PARP and PARG inhibitors--new therapeutic targets in cancer treatment.
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Structures of the Human Poly (ADP-Ribose) Glycohydrolase Catalytic Domain Confirm Catalytic Mechanism and Explain Inhibition by ADP-HPD DerivativesLoss of TRPM2 function protects against irradiation-induced salivary gland dysfunctionComparative toxicogenomic responses of mercuric and methyl-mercury.TRPM2: a multifunctional ion channel for calcium signalling.Review of poly (ADP-ribose) polymerase (PARP) mechanisms of action and rationale for targeting in cancer and other diseases.Insight into the machinery that oils chromatin dynamics.Novel hydrophilic docetaxel (CQMU-0519) analogue inhibits proliferation and induces apoptosis in human A549 lung, SKVO3 ovarian and MCF7 breast carcinoma cell lines.Hydrogen peroxide modulates synaptic transmission in ventral horn neurons of the rat spinal cord.Silencing Poly (ADP-Ribose) glycohydrolase (PARG) expression inhibits growth of human colon cancer cells in vitro via PI3K/Akt/NFκ-B pathway.
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PARP and PARG inhibitors--new therapeutic targets in cancer treatment.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 12 April 2010
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
PARP and PARG inhibitors--new therapeutic targets in cancer treatment.
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PARP and PARG inhibitors--new therapeutic targets in cancer treatment.
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type
label
PARP and PARG inhibitors--new therapeutic targets in cancer treatment.
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PARP and PARG inhibitors--new therapeutic targets in cancer treatment.
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prefLabel
PARP and PARG inhibitors--new therapeutic targets in cancer treatment.
@en
PARP and PARG inhibitors--new therapeutic targets in cancer treatment.
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P2860
P1476
PARP and PARG inhibitors--new therapeutic targets in cancer treatment.
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Nilufer Jasmine Selimah Fauzee
Ya-lan Wang
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P2888
P304
P356
10.1007/S12253-010-9266-6
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2010-04-12T00:00:00Z