about
Tip60 and p400 are both required for UV-induced apoptosis but play antagonistic roles in cell cycle progression.Physical association between the histone acetyl transferase CBP and a histone methyl transferaseTip60 is targeted to proteasome-mediated degradation by Mdm2 and accumulates after UV irradiationFunctional and physical interaction between the histone methyl transferase Suv39H1 and histone deacetylasesTranscriptional repression by the retinoblastoma protein through the recruitment of a histone methyltransferaseThe histone deacetylase HDAC3 targets RbAp48 to the retinoblastoma proteinThe three members of the pocket proteins family share the ability to repress E2F activity through recruitment of a histone deacetylaseThe R438W polymorphism of human DNA polymerase lambda triggers cellular sensitivity to camptothecin by compromising the homologous recombination repair pathwayRbAp48 belongs to the histone deacetylase complex that associates with the retinoblastoma proteinTip60 acetyltransferase activity is controlled by phosphorylationRetinoblastoma protein represses transcription by recruiting a histone deacetylasePhysical interaction between the mitogen-responsive serum response factor and myogenic basic-helix-loop-helix proteinsDeciphering the chromatin landscape induced around DNA double strand breaksInterplay between chromatin-modifying enzymes controls colon cancer progression through Wnt signalingThe E1A-associated p400 protein modulates cell fate decisions by the regulation of ROS homeostasis.CENP-A is required for accurate chromosome segregation and sustained kinetochore association of BubR1.A new isoform of the histone demethylase JMJD2A/KDM4A is required for skeletal muscle differentiation.Coordinated methyl and RNA binding is required for heterochromatin localization of mammalian HP1alpha.Regulating histone acetyltransferases and deacetylases.Stimulation of E2F1/DP1 transcriptional activity by MDM2 oncoprotein.E2F1 and E1A(12S) have a homologous activation domain regulated by RB and CBP.Regulation of transcription by E2F1/DP1.H2A.Z depletion impairs proliferation and viability but not DNA double-strand breaks repair in human immortalized and tumoral cell lines.The chromatin remodeler p400 ATPase facilitates Rad51-mediated repair of DNA double-strand breaks.RB and hbrm cooperate to repress the activation functions of E2F1To die or not to die: a HAT trick.The histone demethylase JMJD2A/KDM4A links ribosomal RNA transcription to nutrients and growth factors availability.Histone demethylases in chromatin cross-talks.Myogenin binds to and represses c-fos promoter.The serum unresponsive Rous sarcoma virus promoter sustains a high serum response factor-dependent transcription in vitro.Universality of c-fos transcriptional regulation: the Dyad Symmetry Element mediates activation by PMA in T lymphocytes.Control of genetic stability by a new heterochromatin compaction pathway involving the Tip60 histone acetyltransferase.Control of alternative end joining by the chromatin remodeler p400 ATPase.A vlincRNA participates in senescence maintenance by relieving H2AZ-mediated repression at the INK4 locus.Control of CBP co-activating activity by arginine methylationThe CBP co-activator stimulates E2F1/DP1 activity.High-resolution profiling of gammaH2AX around DNA double strand breaks in the mammalian genome.Balance between acetylation and methylation of histone H3 lysine 9 on the E2F-responsive dihydrofolate reductase promoter.Physical interaction between the histone acetyl transferase Tip60 and the DNA double-strand breaks sensor MRN complex.Dual role of the arginine methyltransferase CARM1 in the regulation of c-Fos target genes.
P50
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P50
description
hulumtues
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onderzoeker
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հետազոտող
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Didier Trouche
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Didier Trouche
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Didier Trouche
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Didier Trouche
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type
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Didier Trouche
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Didier Trouche
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Didier Trouche
@es
Didier Trouche
@sl
prefLabel
Didier Trouche
@ast
Didier Trouche
@en
Didier Trouche
@es
Didier Trouche
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P214
P106
P21
P214
P31
P496
0000-0003-1398-6481
P735
P7859
viaf-194915270