Literatura académica sobre el tema "Non muscle myosin II A"
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Artículos de revistas sobre el tema "Non muscle myosin II A"
Watanabe, T., H. Hosoya y S. Yonemura. "1P205 Live imaging of Non-muscle myosin II in epithelial cells". Seibutsu Butsuri 45, supplement (2005): S83. http://dx.doi.org/10.2142/biophys.45.s83_1.
Texto completoUbukawa, Kumi, Yong-Mei Guo, Masayuki Takahashi, Makoto Hirokawa, Yoshihiro Michishita, Miho Nara, Hiroyuki Tagawa et al. "Enucleation of human erythroblasts involves non-muscle myosin IIB". Blood 119, n.º 4 (26 de enero de 2012): 1036–44. http://dx.doi.org/10.1182/blood-2011-06-361907.
Texto completoDasbiswas, Kinjal, Shiqiong Hu, Frank Schnorrer, Samuel A. Safran y Alexander D. Bershadsky. "Ordering of myosin II filaments driven by mechanical forces: experiments and theory". Philosophical Transactions of the Royal Society B: Biological Sciences 373, n.º 1747 (9 de abril de 2018): 20170114. http://dx.doi.org/10.1098/rstb.2017.0114.
Texto completoWrighton, Katharine H. "Non-muscle myosin II in kidney morphogenesis". Nature Reviews Nephrology 13, n.º 7 (30 de mayo de 2017): 384. http://dx.doi.org/10.1038/nrneph.2017.77.
Texto completoLevinson, Howard, Blaine Mischen, Bruce Klitzman, Detlev Erdmann y L. Scott Levin. "Non muscle myosin II regulates contractile phenotypes". Journal of the American College of Surgeons 205, n.º 3 (septiembre de 2007): S60—S61. http://dx.doi.org/10.1016/j.jamcollsurg.2007.06.148.
Texto completoMaciver, Sutherland K. "Myosin II function in non-muscle cells". BioEssays 18, n.º 3 (marzo de 1996): 179–82. http://dx.doi.org/10.1002/bies.950180304.
Texto completoPorro, Chiara, Antonio Pennella, Maria Antonietta Panaro y Teresa Trotta. "Functional Role of Non-Muscle Myosin II in Microglia: An Updated Review". International Journal of Molecular Sciences 22, n.º 13 (22 de junio de 2021): 6687. http://dx.doi.org/10.3390/ijms22136687.
Texto completoTakubo, T., S. Wakui, K. Daigo, K. Kurokata, T. Ohashi, K. Katayama y M. Hino. "Expression of non-muscle type myosin heavy polypeptide 9 (MYH9) in mammalian cells". European Journal of Histochemistry 47, n.º 4 (26 de junio de 2009): 345. http://dx.doi.org/10.4081/845.
Texto completoJuanes-García, Alba, Clara Llorente-González y Miguel Vicente-Manzanares. "Molecular control of non-muscle myosin II assembly". Oncotarget 7, n.º 5 (18 de enero de 2016): 5092–93. http://dx.doi.org/10.18632/oncotarget.6936.
Texto completoWan, Xiaohu. "Counting Molecules in Non-Muscle Myosin II Filaments". Biophysical Journal 108, n.º 2 (enero de 2015): 322a. http://dx.doi.org/10.1016/j.bpj.2014.11.1750.
Texto completoTesis sobre el tema "Non muscle myosin II A"
Frei, Ryan. "Regulatory Elements of Drosophila Non-Muscle Myosin II". Thesis, University of Oregon, 2013. http://hdl.handle.net/1794/12954.
Texto completo2015-07-11
Swailes, Nathan. "Actin and non-muscle myosin II in pre-fusion myoblasts". Thesis, University of Leeds, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.416842.
Texto completoPicariello, Hannah Stubbs. "The Diverse Roles of Non-muscle Myosin II in Tumorigenesis". Case Western Reserve University School of Graduate Studies / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1562680454131993.
Texto completoKhan, Protiti. "The Role of Myosin Light Chain Kinase and Non Muscle Myosin II In Ras Signaling to ERK". Scholarly Repository, 2008. http://scholarlyrepository.miami.edu/oa_theses/177.
Texto completoSankara, Narayana Gautham Hari Narayana. "Role of non-muscle myosin-II isoforms in adherens junction biogenesis and collective migration". Thesis, Université de Paris (2019-....), 2019. https://theses.md.univ-paris-diderot.fr/SANKARA_NARAYANA_Gautham_Hari_Naryana_va.pdf.
