Bibliografias temáticas / Tubulins

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Literatura científica selecionada sobre o tema "Tubulins"

Autor: Grafiati
Publicado: 4 de junho de 2021
Última modificação: 29 de julho de 2024

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Artigos de revistas sobre o assunto "Tubulins"

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Shu, H. B., and H. C. Joshi. "Gamma-tubulin can both nucleate microtubule assembly and self-assemble into novel tubular structures in mammalian cells." Journal of Cell Biology 130, no. 5 (September 1, 1995): 1137–47. http://dx.doi.org/10.1083/jcb.130.5.1137.

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alpha-, beta-, and gamma-tubulins are evolutionarily highly conserved members of the tubulin gene superfamily. While the abundant members, alpha- and beta-tubulins, constitute the building blocks of cellular microtubule polymers, gamma-tubulin is a low abundance protein which localized to the pericentriolar material and may play a role in microtubule assembly. To test whether gamma-tubulin mediates the nucleation of microtubule assembly in vivo, and co-assembles with alpha- and beta-tubulins into microtubules or self-assembles into macro-molecular structures, we experimentally elevated the exp
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Burland, T. G., E. C. Paul, M. Oetliker, and W. F. Dove. "A gene encoding the major beta tubulin of the mitotic spindle in Physarum polycephalum plasmodia." Molecular and Cellular Biology 8, no. 3 (March 1988): 1275–81. http://dx.doi.org/10.1128/mcb.8.3.1275-1281.1988.

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The multinucleate plasmodium of Physarum polycephalum is unusual among eucaryotic cells in that it uses tubulins only in mitotic-spindle microtubules; cytoskeletal, flagellar, and centriolar microtubules are absent in this cell type. We have identified a beta-tubulin cDNA clone, beta 105, which is shown to correspond to the transcript of the betC beta-tubulin locus and to encode beta 2 tubulin, the beta tubulin expressed specifically in the plasmodium and used exclusively in the mitotic spindle. Physarum amoebae utilize tubulins in the cytoskeleton, centrioles, and flagella, in addition to the
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Burland, T. G., E. C. Paul, M. Oetliker, and W. F. Dove. "A gene encoding the major beta tubulin of the mitotic spindle in Physarum polycephalum plasmodia." Molecular and Cellular Biology 8, no. 3 (March 1988): 1275–81. http://dx.doi.org/10.1128/mcb.8.3.1275.

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The multinucleate plasmodium of Physarum polycephalum is unusual among eucaryotic cells in that it uses tubulins only in mitotic-spindle microtubules; cytoskeletal, flagellar, and centriolar microtubules are absent in this cell type. We have identified a beta-tubulin cDNA clone, beta 105, which is shown to correspond to the transcript of the betC beta-tubulin locus and to encode beta 2 tubulin, the beta tubulin expressed specifically in the plasmodium and used exclusively in the mitotic spindle. Physarum amoebae utilize tubulins in the cytoskeleton, centrioles, and flagella, in addition to the
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Khabudaev, Kirill V., Darya P. Petrova, Yekaterina D. Bedoshvili, Yelena V. Likhoshway, and Mikhail A. Grachev. "Molecular Evolution of Tubulins in Diatoms." International Journal of Molecular Sciences 23, no. 2 (January 6, 2022): 618. http://dx.doi.org/10.3390/ijms23020618.

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Microtubules are formed by α- and β-tubulin heterodimers nucleated with γ-tubulin. Tubulins are conserved eukaryotic proteins. Previously, it was shown that microtubules are involved in diatom silica frustule morphogenesis. Diatom frustules are varied, and their morphology is species-specific. Despite the attractiveness of the problem of elucidating the molecular mechanisms of genetically programmed morphogenesis, the structure and evolution of diatom tubulins have not been studied previously. Based on available genomic and transcriptome data, we analyzed the phylogeny of the predicted amino a
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Zhou, Yujun, Jianqiang Xu, Yuanye Zhu, Yabing Duan, and Mingguo Zhou. "Mechanism of Action of the Benzimidazole Fungicide on Fusarium graminearum: Interfering with Polymerization of Monomeric Tubulin But Not Polymerized Microtubule." Phytopathology® 106, no. 8 (August 2016): 807–13. http://dx.doi.org/10.1094/phyto-08-15-0186-r.

