Results 31 to 40 of about 7,503,880 (242)

DNA damage checkpoint and repair: From the budding yeast Saccharomyces cerevisiae to the pathogenic fungus Candida albicans

open access: yesComputational and Structural Biotechnology Journal, 2021
Cells are constantly challenged by internal or external genotoxic assaults, which may induce a high frequency of DNA lesions, leading to genome instability.
Shuangyan Yao   +3 more
doaj   +1 more source

DNA damage responses in ageing [PDF]

open access: yesOpen Biology, 2019
Ageing appears to be a nearly universal feature of life, ranging from unicellular microorganisms to humans. Longevity depends on the maintenance of cellular functionality, and an organism's ability to respond to stress has been linked to functional maintenance and longevity.
Paulo F. L. da Silva, Björn Schumacher
openaire   +3 more sources

Utilization of a Strongly Inducible DDI2 Promoter to Control Gene Expression in Saccharomyces cerevisiae

open access: yesFrontiers in Microbiology, 2018
Regulating target gene expression is a common method in yeast research. In Saccharomyces cerevisiae, there are several widely used regulated expression systems, such as the GAL and Tet-off systems.
Aiyang Lin   +8 more
doaj   +1 more source

Phosphorylation-Dependent PIH1D1 Interactions Define Substrate Specificity of the R2TP Cochaperone Complex

open access: yesCell Reports, 2014
The R2TP cochaperone complex plays a critical role in the assembly of multisubunit machines, including small nucleolar ribonucleoproteins (snoRNPs), RNA polymerase II, and the mTORC1 and SMG1 kinase complexes, but the molecular basis of substrate ...
Zuzana Hořejší   +9 more
doaj   +1 more source

A p53-independent role for the MDM2 antagonist Nutlin-3 in DNA damage response initiation. [PDF]

open access: yes, 2011
BACKGROUND: The mammalian DNA-damage response (DDR) has evolved to protect genome stability and maximize cell survival following DNA-damage. One of the key regulators of the DDR is p53, itself tightly regulated by MDM2. Following double-strand DNA breaks
Valentine, Jane M.   +11 more
core   +2 more sources

DNA Damage and DNA Damage Response in Chronic Myeloid Leukemia [PDF]

open access: yesInternational Journal of Molecular Sciences, 2020
DNA damage and alterations in the DNA damage response (DDR) are critical sources of genetic instability that might be involved in BCR-ABL1 kinase-mediated blastic transformation of chronic myeloid leukemia (CML). Here, increased DNA damage is detected by γH2AX foci analysis in peripheral blood mononuclear cells (PBMCs) of de novo untreated chronic ...
Henning D. Popp   +10 more
openaire   +2 more sources

Autophagic Organelles in DNA Damage Response

open access: yesFrontiers in Cell and Developmental Biology, 2021
Autophagy is an important subcellular event engaged in the maintenance of cellular homeostasis via the degradation of cargo proteins and malfunctioning organelles.
Jeongha Kim   +7 more
doaj   +1 more source

Deciphering the DNA Damage Response [PDF]

open access: yesCell, 2015
This year's Albert Lasker Basic Medical Research Award honors Evelyn Witkin and Stephen J. Elledge, two pioneers in elucidating the DNA damage response, whose contributions span more than 40 years.
openaire   +2 more sources

Autophagy in DNA Damage Response [PDF]

open access: yesInternational Journal of Molecular Sciences, 2015
DNA damage response (DDR) involves DNA repair, cell cycle regulation and apoptosis, but autophagy is also suggested to play a role in DDR. Autophagy can be activated in response to DNA-damaging agents, but the exact mechanism underlying this activation is not fully understood, although it is suggested that it involves the inhibition of mammalian target
Czarny, Piotr   +4 more
openaire   +2 more sources

The concerted roles of FANCM and Rad52 in the protection of common fragile sites

open access: yesNature Communications, 2018
Fanconi anemia core proteins have been linked to common fragile site stability. Here the authors shed light into the role of FANCM in common fragile site protection by suppressing double-strand break formation and mitotic recombination.
Hailong Wang   +5 more
doaj   +1 more source

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