Gotowa bibliografia na temat „Myosin A”
Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych
Spis treści
Zobacz listy aktualnych artykułów, książek, rozpraw, streszczeń i innych źródeł naukowych na temat „Myosin A”.
Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.
Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.
Artykuły w czasopismach na temat "Myosin A"
Siththanandan, Verl B., i James R. Sellers. "Regulation of myosin 5a and myosin 7a". Biochemical Society Transactions 39, nr 5 (21.09.2011): 1136–41. http://dx.doi.org/10.1042/bst0391136.
Pełny tekst źródłaBaines, I. C., H. Brzeska i E. D. Korn. "Differential localization of Acanthamoeba myosin I isoforms." Journal of Cell Biology 119, nr 5 (1.12.1992): 1193–203. http://dx.doi.org/10.1083/jcb.119.5.1193.
Pełny tekst źródłaBerg, Jonathan S., Bradford C. Powell i Richard E. Cheney. "A Millennial Myosin Census". Molecular Biology of the Cell 12, nr 4 (kwiecień 2001): 780–94. http://dx.doi.org/10.1091/mbc.12.4.780.
Pełny tekst źródłaHammer, J. A., B. Bowers, B. M. Paterson i E. D. Korn. "Complete nucleotide sequence and deduced polypeptide sequence of a nonmuscle myosin heavy chain gene from Acanthamoeba: evidence of a hinge in the rodlike tail." Journal of Cell Biology 105, nr 2 (1.08.1987): 913–25. http://dx.doi.org/10.1083/jcb.105.2.913.
Pełny tekst źródłaHeintzelman, M. B., T. Hasson i M. S. Mooseker. "Multiple unconventional myosin domains of the intestinal brush border cytoskeleton". Journal of Cell Science 107, nr 12 (1.12.1994): 3535–43. http://dx.doi.org/10.1242/jcs.107.12.3535.
Pełny tekst źródłaBerg, J. S., B. H. Derfler, C. M. Pennisi, D. P. Corey i R. E. Cheney. "Myosin-X, a novel myosin with pleckstrin homology domains, associates with regions of dynamic actin". Journal of Cell Science 113, nr 19 (1.10.2000): 3439–51. http://dx.doi.org/10.1242/jcs.113.19.3439.
Pełny tekst źródłaPost, P. L., G. M. Bokoch i M. S. Mooseker. "Human myosin-IXb is a mechanochemically active motor and a GAP for rho". Journal of Cell Science 111, nr 7 (1.04.1998): 941–50. http://dx.doi.org/10.1242/jcs.111.7.941.
Pełny tekst źródłaWylie, Steven R., i Peter D. Chantler. "Myosin IIC: A Third Molecular Motor Driving Neuronal Dynamics". Molecular Biology of the Cell 19, nr 9 (wrzesień 2008): 3956–68. http://dx.doi.org/10.1091/mbc.e07-08-0744.
Pełny tekst źródłaO'Halloran, T. J., S. Ravid i J. A. Spudich. "Expression of Dictyostelium myosin tail segments in Escherichia coli: domains required for assembly and phosphorylation." Journal of Cell Biology 110, nr 1 (1.01.1990): 63–70. http://dx.doi.org/10.1083/jcb.110.1.63.
Pełny tekst źródłaHasson, T., i M. S. Mooseker. "Porcine myosin-VI: characterization of a new mammalian unconventional myosin." Journal of Cell Biology 127, nr 2 (15.10.1994): 425–40. http://dx.doi.org/10.1083/jcb.127.2.425.
Pełny tekst źródłaRozprawy doktorskie na temat "Myosin A"
Zhu, Jing. "The role of nonmuscle myosin IIA in endothelial cell". Morgantown, W. Va. : [West Virginia University Libraries], 2010. http://hdl.handle.net/10450/11006.
Pełny tekst źródłaTitle from document title page. Document formatted into pages; contains viii, 37 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 33-37).
Stevens, Richard. "Two light chains of the unconventional myosin Myo2p /". Thesis, Connect to this title online; UW restricted, 1997. http://hdl.handle.net/1773/9226.
Pełny tekst źródłaGuimard, Laurent. "Modélisation et synthèse de peptides interagissant avec une protéine cible : application au complexe calmoduline-RS20". Montpellier 1, 1995. http://www.theses.fr/1995MON1T037.
