- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
-
Dynamic interplay of microtubule and actomyosin forces drive tissue extension ; volume:15 ; number:1 ; day:12 ; month:4 ; year:2024 ; pages:1-14 ; date:12.2024
Nature Communications ; 15, Heft 1 (12.4.2024), 1-14, 12.2024
- Creator
-
Singh, Amrita
Thale, Sameedha
Leibner, Tobias
Lamparter, Lucas
Ricker, Andrea
Nüsse, Harald
Klingauf, Jürgen
Galic, Milos
Ohlberger, Mario
Matis, Maja
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41467-024-47596-8
- URN
-
urn:nbn:de:101:1-2406252122413.086535082928
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:56 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Singh, Amrita
- Thale, Sameedha
- Leibner, Tobias
- Lamparter, Lucas
- Ricker, Andrea
- Nüsse, Harald
- Klingauf, Jürgen
- Galic, Milos
- Ohlberger, Mario
- Matis, Maja
- SpringerLink (Online service)
Other Objects (12)
Actomyosin-driven force patterning controls endocytosis at the immune synapse
Vimentin is a key regulator of cell mechanosensing through opposite actions on actomyosin and microtubule networks
Diffusible crosslinkers generate directed forces in microtubule networks
Coupling traction force patterns and actomyosin wave dynamics reveals mechanics of cell motion
Force measurements on ensembles of diffusible microtubule crosslinking proteins
Acto-myosin force organization modulates centriole separation and PLK4 recruitment to ensure centriole fidelity
Modelling the Dynamics of Actomyosin Networks
Actomyosin mechanics at the cell level
Unraveling a Force-Generating Allosteric Pathway of Actomyosin Communication Associated with ADP and Pi Release
Force-extension curves of bacterial flagella
Actin-microtubule coordination at growing microtubule ends
Interplay of physical forces underlying insect gastrulation
Actomyosin-driven force patterning controls endocytosis at the immune synapse
Vimentin is a key regulator of cell mechanosensing through opposite actions on actomyosin and microtubule networks
Diffusible crosslinkers generate directed forces in microtubule networks
Coupling traction force patterns and actomyosin wave dynamics reveals mechanics of cell motion
Force measurements on ensembles of diffusible microtubule crosslinking proteins
Acto-myosin force organization modulates centriole separation and PLK4 recruitment to ensure centriole fidelity
Modelling the Dynamics of Actomyosin Networks
Actomyosin mechanics at the cell level
Unraveling a Force-Generating Allosteric Pathway of Actomyosin Communication Associated with ADP and Pi Release
Force-extension curves of bacterial flagella
Actin-microtubule coordination at growing microtubule ends
Interplay of physical forces underlying insect gastrulation
Actomyosin-driven force patterning controls endocytosis at the immune synapse
Vimentin is a key regulator of cell mechanosensing through opposite actions on actomyosin and microtubule networks
Diffusible crosslinkers generate directed forces in microtubule networks
Coupling traction force patterns and actomyosin wave dynamics reveals mechanics of cell motion
Force measurements on ensembles of diffusible microtubule crosslinking proteins
Acto-myosin force organization modulates centriole separation and PLK4 recruitment to ensure centriole fidelity
Modelling the Dynamics of Actomyosin Networks
Actomyosin mechanics at the cell level
Unraveling a Force-Generating Allosteric Pathway of Actomyosin Communication Associated with ADP and Pi Release
Force-extension curves of bacterial flagella
Actin-microtubule coordination at growing microtubule ends