Texto completoAdherens junction formation and remodeling is essential for many biological processes like embryo compaction, tissue morphogenesis and wound healing. It is now well described that non-muscle myosin II (NMII) acts as a mechanical support and force-generator for E-cadherin junctions during collective migration and morphogenesis. However, the contribution of NMII during early steps of junction formation remains obscure, probably because of the technical difficulty to catch such a transient event. In this work, we investigate the role of non-muscle myosin II isoforms (NMIIA and NMIIB) during adherens junction biogenesis in MDCK cells, using an in vitro reductionist approach. This system, based on chemically switchable micropatterns allows a spatio-temporal control of adherens junction formation. Our observations on MDCK cells show that the cells form irreversible E-cadherin based contacts, junction elongation is accompanied by the repolarization of actin cytoskeleton and nucleus-centrosome axis. Using isoform-specific ShRNA for NMIIA and IIB, we show that they have distinct contributions to junction formation and dynamics. NMIIA and NMIIB differentially regulate biogenesis of AJ through association with distinct actin networks. Analysis of junction dynamics, actin organization, and mechanical forces of control and knockdown cells for myosins revealed that NMIIA provides the mechanical tugging force necessary for cell-cell junction reinforcement and maintenance. NMIIB is involved in E-cadherin clustering, maintenance of a branched actin layer connecting E-cadherin complexes and perijunctional actin fibres leading to the building-up of anisotropic stress. These data reveal unanticipated complementary functions of NMIIA and NMIIB in the biogenesis and integrity of AJ
Ricketson, Derek Lee. "Drosophila non-muscle myosin II bipolar filament formation : importance of charged residues and specific domains for self-assembly /". Connect to title online (Scholars' Bank) Connect to title online (ProQuest), 2009. http://hdl.handle.net/1794/10285.
Texto completoDing, Siyu Serena. "Elucidating the role of non-muscle myosin II in Caenorhabditis elegans stem-like seam cell divisions". Thesis, University of Oxford, 2015. https://ora.ox.ac.uk/objects/uuid:5b5cb805-327a-4a58-b3db-3787f5264efc.
Texto completoRicketson, Derek Lee 1980. "Drosophila non-muscle myosin II bipolar filament formation: Importance of charged residues and specific domains for self-assembly". Thesis, University of Oregon, 2009. http://hdl.handle.net/1794/10285.
Texto completoNon-muscle myosin II generates contractile forces for processes such as cytokinesis, motility, and polarity. Contractility requires assembly of myosin molecules into bipolar mini-filaments through electrostatic interactions between coiled-coil tail domains of the heavy chains. Analyses of myosin II from various organisms have revealed "assembly domains" within the C-terminal portion of the tail domain that mediate filament formation. However, it has been unclear precisely how assembly domains interact with one another, or otherwise contribute to tail-tail interactions, to form the bipolar mini-filament structure. To understand tail domain interactions, we first identified a 90-residue region (1849-1940) of the Drosophila non-muscle myosin II tail domain that was necessary and sufficient for filament formation, using salt-dependent solubility and a novel fluorescence energy transfer assay. We identified residues within this "assembly domain" that were critical for filament assembly by analyzing the effect of point mutations. We found that single point mutations in specific positively charged regions completely disrupt filament assembly. Surprisingly, none of the negatively charged regions within the assembly domain are required for assembly. Most of the mutations in positively charged residues that disrupted filament assembly clustered within a 15-residue segment (1880-1894) that appears to form a critical interaction surface. Using this information, along with known geometrical constraints and electrostatic calculations, we constructed a structural model of the bipolar mini-filament. This model features one favored anti-parallel tail overlap and multiple slightly less stable alternative overlaps. The ability of the positive segment to interact with multiple negative regions explains the lack of required negatively charged residues in the assembly domain. To our knowledge, this structural model of the non- muscle myosin II bipolar filament is consistent with all physical observations and provides a framework for understanding the detailed mechanism by which this fundamental cellular structure is generated. This dissertation contains previously published and unpublished co-authored material.
Committee in charge: Tom Stevens, Chairperson, Chemistry; Kenneth Prehoda, Advisor, Chemistry; J. Andrew Berglund, Member, Chemistry; Christopher Doe, Member, Biology; Karen Guillemin, Outside Member, Biology
Sarkar, Saheli. "Combined Experimental and Mathematical Approach for Development of a Microfabrication-Based Model to Investigate Cell-Cell Interaction during Migration". Case Western Reserve University School of Graduate Studies / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=case1301420667.
Texto completoMessineo, Stefania. "Development of a gene targeting strategy (Recombinase-Mediated CAssette Exchange) to generate cellular models of MYH9-related disease". Doctoral thesis, Università degli studi di Trieste, 2011. http://hdl.handle.net/10077/4603.