Pełny tekst źródłaPetzoldt, Astrid G. "DE-cadherin regulates unconventional myosin ID through myosin IC in Drosophila melanogaster". Nice, 2009. http://www.theses.fr/2009NICE4048.
Pełny tekst źródłaThe accurate establishment of stereotyped L/R asymetry is subject to a strict genetic program and crucial for the functionality of the organism. It is only recently that the mechanism of L/R asymmetry establishment is exploited in the invertebrate species Drosphophila melanogaster (Hozumi et al. , 2006 ; Speder et al. , 2006). The unconventional type ID myosin (MyoID) has been characterised as a dextral determinant accountable for the clockwise (dextral) rotation of the male genital plate during pupae stage. In our attempt to isolate new components of the L/R mechanism, we first focussed on MyoIC, the closest homologue of genitalia, thus L/R axis inversion. We provide evidence that this situs inversus phenotype is du to an inhibition of MyoID function through MyoIC and consequently define MyoIC as an anti-dextral effector of MyoID. An interaction between MyoID and adherents junctions had been suggested by Speder et al. (2006) as the authors could show by two-hybrid screen and GST pull down that MyoID tail and beta-catenin cal physically interact. Our DE-cadherin loss and gain of function studies revealed a linear interaction between DE-cadherin zand the unconventional myosins MyoID and MyoIC. DE-cadherin controls MyoIC expression, acting as inhibitor of MyoIC. As MyoID functionality is regulated by MyoIC expression, myoIC functions as a mediator between DE-cadherin and myoID. In summary, we present in this study a new regulatory network of L/R asymmetry establishment, where DE-cadherin affects MyoID activity through regulation of MyoIC protein expression
Ripoll, Léa. "Role of myosin VI and actin dynamics in membrane remodeling during pigmentation". Thesis, Sorbonne Paris Cité, 2017. http://www.theses.fr/2017USPCB102.
Pełny tekst źródłaIntracellular transport among organelles and the plasma membrane occurs through the formation and transport of vesicular and tubular membrane carriers. The formation of these carriers requires first the bending of membrane and the generation of a bud, followed by its elongation to form the tubule-vesicle. Lastly, the carrier is released from the membrane source by the scission of the membrane. Importantly, all these different steps need an accurate orchestration to properly deform the membrane. The actions exerted by molecular motors onto microtubule and actin cytoskeletons provide forces onto membrane that contribute to its remodeling during the biogenesis of carrier. Actin filaments (F-actin) and myosins are thought to participate in the initiation and the fission of carriers. However, the role of actin machinery during carrier biogenesis remains elusive. We thus decided to address the role of F-actin and the actin-based motor myosin VI in the formation of tubular intermediates at melanosome. Melanosomes are lysosome-related organelles of skin melanocytes and eye pigment cells that function in the synthesis and storage of the melanin pigment. Melanosomes originate from endosomes and progressively mature into fully pigmented compartments, which fate is to be secreted and transferred to neighboring keratinocytes. Melanosomes are dynamic organelles that constantly receive, but also recycle proteins such as the SNARE VAMP7 through the formation and release of tubular intermediates. Our work reveals that myosin VI, together with Arp2/3- and WASH-mediated branched actin localize at specific melanosomal subdomains where they promote the constriction and scission of tubular intermediates. This fission event allows the export of components such as VAMP7 from melanosomes and promotes their maturation and subsequent transfer to keratinocytes. Altogether, our results uncover a new role for myosin VI and F-actin in the constriction and scission of membrane tubules at melanosome that is required for organelle homeostasis and function
Saeki, Nobutaka. "The Function of Myosin IX: the Ninth Class of Myosin Superfamily: a Dissertation". eScholarship@UMMS, 2005. http://escholarship.umassmed.edu/gsbs_diss/294.
Pełny tekst źródłaCartón, García Fernando. "Myosin VB in intestinal pathogenesis". Doctoral thesis, Universitat Autònoma de Barcelona, 2017. http://hdl.handle.net/10803/458251.
