Academic literature on the topic 'Tubuline GTP'

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Journal articles on the topic "Tubuline GTP"

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Yajima, Hiroaki, Toshihiko Ogura, Ryo Nitta, Yasushi Okada, Chikara Sato, and Nobutaka Hirokawa. "Conformational changes in tubulin in GMPCPP and GDP-taxol microtubules observed by cryoelectron microscopy." Journal of Cell Biology 198, no. 3 (2012): 315–22. http://dx.doi.org/10.1083/jcb.201201161.

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Microtubules are dynamic polymers that stochastically switch between growing and shrinking phases. Microtubule dynamics are regulated by guanosine triphosphate (GTP) hydrolysis by β-tubulin, but the mechanism of this regulation remains elusive because high-resolution microtubule structures have only been revealed for the guanosine diphosphate (GDP) state. In this paper, we solved the cryoelectron microscopy (cryo-EM) structure of microtubule stabilized with a GTP analogue, guanylyl 5′-α,β-methylenediphosphonate (GMPCPP), at 8.8-Å resolution by developing a novel cryo-EM image reconstruction al
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Mori, Risa, and Takashi Toda. "The dual role of fission yeast Tbc1/cofactor C orchestrates microtubule homeostasis in tubulin folding and acts as a GAP for GTPase Alp41/Arl2." Molecular Biology of the Cell 24, no. 11 (2013): 1713–24. http://dx.doi.org/10.1091/mbc.e12-11-0792.

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Supplying the appropriate amount of correctly folded α/β-tubulin heterodimers is critical for microtubule dynamics. Formation of assembly-competent heterodimers is remarkably elaborate at the molecular level, in which the α- and β-tubulins are separately processed in a chaperone-dependent manner. This sequential step is performed by the tubulin-folding cofactor pathway, comprising a specific set of regulatory proteins: cofactors A–E. We identified the fission yeast cofactor: the orthologue of cofactor C, Tbc1. In addition to its roles in tubulin folding, Tbc1 acts as a GAP in regulating Alp41/
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Kristensson, Maria Alvarado. "The Game of Tubulins." Cells 10, no. 4 (2021): 745. http://dx.doi.org/10.3390/cells10040745.

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Members of the tubulin superfamily are GTPases; the activities of GTPases are necessary for life. The members of the tubulin superfamily are the constituents of the microtubules and the γ-tubulin meshwork. Mutations in members of the tubulin superfamily are involved in developmental brain disorders, and tubulin activities are the target for various chemotherapies. The intricate functions (game) of tubulins depend on the activities of the GTP-binding domain of α-, β-, and γ-tubulin. This review compares the GTP-binding domains of γ-tubulin, α-tubulin, and β-tubulin and, based on their similarit
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Anders, Kirk R., та David Botstein. "Dominant-Lethal α-Tubulin Mutants Defective in Microtubule Depolymerization in Yeast". Molecular Biology of the Cell 12, № 12 (2001): 3973–86. http://dx.doi.org/10.1091/mbc.12.12.3973.

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The dynamic instability of microtubules has long been understood to depend on the hydrolysis of GTP bound to β-tubulin, an event stimulated by polymerization and necessary for depolymerization. Crystallographic studies of tubulin show that GTP is bound by β-tubulin at the longitudinal dimer-dimer interface and contacts particular α-tubulin residues in the next dimer along the protofilament. This structural arrangement suggests that these contacts could account for assembly-stimulated GTP hydrolysis. As a test of this hypothesis, we examined, in yeast cells, the effect of mutating the α-tubulin
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Al-Bassam, Jawdat. "Revisiting the tubulin cofactors and Arl2 in the regulation of soluble αβ-tubulin pools and their effect on microtubule dynamics". Molecular Biology of the Cell 28, № 3 (2017): 359–63. http://dx.doi.org/10.1091/mbc.e15-10-0694.

