Centrin depletion causes cyst formation and other ciliopathy-related phenotypes in zebrafish
出版年份 2011 全文链接
标题
Centrin depletion causes cyst formation and other ciliopathy-related phenotypes in zebrafish
作者
关键词
-
出版物
CELL CYCLE
Volume 10, Issue 22, Pages 3964-3972
出版商
Informa UK Limited
发表日期
2011-12-07
DOI
10.4161/cc.10.22.18150
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Mapping the NPHP-JBTS-MKS Protein Network Reveals Ciliopathy Disease Genes and Pathways
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- Defective nucleotide excision repair with normal centrosome structures and functions in the absence of all vertebrate centrins
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- The two domains of centrin have distinct basal body functions in Tetrahymena
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- The cilia protein IFT88 is required for spindle orientation in mitosis
- (2011) Benedicte Delaval et al. NATURE CELL BIOLOGY
- Centriole duplication
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- Cdk5 in the centriolar appendages mediates cenexin1 localization and primary cilia formation
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- Polycystic kidney disease protein fibrocystin localizes to the mitotic spindle and regulates spindle bipolarity
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- Mps1 Phosphorylation Sites Regulate the Function of Centrin 2 in Centriole Assembly
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- Dictyostelium discoideumCenB Is a Bona Fide Centrin Essential for Nuclear Architecture and Centrosome Stability
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- Pericentrin, a centrosomal protein related to microcephalic primordial dwarfism, is required for olfactory cilia assembly in mice
- (2009) Ko Miyoshi et al. FASEB JOURNAL
- SUMO-dependent regulation of centrin-2
- (2009) U. R. Klein et al. JOURNAL OF CELL SCIENCE
- Acute kidney injury and aberrant planar cell polarity induce cyst formation in mice lacking renal cilia
- (2008) Vishal Patel et al. HUMAN MOLECULAR GENETICS
- Centrin 2 Localizes to the Vertebrate Nuclear Pore and Plays a Role in mRNA and Protein Export
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- Centrins in retinal photoreceptor cells: Regulators in the connecting cilium
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