Pełny tekst źródłaMyosin VB is a molecular motor protein that uses the energy of ATP to move along actin filaments. It participates in the recycling endosomes trafficking in the subapical cytoplasmic region of non-polarized and polarized cells. It is highly expressed in the small and large intestine, where its role in the establishment of polarized function in enterocytes is also well known. Inactivating mutations of MYO5B have been associated with microvillus inclusion disease (MVID), a rare congenital disorder of the intestinal epithelial cells that presents with persistent life-threatening watery diarrhea. It is characterized by morphological enterocyte abnormalities such as microvillus atrophy and mislocalization of apical and basolateral protein transporters. The molecular pathology of the disease is not well known mainly due to the lack of animal models. In the present study, we report a versatile murine model with targeted inactivation of Myo5b. This model allowed us to generate and characterized a constitutive Myo5b knockout mice and a tamoxifen-inducible intestinal-epithelium-specific Myo5b knockout. In both cases, the mice closely resemble the phenotype of MVID patients, developing watery diarrhea and dehydration causing the death of the animal. Histological study of the intestine showed all the characteristic enterocyte defects observed in MVID patients, including microvillus atrophy and mislocalization of protein markers. Moreover, the inactivation of MYO5B also originated hyperproliferation of the intestinal crypts. Therefore, our mice constitute a useful model to further investigate the underlying molecular mechanism of this disease and to preclinically assess the efficacy of novel therapeutic approaches. In addition, hyperproliferation as well as loss of cell polarity, differentiation, and tissue architecture are hallmarks of advanced metastatic carcinomas and strongly correlate with poor patient prognosis. Specifically, for colorectal cancer, the third most common type of cancer worldwide, we have previously demonstrated that the loss of brush border MYO1A, also involved in cell polarity, promotes cancer progression and has tumor suppressor activity. Other studies have indicated a relationship between MYO5B inactivation and gastric cancer, promoting invasion and motility, but little is known regarding its role in colorectal cancer. To address this question, we have developed novel doxycycline-inducible in vitro models of MYO5B overexpression and downregulation. Moreover, we have generated MYO5B knockout Caco2-BBE cells using CRISPR/Cas9 technology. Our results showed changes in the polarization and differentiation of colon cancer cells, in agreement with previous observations in the normal intestine. Moreover, we have observed a relationship between MYO5B and the motility and invasion capacity of colon cancer cells, indicating a possible role of MYO5B in colon cancer progression. However, the effect of MYO5B loss in cell proliferation observed in our Myo5b knockout mice could not be confirmed in our models in vitro and in vivo, employing cell line-derived xenografts. In addition, using a tissue microarray containing triplicate samples from 155 primary Dukes C colorectal tumors, reduced MYO5B expression was found to be associated with shorter disease-free and overall survival of the patients. Moreover, poorly differentiated tumors showed significantly reduced expression of MYO5B. Collectively, our results indicate that MYO5B plays an important role in the differentiation of the normal intestinal epithelium and colon cancer cells, as well as a possible role in cancer progression promoting cell motility and invasion.
Tyrrell, Graham Philip. "Modelling the myosin molecular motor". Thesis, University of York, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.247144.
Pełny tekst źródłaThomas, Daniel G. "The self-interaction of myosin". Thesis, University of Leicester, 1992. http://hdl.handle.net/2381/35170.
Pełny tekst źródłaCarrington, Glenn Stuart Peter. "The flexibility of myosin 7a". Thesis, University of Leeds, 2018. http://etheses.whiterose.ac.uk/22504/.
Pełny tekst źródłaKsiążki na temat "Myosin A"
Sellers, James R. Motor proteins 2: myosin. London: Academic Press, 1995.
Znajdź pełny tekst źródłaMyosins. Wyd. 2. Oxford: Oxford University Press, 1999.
Znajdź pełny tekst źródłaSyrový, Ivo. Kontraktilní bílkoviny a funkční požadavky svalu. Praha: Academia, 1985.
Znajdź pełny tekst źródła1933-, Sugi Haruo, i Pollack Gerald H, red. Mechanism of myofilament sliding in muscle contraction. New York: Plenum Press, 1993.
Znajdź pełny tekst źródłaGriffiths, Hazel Sylvia. Studies on the properties and function of myosin light chain kinase. Birmingham: University of Birmingham, 1986.
