Relevant bibliographies by topics / CDw44

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'CDw44'

Author: Grafiati
Published: 4 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "CDw44"

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Štefanová, Irena, Ivan Hilgert, Vladimír Bažil, Hana Krištofová, and Václav Hořejší. "Human leucocyte surface glycoprotein CDw44 and lymphocyte homing receptor are identical molecules." Immunogenetics 29, no. 6 (1989): 402–4. http://dx.doi.org/10.1007/bf00375869.

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Rogers, Ian, Giacomo D'Agostaro, Sonia Vera, and Michelle Letarte. "Several epitopes of p85 glycoprotein (CDw44) are dependent on intact disulphide bonds. Isolation of cDNA clones requires a polyclonal antibody raised against the reduced protein." Bioscience Reports 8, no. 4 (1988): 359–68. http://dx.doi.org/10.1007/bf01115227.

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Monoclonal antibodies 50B4 and 50E6 recognize two distinct epitopes of human p85 glycoprotein (CDw44). Both epitopes are destroyed by reduction of the purified gycoprotein as demonstrated by inhibition of cellular radioimmunoassay and Western blot analysis. Endoglycosidase F treated p85 glycoprotein, with an apparent molecular weight of 73,000 is still reactive with both monoclonal antibodies. Thus both epitopes are conformational determinats of the polypeptide chain. A rabbit antibody produced against purified native p85 glycoprotein also reacted only with the non-reduced form of p85. Repeate
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Dorn, G. W., M. G. Davis, and D. D. D'Angelo. "Gene expression during phorbol ester-induced differentiation of cultured human megakaryoblastic cells." American Journal of Physiology-Cell Physiology 266, no. 5 (1994): C1231—C1239. http://dx.doi.org/10.1152/ajpcell.1994.266.5.c1231.

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Platelet protein makeup is determined during transformation of megakaryoblasts to mature megakaryocytes, the immediate precursor of circulating platelets. To better understand the molecular mechanisms of megakaryocyte formation, gene expression was characterized by Northern analysis and RNA fingerprinting of cultured human CHRF-288 megakaryoblastic cells undergoing phorbol ester-stimulated megakaryocytic differentiation or serum-stimulated megakaryoblast proliferation. Protooncogenes c-fos and c-jun were coordinately upregulated in both proliferating and differentiating cells, whereas c-myc tr
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Naraoka, Yuna, Yo Mabuchi, Mai Kiuchi, et al. "Quality Control of Stem Cell-Based Cultured Meat According to Specific Differentiation Abilities." Cells 13, no. 2 (2024): 135. http://dx.doi.org/10.3390/cells13020135.

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The demand for stem cell-based cultured meat as an alternative protein source is increasing in response to global food scarcity. However, the definition of quality controls, including appropriate growth factors and cell characteristics, remains incomplete. Cluster of differentiation (CD) 29 is ubiquitously expressed in bovine muscle tissue and is a marker of progenitor cells in cultured meat. However, CD29+ cells are naturally heterogeneous, and this quality control issue must be resolved. In this study, the aim was to identify the subpopulation of the CD29+ cell population with potential util
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Yoo, Jeong Joon, Kwang Woo Nam, Kyung Hoi Koo, Kang Sup Yoon, and Hee Joong Kim. "Expression Patterns of Cell Surface Molecules on Human Bone Marrow Stromal Cells from Multi-Donors." Key Engineering Materials 361-363 (November 2007): 1153–56. http://dx.doi.org/10.4028/www.scientific.net/kem.361-363.1153.

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The unique characteristics of cell surface molecules on human bone marrow stromal cells (hBMSCs) have not been clearly elucidated. The authors characterized 19 cell surface molecules on culture-expanded hBMSCs obtained from 10 human donors, by flow cytometry, calculated the averages and standard deviations of the expression frequencies of individual surface molecules, and evaluated their expression patterns with respect to donor-dependent variations. Surface molecules expressed at frequencies of more than 80% on cells included, CD49e, CD29, CD90, CD73, CD44, CD105, and CD146, those expressed a
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White, Cristiana Pérez, and Lisa López Levers. "Parent–Teacher Engagement during Child-Centered Pedagogical Change in Elementary School." Children & Schools 39, no. 1 (2016): 15–24. http://dx.doi.org/10.1093/cs/cdw044.

