WordNet

(immunology) a technique that uses antibodies linked to a fluorescent dye in order to study antigens in a sample of tissue
the act of spotting or staining something (同)spotting, maculation
(histology) the use of a dye to color specimens for microscopic study

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1. 腎同種移植片のC4d染色および抗体媒介性拒絶反応の治療 c4d staining in renal allografts and treatment of antibody mediated rejection
2. 膜性増殖性糸球体腎炎の臨床像、分類、および原因 clinical presentation classification and causes of membranoproliferative glomerulonephritis
3. 免疫グロブリン軽鎖（AL）アミロイドーシスおよび軽鎖重鎖沈着症の病因 pathogenesis of immunoglobulin light chain al amyloidosis and light and heavy chain deposition diseases
4. 後天性表皮水疱症 epidermolysis bullosa acquisita
5. 抗好中球細胞質抗体の臨床的な意味 clinical spectrum of antineutrophil cytoplasmic antibodies

Fluorescence imaging of in vivo miR-124a-induced neurogenesis of neuronal progenitor cells using neuron-specific reporters.

Jang J1,2, Lee S1, Oh HJ1,2, Choi Y1, Choi JH1, Hwang DW3,4, Lee DS5,6.
EJNMMI research.EJNMMI Res.2016 Dec;6(1):38. doi: 10.1186/s13550-016-0190-y. Epub 2016 Apr 26.
BACKGROUND: Facilitation of the differentiation of the stem cells toward neuronal lineage is crucial for enhancing the differentiation efficacy of grafted stem cells for the possible treatment of neurodegenerative disorders. MicroRNA124a (miR-124a) has been considered as a neuronal lineage regulator
PMID 27115744

Quercetin and vitamin E attenuate Bonny Light crude oil-induced alterations in testicular apoptosis, stress proteins and steroidogenic acute regulatory protein in Wistar rats.

Ebokaiwe AP1, Mathur PP2, Farombi EO3.
Drug and chemical toxicology.Drug Chem Toxicol.2016 Oct;39(4):424-31. doi: 10.3109/01480545.2015.1137303. Epub 2016 Jan 28.
Studies have shown the reproductive effects of Bonny Light crude oil (BLCO) via the mechanism of oxidative stress and testicular apoptosis. We investigated the protective role of quercetin and vitamin E on BLCO-induced testicular apoptosis. Experimental rats were divided into four groups of four eac
PMID 26821606

Exopolysaccharide from Trichoderma pseudokoningii induces macrophage activation.

Wang G1, Zhu L2, Yu B3, Chen K3, Liu B3, Liu J3, Qin G2, Liu C2, Liu H4, Chen K5.
Carbohydrate polymers.Carbohydr Polym.2016 Sep 20;149:112-20. doi: 10.1016/j.carbpol.2016.04.093. Epub 2016 Apr 26.
In this study, we evaluated the immunomodulatory activity of an exopolysaccharide (EPS) derived from Trichoderma pseudokoningii and investigated the molecular mechanism of EPS-mediated activation of macrophages. Results revealed that EPS could significantly induce the production of nitric oxide (NO)
PMID 27261736

Direct Infection of Primary Salivary Gland Epithelial Cells by Human T Lymphotropic Virus Type I in Patients With Sjögren's Syndrome

Nakamura Hideki,Takahashi Yoshiko,Yamamoto-Fukuda Tomomi,Horai Yoshiro,Nakashima Yoshikazu,Arima Kazuhiko,Nakamura Tatsufumi,Koji Takehiko,Kawakami Atsushi
Arthritis & Rheumatology 67(4), 1096-1106, 2015-04
… Antibody arrays, immunofluorescence analysis, and enzyme-linked immunosorbent assay (ELISA) were used to determine the profiles of inflammation-related molecules, and the profiles of apoptosis-related molecules were determined by antibody array and immunofluorescence analysis. … The presence of HTLV-I-related molecules was assessed by immunofluorescence analysis and in situ polymerase chain reaction. … Apoptosis of SGECs was evaluated by TUNEL staining. …
NAID 120005603845

Microfluidic devices for construction of contractile skeletal muscle microtissues(CELL AND TISSUE ENGINEERING)

Shimizu Kazunori,Araki Hiroyuki,Sakata Kohei [他],Tonomura Wataru,Hashida Mitsuru,Konishi Satoshi
Journal of bioscience and bioengineering 119(2), 212-216, 2015-02
… Skeletal muscle microtissues cultured in the microchannel for a week consisted of myotubes were confirmed by histological analysis and immunofluorescence staining. …
NAID 110009922584

WANG JUAN,ASANUMA KATSUHIKO,HIDAKA TERUO,SASAKI YU,TANAKA ERIKO,TAKAGI-AKIBA MIYUKI,ALEJANDRO OLIVA TREJO JUAN,TOMINO YASUHIKO
順天堂醫事雑誌 61(1), 34-40, 2015
… To confirm the changes in mRNA levels and their protein expression, ADR was added to cultured mouse podocytes and analyzed at 1, 2, 6, and 24 hours using real-time PCR and immunofluorescence. … Finally, we also confirmed the expression of both proteins in vivo, by staining mouse kidney tissue at 0, 3, and 15 days after ADR injection.Results: Microarray data showed that after ADR treatment, FOSL1 was up-regulated, while RGS2 was down-regulated. …
NAID 130005085651