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Tubulins are the proposed target of clinically relevant anticancer drugs, anthelmintic, and fungicide. β2-tubulin of the plant pathogen Fusarium graminearum was considered as the target of benzimidazole compounds by homology modeling in our previous work. In this study, α1-, α2-, and β2-tubulin of F. graminearum were produced in Escherichia coli. Three benzimidazole compounds (carbendazim, benomyl, and thiabendazole) interacted with the recombinant β2-tubulin and reduced the maximum fluorescence intensity of 2 μM β2-tubulin 47, 50, and 25%, respectively, at saturation of compound-tubulin compl
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Rudolph, J. E., M. Kimble, H. D. Hoyle, M. A. Subler, and E. C. Raff. "Three Drosophila beta-tubulin sequences: a developmentally regulated isoform (beta 3), the testis-specific isoform (beta 2), and an assembly-defective mutation of the testis-specific isoform (B2t8) reveal both an ancient divergence in metazoan isotypes and structural constraints for beta-tubulin function." Molecular and Cellular Biology 7, no. 6 (June 1987): 2231–42. http://dx.doi.org/10.1128/mcb.7.6.2231-2242.1987.

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The genomic DNA sequence and deduced amino acid sequence are presented for three Drosophila melanogaster beta-tubulins: a developmentally regulated isoform beta 3-tubulin, the wild-type testis-specific isoform beta 2-tubulin, and an ethyl methanesulfonate-induced assembly-defective mutation of the testis isoform, B2t8. The testis-specific beta 2-tubulin is highly homologous to the major vertebrate beta-tubulins, but beta 3-tubulin is considerably diverged. Comparison of the amino acid sequences of the two Drosophila isoforms to those of other beta-tubulins indicates that these two proteins are
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Rudolph, J. E., M. Kimble, H. D. Hoyle, M. A. Subler, and E. C. Raff. "Three Drosophila beta-tubulin sequences: a developmentally regulated isoform (beta 3), the testis-specific isoform (beta 2), and an assembly-defective mutation of the testis-specific isoform (B2t8) reveal both an ancient divergence in metazoan isotypes and structural constraints for beta-tubulin function." Molecular and Cellular Biology 7, no. 6 (June 1987): 2231–42. http://dx.doi.org/10.1128/mcb.7.6.2231.

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The genomic DNA sequence and deduced amino acid sequence are presented for three Drosophila melanogaster beta-tubulins: a developmentally regulated isoform beta 3-tubulin, the wild-type testis-specific isoform beta 2-tubulin, and an ethyl methanesulfonate-induced assembly-defective mutation of the testis isoform, B2t8. The testis-specific beta 2-tubulin is highly homologous to the major vertebrate beta-tubulins, but beta 3-tubulin is considerably diverged. Comparison of the amino acid sequences of the two Drosophila isoforms to those of other beta-tubulins indicates that these two proteins are
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Xie, Yixin, and Lin Li. "Computational Study on E-Hooks of Tubulins in the Binding Process with Kinesin." International Journal of Molecular Sciences 23, no. 4 (February 12, 2022): 2035. http://dx.doi.org/10.3390/ijms23042035.

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Cargo transport within cells is essential to healthy cells, which requires microtubules-based motors, including kinesin. The C-terminal tails (E-hooks) of alpha and beta tubulins of microtubules have been proven to play important roles in interactions between the kinesins and tubulins. Here, we implemented multi-scale computational methods in E-hook-related analyses, including flexibility investigations of E-hooks, binding force calculations at binding interfaces between kinesin and tubulins, electrostatic potential calculations on the surface of kinesin and tubulins. Our results show that E-h
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Lajoie-Mazenc, I., C. Detraves, V. Rotaru, M. Gares, Y. Tollon, C. Jean, M. Julian, M. Wright, and B. Raynaud-Messina. "A single gamma-tubulin gene and mRNA, but two gamma-tubulin polypeptides differing by their binding to the spindle pole organizing centres." Journal of Cell Science 109, no. 10 (October 1, 1996): 2483–92. http://dx.doi.org/10.1242/jcs.109.10.2483.

