Involvement of DNA-dependent protein kinase in normal cell cycle progression through mitosis. - Wikidata - wikimedia - TriplyDB

Involvement of DNA-dependent protein kinase in normal cell cycle progression through mitosis.

Involvement of DNA-dependent protein kinase in normal cell cycle progression through mitosis.

http://www.wikidata.org/entity/Q34752724

about

DNA-dependent protein kinase (DNA-PK) permits vascular smooth muscle cell proliferation through phosphorylation of the orphan nuclear receptor NOR1 Beyond DNA repair: DNA-PK function in cancer The DNA-dependent protein kinase: A multifunctional protein kinase with roles in DNA double strand break repair and mitosis RNF144A, an E3 ubiquitin ligase for DNA-PKcs, promotes apoptosis during DNA damage Role of DNA-dependent protein kinase catalytic subunit in cancer development and treatment Cell cycle-dependent localization of CHK2 at centrosomes during mitosis.Ectopic TLX1 expression accelerates malignancies in mice deficient in DNA-PK.DNA double strand break repair in mitosis is suppressed by phosphorylation of XRCC4 The Catalytic Subunit of DNA-Dependent Protein Kinase Coordinates with Polo-Like Kinase 1 to Facilitate Mitotic Entry.Targeting MPS1 Enhances Radiosensitization of Human Glioblastoma by Modulating DNA Repair Proteins DNA-PKcs phosphorylates hnRNP-A1 to facilitate the RPA-to-POT1 switch and telomere capping after replication.DNA double-strand break repair is impaired in presenescent Syrian hamster fibroblasts Nuclear basic fibroblast growth factor regulates triple-negative breast cancer chemo-resistance DNA-PKcs Negatively Regulates Cyclin B1 Protein Stability through Facilitating Its Ubiquitination Mediated by Cdh1-APC/C Pathway.Phosphorylation of SAF-A/hnRNP-U Serine 59 by Polo-Like Kinase 1 Is Required for Mitosis.Elevated cyclin G2 expression intersects with DNA damage checkpoint signaling and is required for a potent G2/M checkpoint arrest response to doxorubicin.DNA-PKcs plays role in cancer metastasis through regulation of secreted proteins involved in migration and invasion.A genomic Multiprocess survey of machineries that control and link cell shape, microtubule organization, and cell-cycle progression Steroidogenic factor 1 (NR5A1) maintains centrosome homeostasis in steroidogenic cells by restricting centrosomal DNA-dependent protein kinase activation DNA-PK triggers histone ubiquitination and signaling in response to DNA double-strand breaks produced during the repair of transcription-blocking topoisomerase I lesions.Deregulation of DNA-dependent protein kinase catalytic subunit contributes to human hepatocarcinogenesis development and has a putative prognostic value.DNA-PKcs activates the Chk2-Brca1 pathway during mitosis to ensure chromosomal stability.PIG3 promotes NSCLC cell mitotic progression and is associated with poor prognosis of NSCLC patients Getting down to the core of histone modifications.Interplay between the DNA damage proteins MDC1 and ATM in the regulation of the spindle assembly checkpoint.Synergy between Prkdc and Trp53 regulates stem cell proliferation and GI-ARS after irradiation.DNA-PK/Chk2 induces centrosome amplification during prolonged replication stress.Polo-like kinase 1 (PLK1) and protein phosphatase 6 (PP6) regulate DNA-dependent protein kinase catalytic subunit (DNA-PKcs) phosphorylation in mitosis.Inhibition of c-Myc expression accounts for an increase in the number of multinucleated cells in human cervical epithelial cells.The Ku70 DNA-repair protein is involved in centromere function in a grasshopper species.Regulation of the DNA Damage Response by DNA-PKcs Inhibitory Phosphorylation of ATM.Polyploidy and Mitotic Cell Death Are Two Distinct HIV-1 Vpr-Driven Outcomes in Renal Tubule Epithelial Cells.DNA-PKcs associates with PLK1 and is involved in proper chromosome segregation and cytokinesis.

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Involvement of DNA-dependent protein kinase in normal cell cycle progression through mitosis.

http://www.wikidata.org/entity/Q34752724

description

2011 nî lūn-bûn

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2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի փետրվարին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Involvement of DNA-dependent p ...... e progression through mitosis.

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Involvement of DNA-dependent p ...... e progression through mitosis.

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Involvement of DNA-dependent p ...... e progression through mitosis.

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Involvement of DNA-dependent p ...... e progression through mitosis.

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Involvement of DNA-dependent p ...... e progression through mitosis.

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Involvement of DNA-dependent p ...... e progression through mitosis.

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Involvement of DNA-dependent p ...... e progression through mitosis.

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Involvement of DNA-dependent p ...... e progression through mitosis.

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Involvement of DNA-dependent p ...... e progression through mitosis.

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JBC.M110.212969

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Journal of Biological Chemistry

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Involvement of DNA-dependent p ...... e progression through mitosis.

@en

P2093

Benjamin P C Chen

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

Han-Yi Chou

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Hirohiko Yajima

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Kazi R Fattah

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Kyung-Jong Lee

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Sheng-Chung Lee

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Yu-Fen Lin

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P2860

E2F-dependent accumulation of hEmi1 regulates S phase entry by inhibiting APC(Cdh1)

Proteomic characterization of the human centrosome by protein correlation profiling

Phosphorylation of Cdc20 by Bub1 provides a catalytic mechanism for APC/C inhibition by the spindle checkpoint

A role of DNA-PK for the metabolic gene regulation in response to insulin

Plk is an M-phase-specific protein kinase and interacts with a kinesin-like protein, CHO1/MKLP-1

Cell cycle regulation of the activity and subcellular localization of Plk1, a human protein kinase implicated in mitotic spindle function

HURP controls spindle dynamics to promote proper interkinetochore tension and efficient kinetochore capture.

Cyclin A is destroyed in prometaphase and can delay chromosome alignment and anaphase

Identification of in vitro and in vivo phosphorylation sites in the catalytic subunit of the DNA-dependent protein kinase.

Autophosphorylation of the DNA-dependent protein kinase catalytic subunit is required for rejoining of DNA double-strand breaks.

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12796-12802

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10.1074/JBC.M110.212969

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14

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286

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2011-02-17T00:00:00Z

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21330363

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3069479

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