Texto completoLa malattia MYH9-correlata (MYH9-RD) è una malattia autosomica dominante, caratterizzata da trombocitopenia congenita con piastrine di grandi dimensioni, aggregati nei neutrofili, sordità progressiva, cataratta e nefropatia. La MYH9-RD è causata da mutazioni nel gene MYH9 che codifica per la catena pesante della miosina non muscolare di classe II (miosina-9). I meccanismi patogenetici che causano questa malattia non sono ancora stati chiaramente identificati e il loro studio è complicato dalla mancanza di adeguati modelli cellulari e animali. Lo scopo di questo progetto è stato di generare un modello in vitro per studiare la funzione della miosina-9 e il ruolo di due mutazioni che incorrono nel gene MYH9: la R702C e la R1933X, che correlano rispettivamente con un fenotipo grave e lieve. Per questo motivo abbiamo deciso di manipolare le cellule staminali embrionali murine (ES), che sono pluripotenti e possono essere differenziate in diversi linee cellulari, compresa la linea megacariocitica. Per ingegnerizzare queste cellule ad alta efficienza abbiamo messo a punto una strategia nota come "scambio di cassette mediato da ricombinasi" (RMCE). Dopo l'integrazione di una cassetta fiancheggiata da siti FRT (sequenze di riconoscimento per l'enzima flippasi), il sistema ci ha permesso di scambiare diverse sequenze di DNA in presenza dell'enzima flippasi. Quindi il primo esone codificante del gene Myh9 è stato distrutto dall'inserimento, mediante ricombinazione omologa, di una cassetta fiancheggiata da due siti FRT contenente il gene reporter Beta-galattosidasi. Successivamente abbiamo scambiato questa cassetta con altre tre contenenti il cDNA Myh9 murino wild-type e i due mutati, generando i cloni ES che esprimono queste sequenze esogene sotto il controllo del promotore Myh9 endogeno. La caratterizzazione a livello dell'RNA e delle proteine di questi cloni ci ha portato a stabilire che gli alleli mutati e wild-type sono espressi allo stesso livello, suggerendo che le manipolazioni genetiche non interferiscono con i corretti meccanismi fisiologici di trascrizione e traduzione del gene Myh9. Tuttavia, mediante Western Blot abbiamo mostrato che la proteina miosina-9 è espressa a livello inferiore nei cloni mutati rispetto ai wild-type. Le analisi di immunofluorescenza per indagare la presenza di aggregati di miosina-9, che sono sempre presenti nei neutrofili di pazienti, non hanno rilevato alcuna variazione nella distribuzione della miosina-9, fatta eccezione per un segnale di intensità minore. Questi risultati indicano che, nonostante l'espressione dell'allele ingegnerizzato sia normale, la proteina mutata sembra essere degradata, almeno nelle cellule ES murine, determinando un effetto di aploinsufficienza delle mutazioni R702C e R1933X. Per accertare la loro pluripotenza, abbiamo differenziato dei cloni ES in corpi embrioidi e cardiomiociti, senza rivelare alcuna differenza tra i cloni mutanti e i wild-type. Dal momento che una caratteristica congenita dei pazienti MYH9-RD è la macrotrombocitopenia, abbiamo sviluppato un protocollo per differenziare i cloni mutati ES in megacariociti per indagare come le mutazioni in MYH9 portino a una impropria produzione di piastrine. In conclusione, per studiare la MYH9-RD abbiamo sviluppato una strategia che ci ha permesso di esprimere sequenze di interesse in cellule ES di topo sotto il controllo del promotore Myh9 endogeno. La differenziazione in vitro di queste cellule ci permetterà di studiare l'effetto delle mutazioni nel corso della megacariocitopoiesi. Inoltre, poiché le cellule ES possono anche essere usate per generare modelli animali, questa strategia ci permetterà di testare diverse ipotesi patogenetiche in vitro, prima di passare a studi in vivo.
XXIII Ciclo
1982
Libros sobre el tema "Non muscle myosin II A"
Turner, Neil y Bertrand Knebelmann. MYH9 and renal disease. Editado por Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0342_update_001.
Texto completoBarker, Alan R. y Neil Armstrong. Pulmonary oxygen uptake kinetics. Editado por Neil Armstrong y Willem van Mechelen. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198757672.003.0013.
Texto completoCapítulos de libros sobre el tema "Non muscle myosin II A"
Betapudi, Venkaiah. "Non-muscle Myosin II Motor Proteins in Human Health and Diseases". En Genome Analysis and Human Health, 79–107. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-4298-0_5.
Texto completoGoonewardene, Sanchia S., Raj Persad, Hanif Motiwala y David Albala. "NMIBC and Intravesical Chemotherapy—HIVEC I and HIVEC II". En Management of Non-Muscle Invasive Bladder Cancer, 223–24. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-28646-0_43.