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Cells of eukaryotic organisms exhibit microtubules with various functions during the different developmental stages. The identification of multiple forms of alpha- and beta-tubulins had raised the question of their possible physiological roles. In the myxomycete Physarum polycephalum a complex polymorphism for alpha- and beta-tubulins has been correlated with a specific developmental expression pattern. Here, we have investigated the potential heterogeneity of gamma-tubulin in this organism. A single gene, with 3 introns and 4 exons, and a single mRNA coding for gamma-tubulin were detected. Th
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Chumová, Jana, Hana Kourová, Lucie Trögelová, Petr Halada та Pavla Binarová. "Microtubular and Nuclear Functions of γ-Tubulin: Are They LINCed?" Cells 8, № 3 (19 березня 2019): 259. http://dx.doi.org/10.3390/cells8030259.

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γ-Tubulin is a conserved member of the tubulin superfamily with a function in microtubule nucleation. Proteins of γ-tubulin complexes serve as nucleation templates as well as a majority of other proteins contributing to centrosomal and non-centrosomal nucleation, conserved across eukaryotes. There is a growing amount of evidence of γ-tubulin functions besides microtubule nucleation in transcription, DNA damage response, chromatin remodeling, and on its interactions with tumor suppressors. However, the molecular mechanisms are not well understood. Furthermore, interactions with lamin and SUN pr
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Teses / dissertações sobre o assunto "Tubulins"

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Nacoulma, Aminata. "Reprogrammation métabolique induite dans les tissus hyperplasiques formés chez le tabac infecté par Rhodococcus fascians: aspects fondamentaux et applications." Doctoral thesis, Universite Libre de Bruxelles, 2013. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/209429.

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Les pathosystèmes, plante-bactérie, aboutissent souvent au niveau de la plante à de profondes reprogrammations tant au niveau de la morphogenèse que du métabolome. Dans le cas de l’interaction plante-Rhodococcus fascians, une bactérie phytopathogène, il se développe au niveau du site d’infection, une structure morphologique particulière nommée « galle feuillée ». <p>Au sein de cette hyperplasie, les altérations métaboliques induites concernent non seulement les produits du métabolisme primaire mais également le métabolisme secondaire et plus particulièrement des composés qui interviennent dans
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2

Bladh, Håkan. "Structure-activity studies of novel colchicine analogs synthesis, conformation and tublin binding /." Lund : Lund University, 1998. http://books.google.com/books?id=1sBqAAAAMAAJ.

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Lo, Wai Hong. "Biochemical, structural and functional characterization of the light chains of the microtubule-based motor dynein /." View Abstract or Full-Text, 2003. http://library.ust.hk/cgi/db/thesis.pl?BICH%202003%20LO.

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Thesis (Ph. D.)--Hong Kong University of Science and Technology, 2003.<br>Includes bibliographical references (leaves 133-154). Also available in electronic version. Access restricted to campus users.
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Tang, Liang. "Characterization of tubulins from parasitic nematodes (Brugia malayi, B. pahangi and Nippostrongylus brasiliensis) and comparison with mammalian brain tubulin." Thesis, McGill University, 1988. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=75933.

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The properties of tubulins from Brugia malayi, B. pahangi, Nippostrongylus brasiliensis and rat brain were compared. Tubulins from all nematodes and rat brain were partially purified by polylysine agarose chromatography, those of brain also by cycles of assembly/disassembly, and all by taxol-induced assembly. The tubulins were compared with respect to concentration ($ mu$g tubulin/mg soluble protein), drugs binding and isoforms. The tubulins of B. malayi and B. pahangi were similar. However, the tubulin from these filariae were different from those of N. brasiliensis. Even larger differences w
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Akkari, Yassmine M. Nazih. "Investigation of tubulins in Aspergillus nidulans and Cyanidium caldarium /." The Ohio State University, 1997. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487942739806417.

