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Готові списки джерел за темами / Standard Stained Shingle Co

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Добірка наукової літератури з теми "Standard Stained Shingle Co"

Автор: Grafiati

Опубліковано: 25 липня 2024

Оновлено: 31 липня 2025

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Статті в журналах з теми "Standard Stained Shingle Co"

1

Quddus, Iram, Farhana Samir, Humera Waqar, and Sarwer Qureshi. "Concomitant Use Of L-arginine With High Butter And Corn Oil Diet Prevent Their Harmful Effects On Adrenocortical Cells Of Albino Rats." Journal of Bahria University Medical and Dental College 08, no. 01 (2017): 35–39. http://dx.doi.org/10.51985/jbumdc2018009.

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Objective: To compare the bichemical and morphological effects of L -Arginine against the changes caused by butter and corn oil supplementation Study design: A prospective experimental study Place: Department of Anatomy BMSI, JPMC Duration: August to October 2008. Methodology:Male Albino rats weighing 200 - 240gm were selected and divided into 5 groups. Group ‘CL’ received standard laboratory diet. Group ‘Bu’ received 20% added unsalted butter in diet. Group ‘Co’ received 20% added corn oil in diet. Group ‘BuAr’ received 20% Butter with L-Arginine 300mg /kg body weight /day orally .Group‘CoAr’

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2

Monge, Florencia A., Adeline M. Fanni, Patrick L. Donabedian, et al. "Selective In Vitro and Ex Vivo Staining of Brain Neurofibrillary Tangles and Amyloid Plaques by Novel Ethylene Ethynylene-Based Optical Sensors." Biosensors 13, no. 2 (2023): 151. http://dx.doi.org/10.3390/bios13020151.

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The identification of protein aggregates as biomarkers for neurodegeneration is an area of interest for disease diagnosis and treatment development. In this work, we present novel super luminescent conjugated polyelectrolyte molecules as ex vivo sensors for tau-paired helical filaments (PHFs) and amyloid-β (Aβ) plaques. We evaluated the use of two oligo-p-phenylene ethynylenes (OPEs), anionic OPE12- and cationic OPE24+, as stains for fibrillar protein pathology in brain sections of transgenic mouse (rTg4510) and rat (TgF344-AD) models of Alzheimer’s disease (AD) tauopathy, and post-mortem brai

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3

Tantisatirapong, Suchada, and Wongsakorn Preedanan. "Texture Based Classification of Malaria Parasites from Giemsa-Stained Thin Blood Films." ECTI Transactions on Electrical Engineering, Electronics, and Communications 18, no. 1 (2020): 9–16. http://dx.doi.org/10.37936/ecti-eec.2020181.208115.

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Quantification of parasitemia is an important part of a microscopic malaria diagnosis. Giemsa-stained thin blood smear is the gold standard method for detecting malaria parasite enumeration. However, manual counting reveals the limitations of human inconsistency and fatigue, as well as the unreliability of accuracy and non-reproducibility. Inaccurate parasitemia affects clinical diagnosis and therapeutic procedure. Automated quantification is therefore useful to improve the performance of quantifying parasite density. In this paper, the texture-based classification approach is investigated. Th

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4

Hwang, Kevin, Grace Vezeau, Edyta Olejnik, et al. "Abstract 3767: A novel method to minimize HIER-induced alterations on H&E staining in an integrated mIF-H&E workflow." Cancer Research 84, no. 6_Supplement (2024): 3767. http://dx.doi.org/10.1158/1538-7445.am2024-3767.

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Abstract Background: Hematoxylin and eosin staining (H&E) is widely used as an anatomical assay for clinical diagnosis. Researchers and clinicians also rely on molecular in situ techniques, such as multiplexed immunofluorescence (mIF), to gain deeper insights on cellular phenotypes and tissue microenvironment. As a result, there has been significant interest in combining anatomical stains with molecular imaging techniques, most commonly by using a terminal H&E stain after mIF staining. This allows a combination of the two assays but has been observed to show alterations in the H&E

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5

Alatrash, Gheath, Pariya Sukhumalchandra, Mao Zhang, et al. "PR1 Is Cross-Presented By Multiple Myeloma Cells in Patients and Renders Multiple Myeloma Susceptible to PR1-CTL and Anti-PR1/HLA-A2 Antibody." Blood 124, no. 21 (2014): 2133. http://dx.doi.org/10.1182/blood.v124.21.2133.2133.

