CREM gene: use of alternative DNA-binding domains generates multiple antagonists of cAMP-induced transcription.
about
The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factorsHuman Cdc34 and Rad6B ubiquitin-conjugating enzymes target repressors of cyclic AMP-induced transcription for proteolysisCREB-H: a novel mammalian transcription factor belonging to the CREB/ATF family and functioning via the box-B element with a liver-specific expressionIg/EBP (C/EBP gamma) is a transdominant negative inhibitor of C/EBP family transcriptional activatorsIndividual CREB-target genes dictate usage of distinct cAMP-responsive coactivation mechanismsAn alternatively spliced mRNA from the AP-2 gene encodes a negative regulator of transcriptional activation by AP-2DNA binding and transcriptional repression by DAX-1 blocks steroidogenesisCyclin-dependent kinase 3-mediated activating transcription factor 1 phosphorylation enhances cell transformationAlternative splicing of Pax-8 gene transcripts is developmentally regulated and generates isoforms with different transactivation propertiesKv8.1, a new neuronal potassium channel subunit with specific inhibitory properties towards Shab and Shaw channelsLuman, a new member of the CREB/ATF family, binds to herpes simplex virus VP16-associated host cellular factorTranscriptional repression by a novel member of the bZIP family of transcription factorsA family of LIM-only transcriptional coactivators: tissue-specific expression and selective activation of CREB and CREMDREAM-alphaCREM interaction via leucine-charged domains derepresses downstream regulatory element-dependent transcriptionRole of tissue-specific transcription factor LFB3 in a cyclic AMP-responsive enhancer of the urokinase-type plasminogen activator gene in LLC-PK1 cellsCa2+-dependent block of CREB-CBP transcription by repressor DREAM.Dual roles of RNA helicase A in CREB-dependent transcriptionMolecular cloning of human CREB-2: an ATF/CREB transcription factor that can negatively regulate transcription from the cAMP response elementThyroid-stimulating hormone (TSH)-directed induction of the CREM gene in the thyroid gland participates in the long-term desensitization of the TSH receptorAn isoform of transcription factor CREM expressed during spermatogenesis lacks the phosphorylation domain and represses cAMP-induced transcriptionMore potent transcriptional activators or a transdominant inhibitor of the HNF1 homeoprotein family are generated by alternative RNA processingMultiple and cooperative phosphorylation events regulate the CREM activator functionThe Sendai virus P gene expresses both an essential protein and an inhibitor of RNA synthesis by shuffling modules via mRNA editingH1TF2A, the large subunit of a heterodimeric, glutamine-rich CCAAT-binding transcription factor involved in histone H1 cell cycle regulationAsynchronous oscillations of two zebrafish CLOCK partners reveal differential clock control and functionGlobal gene expression profiling of cells overexpressing SMC3.Novel insights into the downstream pathways and targets controlled by transcription factors CREM in the testisACR1, a yeast ATF/CREB repressor.The cyclic AMP response element modulator family regulates the insulin gene transcription by interacting with transcription factor IIDSAF-2, a splice variant of SAF-1, acts as a negative regulator of transcriptionHuman nuclear transcription factor gene CREM: genomic organization, mutation screening, and association analysis in panic disorderTranscription repression of human hepatitis B virus genes by negative regulatory element-binding protein/SONAttenuated function of a variant form of the helix-loop-helix protein, Id-3, generated by an alternative splicing mechanismActivating transcription factor 1 and cyclic AMP response element modulator can modulate the activity of the immunoglobulin kappa 3' enhancerDifferential activation of viral and cellular promoters by human T-cell lymphotropic virus-1 tax and cAMP-responsive element modulator isoformsAs the proliferation promoter noradrenaline induces expression of ICER (induced cAMP early repressor) in proliferative brown adipocytes, ICER may not be a universal tumour suppressorIdentification and characterization of a tissue-specific coactivator, GT198, that interacts with the DNA-binding domains of nuclear receptors.Breakpoint analysis of transcriptional and genomic profiles uncovers novel gene fusions spanning multiple human cancer typesStress-induced stimulation of early growth response gene-1 by p38/stress-activated protein kinase 2 is mediated by a cAMP-responsive promoter element in a MAPKAP kinase 2-independent mannerTranscription factor CREM coordinates the timing of hepatocyte proliferation in the regenerating liver.