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Bittermann, Elizabeth A. "The Roles of Tubulins in the Developing Mouse Brain." University of Cincinnati / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1523630790076922.

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Cheung, Po Yan. "Interaction between MKK6 and p150 glued dynactin is required for microtubule-mediated p38 MAPK activation /." View Abstract or Full-Text, 2002. http://library.ust.hk/cgi/db/thesis.pl?BICH%202002%20CHEUNG.

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Thesis (M. Phil.)--Hong Kong University of Science and Technology, 2002.<br>On t.p. glued is superscript. Includes bibliographical references (leaves 84-94). Also available in electronic version. Access restricted to campus users.
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Washington, Ashley L. "FUNCTIONAL TESTS OF β TUBULINS IN DROSOPHILA SPERM TAIL MORPHOLOGY". University of Dayton / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=dayton1229709260.

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Washington, Ashley. "Functional tests of [beta] tubulins in Drosophila sperm tail morphology." Dayton, Ohio : University of Dayton, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=dayton1229709260.

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Cushion, Thomas David. "Tubulin genes in human disorders of cerebral cortex development." Thesis, Swansea University, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.678290.

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Livros sobre o assunto "Tubulins"

1

Jesús, Avila, ed. Microtubule proteins. Boca Raton, Fla: CRC Press, 1990.

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2

Poetsch, Bettina. Zur Expression und Funktion von Aktin und Tubulin in der Photomorphogenese von Physarum polycephalum. Gauting bei München: Intemann, 1989.

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3

Thomas, Kreis, and Vale Ronald, eds. Guidebook to the cytoskeletal and motor proteins. Oxford: Oxford University Press, 1993.

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4

A, Cross R., and Kendrick-Jones J, eds. Motor proteins: A volume based on the EMBO Workshop, Cambridge, September 1990. Cambridge [England]: Company of Biologists, 1991.

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5

Thomas, Scheibel, ed. Fibrous proteins. Austin, Tex: Landes Bioscience, 2008.

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6

Carlomagno, Teresa, ed. Tubulin-Binding Agents. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-69039-9.

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Jesús, Avila de Grado, Brandt Roland, and Kosik K. S. 1950-, eds. Brain microtubule associated proteins: Modifications in disease. Amsterdam: Harwood Academic Publishers, 1997.

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Yamauchi, Wei. Tubulin: Structure, functions, and roles in disease. Hauppauge, N.Y: Nova Science, 2011.

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Read, M. Tubulin in the erythrocytic stages of phasmodium falciparum. Manchester: UMIST, 1995.

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service), SpringerLink (Online, ed. Tubulin-binding agents: Synthetic, structural and mechanistic insights. Berlin: Springer, 2009.

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Capítulos de livros sobre o assunto "Tubulins"

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Morejohn, Louis C., and Donald E. Fosket. "Tubulins from Plants, Fungi, and Protists." In Cell and Molecular Biology of the Cytoskeleton, 257–329. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4613-2151-4_11.

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Yu, Nuo, and Niels Galjart. "Purification of Mammalian Tubulins and Tubulin-Associated Proteins Using a P2A-Based Expression System." In Methods in Molecular Biology, 1–17. New York, NY: Springer US, 2019. http://dx.doi.org/10.1007/978-1-0716-0219-5_1.

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Burns, Roy G., Kevin W. Farrell, and Christopher D. Surridge. "Should the Tubulins be Members of the GTPase Superfamily?" In Ciba Foundation Symposium 176 - The GTPase Superfamily, 248–77. Chichester, UK: John Wiley & Sons, Ltd., 2007. http://dx.doi.org/10.1002/9780470514450.ch16.

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O’Connell, Paul A., and Thomas H. MacRae. "Preparation and Characterization of Posttranslationally Modified Tubulins From Artemia franciscana." In Methods in Molecular Medicine™, 45–63. Totowa, NJ: Humana Press, 2007. http://dx.doi.org/10.1007/978-1-59745-442-1_4.