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Wang, Yang, Huiling Zhong, Xiaodan Xie, et al. "Long noncoding RNA derived from CD244 signaling epigenetically controls CD8+ T-cell immune responses in tuberculosis infection." Proceedings of the National Academy of Sciences 112, no. 29 (2015): E3883—E3892. http://dx.doi.org/10.1073/pnas.1501662112.

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Molecular mechanisms for T-cell immune responses modulated by T cell-inhibitory molecules during tuberculosis (TB) infection remain unclear. Here, we show that active human TB infection up-regulates CD244 and CD244 signaling-associated molecules in CD8+ T cells and that blockade of CD244 signaling enhances production of IFN-γ and TNF-α. CD244 expression/signaling in TB correlates with high levels of a long noncoding RNA (lncRNA)-BC050410 [named as lncRNA-AS-GSTT1(1-72) or lncRNA-CD244] in the CD244+CD8+ T-cell subpopulation. CD244 signaling drives lncRNA-CD244 expression via sustaining a permi
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Ylagan, Lourdes R., John Scholes, and Rita Demopoulos. "CD44." Archives of Pathology & Laboratory Medicine 124, no. 2 (2000): 212–15. http://dx.doi.org/10.5858/2000-124-0212-c.

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Abstract Objective.—To test the hypothesis that CD44 standard (CD44[s]) and its other variants, CD44v6 and CD44v7-8, might be useful markers of squamous differentiation in epithelial tumors. Design.—We studied expression of CD44(s), CD44v6, and CD44v7-8 using immunohistochemistry in human tumors that had squamous differentiation, glandular differentiation, or both arising in the colon, stomach, esophagus, lung, pancreas, gallbladder, or uterus/cervix, as well as in adjacent nonneoplastic tissues. Formalin-fixed, paraffin-embedded archival tissue specimens of 33 adenosquamous tumors were used.
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Jawhari, Ahmed Hussain. "One-Pot Facile Synthesis of ZrO2-CdWO4: A Novel Nanocomposite for Hydrogen Production via Photocatalytic Water Splitting." Applied Sciences 13, no. 24 (2023): 13344. http://dx.doi.org/10.3390/app132413344.

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ZrO2-based nanocomposites are highly versatile materials with huge potential for photocatalysis. In this study, ZrO2-CdWO4 nanocomposites (NC) were prepared via the green route using aqueous Brassica rapa leaf extract, and its photocatalytic water-splitting application was evaluated. Brassica rapa leaf extract acts as a reducing agent and abundant phytochemicals are adsorbed onto the nanoparticle surfaces, improving the properties of ZrO2-CdWO4 nanocomposites. As-prepared samples were characterized by using various spectroscopic and microscopic techniques. The energy of the direct band gap (Eg
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Sun, Xugang, Jun Yu, Tiansuo Zhao, and Jihui Hao. "Abstract 1597: CD144+cancer-associated fibroblasts drive the malignancy of pancreatic cancer via stimulating inflammatory paracrine." Cancer Research 84, no. 6_Supplement (2024): 1597. http://dx.doi.org/10.1158/1538-7445.am2024-1597.