Texto completoBandman, E., D. L. Bourke y M. Wick. "Regulation of Myosin Heavy Chain Expression during Development, Maturation, and Regeneration in Avian Muscles: The Role of Myogenic and Non-Myogenic Factors". En The Dynamic State of Muscle Fibers, editado por Dirk Pette, 127–38. Berlin, Boston: De Gruyter, 1990. http://dx.doi.org/10.1515/9783110884784-013.
Texto completoZolty, Ronald. "The Role of Neurohormonal Systems, Inflammatory Mediators and Oxydative Stress in Cardiomyopathy". En Cardiomyopathy - Disease of the Heart Muscle. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.97345.
Texto completoLee-Gannon, Theo, Hannah Lehrenbaum, Rahul Sheth y Pradeep P.A. Mammen. "Clinical Management of DMD-Associated Cardiomyopathy". En Cardiomyopathy - Disease of the Heart Muscle. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.98919.
Texto completoPartanen, Juhani, Urho Sompa y Miguel Muñoz-Ruiz. "Recording of Proprioceptive Muscle Reflexes in the Lower Extremity". En Proprioception [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.95575.
Texto completoActas de conferencias sobre el tema "Non muscle myosin II A"
Zhang, Wenwu, Yidi Wu y Susan J. Gunst. "The Small GTPase RhoA Regulates Non-Muscle Myosin II Activity During Contractile Stimulation In Canine Tracheal Smooth Muscle". En American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a4131.
Texto completoLi, Xiaona, Meiwen An, Li Wang y Wenzhou Wu. "The Experimental Study on the Functions of Non-Muscle Myosin II in Dividing Mammalian Cells". En 2009 3rd International Conference on Bioinformatics and Biomedical Engineering (iCBBE 2009). IEEE, 2009. http://dx.doi.org/10.1109/icbbe.2009.5163614.
Texto completoHsu, Hui-Ju, Andrea Locke, Susan Q. Vanderzyl y Roland Kaunas. "Stretch-Induced Stress Fiber Remodeling and MAPK Activations Depend on Mechanical Strain Rate". En ASME 2011 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2011. http://dx.doi.org/10.1115/sbc2011-53464.
Texto completoSiegler, Jessica, Biji Mathew, Ting Wang, Tong Zhou, Michael S. Wade, Ralph Weichselbaum, Liliana Moreno-Vinasco y Joe G. Garcia. "Non-Muscle Myosin Light Chain Kinase Participates In Tumor Metastasis In Mice". En American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a5084.
Texto completoAprodu, Iuliana, Alberto Redaelli, Franco Maria Montevecchi y Monica Soncini. "Mechanical Characterization of Myosin II, Actin and Their Complexes by Molecular Mechanics Approach". En ASME 8th Biennial Conference on Engineering Systems Design and Analysis. ASMEDC, 2006. http://dx.doi.org/10.1115/esda2006-95670.
Texto completoSiegler, Jessica, Biji Mathew, Frances Lennon, Lynnette Gerhold, Chin-tu Chen, Patrick La Riviere, Christian Wietholt et al. "Non-Muscle Myosin Light Chain Kinase Promotes The Development Of Non-Small-Cell Lung Cancer". En American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a2062.
Texto completoAlanazi, Samar M., Rosalin Mishra, Long Yuan, Hima Patel y Joan Garrett. "Abstract 4205: The role of non-muscle myosin IIA in HER2+ breast cancers". En 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.am2020-4205.
Texto completoMartin, Ryan D., Jayashree Banerjee, Meenakshi Lakshminarayanan, Yuxia Cao y Maria I. Ramirez. "T1± Interacts With Myh9, A Non-Muscle Myosin, In Type I Lung Epithelial Cells". En American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a6310.
Texto completoBowers, Robert, Danyelle M. Townsend, Yefim Manevich y Kenneth D. Tew. "Abstract 5136: Sulfiredoxin promotes cell migration through direct interaction with non muscle myosin IIa". En 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.am10-5136.
Texto completoMoreno-Vinasco, Liliana, Syed R. Zaidi, Saad Sammani, Tamara Mirzapoiazova, Roberto F. Machado y Joe G. N. Garcia. "Role Of Non-muscle Myosin Light Chain Kinase In Hypoxia-induced Murine Pulmonary Hypertension". En American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a5245.
Texto completoInformes sobre el tema "Non muscle myosin II A"
Kanner, Joseph, Edwin Frankel, Stella Harel y Bruce German. Grapes, Wines and By-products as Potential Sources of Antioxidants. United States Department of Agriculture, enero de 1995. http://dx.doi.org/10.32747/1995.7568767.bard.
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