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Soluble αβ-tubulin heterodimers are maintained at high concentration inside eukaryotic cells, forming pools that fundamentally drive microtubule dynamics. Five conserved tubulin cofactors and ADP ribosylation factor–like 2 regulate the biogenesis and degradation of αβ-tubulins to maintain concentrated soluble pools. Here I describe a revised model for the function of three tubulin cofactors and Arl2 as a multisubunit GTP-hydrolyzing catalytic chaperone that cycles to promote αβ-tubulin biogenesis and degradation. This model helps explain old and new data indicating these activities enhance mic
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Chu, Chih-Wen, Fajian Hou, Junmei Zhang та ін. "A novel acetylation of β-tubulin by San modulates microtubule polymerization via down-regulating tubulin incorporation". Molecular Biology of the Cell 22, № 4 (2011): 448–56. http://dx.doi.org/10.1091/mbc.e10-03-0203.

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Dynamic instability is a critical property of microtubules (MTs). By regulating the rate of tubulin polymerization and depolymerization, cells organize the MT cytoskeleton to accommodate their specific functions. Among many processes, posttranslational modifications of tubulin are implicated in regulating MT functions. Here we report a novel tubulin acetylation catalyzed by acetyltransferase San at lysine 252 (K252) of β-tubulin. This acetylation, which is also detected in vivo, is added to soluble tubulin heterodimers but not tubulins in MTs. The acetylation-mimicking K252A/Q mutants were inc
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Lin, Chii M., and Ernest Hamel. "Interrelationships of tubulin-GDP and tubulin-GTP in microtubule assembly." Biochemistry 26, no. 22 (1987): 7173–82. http://dx.doi.org/10.1021/bi00396a045.

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Zabala, J. C., A. Fontalba, and J. Avila. "Tubulin folding is altered by mutations in a putative GTP binding motif." Journal of Cell Science 109, no. 6 (1996): 1471–78. http://dx.doi.org/10.1242/jcs.109.6.1471.

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Tubulins contain a glycine-rich loop, that has been implicated in microtubule dynamics by means of an intramolecular interaction with the carboxy-terminal region. As a further extension of the analysis of the role of the carboxy-terminal region in tubulin folding we have mutated the glycine-rich loop of tubulin subunits. An alpha-tubulin point mutant with a T150-->G substitution (the corresponding residue present in beta-tubulin) was able to incorporate into dimers and microtubules. On the other hand, four beta-tubulin point mutants, including the G148-->T substitution, did not i
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Luduena, Richard F., Mary Carmen Roach, Thomas H. MacRae, and George M. Langford. "N,N′-Ethylene-bis(iodoacetamide) as a probe for structural and functional characteristics of brine shrimp, squid, and bovine tubulins." Canadian Journal of Biochemistry and Cell Biology 63, no. 6 (1985): 439–47. http://dx.doi.org/10.1139/o85-063.

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We have developed a simple probe for certain functionally significant features of the tubulin molecule. When bovine brain tubulin is treated with N,N′-ethylene-bis(iodoacetamide) (EBI), two intrachain cross-links, designated βs and β*, are formed in β-tubulin, each one with a unique effect on the electrophoretic mobility of β on gels containing sodium dodecyl sulfate. Formation of the β* cross-link, which involves at least one assembly-critical sulfhydryl, is completely inhibited by colchicine and its congeners, while that of βs is inhibited completely by maytansine and GTP and partly by vinbl
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Caplow, Michael, and Lanette Fee. "Dissociation of the Tubulin Dimer Is Extremely Slow, Thermodynamically Very Unfavorable, and Reversible in the Absence of an Energy Source." Molecular Biology of the Cell 13, no. 6 (2002): 2120–31. http://dx.doi.org/10.1091/mbc.e01-10-0089.

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The finding that exchange of tubulin subunits between tubulin dimers (α-β + α′β′ ↔ α′β + αβ′) does not occur in the absence of protein cofactors and GTP hydrolysis conflicts with the assumption that pure tubulin dimer and monomer are in rapid equilibrium. This assumption underlies the many physical chemical measurements of the K d for dimer dissociation. To resolve this discrepancy we used surface plasmon resonance to determine the rate constant for dimer dissociation. The half-time for dissociation was ∼9.6 h with tubulin-GTP, 2.4 h with tubulin-GDP, and 1.3 h in the absence of nucleotide. AK
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Dissertations / Theses on the topic "Tubuline GTP"

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Cormier, Anthony. "Interaction tubuline-nucléotide : structure et biochimie." Paris 6, 2009. http://www.theses.fr/2009PA066030.