Znajdź pełny tekst źródłaThomas, D. D. Molecular Interactions of Actin: Actin-Myosin Interaction and Actin-Based Regulation. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002.
Znajdź pełny tekst źródłaKeane, Anita M. Peptide mimetics of an actin-binding site on the myosin head. Birmingham: University of Birmingham, 1991.
Znajdź pełny tekst źródłaMilankov, Kosta. Immunocytochemical localization of actin and myosin within interphase nuclei in situ. Ottawa: National Library of Canada, 1993.
Znajdź pełny tekst źródłaEpp, Trevor Allan. Characterization of the human cardiac gas-myosin heavy chain gene. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1993.
Znajdź pełny tekst źródłaEastwood, Anthony Michael. The use of peptide mimetics in defining the actin-myosin interaction. Birmingham: University of Birmingham, 1994.
Znajdź pełny tekst źródłaCzęści książek na temat "Myosin A"
Gewies, Andreas, Jürgen Ruland, Alexey Kotlyarov, Matthias Gaestel, Shiri Procaccia, Rony Seger, Shin Yasuda i in. "Myosin II, “Conventional” Myosin". W Encyclopedia of Signaling Molecules, 1169. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-0461-4_100886.
Pełny tekst źródłaLackner, K. J., i D. Peetz. "Myosin". W Lexikon der Medizinischen Laboratoriumsdiagnostik, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-49054-9_2210-1.
Pełny tekst źródłaLackner, K. J., i D. Peetz. "Myosin". W Springer Reference Medizin, 1711. Berlin, Heidelberg: Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-48986-4_2210.
Pełny tekst źródłaWard, Tony Milford. "Myosin". W Proteins and Tumour Markers May 1995, 1286–87. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0681-8_54.
Pełny tekst źródłaAitchison Smith, David. "Myosin Motors". W The Sliding-Filament Theory of Muscle Contraction, 237–91. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-03526-6_6.
Pełny tekst źródłaTokuo, Hiroshi. "Myosin X". W Advances in Experimental Medicine and Biology, 391–403. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-38062-5_17.
Pełny tekst źródłaBugyi, Beáta, i András Kengyel. "Myosin XVI". W Advances in Experimental Medicine and Biology, 405–19. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-38062-5_18.
Pełny tekst źródłaTaft, Manuel H., i Sharissa L. Latham. "Myosin XVIII". W Advances in Experimental Medicine and Biology, 421–38. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-38062-5_19.
Pełny tekst źródłaSweeney, H. Lee, Anne Houdusse i Julien Robert-Paganin. "Myosin Structures". W Advances in Experimental Medicine and Biology, 7–19. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-38062-5_2.
Pełny tekst źródłaBocanegra, Jennifer L., Rebecca Adikes i Omar A. Quintero. "Myosin XIX". W Advances in Experimental Medicine and Biology, 439–51. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-38062-5_20.
Pełny tekst źródłaStreszczenia konferencji na temat "Myosin A"
Egan, Paul F., Philip R. LeDuc, Jonathan Cagan i Christian Schunn. "A Design Exploration of Genetically Engineered Myosin Motors". W ASME 2011 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. ASMEDC, 2011. http://dx.doi.org/10.1115/detc2011-48568.
Pełny tekst źródłaEgan, Paul F., Jonathan Cagan, Christian Schunn i Philip R. LeDuc. "Design of Complex Nano-Scale Systems Using Multi-Agent Simulations and Structure-Behavior-Function Representations". W ASME 2012 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/detc2012-70291.
Pełny tekst źródłaAprodu, Iuliana, Alberto Redaelli, Franco Maria Montevecchi i Monica Soncini. "Mechanical Characterization of Myosin II, Actin and Their Complexes by Molecular Mechanics Approach". W ASME 8th Biennial Conference on Engineering Systems Design and Analysis. ASMEDC, 2006. http://dx.doi.org/10.1115/esda2006-95670.
Pełny tekst źródłaDaniel, J. L., i M. Rigmaiden. "Evidence for Ca2+-independent phosphorylation of human platelet myosin". W XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644527.
Pełny tekst źródłaHaghshenas-Jaryani, Mahdi, i Alan Bowling. "Multiscale Dynamic Modeling of Flexibility in Myosin V". W ASME 2013 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/detc2013-13154.
