about
NF-κB-dependent role for cold-inducible RNA binding protein in regulating interleukin 1βUltraviolet light-induced apoptosis is associated with S-phase in primary human fibroblasts.UV light-induced degradation of RNA polymerase II is dependent on the Cockayne's syndrome A and B proteins but not p53 or MLH1.Decreased transcription-coupled nucleotide excision repair capacity is associated with increased p53- and MLH1-independent apoptosis in response to cisplatin.Loss of periostin/OSF-2 in ErbB2/Neu-driven tumors results in androgen receptor-positive molecular apocrine-like tumors with reduced Notch1 activity.A Temperature Sensitive Variant of p53 Drives p53-Dependent MicroRNA Expression without Evidence of Widespread Post-Transcriptional Gene SilencingCompromised genomic integrity impedes muscle growth after Atrx inactivation.A novel cis-acting element from the 3'UTR of DNA damage-binding protein 2 mRNA links transcriptional and post-transcriptional regulation of gene expressionPost-transcriptional regulation of DNA damage-responsive gene expressionDDB2-independent role for p53 in the recovery from ultraviolet light-induced replication arrest.The p53 protein induces stable miRNAs that have the potential to modify subsequent p53 responses.Preferential estrogen receptor β ligands reduce Bcl-2 expression in hormone-resistant breast cancer cells to increase autophagy.Lack of functional pRb results in attenuated recovery of mRNA synthesis and increased apoptosis following UV radiation in human breast cancer cells.Focal adhesion kinase inhibitors are potent anti-angiogenic agents.P53 plays a protective role against UV- and cisplatin-induced apoptosis in transcription-coupled repair proficient fibroblasts.In vitro selections of mammaglobin A and mammaglobin B aptamers for the recognition of circulating breast tumor cells.The anti-apoptotic role for p53 following exposure to ultraviolet light does not involve DDB2.Flow cytometric analysis identifies changes in S and M phases as novel cell cycle alterations induced by the splicing inhibitor isoginkgetin.Rapid Decrease in KRT14 and TP53 mRNA Expression in the Buccal Mucosa of Patients Receiving Total-Body Irradiation for Allogeneic Stem Cell Transplantation.Heavy metal sensitivities of gene deletion strains for ITT1 and RPS1A connect their activities to the expression of URE2, a key gene involved in metal detoxification in yeastManganese-induced cellular disturbance in the baker's yeast, Saccharomyces cerevisiae with putative implications in neuronal dysfunctionDose-dependent effects of DNA-damaging agents on p53-mediated cell cycle arrestInhibition of RNA polymerase II as a trigger for the p53 responseComparative genomic analysis of the 3' UTR of human MDM2 identifies multiple transposable elements, an RLP24 pseudogene and a cluster of novel repeat sequences that arose during primate evolutionMode of action of nisin on Escherichia coli
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description
researcher ORCID ID = 0000-0002-7921-1331
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wetenschapper
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name
Bruce C McKay
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Bruce C McKay
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Bruce C McKay
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Bruce C McKay
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type
label
Bruce C McKay
@ast
Bruce C McKay
@en
Bruce C McKay
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Bruce C McKay
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prefLabel
Bruce C McKay
@ast
Bruce C McKay
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Bruce C McKay
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Bruce C McKay
@nl
P106
P1153
57197295868
P21
P31
P496
0000-0002-7921-1331