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Abstract Purpose: Cancer-associated fibroblasts (CAFs) are highly heterogeneous in pancreatic ductal adenocarcinoma (PDAC). We previously reported that CAFs can acquire an endothelial phenotype under stress. Thus, we hypothesized that there are CAFs highly expressing endothelial markers and substantiated a novel subtype of CAFs promoting tumor progression. Experimental design: We performed single-cell RNA sequencing to identify the existence of CD144+CAFs. The prospective and retrospective analysis were combined to figure out the correlation between CD144+CAFs proportion and clinical outcome.
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Dissertations / Theses on the topic "CDw44"

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Georg, Christian. "Die Bedeutung der Expression von CD44-h und seiner Isoformen CD44-v3, CD44-v6 und CD44-v9 sowie von E-Cadherin und PCNA für die klinische Progressionstendenz des Nierenzellkarzinoms." [S.l.] : [s.n.], 1999. http://deposit.ddb.de/cgi-bin/dokserv?idn=959324232.

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Ibrahim, Emad Moussa. "CD44 in cervical cancer." Thesis, University of Sheffield, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.269370.

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Kastilan, Thor. "Der Ko-Rezeptor CD44 v6 ein Beitrag zur Signaltransduktion und Etablierung einer CD44-negativen Maus /." Karlsruhe : Forschungszentrum Karlsruhe, 2007. http://d-nb.info/985061790/34.

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Rudzki, Zbigniew. "Relevance of CD44 to cancer biology." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ37162.pdf.

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Taher, Taher Elamin Imam. "CD44 and Met: the signaling perspective." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2002. http://dare.uva.nl/document/61689.

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Rudzki, Zbigniew. "Revelance of CD44 to cancer biology." Thesis, McGill University, 1997. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=27903.

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This thesis explores the role of an adhesion protein, CD44, in the biology of colon cancer. CD44 glycoprotein is a main extracellular receptor for hyaluronic acid. A single CD44 gene composed of 20 exons encodes a variety of isoforms due to alternative splicing of 10 middle exons. Overexpression of CD44 and appearance of abnormal isoforms containing products of variant exons have been implicated in the origin and progression of cancer, including human colon carcinoma.<br>Of two main parts comprising the dissertation, the first one ("CD44 and the adhesion of neoplastic cells" by Z. Rudzki and S
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Kastilan, Thor [Verfasser]. "Der Ko-Rezeptor CD44 v6 : ein Beitrag zur Signaltransduktion und Etablierung einer CD44-negativen Maus / Thor Kastilan." Karlsruhe : Forschungszentrum Karlsruhe, 2007. http://d-nb.info/985061790/34.

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Engel, Peter. "CD44 und variante Isoformen im murinen System." [S.l.] : [s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=968031609.

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Sidorchuk, Janine. "Expression of CD44 in human breast cancer." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape11/PQDD_0004/MQ41778.pdf.

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Maeshima, Nina Miharu. "Hyaluronan binding by CD44 on T cells." Thesis, University of British Columbia, 2010. http://hdl.handle.net/2429/27275.

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CD44 is a transmembrane protein that binds to hyaluronan, a component of the extracellular and pericellular matrices. Hyaluronan supports cell migration and proliferation during embryonic development, wound repair, as well as tumourigenesis. Hyaluronan binding to CD44 can also regulate leukocyte migration and adhesion. On naïve CD4 and CD8 T cells, CD44 is in its inactive form, but it is upregulated and induced to bind hyaluronan upon T cell activation. High CD44 expression is used as a marker for effector and memory T cells, and recent evidence has implicated CD44 in the formation of CD4
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Books on the topic "CDw44"

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Hannover, Tierärztliche Hochschule, ed. CD44-Expression in Gliomzellen des Menschen unter verschiedenen Wachstumsbedingungen. [s.n.], 1999.

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Shatirishvili, Marine. Conditional inactivation of CD44 in the skin reveals impaired epidermal repair. s.n.], 2013.

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Tölg, Cornelia. Die Genstruktur von CD44: Versuche zur Elimination der Funktion diskreter Isoformen. Forschungszentrum Karlsruhe GmbH, 1995.

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Owh, Phillip. Myelin basic protein up-regulates CD44 levels in an astrocytoma cell line in vitro. National Library of Canada, 1996.

