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anti-Mouse (Murine) PPM1D Antibodies:
anti-Human PPM1D Antibodies:
anti-Rat (Rattus) PPM1D Antibodies:
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Human Polyclonal PPM1D Primary Antibody for WB - ABIN392853
Song, Han, Sabapathy, Lee, Yu, Choi: Expression of a homeostatic regulator, Wip1 (wild-type p53-induced phosphatase), is temporally induced by c-Jun and p53 in response to UV irradiation. in The Journal of biological chemistry 2010
Show all 7 Pubmed References
Human Polyclonal PPM1D Primary Antibody for IP, WB - ABIN151547
Lee, Lee, Moon, Shim, Fornace, Cha: Senescent growth arrest in mesenchymal stem cells is bypassed by Wip1-mediated downregulation of intrinsic stress signaling pathways. in Stem cells (Dayton, Ohio) 2009
Show all 4 Pubmed References
Human Polyclonal PPM1D Primary Antibody for IF (p), IHC (p) - ABIN740415
Wang, Cui, Wen, Guo, Zhang, Chen: Cisplatin induces HepG2 cell cycle arrest through targeting specific long noncoding RNAs and the p53 signaling pathway. in Oncology letters 2017
Findings indicate that the PPM1D-Ulk1 (show ULK1 Antibodies) axis plays a pivotal role in genotoxic stress-induced autophagy.
This suggests an important cross-talk between SHH and WIP1 pathways that accelerates tumorigenesis and supports WIP1 inhibition as a potential treatment strategy for MB.
WIP1 phosphatase plays a pro-adipogenic role by interacting directly with PPARgamma (show PPARG Antibodies) and dephosphorylating p-PPARgamma (show PPARG Antibodies) S112 in vitro and in vivo.
this study shows that knock out of Wip1 in mouse aggravates colonic inflammation and increases neutrophils migration
the data indicate that the WIP1 phosphatase functions to maintain insulin (show INS Antibodies) sensitivity and glucose homeostasis.
Study suggests a potential protective function of p53 (show TP53 Antibodies)-induced phosphatase 1 in mood stabilization.
loss of Wip1 phosphatase induces a p53 (show TP53 Antibodies)-dependent, but p21 (show D4S234E Antibodies)-independent, mechanism that impairs B-cell development by enhancing apoptosis in early B-cell precursors
our findings identify Wip1 as an intrinsic negative regulator of neutrophil inflammation in intestinal I/R injury process
the principal function of Wip1 in MSCs transformation is the maintenance of proliferative capacity; but knocking out Wip1 increases the migratory capacity of MSCs; this dual effect of Wip1 provides the potential for purposeful routing of MSCs
Wip1 inhibition can activate the mTORC1 pathway and enhance hepatocyte proliferation after hepatectomy.
Wip1 activity and its relevance to cancer as an oncoprotein is reviewed
The authors show that a global spread of ATM (show ATM Antibodies) activity on chromatin and phosphorylation of ATM (show ATM Antibodies) targets including KAP1 (show CDKN3 Antibodies) control Plk1 (show PLK1 Antibodies) re-activation. These phosphorylations are rapidly counteracted by the chromatin-bound phosphatase Wip1, allowing cell cycle restart despite persistent ATM (show ATM Antibodies) activity present at DNA lesions.
Truncating and missense PPM1D mutations are associated with prostate cancer.
this study shows that expression of Wip1 is decreased in patients with active inflammatory bowel disease
Wip1 is frequently overexpressed in nonsmall cell lung cancer, which may serve an essential role in the p38MAPK (show MAPK14 Antibodies)/p53 (show TP53 Antibodies)/p16 (show CDKN2A Antibodies) signaling pathway.
Study identified 14 individuals with mild to severe Intellectual Disability (ID) and/or developmental delay and de novo truncating PPM1D mutations; all mutations were located in the last or penultimate exon, suggesting escape from nonsense-mediated mRNA decay.
PPM1D gene silencing combined with TMZ eradicates glioma cells through cell apoptosis and cell cycle arrest
High PPM1D expression is associated with breast cancer.
PPM1D in the chromosomal location 17q22-24 might be the most relevant candidate gene with respect to a potential functional implication in meningioma progression.
The protein encoded by this gene is a member of the PP2C family of Ser/Thr protein phosphatases. PP2C family members are known to be negative regulators of cell stress response pathways. The expression of this gene is induced in a p53-dependent manner in response to various environmental stresses. While being induced by tumor suppressor protein TP53/p53, this phosphatase negatively regulates the activity of p38 MAP kinase, MAPK/p38, through which it reduces the phosphorylation of p53, and in turn suppresses p53-mediated transcription and apoptosis. This phosphatase thus mediates a feedback regulation of p38-p53 signaling that contributes to growth inhibition and the suppression of stress induced apoptosis. This gene is located in a chromosomal region known to be amplified in breast cancer. The amplification of this gene has been detected in both breast cancer cell line and primary breast tumors, which suggests a role of this gene in cancer development.
, p53-induced protein phosphatase 1
, protein phosphatase 1D
, protein phosphatase 2C isoform delta
, protein phosphatase magnesium-dependent 1 delta
, protein phosphatase 1D magnesium-dependent, delta isoform
, protein phosphatase 2C delta isoform
, protein phosphatase Wip1
, wild-type p53-induced phosphatase 1