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Abstract PR1 is an HLA-A2-retricted, nonameric peptide that is derived from the azurophil granule proteases neutrophil elastase (NE) and proteinase 3 (P3). PR1 has been targeted successfully in acute (AML) and chronic (CML) myeloid leukemia using anti-PR1/HLA-A2 antibody (8F4), PR1-peptide vaccine and PR1-specific cytotoxic T lymphocytes (PR1-CTL). We have previously reported that NE and P3 are cross-presented by normal B cells and dendritic cells (DC), leading to PR1 expression by HLA-A2. Since multiple myeloma (MM) is a B cell malignancy, we investigated whether MM cells can cross-present PR

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6

Nikolskiy, I., V. Nikolskaya, D. Demchenko, and D. Zubov. "Potentiation of directed osteogenic differentiation of thymic multipotent stromal cells by prior co-cultivation with thymocytes." Cell and Organ Transplantology 4, no. 2 (2016): 220–23. http://dx.doi.org/10.22494/cot.v4i2.59.

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It is known that multipotent stromal cells (MSCs) and thymocytes possess membrane affinity and interaction in the thymic niches that is essentially important for thymocytes differentiation. However there are no data about possible influence of intercellular contacts in the reverse direction: from the thymocytes to the MSCs.Materials and methods. The MSCs were obtained from the thymuses of С57ВL mice, using the explants technique, and cultivated under standard conditions during 8-12 passages. Thymocytes or bone marrow cells (106) were added to 4×104 MSCs for 24 hours. Thereafter they were elimi

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7

DOONABOYINA, RAGHAVA, Abhilasha Mittal, and Sridhar Babu Gummadi. "IN VITRO SULFORHODAMINE B ASSAY EVALUATION OF NOVEL 2-PHENYL BENZOFURANONE DERIVATIVES ON HUMAN SKIN CANCER CELL LINE G361." Journal of Drug Delivery and Therapeutics 9, no. 4-A (2019): 385–89. http://dx.doi.org/10.22270/jddt.v9i4-a.3434.

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The newly synthesized compounds are being tested for in vitro anticancer activity. The method used for In Vitro testing is Sulforhodamine B assay also known SRB assay. Cell lines were prepared and homogenized and disassociated with the help of trypsin. Then trypsin was inactivated with fetal bovine serum. Then cell concentration was determined. Synthesized molecules were prepared into four different dilutions and exposed to cell lines. The procedure was also compared with standard drug doxorubicin. All the cell medium were incubated 37 degrees centigrade in a humidified incubator with 5 percen

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8

Aertker, Benjamin M., Akshita Kumar, Fanni Cardenas, et al. "PET Imaging of Peripheral Benzodiazepine Receptor Standard Uptake Value Increases After Controlled Cortical Impact, a Rodent Model of Traumatic Brain Injury." ASN Neuro 13 (January 2021): 175909142110141. http://dx.doi.org/10.1177/17590914211014135.

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Traumatic brain injury (TBI) is a chronic, life threatening injury for which few effective interventions are available. Evidence in animal models suggests un-checked immune activation may contribute to the pathophysiology. Changes in regional density of active brain microglia can be quantified in vivo with positron emission topography (PET) with the relatively selective radiotracer, peripheral benzodiazepine receptor 28 (11 C-PBR28). Phenotypic assessment (activated vs resting) can subsequently be assessed (ex vivo) using morphological techniques. To elucidate the mechanistic contribution of i

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9

Thongheang, Kanyarat, Thanathat Pamonsupornwichit, Kanokporn Sornsuwan, et al. "Potentiating Antibody-Dependent Cellular Cytotoxicity in Triple-Negative Breast Cancer via the Humanized Anti-CD147 Antibody." Antibodies 14, no. 2 (2025): 36. https://doi.org/10.3390/antib14020036.

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Background: Triple-negative breast cancer (TNBC) is an aggressive subtype with high metastatic potential, poor prognosis, and the absence of estrogen receptors, progesterone receptors, and human epidermal growth factor receptor 2 (HER2). The lack of these receptors limits the standard treatments, such as hormone therapies and HER2-targeted antibodies like trastuzumab. These challenges highlight the critical need for novel therapeutic strategies. CD147, a transmembrane glycoprotein overexpressed in TNBC, promotes tumor progression, metastasis, and chemoresistance, making it a promising therapeu

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10

Pantic, Igor, Sanja Dacic, Predrag Brkic, et al. "Application of Fractal and Grey Level Co-Occurrence Matrix Analysis in Evaluation of Brain Corpus Callosum and Cingulum Architecture." Microscopy and Microanalysis 20, no. 5 (2014): 1373–81. http://dx.doi.org/10.1017/s1431927614012811.

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AbstractThis aim of this study was to assess the discriminatory value of fractal and grey level co-occurrence matrix (GLCM) analysis methods in standard microscopy analysis of two histologically similar brain white mass regions that have different nerve fiber orientation. A total of 160 digital micrographs of thionine-stained rat brain white mass were acquired using a Pro-MicroScan DEM-200 instrument. Eighty micrographs from the anterior corpus callosum and eighty from the anterior cingulum areas of the brain were analyzed. The micrographs were evaluated using the National Institutes of Health

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