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The present study was designed to investigate the source of AVP in the rat NRM during pain process using the methods of nucleus push pull perfusion and radioimmunoassay.
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This paper presents the METINUS Plus (METhod of Immunohistochemical NUclei Segmentation Plus) method that has been developed for localization and quantification of the regulatory T cells' nuclei.
This paper describes in vitro methods developed to remove as much nucleus as possible from discs for studies of nucleus replacement.
The first method was a single-cell digital imaging-based method employing fluorescent staining of nuclei.
In this paper, we proposed a quantitative image analysis method to analyze subcellular cytoskeletal changes using a texture analysis method preceded by segmentation of nuclei, cytoplasm and ruffling regions (area except nuclei and cytoplasm).
For image processing of the dentate nuclei, a recently developed region of interest (ROI) driven normalization method of the dentate nuclei was applied (Diedrichsen et al., 2011).
SPIRAL2 will complement FAIR by using an alternative method of generating unstable nuclei.
Our methods of podocyte counting relied on accurately identifying podocyte nuclei (WT-1) or cytoplasm (GLEPP1).
In this phase, we introduce the methods of extracting these features from the segmented epithelial nuclei.
Many studies have found that caudate nucleus (CdN) enriches OXT and OXT receptors by the methods of historadioautograph and gene expression.
As far as we know, this is a novel rapid and high-accuracy method for determining the number of nuclei per spores in AMF.
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