Inflammatory Proteomic Analysis of 22q11.2 Deletion Syndrome. J Clin Immunol. 2024 03 15; 44(3):82.
-
Afzal Z, Lange JJ, Nolte C, McKinney S, Wood C, Paulson A, De Kumar B, Unruh J, Slaughter BD, Krumlauf R. Shared retinoic acid responsive enhancers coordinately regulate nascent transcription of Hoxb coding and non-coding RNAs in the developing mouse neural tube. Development. 2023 05 15; 150(10).
-
Diaz VD, Hermann BP. Single-Molecule Fluorescence In Situ Hybridization for Spatial Detection of mRNAs in Sections of Mammalian Testes. Methods Mol Biol. 2023; 2656:21-35.
-
Bahry E, Breimann L, Zouinkhi M, Epstein L, Kolyvanov K, Mamrak N, King B, Long X, Harrington KIS, Lionnet T, Preibisch S. RS-FISH: precise, interactive, fast, and scalable FISH spot detection. Nat Methods. 2022 12; 19(12):1563-1567.
-
Yin Q, Zhao YJ, Ni WJ, Tang TT, Wang Y, Cao JY, Yin D, Wen Y, Li ZL, Zhang YL, Jiang W, Zhang Y, Lu XY, Zhang AQ, Gan WH, Lv LL, Liu BC, Wang B. MiR-155 deficiency protects renal tubular epithelial cells from telomeric and genomic DNA damage in cisplatin-induced acute kidney injury. Theranostics. 2022; 12(10):4753-4766.
-
Blanchard EL, Argyropoulou D, Zurla C, Bhosle SM, Vanover D, Santangelo PJ. Quantification and Localization of Protein-RNA Interactions in Patient-Derived Archival Tumor Tissue. Cancer Res. 2019 10 15; 79(20):5418-5431.
-
Nwokafor C, Singer RH, Lim H. Imaging cell-type-specific dynamics of mRNAs in living mouse brain. Methods. 2019 03 15; 157:100-105.
-
Barry JC, Crowley TB, Jyonouchi S, Heimall J, Zackai EH, Sullivan KE, McDonald-McGinn DM. Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency. J Clin Immunol. 2017 Jul; 37(5):476-485.