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Les microtubules sont des composants clefs du cytosquelette des cellules eucaryotes, ils alternent des phases d’assemblage et de désassemblage, un processus appelé instabilité dynamique. La tubuline qui constitue les microtubules est une protéine hétérodimérique liant deux nucléotides guanosine, l’un au site non-échangeable, l’autre au site échangeable. Au cycle de polymérisation/dépolymérisation des microtubules est associé un cycle nucléotidique au cours duquel la tubuline échange son nucléotide en solution et l’hydrolyse ensuite lors de son assemblage. L’objectif de ma thèse a été de caract
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Quesnoit, Mélanie. "Régulation de la dynamique microtubulaire : implication de la tubuline GTP et de protéines associées aux microtubules." Paris 11, 2007. http://www.theses.fr/2007PA114811.

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Les microtubules (MTs) sont un des composants clés du cytosquelette, dont la dynamique est indispensable à la fonction. Dans ce projet, nous cherchons à aborder sous plusieurs angles la régulation de la dynamique microtubulaire, liée au comportement de la tubuline elle-même ou par l'intermédiaire de protéines associées aux MTs. Nous avons construit un outil dans le but d'avancer dans la caractérisation de l'importance de l'hydrolyse du GTP par la tubuline pour la stabilisation du polymère. Cet outil est un anticorps recombinant qui permet de détecter la tubuline liée au GTP et nous a conduit à
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Lemoyne, de Forges Hélène. "Organisation et dynamique des microtubules : rôles de la tubuline-GTP et de CLIP-170." Paris 6, 2013. http://www.theses.fr/2013PA066219.

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Les microtubules sont des polymères de tubuline, très dynamiques, essentiels à de nombreuses fonctions cellulaires telles que la division, le trafic intracellulaire et la migration. Ils alternent entre des phases de croissance et décroissance, séparées par des événements de catastrophe et de sauvetage. L’équipe a montré que la tubuline-GTP est présente sous forme d’îlots le long des microtubules. Nous avons proposé un nouveau modèle d’instabilité dynamique selon lequel les îlots de tubuline-GTP, exposés lors de la dépolymérisation des microtubules, favoriseraient les sauvetages. Durant ma thès
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Yuan, Wenjue. "Sas4 N terminal as a potential binding probe for tubulin-GDP." University of Toledo / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1399559850.

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Farr, George William. "Site-directed mutagenesis of beta tubulin's putative GTP-binding domain." Case Western Reserve University School of Graduate Studies / OhioLINK, 1993. http://rave.ohiolink.edu/etdc/view?acc_num=case1060367517.

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Pomel, Sébastien. "Squelette menbranaire chez Paramecium tetraurelia : caractérisation d'une nouvelle famille multigénique et analyse par les approche GFP et RNAi." Clermont-Ferrand 2, 2005. https://tel.archives-ouvertes.fr/tel-00686966/document.

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Chez la paramécie, l'épiplasme se présente sous forme d'écailles indépendantes disposées autour de chaque appareil ciliaire et composées d'une multitude de protéines appelées épiplasmines. Dans une première partie, nous avons contribué à l'annotation du génome macronucléaire de Paramecium tetraurelia à partir de la séquence de 2 épiplasmines (EPI-1 et EPI-2) et identifié 39 gènes supplémentaires. L'analyse des séquences indique que la signature de cette nouvelle famille est un domaine de 79 acides aminés. L'expression de l'épiplasmine 1 couplée à la GFP confirme la localisation de cette protéi
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Läppchen, Tilman. "Synthesis of GTP analogues and evaluation of their effect on the antibiotic target FtsZ and its eukaryotic homologue tubulin." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2007. http://dare.uva.nl/document/42388.

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Pomel, Sébastien. "Squelette membranaire chez Paramecium tetraurelia : caractérisation d'une nouvelle famille multigénique et analyse par les approches GFP et RNAi." Phd thesis, Université Blaise Pascal - Clermont-Ferrand II, 2005. http://tel.archives-ouvertes.fr/tel-00686966.