Pełny tekst źródłaKostcheeva, O. I., V. Yu Ostchepkova, M. R. Sharipov, D. V. Stchepkin i G. V. Kopylova. "Influence of the myosin activator omecamptive-mecarbil onto the actin-myosin interaction in the myocard". W VI Information school of a young scientist. Central Scientific Library of the Urals Branch of the Russian Academy of Sciences, 2018. http://dx.doi.org/10.32460/ishmu-2018-6-0023.
Pełny tekst źródłaNikmaneshi, Mohammad Reza, Bahar Firoozabadi i Mohammad Said Saidi. "Continuum model of actin-myosin flow". W 2013 20th Iranian Conference on Biomedical Engineering (ICBME). IEEE, 2013. http://dx.doi.org/10.1109/icbme.2013.6782200.
Pełny tekst źródłaLE GOFF, L., F. AMBLARD i E. M. FURST. "VISCOELASTICITY OF ACTIVE ACTIN-MYOSIN NETWORKS". W Proceedings of the International Symposium. WORLD SCIENTIFIC, 2003. http://dx.doi.org/10.1142/9789812704931_0010.
Pełny tekst źródłaBidone, Tamara Carla, Haosu Tang i Dimitrios Vavylonis. "Insights Into the Mechanics of Cytokinetic Ring Assembly Using 3D Modeling". W ASME 2014 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/imece2014-39006.
Pełny tekst źródłaChin, LY, Y. Bosse, PD Pare i CY Seow. "Myosin Filament Assembly in Airway Smooth Muscle." W American Thoracic Society 2009 International Conference, May 15-20, 2009 • San Diego, California. American Thoracic Society, 2009. http://dx.doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a2063.
Pełny tekst źródłaRaporty organizacyjne na temat "Myosin A"
Sadot, Einat, Christopher Staiger i Mohamad Abu-Abied. Studies of Novel Cytoskeletal Regulatory Proteins that are Involved in Abiotic Stress Signaling. United States Department of Agriculture, wrzesień 2011. http://dx.doi.org/10.32747/2011.7592652.bard.
Pełny tekst źródłaSanders, Luraynne. Cell Adhesion, Signaling and Myosin in Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, sierpień 2000. http://dx.doi.org/10.21236/ada392857.
Pełny tekst źródłaSanders, Luraynne C. Cell Adhesion, Signaling and Myosin in Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, sierpień 1999. http://dx.doi.org/10.21236/ada382496.
Pełny tekst źródłaChew, Teng-Leong. Regulation of Actin-Myosin Cytoskeletal Changes Involved in Cancer Metastasis. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2001. http://dx.doi.org/10.21236/ada396798.
Pełny tekst źródłaHofmann, Wilma A. The Role of a Novel Myosin Isoform in Prostate Cancer Metastasis. Fort Belvoir, VA: Defense Technical Information Center, październik 2013. http://dx.doi.org/10.21236/ada593300.
Pełny tekst źródłaZhang, John Q. Post-Myocardial Infarction and Exercise Training on Myosin Heavy Chain and Cardiac Function. Science Repository, kwiecień 2019. http://dx.doi.org/10.31487/j.jicoa.2019.01.08.
Pełny tekst źródłaSchiefelbein, J. Molecular genetics of myosin motors in Arabidopsis. Final report, July 1, 1992--June 30, 1996. Office of Scientific and Technical Information (OSTI), luty 1997. http://dx.doi.org/10.2172/486111.
Pełny tekst źródłaStaiger, Christopher. Regulation of Cell Wall Assembly: Myosin and Exocyst Involvement in Cellulose Synthase Delivery to the Plasma Membrane. Office of Scientific and Technical Information (OSTI), styczeń 2022. http://dx.doi.org/10.2172/1840725.
Pełny tekst źródłaGabaix, Xavier, i David Laibson. Myopia and Discounting. Cambridge, MA: National Bureau of Economic Research, marzec 2017. http://dx.doi.org/10.3386/w23254.
Pełny tekst źródłaAngeletos, George-Marios, i Zhen Huo. Myopia and Anchoring. Cambridge, MA: National Bureau of Economic Research, kwiecień 2018. http://dx.doi.org/10.3386/w24545.
Pełny tekst źródła