The contribution of the N- and C-terminal regions of steroid receptors to activation of transcription is both receptor and cell-specific.
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Cloning and characterization of androgen receptor coactivator, ARA55, in human prostateThe ubiquitin-conjugating enzyme UBCH7 acts as a coactivator for steroid hormone receptorsThe coactivator TIF2 contains three nuclear receptor-binding motifs and mediates transactivation through CBP binding-dependent and -independent pathwaysThe Angelman syndrome-associated protein, E6-AP, is a coactivator for the nuclear hormone receptor superfamilyThe opposing transcriptional activities of the two isoforms of the human progesterone receptor are due to differential cofactor bindingTIF2, a 160 kDa transcriptional mediator for the ligand-dependent activation function AF-2 of nuclear receptorsTwo mutations in the hormone binding domain of the vitamin D receptor cause tissue resistance to 1,25 dihydroxyvitamin D3Increase of androgen-induced cell death and androgen receptor transactivation by BRCA1 in prostate cancer cellsEstrogen receptor transcription and transactivation: Estrogen receptor alpha and estrogen receptor beta: regulation by selective estrogen receptor modulators and importance in breast cancer.Coactivator/corepressor ratios modulate PR-mediated transcription by the selective receptor modulator RU486PIAS3 (protein inhibitor of activated STAT-3) modulates the transcriptional activation mediated by the nuclear receptor coactivator TIF2p65 Negatively regulates transcription of the cyclin E geneThe N-terminal part of TIF1, a putative mediator of the ligand-dependent activation function (AF-2) of nuclear receptors, is fused to B-raf in the oncogenic protein T18Cloning of a mouse glucocorticoid modulatory element binding protein, a new member of the KDWK familyThe AF-1 domain of the orphan nuclear receptor NOR-1 mediates trans-activation, coactivator recruitment, and activation by the purine anti-metabolite 6-mercaptopurineOestrogen receptor facilitates the formation of preinitiation complex assembly: involvement of the general transcription factor TFIIBIdentification of a conserved region required for hormone dependent transcriptional activation by steroid hormone receptorsA mutation mimicking ligand-induced conformational change yields a constitutive RXR that senses allosteric effects in heterodimers.Agonistic and antagonistic activities of RU486 on the functions of the human progesterone receptor.Negative regulation of the rat stromelysin gene promoter by retinoic acid is mediated by an AP1 binding siteBinding-folding induced regulation of AF1 transactivation domain of the glucocorticoid receptor by a cofactor that binds to its DNA binding domain.The patterns of binding of RAR, RXR and TR homo- and heterodimers to direct repeats are dictated by the binding specificites of the DNA binding domains.Molecular basis of androgen resistance in a family with a qualitative abnormality of the androgen receptor and responsive to high-dose androgen therapy.Progesterone receptors, their isoforms and progesterone regulated transcriptionCharacterization of the AB (AF-1) region in the muscle-specific retinoid X receptor-gamma: evidence that the AF-1 region functions in a cell-specific mannerDefinition of the DNA-binding site repertoire for the Drosophila transcription factor SNAIL.Spatiotemporal expression patterns of chicken ovalbumin upstream promoter-transcription factors in the developing mouse central nervous system: evidence for a role in segmental patterning of the diencephalon.Promoter specificity of the two transcriptional activation functions of the human oestrogen receptor in yeast.From estrogen to androgen receptor: a new pathway for sex hormones in prostate.Separation of retinoid X receptor homo- and heterodimerization functionsGlucocorticoid receptor-mediated suppression of the interleukin 2 gene expression through impairment of the cooperativity between nuclear factor of activated T cells and AP-1 enhancer elements.Phosphorylation at serines 104 and 106 by Erk1/2 MAPK is important for estrogen receptor-alpha activity.Interaction of human thyroid hormone receptor beta with transcription factor TFIIB may mediate target gene derepression and activation by thyroid hormoneProbing the structure and function of the estrogen receptor ligand binding domain by analysis of mutants with altered transactivation characteristics.A steroid hormone response unit in the late leader of the noncoding control region of the human polyomavirus BK confers enhanced host cell permissivity.The A and B isoforms of the human progesterone receptor operate through distinct signaling pathways within target cellsLKB1 catalytic activity contributes to estrogen receptor alpha signalingMultiple promoters direct the tissue-specific expression of novel N-terminal variant human vitamin D receptor gene transcripts.Differential regulation of the transcriptional activity of the glucocorticoid receptor through site-specific phosphorylation.RAR-specific agonist/antagonists which dissociate transactivation and AP1 transrepression inhibit anchorage-independent cell proliferation.
P2860
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P2860
The contribution of the N- and C-terminal regions of steroid receptors to activation of transcription is both receptor and cell-specific.
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年学术文章
@wuu
1989年学术文章
@zh-cn
1989年学术文章
@zh-hans
1989年学术文章
@zh-my
1989年学术文章
@zh-sg
1989年學術文章
@yue
1989年學術文章
@zh
1989年學術文章
@zh-hant
name
The contribution of the N- and ...... th receptor and cell-specific.
@en
type
label
The contribution of the N- and ...... th receptor and cell-specific.
@en
prefLabel
The contribution of the N- and ...... th receptor and cell-specific.
@en
P2093
P2860
P356
P1476
The contribution of the N- and ...... th receptor and cell-specific.
@en
P2093
P2860
P304
P356
10.1093/NAR/17.7.2581
P577
1989-04-01T00:00:00Z