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Chez la paramécie, l'épiplasme se présente sous forme d'écailles indépendantes disposées autour de chaque appareil ciliaire et composées d'une multitude de protéines appelées épiplasmines. Dans une première partie, nous avons contribué à l'annotation du génome macronucléaire de Paramecium tetraurelia à partir de la séquence de 2 épiplasmines (EPI-1 et EPI-2) et identifié 39 gènes supplémentaires. L'analyse des séquences indique que la signature de cette nouvelle famille est un domaine de 79 acides aminés. L'expression de l'épiplasmine 1 couplée à la GFP confirme la localisation de cette protéi
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Borrmann, Claudia [Verfasser], та Georg [Akademischer Betreuer] Reiser. "Interaction of the brain-specific Arf-GAP protein p42 I P 4 (centaurin α1, ADAP1) with the metalloendopeptidase nardilysin and modulation by tubulin / Claudia Borrmann. Betreuer: Georg Reiser". Magdeburg : Universitätsbibliothek, 2011. http://d-nb.info/1051502381/34.

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Tardif, Valérie. "GLP, une nouvelle protéine associée au récepteur AT1, induit de l'hypertrophie dans les cellules du tubule proximal du rein du rat." Thèse, 2004. http://hdl.handle.net/1866/15275.

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Books on the topic "Tubuline GTP"

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Halperin, Mitchell L., and Kamel S. Kamel. Approach to the patient with metabolic acidosis or alkalosis. Edited by Robert Unwin. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0035_update_001.

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The pathophysiology, clinical approach, and management of the common causes of metabolic acidosis and alkalosis are discussed. In metabolic acidosis, a quantitative estimate of the extracellular volume (ECFV) is required to determine its content of bicarbonate in a patient with ECFV contraction. Buffering of H+ must occur by the bicarbonate buffer system in muscle to avoid binding to intracellular proteins, this requires low muscle capillary PCO2; acid gain type of metabolic acidosis is detected by the finding of new anions in blood and/or urine. The urine osmolal gap is the best indirect test
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Servais, Aude, and Bertrand Knebelmann. Cystinuria. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0024.

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Cystinuria (OMIM #220100) is an autosomal recessive disorder of a dibasic amino acid transport in the apical membrane of epithelial cells of the renal proximal tubule and small intestine. It leads to increased urinary cystine excretion and recurrent urolithiasis. The cystine transporter is an heterodimeric transporter which is composed of a heavy subunit, rBAT, linked to a light subunit, b0,+AT. Two genes, SLC3A1 (solute carrier family 3 member 1) and SLC7A9, coding for rBAT and b0,+AT, account for the genetic basis of cystinuria. Cystinuria may lead to obstruction, infections, and ultimately
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Book chapters on the topic "Tubuline GTP"

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Carlier, Marie-France, and Dominique Pantaloni. "Tubulin as a G-Protein: Regulation of Tubulin-Tubulin Interactions by GTP Hydrolysis." In The Guanine — Nucleotide Binding Proteins. Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-2037-2_37.

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FitzHarris, Greg. "Monitoring Microtubule Dynamics in the Mouse Egg Using Photoactivatable-GFP-Tubulin." In Methods in Molecular Biology. Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-8603-3_14.

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Samora, Catarina P., and Andrew D. McAinsh. "Photoactivatable-GFP-α-Tubulin as a Tool to Study Microtubule Plus-End Turnover in Living Human Cells." In Methods in Molecular Biology. Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-252-6_16.

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Sato, Masamitsu, Mika Toya, and Takashi Toda. "Visualization of Fluorescence-Tagged Proteins in Fission Yeast: The Analysis of Mitotic Spindle Dynamics Using GFP-Tubulin Under the Native Promoter." In Methods in Molecular Biology. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-993-2_11.

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de Forges, Hélène, Antoine Pilon, Christian Poüs, and Franck Perez. "Imaging GTP-Bound Tubulin." In Methods in Cell Biology. Elsevier, 2013. http://dx.doi.org/10.1016/b978-0-12-407757-7.00010-4.

