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CHK2 kinase promotes pre-mRNA splicing via phosphorylating CDK11(p110)
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
23178491
retrieved
4 January 2017
title
CHK2 kinase promotes pre-mRNA splicing via phosphorylating CDK11(p110)
(English)
1 reference
stated in
PubMed
PubMed ID
23178491
retrieved
4 January 2017
main subject
phosphorylation
0 references
author name string
H.-H. Choi
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
23178491
retrieved
4 January 2017
H.-K. Choi
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2
1 reference
stated in
PubMed
PubMed ID
23178491
retrieved
4 January 2017
S. Y. Jung
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
23178491
retrieved
4 January 2017
J. Hyle
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4
1 reference
stated in
PubMed
PubMed ID
23178491
retrieved
4 January 2017
B.-J. Kim
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5
1 reference
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PubMed
PubMed ID
23178491
retrieved
4 January 2017
K. Yoon
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6
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PubMed
PubMed ID
23178491
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4 January 2017
E.-J. Cho
series ordinal
7
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PubMed
PubMed ID
23178491
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4 January 2017
H.-D. Youn
series ordinal
8
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PubMed
PubMed ID
23178491
retrieved
4 January 2017
J. M. Lahti
series ordinal
9
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PubMed
PubMed ID
23178491
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4 January 2017
J. Qin
series ordinal
10
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PubMed
PubMed ID
23178491
retrieved
4 January 2017
S.-T. Kim
series ordinal
11
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stated in
PubMed
PubMed ID
23178491
retrieved
4 January 2017
language of work or name
English
0 references
publication date
2 January 2014
1 reference
stated in
PubMed
PubMed ID
23178491
retrieved
4 January 2017
published in
Oncogene
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stated in
PubMed
PubMed ID
23178491
retrieved
4 January 2017
volume
33
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PubMed
PubMed ID
23178491
retrieved
4 January 2017
page(s)
108–115
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stated in
PubMed
PubMed ID
23178491
retrieved
4 January 2017
issue
1
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PubMed
PubMed ID
23178491
retrieved
4 January 2017
cites work
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The CHK2-BRCA1 tumour suppressor pathway ensures chromosomal stability in human somatic cells
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PML-dependent apoptosis after DNA damage is regulated by the checkpoint kinase hCds1/Chk2
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20 March 2017
CDK11 complexes promote pre-mRNA splicing
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PubMed Central
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The PITSLRE/CDK11p58 protein kinase promotes centrosome maturation and bipolar spindle formation
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The human homologs of checkpoint kinases Chk1 and Cds1 (Chk2) phosphorylate p53 at multiple DNA damage-inducible sites
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Chk2/hCds1 functions as a DNA damage checkpoint in G(1) by stabilizing p53
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The pathobiology of splicing
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PubMed Central
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Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations
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PITSLRE p110 protein kinases associate with transcription complexes and affect their activity
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hCds1-mediated phosphorylation of BRCA1 regulates the DNA damage response
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DNA damage-induced activation of p53 by the checkpoint kinase Chk2
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Mammalian Chk2 is a downstream effector of the ATM-dependent DNA damage checkpoint pathway
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ATR-Chk2 signaling in p53 activation and DNA damage response during cisplatin-induced apoptosis
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CDK11(p58) is required for centriole duplication and Plk4 recruitment to mitotic centrosomes
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Thr-370 is responsible for CDK11(p58) autophosphorylation, dimerization, and kinase activity
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Rapid-response splicing reporter screens identify differential regulators of constitutive and alternative splicing.
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Death receptor-induced activation of the Chk2- and histone H2AX-associated DNA damage response pathways
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Characterization of cyclin L1 and L2 interactions with CDK11 and splicing factors: influence of cyclin L isoforms on splice site selection.
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Cyclin D3/CDK11p58 complex is involved in the repression of androgen receptor
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CDK11(p58) is required for the maintenance of sister chromatid cohesion
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HIV-1 mRNA 3' end processing is distinctively regulated by eIF3f, CDK11, and splice factor 9G8.
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Distinct Chk2 activation pathways are triggered by genistein and DNA-damaging agents in human melanoma cells
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Destabilization of CHK2 by a missense mutation associated with Li-Fraumeni Syndrome
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23178491
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1038/ONC.2012.535
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4971336
Dimensions Publication ID
1048771227
0 references
OpenCitations bibliographic resource ID
4971336
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4971336
PMCID
4131284
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4971336
PubMed ID
23178491
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4971336
ResearchGate publication ID
233768528
0 references
Springer Nature article ID
10.1038/onc.2012.535
0 references
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