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Tian, Huaize, and Sanetaka Shirahata. "Some Characteristics of UNC-51 Phosphorylations of Both Actins and Tubulins." In Animal Cell Technology: Basic & Applied Aspects, 333–39. Dordrecht: Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-9646-4_50.

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Yariv, Joseph. "Tubulin." In The Discreet Charm of Protein Binding Sites, 19–26. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-24996-4_2.

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Schatten, Heide, and Qing-Yuan Sun. "Posttranslationally Modified Tubulins and Other Cytoskeletal Proteins: Their Role in Gametogenesis, Oocyte Maturation, Fertilization and Pre-implantation Embryo Development." In Advances in Experimental Medicine and Biology, 57–87. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-0817-2_4.

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Tian, Huaize, and Sanetaka Shirahata. "Protein Phosphotase 1α Reverses UNC-51 Phosphorylations of Both Actins and Tubulins and a New Model of UNC-51-Inducing Axon Formation." In Animal Cell Technology: Basic & Applied Aspects, 341–45. Dordrecht: Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-9646-4_51.

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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, 379–84. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-2037-2_37.

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Stephens, R. E. "Ciliary Membrane Tubulin." In Ciliary and Flagellar Membranes, 217–40. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-0515-6_9.

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Trabalhos de conferências sobre o assunto "Tubulins"

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Deriu, Marco A., Monica Soncini, Mario Orsi, Mishal Patel, Jonathan W. Essex, Franco M. Montevecchi, and Alberto Redaelli. "Elastic Network Normal Mode Analysis for Microtubule Mechanics." In ASME 2009 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2009. http://dx.doi.org/10.1115/sbc2009-206618.

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The cellular microtubules MTs are hollow cylinder-shaped biopolymers with inner and outer diameter of about 17 and 25 nm and length ranging from 1 to 10 μm. They are constituted by αβ-tubulins arranged in protofilaments with a head-to-tail motif [1]. 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 (Fig.1a). The building-block of the MT, the αβ-tubulin, is a hetero-dimer made of two globular monomers, α- and β-tubulin, each of them consisting of about 450 residues with high degree of sequence
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2

Das, Somenath, Ramana Pidaparti, and Preetam Ghosh. "Modeling Self-organization of Microtubules from Tubulins." In 8th International Conference on Bio-inspired Information and Communications Technologies (formerly BIONETICS). ACM, 2015. http://dx.doi.org/10.4108/icst.bict.2014.257891.

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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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Singh, Shivendra V., Marie Lue Antony, Joomin Lee, Eun-Ryeong Hahm, Su-Hyeong Kim, Guillermo Romero, Adam I. Marcus та ін. "Abstract 228: Withaferin A downregulates tubulins and covalently binds β-tubulin at cysteine-303 in human breast cancer cells". У Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-228.

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Yang, Chia-Ping H., Hui Xiao, and Susan Band Horwitz. "Abstract 4496: Differential inhibition by microtubule stabilizing agents of 2-(m-azidobenzoyl)Taxol photoaffinity labeling of tubulins from different eukaryotic sources." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-4496.

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Sohrabi, Salman, Seyyed Mahdi Nemati Mehr, and Pedram Falsafi. "A Novel Approach for Compensating the Significance of Tubule’s Architecture in Urine Concentrating Mechanism of Renal Medulla." In ASME 2013 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/imece2013-63747.

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Many theories and mathematical simulations have been proposed concerning urine concentrating mechanism (UCM). The WKM and region approach are the two most valuable methods for compensating the effect of tubule’s architecture in renal medulla. They both have tried to simulate tubule’s confinement within a particular region mathematically in one spatial dimension. In this study, continuity, momentum and species transport equations along with standard expressions for transtubular solutes and water transports on tubule’s membrane were solved numerically in three spatial dimensions which practicall
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Stewart, R. B., F. Marketz, W. C. M. Lohbeck, F. D. Fischer, W. Daves, F. G. Rammerstorfer, and H. J. Böhm. "Expandable Wellbore Tubulars." In SPE Technical Symposium. Society of Petroleum Engineers, 1999. http://dx.doi.org/10.2118/60766-ms.

