SH2D4A promotes centrosome maturation to support spindle microtubule formation and mitotic progression
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2045-2322
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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SH2D4A promotes centrosome maturation to support spindle microtubule formation and mitotic progression ; volume:13 ; number:1 ; day:4 ; month:2 ; year:2023 ; pages:1-15 ; date:12.2023
Scientific reports ; 13, Heft 1 (4.2.2023), 1-15, 12.2023
- Creator
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Yuki, Ryuzaburo
Ikeda, Yuki
Yasutake, Ryuji
Saito, Youhei
Nakayama, Yuji
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41598-023-29362-w
- URN
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urn:nbn:de:101:1-2023040909081473290568
- Rights
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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
- Yuki, Ryuzaburo
- Ikeda, Yuki
- Yasutake, Ryuji
- Saito, Youhei
- Nakayama, Yuji
- SpringerLink (Online service)
Other Objects (12)
Publisher Correction: SH2D4A promotes centrosome maturation to support spindle microtubule formation and mitotic progression
Cell type-dependent functions of centrosome linker components and their role in centrosome clustering and mitotic spindle formation
Theoretical model of mitotic spindle microtubule growth for FRAP curve interpretation
The mitotic spindle is chiral due to torques within microtubule bundles
Force-transducing molecular ensembles at growing microtubule tips control mitotic spindle size
Human Mps1 kinase is required for the mitotic spindle checkpoint, but not for centrosome duplication
Automatic quantification of microtubule dynamics enables RNAi-screening of new mitotic spindle regulators
Aurora-A inactivation causes mitotic spindle pole fragmentation by unbalancing microtubule-generated forces
A functional assay for the identification and characterization of microtubule-associated proteins involved in the regulation of microtubule dynamics and mitotic spindle assembly
Dynamics and forces in the mitotic spindle
Phosphoproteome studies of human mitotic spindle proteins
The mitotic spindle assembly in C. elegans embryos
Publisher Correction: SH2D4A promotes centrosome maturation to support spindle microtubule formation and mitotic progression
Cell type-dependent functions of centrosome linker components and their role in centrosome clustering and mitotic spindle formation
Theoretical model of mitotic spindle microtubule growth for FRAP curve interpretation
The mitotic spindle is chiral due to torques within microtubule bundles
Force-transducing molecular ensembles at growing microtubule tips control mitotic spindle size
Human Mps1 kinase is required for the mitotic spindle checkpoint, but not for centrosome duplication
Automatic quantification of microtubule dynamics enables RNAi-screening of new mitotic spindle regulators
Aurora-A inactivation causes mitotic spindle pole fragmentation by unbalancing microtubule-generated forces
A functional assay for the identification and characterization of microtubule-associated proteins involved in the regulation of microtubule dynamics and mitotic spindle assembly
Dynamics and forces in the mitotic spindle
Phosphoproteome studies of human mitotic spindle proteins
The mitotic spindle assembly in C. elegans embryos
Publisher Correction: SH2D4A promotes centrosome maturation to support spindle microtubule formation and mitotic progression
Cell type-dependent functions of centrosome linker components and their role in centrosome clustering and mitotic spindle formation
Theoretical model of mitotic spindle microtubule growth for FRAP curve interpretation
The mitotic spindle is chiral due to torques within microtubule bundles
Force-transducing molecular ensembles at growing microtubule tips control mitotic spindle size
Human Mps1 kinase is required for the mitotic spindle checkpoint, but not for centrosome duplication
Automatic quantification of microtubule dynamics enables RNAi-screening of new mitotic spindle regulators
Aurora-A inactivation causes mitotic spindle pole fragmentation by unbalancing microtubule-generated forces
A functional assay for the identification and characterization of microtubule-associated proteins involved in the regulation of microtubule dynamics and mitotic spindle assembly
Dynamics and forces in the mitotic spindle
Phosphoproteome studies of human mitotic spindle proteins