Gradient of increasing Aurora B kinase activity is required for cells to execute mitosis - Test2 - elhamkhani - TriplyDB

Gradient of increasing Aurora B kinase activity is required for cells to execute mitosis

Gradient of increasing Aurora B kinase activity is required for cells to execute mitosis

http://www.wikidata.org/entity/Q39642698

about

Phosphorylation at serine 331 is required for Aurora B activation.A small-molecule inhibitor of Haspin alters the kinetochore functions of Aurora B Cell division: control of the chromosomal passenger complex in time and space The Renaissance or the cuckoo clock Selective disruption of aurora C kinase reveals distinct functions from aurora B kinase during meiosis in mouse oocytes Overexpression of hnRNPC2 induces multinucleation by repression of Aurora B in hepatocellular carcinoma cells Targeting the INCENP IN-box-Aurora B interaction to inhibit CPC activity in vivo.Bistability of a coupled Aurora B kinase-phosphatase system in cell division.A chemical biology strategy to analyze rheostat-like protein kinase-dependent regulation Polo-like kinase-1 triggers histone phosphorylation by Haspin in mitosis.Basal aurora kinase B activity is sufficient for histone H3 phosphorylation in prophase Large tumor suppressors 1 and 2 regulate Aurora-B through phosphorylation of INCENP to ensure completion of cytokinesis.High-resolution temporal analysis reveals a functional timeline for the molecular regulation of cytokinesis.Targeting hepatocarcinogenesis model in C56BL6 mice with pan-aurora kinase inhibitor Danusertib.Measuring NDC80 binding reveals the molecular basis of tension-dependent kinetochore-microtubule attachments

P2860

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P2860

Gradient of increasing Aurora B kinase activity is required for cells to execute mitosis

http://www.wikidata.org/entity/Q39642698

description

2010 nî lūn-bûn

@nan

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

2010年论文

@zh

2010年论文

@zh-cn

name

Gradient of increasing Aurora B kinase activity is required for cells to execute mitosis

@en

Gradient of increasing Aurora B kinase activity is required for cells to execute mitosis.

@nl

type

label

Gradient of increasing Aurora B kinase activity is required for cells to execute mitosis

@en

Gradient of increasing Aurora B kinase activity is required for cells to execute mitosis.

@nl

prefLabel

Gradient of increasing Aurora B kinase activity is required for cells to execute mitosis

@en

Gradient of increasing Aurora B kinase activity is required for cells to execute mitosis.

@nl

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JBC.M110.181545

P1433

Journal of Biological Chemistry

P1476

Gradient of increasing Aurora B kinase activity is required for cells to execute mitosis

@en

P2093

Hiromi Ogawa

http://www.w3.org/2001/XMLSchema#string

Kumiko Samejima

http://www.w3.org/2001/XMLSchema#string

Paola Vagnarelli

http://www.w3.org/2001/XMLSchema#string

Zhenjie Xu

http://www.w3.org/2001/XMLSchema#string

P2860

Structure of a Survivin-Borealin-INCENP core complex reveals how chromosomal passengers travel together

Survivin mediates targeting of the chromosomal passenger complex to the centromere and midbody

Phosphoproteome analysis of the human mitotic spindle

Centromere targeting of the chromosomal passenger complex requires a ternary subcomplex of Borealin, Survivin, and the N-terminal domain of INCENP

A quantitative atlas of mitotic phosphorylation

Exploring the functional interactions between Aurora B, INCENP, and survivin in mitosis

Aurora B couples chromosome alignment with anaphase by targeting BubR1, Mad2, and Cenp-E to kinetochores

Chromosomal passengers: conducting cell division

Aurora B kinase exists in a complex with survivin and INCENP and its kinase activity is stimulated by survivin binding and phosphorylation.

Perturbation of Incenp function impedes anaphase chromatid movements and chromosomal passenger protein flux at centromeres

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40163-40170

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scholarly article

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10.1074/JBC.M110.181545

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51

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285

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William Charles Earnshaw

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2010-10-18T00:00:00Z

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47459506

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3000998

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