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Emmett, Stevan R., Nicola Hill, and Federico Dajas-Bailador. "Renal medicine." In Clinical Pharmacology for Prescribing. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780199694938.003.0013.

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The kidneys are of fundamental importance in the regu­lation of fluid and electrolytes, maintaining permissive extracellular fluid composition (salts and water), pH, and volume, while also mediating the removal of waste prod­ucts. Based on the anatomy of the nephron, three main processes occur in order to deliver this balance: glom­erular filtration, tubular secretion, and tubular resorption. Drugs can act at different sites within this system, so that functional equilibrium can be restored in various disease states (e.g. hypertension, heart failure, liver failure, neph­rotic syndrome). CKD is a long- term condition that lasts more than 3 months and affects the function of both kidneys. It results from any pathology that reduces renal functional capacity and produces a decrease in GFR to less than 60 mL/ min/ 1.73 m<sup>2</sup>. Prevalence within the UK is high, particularly in the elderly and affects 6– 8% of the population. The most common cause of CKD is idiopathic (unknown, usually with small kidneys), then diabetes mellitus. In both, glom­erular damage and mesangial injury (causing metabolic and haemodynamic effects) occur. Mild- moderate essen­tial hypertension does not cause CKD. Knowledge of the functional anatomy of the proximal tubule and loop of Henle is essential in understanding therapeutic targets and treatment of pathologies, as each region and transporter system has a key role. In brief, the journey of solutes from the blood to the production of urine occurs at five main anatomical sites— the glom­erulus, the proximal tubule, the loop of Henle, the distal tubule (proximal part and distal part), and the collecting ducts (Figures 5.1 and 5.2). The glomerulus is a network of capillaries (like a ball of string), which merge with the nephron via Bowman’s cap­sule. It is the first site of filtration and the place where solutes, toxins, and small proteins are removed from the wider circulatory system, after delivery by the renal ar­teries (via an afferent arteriole). Blood and larger proteins remain in the arteriole and leave via an efferent branch, while the filtrate enters the proximal convoluted tubule. The afferent:efferent system ensures that a constant filtration pressure is maintained irrespective of variations in arterial pressure. The capillary bed is very large, so that permeability and filtration rates are high. A normal glomerular filtration rate (GFR) i.e. 90– 120 mL/ min/ 1.73 m<sup>2</sup>, depends on hydrostatic pressure, the colloid osmotic pressure and hydraulic per¬meability.
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Conference papers on the topic "Tubuline GTP"

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Deriu, Marco A., Søren Enemark, Emiliano Votta, Franco M. Montevecchi, Alberto Redaelli, and Monica Soncini. "Bottom-Up Mesoscale Model of Microtubule." In ASME 2007 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2007. http://dx.doi.org/10.1115/sbc2007-176115.

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Microtubules (MTs) are fundamental structural elements in the cytoskeleton of all eukaryotic cells. The MTs are hollow cylinder-shaped biopolymers with inner and outer diameter of about 18 and 30 nm respectively and length ranging from 1 to 10 μm. They are constituted by αβ-tubulins arranged in protofilaments with head-to-tail motif. The protofilaments bind together laterally along the MT’s long axis with a slight shift generating a spiral with a pitch of 2, 3 or 4 monomers’ length [1]. The building-block of the MT, αβ-tubulin, is a hetero-dimer made of two globular monomers, α- and β-tubulin.
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Radomsky, R. W., and K. A. Thole. "High Freestream Turbulence Effects on Endwall Heat Transfer for a Gas Turbine Stator Vane." In ASME Turbo Expo 2000: Power for Land, Sea, and Air. American Society of Mechanical Engineers, 2000. http://dx.doi.org/10.1115/2000-gt-0201.

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High freestream turbulence along a gas turbine airfoil and strong secondary flows along the endwall have both been reported to significantly increase convective heat transfer. This study superimposes high freestream turbulence on the naturally occurring secondary flow vortices to determine the effects on the flowfield and the endwall convective heat transfer. Measured flowfield and heat transfer data were compared between low freestream turbulence levels (0.6%) and combustor simulated turbulence levels (19.5%) that were generated using an active grid. These experiments were conducted using a s
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