P2860
Q21092455-81947489-1672-4529-9A69-DCFB22263688Q22010136-04C3A71A-E1D1-407B-AB4B-1599EAEB2CC1Q24291231-84B6DCCF-C49D-42E6-B54C-BF784267DCF3Q24304434-C23D6010-508D-45BC-A643-D4043F789C50Q24306838-8EAC00C9-4E81-43F1-A321-5BD28C43AA40Q24308857-1B4DBAB0-4C15-4391-A1EC-50191B94EC76Q24310202-55769239-9536-4F5E-BB01-00F2FF0AFC44Q24312766-9DB9FAE7-847D-43DF-B8AF-DB246E33F200Q24318806-FF8FB40A-BD69-4BA9-8E21-C2E7D7F69D8BQ24324152-9E9B9959-3BFA-4136-963E-E32678DFD49CQ24336173-E51407C3-0220-4684-ADD2-A7D8991931ACQ24337465-1590522B-8F1D-4C9F-AEF7-10CBBB3352ADQ24515126-5ECC5E74-057D-4A71-AAA9-4844AD0F728BQ24515142-958497DB-3F8A-4148-95A3-37077C5CBB0EQ24522603-58DCCD0B-8255-45D7-B33C-6B7417D08E0FQ24534305-07BD981B-8053-4EEE-97BE-4742E4589EB6Q24550936-3A20792D-52FE-44ED-9829-065215E62E79Q24561653-4D3F5911-C7F6-4CD3-AED3-05CBA7F408BFQ24563137-A34BC9EE-4FDF-45AF-B601-85B99086F83AQ24564217-13BF3CD7-401D-4BB8-9029-0E61AE456B67Q24564329-4B6DD60F-8E13-4BCA-ACAC-3C28ADA1C9B9Q24564372-F505E9E2-3844-4DD8-A216-28D81C06A5F6Q24564716-FB8D7F9E-7076-4439-AA18-22DEB30574E1Q24607656-6B3F5F99-4B54-47AF-ABA2-2B357020C7AFQ24679485-FFC0554C-27FF-4970-8B45-D5C2A130E190Q24814467-CD414B92-188F-478A-9D74-BF8DA095DBC1Q27308857-9D21FDA5-CAE9-4BBC-A9D6-EFE237378403Q27932635-F1A6A716-3357-4F43-8A98-6A963CE2FF86Q28139930-119F08EA-F6C9-4754-A64F-F87B74BD0744Q28203442-A21BAC59-DE32-4329-92C2-48BD31210A2CQ28205793-863CB1FD-D513-462E-BB9D-CC37510C42B6Q28212953-CC4351DE-C790-4142-96A7-2233BC0DF1B7Q28289616-071873CC-4DDF-4192-AD64-97AB2922B3AAQ28300492-5E101B8C-2789-418A-9ACF-4488CA24F869Q28302012-D731F7D5-DB75-41F2-8F7E-5444E3B3250FQ28348127-CADF0ABD-D12A-4DC7-A26C-9866727190D4Q28366099-A54519B0-0371-4771-BBB0-A0EC2AF92A11Q28486949-9FCBCDCD-E076-4EC4-B76C-24116CCA5767Q28611349-59B56623-E6A7-4F39-A5BB-62C37E9C8B4CQ30448764-9CA2A0B7-AD34-46FC-AC0A-AACB2CAA1C73
P2860
CREM gene: use of alternative DNA-binding domains generates multiple antagonists of cAMP-induced transcription.
description
1991 nî lūn-bûn
@nan
1991 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
CREM gene: use of alternative ...... of cAMP-induced transcription.
@ast
CREM gene: use of alternative ...... of cAMP-induced transcription.
@en
CREM gene: use of alternative ...... of cAMP-induced transcription.
@nl
type
label
CREM gene: use of alternative ...... of cAMP-induced transcription.
@ast
CREM gene: use of alternative ...... of cAMP-induced transcription.
@en
CREM gene: use of alternative ...... of cAMP-induced transcription.
@nl
prefLabel
CREM gene: use of alternative ...... of cAMP-induced transcription.
@ast
CREM gene: use of alternative ...... of cAMP-induced transcription.
@en
CREM gene: use of alternative ...... of cAMP-induced transcription.
@nl
P1433
P1476
CREM gene: use of alternative ...... of cAMP-induced transcription.
@en
P2093
Borrelli E
Foulkes NS
P304
P356
10.1016/0092-8674(91)90503-Q
P407
P577
1991-02-01T00:00:00Z