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Walsh, Thomas J. "Flexible Composite Tubulars." In ASME 1996 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 1996. http://dx.doi.org/10.1115/imece1996-0615.

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Abstract Flexibility requirements for long length tubes (1000–10,000 meters) are driven not only by in-service environments, but also restrictions on the outer dimensions of a package destined for transport. Long lengths of tube are required to be spooled onto reels with small inner diameters. The ratio of tube outer diameter to the spooling diameter provides an estimate of the flexure strain. For example, a 50 mm OD tube spooled onto a 1 meter ID reel would impose 5% strain in the tube during storage. In extreme oilfield downhole environments, the flexible tube must not only survive the requi
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Sheldon, Kely L., and Dan L. Sackett. "Abstract 3044: The ability of tubulin to close mitochondrial VDAC pores depends on beta tubulin isotype." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-3044.

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10

Yang, Chia-Ping H., та Susan B. Horwitz. "Abstract 664: Polymerization of human βIII-tubulin is distinct from βI-tubulin in a cell-free system". У 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.am2011-664.

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Relatórios de organizações sobre o assunto "Tubulins"

1

Banerjee, Asok. Characterization of Tubulin Isoforms in Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, May 2000. http://dx.doi.org/10.21236/ada393136.

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2

Banerjee, Asok. Characterization of Tubulin Isoforms in Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, May 1999. http://dx.doi.org/10.21236/ada381325.

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3

Yang, KyoungLang, and Gunda I. Georg. Synthesis of Cryptophycin Affinity Labels and Tubulin Labeling. Fort Belvoir, VA: Defense Technical Information Center, May 2005. http://dx.doi.org/10.21236/ada443679.

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4

Banerjee, Asok. Characterization of Tubulin Isoforms in Breast Cancer Cells. Fort Belvoir, VA: Defense Technical Information Center, May 2001. http://dx.doi.org/10.21236/ada395082.

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5

Yang, Kyounglang, and AGunda I. Georg. Synthesis of Cryptophycin Affinity Labels and Tubulin Labeling. Fort Belvoir, VA: Defense Technical Information Center, May 2004. http://dx.doi.org/10.21236/ada432471.

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6

Ramadas, Vidya. Synthesis of Cryptophycin Affinity Labels and Tubulin Labeling. Fort Belvoir, VA: Defense Technical Information Center, May 2003. http://dx.doi.org/10.21236/ada416994.

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7

Luduena, Richard. Nuclear Tubulin: A Novel for Breast Cancer Chemotherapy. Fort Belvoir, VA: Defense Technical Information Center, May 2000. http://dx.doi.org/10.21236/ada392981.

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8

Yang, KyoungLang, and Gunda I. Georg. Synthesis of Cryptophycin Affinity Labels and Tubulin Labeling. Fort Belvoir, VA: Defense Technical Information Center, May 2006. http://dx.doi.org/10.21236/ada474734.

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9

Ratigan. L52293 Brine String Integrity Survey and Model Evaluation. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), January 2009. http://dx.doi.org/10.55274/r0010206.

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Resumo:
Brine strings are essential components of both natural gas and liquid hydrocarbon storage caverns. Both the natural gas and liquid hydrocarbon storage industries are well aware that a limit exists for the fluid velocity in the injection tubulars in their storage caverns. If the brine injection or brine withdrawal velocity is gradually increased, eventually, the hanging tubular will experience flow-induced vibration, resulting in the potential for the hanging tubulars to bend and/or break. Additionally, in both types of hydrocarbon storage, salt falls can impact the brine string integrity.Resul
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10

Susan M. Wick. Growth and development of maize that contains mutant tubulin genes. Office of Scientific and Technical Information (OSTI), July 2004. http://dx.doi.org/10.2172/826290.

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