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Paiwand, Frouz Frozan. RHAMM, CD44 expression and erk activation are linked in malignant human breast cancer cells and are associated with cell motility. National Library of Canada, 1999.

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D, Stern Robert M., ed. Hyaluronan in cancer biology. Academic Press, 2009.

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Scheunemann, Peter. Inzidenz und prognostische Bedeutung der Expression von Intercellular Adhesion Molecule-1 (ICAM-1, Human Leucocyte Antigen (HLA) Class I, Adhäsionsmolekül CD44 und Tumorsuppressorprotein p53 bei Lebermetastasen kolorektaler Karzinome und kolorektaler Primärtumoren: Inzidenz der Expression des Oberflächenmoleküls 17-1A bei Lebermetastasen und Lebermetastasenrezidiven. [s.n.], 1997.

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Hoffmann, Isabel. Einfluss der CD44-Standardisoform und der CD44-varianten Isoformen auf den Erhalt des hämatopoetischen und leukämischen Stammzellpotenzials. 2011.

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Taxis, Sabine. Modulation von CD44 Isoformen auf migrierenden Langerhans-Zellen. 1998.

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Lakshman, Minalini. CD44 is anti-apoptotic in the murine colonic epithelium. 2006.

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Book chapters on the topic "CDw44"

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van Roy, Frans, Volker Nimmrich, Anton Bespalov, et al. "CDW40." In Encyclopedia of Signaling Molecules. Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-0461-4_100241.

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Swain, Niharika, Samapika Routray, and Rashmi Maruti Hosalkar. "CD44." In Encyclopedia of Signaling Molecules. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-67199-4_101999.

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Günthert, Ursula. "CD44." In Encyclopedia of Cancer. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-27841-9_930-2.

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Swain, Niharika, Samapika Routray, and Rashmi Maruti Hosalkar. "CD44." In Encyclopedia of Signaling Molecules. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4614-6438-9_101999-1.

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Günthert, Ursula. "CD44." In Encyclopedia of Cancer. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-46875-3_930.

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Seeneevassen, Lornella, Anissa Zaafour, and Christine Varon. "CD44-Based Detection of CSCs: CD44 Immunodetection by Flow Cytometry." In Methods in Molecular Biology. Springer US, 2024. http://dx.doi.org/10.1007/978-1-0716-3730-2_5.

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Günthert, U. "CD44 in Maligant Disorders." In Attempts to Understand Metastasis Formation I. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61107-0_16.

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Herrlich, Peter, Wolfgang Rudy, Martin Hofmann, et al. "Cd44 and Splice Variants of Cd44 in Normal Differentiation and Tumor Progression." In Cell Adhesion Molecules. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2830-2_17.

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Knudson, Cheryl B., Kathleen T. Rousche, Richard S. Peterson, Geraldine Chow, and Warren Knudson. "CD44 and cartilage matrix stabilization." In The Many Faces of Osteoarthritis. Birkhäuser Basel, 2002. http://dx.doi.org/10.1007/978-3-0348-8133-3_22.

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Haegel-Kronenberger, Hélène, Henri de la Salle, Alain Bohbot, et al. "Regulation of CD44 Isoform Expression and CD44-Mediated Signaling in Human Dendritic Cells." In Advances in Experimental Medicine and Biology. Springer US, 1997. http://dx.doi.org/10.1007/978-1-4757-9966-8_14.

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Conference papers on the topic "CDw44"

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Nielson, Megan F., Brittany E. Knighton, Lauren M. Davis, Aldair Alejandro, Emma Nelson, and Jeremy A. Johnson. "Quantification of Nonlinear Photonic and Phononic Excitation in CdWO4 Using 2D Spectroscopy." In CLEO: Applications and Technology. Optica Publishing Group, 2022. http://dx.doi.org/10.1364/cleo_at.2022.jtu3a.28.

