Gotowa bibliografia na temat „Concomitant morphogenesis”
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Artykuły w czasopismach na temat "Concomitant morphogenesis"
Soffer, Arad, Adnan Mahly, Krishnanand Padmanabhan, Jonathan Cohen, Orit Adir, Eidan Loushi, Yaron Fuchs, Scott E. Williams i Chen Luxenburg. "Apoptosis and tissue thinning contribute to symmetric cell division in the developing mouse epidermis in a nonautonomous way". PLOS Biology 20, nr 8 (15.08.2022): e3001756. http://dx.doi.org/10.1371/journal.pbio.3001756.
Pełny tekst źródłaWu, Wei, Shinji Kitamura, David M. Truong, Timo Rieg, Volker Vallon, Hiroyuki Sakurai, Kevin T. Bush, David R. Vera, Robert S. Ross i Sanjay K. Nigam. "β1-Integrin is required for kidney collecting duct morphogenesis and maintenance of renal function". American Journal of Physiology-Renal Physiology 297, nr 1 (lipiec 2009): F210—F217. http://dx.doi.org/10.1152/ajprenal.90260.2008.
Pełny tekst źródłaCorellou, Florence, Colin Brownlee, Bernard Kloareg i François-Yves Bouget. "Cell cycle-dependent control of polarised development by a cyclin-dependent kinase-like protein in theFucuszygote". Development 128, nr 21 (1.11.2001): 4383–92. http://dx.doi.org/10.1242/dev.128.21.4383.
Pełny tekst źródłaHsu, Tzu-Han, Rey-Huei Chen, Yun-Hsin Cheng i Chao-Wen Wang. "Lipid droplets are central organelles for meiosis II progression during yeast sporulation". Molecular Biology of the Cell 28, nr 3 (luty 2017): 440–51. http://dx.doi.org/10.1091/mbc.e16-06-0375.
Pełny tekst źródłaGambley, RL, i W. Dodd. "Effect of Hypocotyl Length on Morphogenesis of Explants of Cucumber (Cucumis sativus L.) in vitro". Functional Plant Biology 19, nr 2 (1992): 165. http://dx.doi.org/10.1071/pp9920165.
Pełny tekst źródłaPanteris, Emmanuel, i Ioannis-Dimosthenis S. Adamakis. "Double Puzzle: Morphogenesis of the Bi-Layered Leaf Adaxial Epidermis of Magnolia grandiflora". Plants 11, nr 24 (9.12.2022): 3437. http://dx.doi.org/10.3390/plants11243437.
Pełny tekst źródłaKim, J. Y., Y. G. Cha, S. W. Cho, E. J. Kim, M. J. Lee, J. M. Lee, J. Cai, H. Ohshima i H. S. Jung. "Inhibition of Apoptosis in Early Tooth Development Alters Tooth Shape and Size". Journal of Dental Research 85, nr 6 (czerwiec 2006): 530–35. http://dx.doi.org/10.1177/154405910608500610.
Pełny tekst źródłaUlanova, V. I., V. I. Mazurov i V. A. Zinzerling. "Clinical and morphological characteristics of infective endocarditis". Clinical Medicine (Russian Journal) 98, nr 2 (15.07.2020): 115–21. http://dx.doi.org/10.30629/0023-2149-2020-98-2-115-121.
Pełny tekst źródłaProksch, S., T. Steinberg, S. Schulz, S. Sauerbier, E. Hellwig i P. Tomakidi. "Environmental Biomechanics Substantiated by Defined Pillar Micropatterns Govern Behavior of Human Mesenchymal Stem Cells". Cell Transplantation 21, nr 11 (listopad 2012): 2455–69. http://dx.doi.org/10.3727/096368912x637037.
Pełny tekst źródłaChen, Yen-Ju, Kuan-Yi Wu, Shu-Fan Lin, Sung-Hsi Huang, Heng-Cheng Hsu i Hong-Ming Hsu. "PIP2 regulating calcium signal modulates actin cytoskeleton-dependent cytoadherence and cytolytic capacity in the protozoan parasite Trichomonas vaginalis". PLOS Pathogens 19, nr 12 (18.12.2023): e1011891. http://dx.doi.org/10.1371/journal.ppat.1011891.
Pełny tekst źródłaRozprawy doktorskie na temat "Concomitant morphogenesis"
John, Alphy. "Propriétés subcellulaires et dynamique à l'échelle de l'embryon gouvernant la morphogenèse". Electronic Thesis or Diss., Université Côte d'Azur, 2021. http://theses.univ-cotedazur.fr/2021COAZ6017.
Pełny tekst źródłaMorphogenesis is the process of reshaping single-cell zygotes to the final form of a developed animal. Embryonic gene patterning systems determine the body axes and lay down the spatiotemporal specification coordinates for cells. Gene patterning systems also affect the organization of cytoskeletal components in order to drive tissue morphogenesis. While much work was done to understand how AP and DV patterning independently control morphogenesis, little is known on how cross-patterning functions. We use the Drosophila embryo as a model system and focus on the process of tissue folding, a process that is vital for the animal since folding defects can impair neurulation in vertebrates and gastrulation in all animals which are organized into the three germ layers. Past work has shown that an actomyosin meshwork spanning the apical-medial side of prospective mesoderm cells and under the control of the embryo DV patterning plays a key role in mesoderm invagination. Nevertheless, both experimental and theoretical pieces of evidence have argued against apical constriction being the sole mechanism driving invagination. In this study, I have uncovered a lateral cell junctional network under the control of both AP and DV patterning. This contractile network generates tension along the apical-basal axis and within the tissue plane, 10-15 μm inside the mesoderm epithelium initiating lateral cell intercalation. Lateral forces in mesoderm cells seem to play a multivalent role in both driving mesoderm extension and invagination. Finally, by implementing 4D multi-view light-sheet imaging, infra-red femtosecond ablation to perturb the cytoskeleton, and optogenetics to synthetically control tissue morphology, this work shines new light on the origin and functions of a novel mechanism responsible for coordinated tissue elongation and folding
Książki na temat "Concomitant morphogenesis"
Campione, Marina, Amelia Aranega i Diego Franco. Cardiac looping and laterality. Redaktorzy José Maria Pérez-Pomares, Robert G. Kelly, Maurice van den Hoff, José Luis de la Pompa, David Sedmera, Cristina Basso i Deborah Henderson. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198757269.003.0014.
Pełny tekst źródłaCzęści książek na temat "Concomitant morphogenesis"
Pasick, J. M. M., i S. Dales. "Epigenetic Factors Influencing the Morphogenesis of Primary Neural Cell Cultures and the Concomitant Effects on Establishing JHMV Infections". W Advances in Experimental Medicine and Biology, 655–67. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4684-5823-7_89.
Pełny tekst źródłaRoskelley, Calvin D., i Shoukat Dedhar. "Extracellular matrix protocols for the study of complex phenotypes". W Essential Cell Biology, 349–64. Oxford University PressOxford, 1992. http://dx.doi.org/10.1093/oso/9780199638314.003.0011.
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