# |
PMID |
Sentence |
1 |
15187252
|
The checkpoint kinase Chk2 is activated in response to DNA damage through pathways requiring protein kinases ATM and/or ATR.
|
2 |
18032786
|
The increase of cell-membranous phosphatidylcholines containing polyunsaturated fatty acid residues induces phosphorylation of p53 through activation of ATR.
|
3 |
18032786
|
We show that specific inhibition of iPLA(2) induces a time dependent phosphorylation of Ser15 in p53 in the absence of DNA damage.
|
4 |
18032786
|
This phosphorylation requires the kinase ataxia-telangiectasia and Rad-3-related (ATR) but not the ataxia-telangiectasia-mutated (ATM) kinase.
|
5 |
18032786
|
We further demonstrate that the PCs with linoleic acid in their sn-2 position (18:2n6) induce phosphorylation of Ser15 in p53 in an ATR-dependent manner.
|
6 |
18032786
|
The increase of cell-membranous phosphatidylcholines containing polyunsaturated fatty acid residues induces phosphorylation of p53 through activation of ATR.
|
7 |
18032786
|
We show that specific inhibition of iPLA(2) induces a time dependent phosphorylation of Ser15 in p53 in the absence of DNA damage.
|
8 |
18032786
|
This phosphorylation requires the kinase ataxia-telangiectasia and Rad-3-related (ATR) but not the ataxia-telangiectasia-mutated (ATM) kinase.
|
9 |
18032786
|
We further demonstrate that the PCs with linoleic acid in their sn-2 position (18:2n6) induce phosphorylation of Ser15 in p53 in an ATR-dependent manner.
|
10 |
18032786
|
The increase of cell-membranous phosphatidylcholines containing polyunsaturated fatty acid residues induces phosphorylation of p53 through activation of ATR.
|
11 |
18032786
|
We show that specific inhibition of iPLA(2) induces a time dependent phosphorylation of Ser15 in p53 in the absence of DNA damage.
|
12 |
18032786
|
This phosphorylation requires the kinase ataxia-telangiectasia and Rad-3-related (ATR) but not the ataxia-telangiectasia-mutated (ATM) kinase.
|
13 |
18032786
|
We further demonstrate that the PCs with linoleic acid in their sn-2 position (18:2n6) induce phosphorylation of Ser15 in p53 in an ATR-dependent manner.
|
14 |
18543256
|
Cell cycle arrest is mediated by ATR kinase and results in phosphorylation of Chk1 and SMC1.
|
15 |
18543256
|
Thus, MMR can act as a direct sensor of FdU-mediated DNA lesions eliciting cell cycle arrest via the ATR/Chk1 pathway.
|
16 |
19710035
|
ATM and ATR protect the genome against two different types of tandem repeat instability in Fragile X premutation mice.
|
17 |
19710035
|
We have previously shown that the ATM and Rad3-related (ATR) checkpoint kinase protects the genome against one type of repeat expansion in a FX premutation mouse model.
|
18 |
19710035
|
However, our data suggest that the ATM-sensitive mechanism is different from the ATR-sensitive one.
|
19 |
19710035
|
Our data thus support the hypothesis that two different mechanisms of FX repeat expansion exist, an ATR-sensitive mechanism seen on maternal transmission and an ATM-sensitive mechanism that shows a male expansion bias.
|
20 |
19710035
|
ATM and ATR protect the genome against two different types of tandem repeat instability in Fragile X premutation mice.
|
21 |
19710035
|
We have previously shown that the ATM and Rad3-related (ATR) checkpoint kinase protects the genome against one type of repeat expansion in a FX premutation mouse model.
|
22 |
19710035
|
However, our data suggest that the ATM-sensitive mechanism is different from the ATR-sensitive one.
|
23 |
19710035
|
Our data thus support the hypothesis that two different mechanisms of FX repeat expansion exist, an ATR-sensitive mechanism seen on maternal transmission and an ATM-sensitive mechanism that shows a male expansion bias.
|
24 |
19710035
|
ATM and ATR protect the genome against two different types of tandem repeat instability in Fragile X premutation mice.
|
25 |
19710035
|
We have previously shown that the ATM and Rad3-related (ATR) checkpoint kinase protects the genome against one type of repeat expansion in a FX premutation mouse model.
|
26 |
19710035
|
However, our data suggest that the ATM-sensitive mechanism is different from the ATR-sensitive one.
|
27 |
19710035
|
Our data thus support the hypothesis that two different mechanisms of FX repeat expansion exist, an ATR-sensitive mechanism seen on maternal transmission and an ATM-sensitive mechanism that shows a male expansion bias.
|
28 |
19710035
|
ATM and ATR protect the genome against two different types of tandem repeat instability in Fragile X premutation mice.
|
29 |
19710035
|
We have previously shown that the ATM and Rad3-related (ATR) checkpoint kinase protects the genome against one type of repeat expansion in a FX premutation mouse model.
|
30 |
19710035
|
However, our data suggest that the ATM-sensitive mechanism is different from the ATR-sensitive one.
|
31 |
19710035
|
Our data thus support the hypothesis that two different mechanisms of FX repeat expansion exist, an ATR-sensitive mechanism seen on maternal transmission and an ATM-sensitive mechanism that shows a male expansion bias.
|
32 |
20372103
|
An early response to the induction of DSBs is phosphorylation of the H2A histone variant, H2AX, at the serine-139 residue, in the highly conserved C-terminal SQEY motif, forming gammaH2AX(1).
|
33 |
20372103
|
Following induction of DSBs, H2AX is rapidly phosphorylated by the phosphatidyl-inosito 3-kinase (PIKK) family of proteins, ataxia telangiectasia mutated (ATM), DNA-protein kinase catalytic subunit and ATM and RAD3-related (ATR)(2).
|
34 |
20372103
|
Phosphorylation of H2AX mediated predominantly by ATM spreads to adjacent areas of chromatin, affecting approximately 0.03% of total cellular H2AX per DSB(2,3).
|
35 |
20613712
|
Phosphorylation of the H2A histone variant, H2AX, at the serine-139 residue, in the highly conserved C-terminal SQEY motif, forming gammaH2AX, is an early response to DNA double-strand breaks.
|
36 |
20613712
|
This phosphorylation event is mediated by the phosphatidyl-inosito 3-kinase (PI3K) family of proteins, ataxia telangiectasia mutated (ATM), DNA-protein kinase catalytic subunit and ATM and RAD3-related (ATR).
|
37 |
20736911
|
This phosphorylation of H2AX is mediated by the phosphatidyl-inosito 3-kinase (PI3K) family of proteins, ataxia telangiectasia mutated (ATM), DNA-protein kinase catalytic subunit and ATM and RAD3-related (ATR).
|