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Ahmad, Salma, Hanan Nazar, Nouralhuda Alatieh, et al. "Validation of Novel Transcriptional Targets that Underpin CD44-promoted breast cancer cell invasion." In Qatar University Annual Research Forum & Exhibition. Qatar University Press, 2021. http://dx.doi.org/10.29117/quarfe.2021.0153.

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Introduction: Breast cancer (BC) is the most common cancer worldwide, and metastasis is its worst aspect and the first cause of death. Metastasis is a multistep process, where an invasion is a recurring event. The process of BC cell invasion involves three major factors, including cell adhesion molecules (CAM), proteinases and Growth factors.CD44, a family of CAM proteins and the hyaluronic acid (HA) cell surface receptor, acts as cell differentiation, cell migration/invasion and apoptosis regulator. Rationale: We have previously established a tetracycline (Tet)-OFF-regulated expression system
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Nielson, Megan F., Brittany E. Knighton, Lauren M. Davis, Aldair Alejandro, Emma Nelson, and Jeremy A. Johnson. "Unpacking Nonlinear Vibrational Excitations in CdWO4." In Laser Science. OSA, 2021. http://dx.doi.org/10.1364/ls.2021.lth6e.3.

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Sukhinina, E. V., P. K. Kozlova, K. V. Nevskaya, N. V. Litvyakov, and A. G. Pershina. "EFFECT OF ACTIVATION OF MYC GENE EXPRESSION ON A METASTASIS POTENTIAL OF A BREAST CANCER CELL LINE." In X Международная конференция молодых ученых: биоинформатиков, биотехнологов, биофизиков, вирусологов и молекулярных биологов — 2023. Novosibirsk State University, 2023. http://dx.doi.org/10.25205/978-5-4437-1526-1-377.

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The overexpression of the MYC gene plays a crucial role in the advancement of tumors and the plasticity of malignant cells. This study aimed to create breast cancer cell line BT-549 with activated MYC gene, using the CRISPR/Cas9-based SAM activation technique. The modified cell line demonstrates an increase in the fraction of CD44+ CD24– cells, as well as increase in the number and diameter of mammospheres formed. These studies open new opportunities for investigation of the mechanisms related to metastasis.
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Sasaki, Masaru, Norikatsu Miyoshi, Shiki Fujino, et al. "Abstract 6170: Newly emerging CD44 negative cells after irradiation reproduce CD44 positive cells and promote radioresistance." In Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-6170.

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Abou Nada, Fahd, Johan Hult, Christoph Knappe, Mattias Richter, Stefan Mayer, and Marcus Aldén. "A First Application of Thermographic Phosphors in a Marine Two-Stroke Diesel Engine for Surface Temperature Measurement." In ASME 2014 Internal Combustion Engine Division Fall Technical Conference. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/icef2014-5417.

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Phosphor thermometry is applied for the first time in a large-bore two-stroke diesel engine. The work proves the practicality of phosphor thermometry in large-bore engines. The experiments were conducted on the MAN 4T50ME-X marine research engine equipped with an optical cylinder head. By employing a thin surface coating of CdWO4 phosphor, cycle resolved temperature measurements of the cylinder wall were obtained. Motored and fired engine operations were tested at engine loads covering the low and medium engine load range. Phosphor thermometry proved to be successful in retrieving the temperat
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Henry, Jon C., Jong-Kook Park, Jinmai Jiang, et al. "Abstract 1183: miR-199a-3p targets CD44 and reduces proliferation of CD44 positive hepatocellular carcinoma cell lines." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-1183.

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Meloni, Federica, Monica Morosini, Veronica Codullo, et al. "The antifibrotic effect of Imatinib loaded CD44 targeted gold nanoparticles (Im-CD44-GNP) relies on alveolar macrophage regulation." In ERS International Congress 2018 abstracts. European Respiratory Society, 2018. http://dx.doi.org/10.1183/13993003.congress-2018.pa3660.

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Klamra, W., T. Szczesniak, M. Moszynski, et al. "Properties of CdWO4 and ZnWO4 at liquid nitrogen temperature." In 2009 IEEE Nuclear Science Symposium and Medical Imaging Conference (NSS/MIC 2009). IEEE, 2009. http://dx.doi.org/10.1109/nssmic.2009.5402262.

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Damaj, Bassam B., Francesca Incardonna, Randy Piotrowicz, Stephen B. Howell, and Malcolm Finlayson. "Abstract 5120: A6 peptide binds to CD44 and inhibits migration and metastasis of CD44+ cell lines inin vitroandin vivostudies." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-5120.

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Reports on the topic "CDw44"

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เทียนไทย, ไพศาล, та พรชลิต อัศวชีพ. การปรากฏของไกลโคสอะมิโนไกลแคนส์และกลไกการทำงานของระบบ Fas-Fas ligand ในท่อนำไข่ของกระบือปลักไทย ในระยะฟอลลิคูลาร์และระยะลูเทียล : รายงานวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 2011. https://doi.org/10.58837/chula.res.2011.106.

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การศึกษานี้ มีวัตถุประสงค์เพื่อศึกษาการปรากฏของไกลโคสอะมิโนไกลแคนส์ชนิดที่ไม่มีซัลเฟต (ไฮยาลูโรแนน) และชนิดที่มีซัลเฟต (syndecan-1, syndecan-2) การปรากฏของตัวรับ CD44 การปรากฏของโปรตีน Fas และ Fas ligand (FasL) รวมทั้งการแสดงออกของ FasL mRNA ภายในท่อนำไข่กระบือปลักไทย ซึ่งสัมพันธ์กับการทำงานของรังไข่ เก็บอวัยวะสืบพันธุ์เพศเมียของกระบือปลักจากโรงฆ่าสัตว์จำนวนทั้งหมด 40 ตัว แบ่งกลุ่มของกระบือปลักออกเป็น 2 กลุ่ม ตามลักษณะที่พบทางมหกายภาคของรังไข่ทั้งสองข้างคือ ระยะฟอลลิคูลาร์ (จำนวน 20 ตัว) และระยะลูเทียลช่วงกลาง (จำนวน 20 ตัว) อวัยวะสืบพันธุ์เพศเมียที่เก็บได้จะนำมาตรวจสอบและไม่มีความผิดปกติทางพย
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Underhill, Charles. Role of CD44 in Tumor Progression. Defense Technical Information Center, 1996. http://dx.doi.org/10.21236/ada319968.

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Z. W. Bell and M. W. Moyer. CdWO4-Boron FY 2000 Task 4 Completion Report. Office of Scientific and Technical Information (OSTI), 2001. http://dx.doi.org/10.2172/775527.

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Berget, Susan M. Metastatic Regulation of Differential Splicing of CD44. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada377159.

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Berget, Susan. Metastic Regulation of Differential Splicing of CD44. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada383934.

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Iczkowski, Kenneth A. Alternate Splicing of CD44 Messenger RNA in Prostate Cancer Growth. Defense Technical Information Center, 2008. http://dx.doi.org/10.21236/ada483366.

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Iczkowski, Kenneth A., Eric W. Robbins, Kui Yang, Alina Handorean, and Yaqiong Tang. Alternate Splicing of CD44 Messenger RNA in Prostate Cancer Growth. Defense Technical Information Center, 2009. http://dx.doi.org/10.21236/ada525215.

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Lopez, Jose I. Hyaluronan-CD44 Interactions Decrease the Metastatic Potential of Breast Cancer Cells. Defense Technical Information Center, 2008. http://dx.doi.org/10.21236/ada572527.

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Lopez, Jose I. Hyaluronan-CD44 Interactions Decrease the Metastatic Potential of Breast Cancer Cells. Defense Technical Information Center, 2007. http://dx.doi.org/10.21236/ada475070.

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Sherman, Larry S. Role of CD44 in Malignant Peripheral Nerve Sheath Tumor Growth and Metastasis. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada411293.

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