Terminal renal failure in mice lacking transcription factor AP-2 beta
about
The AP-2 family of transcription factorsComparative expression profiling identifies an in vivo target gene signature with TFAP2B as a mediator of the survival function of PAX3/FKHRA heart-hand syndrome gene: Tfap2b plays a critical role in the development and remodeling of mouse ductus arteriosus and limb patterningGlomerulocystic kidney disease in mice with a targeted inactivation of Wwtr1Identification and embryonic expression of a new AP-2 transcription factor, AP-2 epsilonAP-2δ is a crucial transcriptional regulator of the posterior midbrain.The kidney transcriptome and proteome defined by transcriptomics and antibody-based profilingAberrant expressions of AP-2α splice variants in pancreatic cancerActivator protein-2 in carcinogenesis with a special reference to breast cancer--a mini review.Polycystic kidney diseases: from molecular discoveries to targeted therapeutic strategiesTranscriptional regulation during development of the ductus arteriosus.Dlx1 and Rgs5 in the ductus arteriosus: vessel-specific genes identified by transcriptional profiling of laser-capture microdissected endothelial and smooth muscle cells.Roles of AP-2 transcription factors in the regulation of cartilage and skeletal development.Comparative transcriptomic analysis identifies evolutionarily conserved gene products in the vertebrate renal distal convoluted tubule.Aberrant polycystin-1 expression results in modification of activator protein-1 activity, whereas Wnt signaling remains unaffected.Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 I27N mutant mice.CDK inhibitors R-roscovitine and S-CR8 effectively block renal and hepatic cystogenesis in an orthologous model of ADPKD.Microarray analysis of gene expression patterns in human proximal tubule cells over a short and long time course of cadmium exposure.Familial nonsyndromic patent ductus arteriosus caused by mutations in TFAP2B.AP-2ε Expression in Developing Retina: Contributing to the Molecular Diversity of Amacrine Cells.A mouse model for cystic biliary dysgenesis in autosomal recessive polycystic kidney disease (ARPKD)
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P2860
Terminal renal failure in mice lacking transcription factor AP-2 beta
description
2003 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի ապրիլին հրատարակված գիտական հոդված
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artículu científicu espublizáu en 2003
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im April 2003 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
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vedecký článok (publikovaný 2003/04/01)
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vědecký článek publikovaný v roce 2003
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wetenschappelijk artikel (gepubliceerd op 2003/04/01)
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наукова стаття, опублікована у квітні 2003
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مقالة علمية (نشرت في أبريل 2003)
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name
Terminal renal failure in mice lacking transcription factor AP-2 beta
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Terminal renal failure in mice lacking transcription factor AP-2 beta
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Terminal renal failure in mice lacking transcription factor AP-2 beta
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type
label
Terminal renal failure in mice lacking transcription factor AP-2 beta
@ast
Terminal renal failure in mice lacking transcription factor AP-2 beta
@en
Terminal renal failure in mice lacking transcription factor AP-2 beta
@nl
prefLabel
Terminal renal failure in mice lacking transcription factor AP-2 beta
@ast
Terminal renal failure in mice lacking transcription factor AP-2 beta
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Terminal renal failure in mice lacking transcription factor AP-2 beta
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P2093
P2860
P921
P1476
Terminal renal failure in mice lacking transcription factor AP-2 beta
@en
P2093
Dagmar Kunz
Hermann Gröne
Judith Dahmen
Markus Moser
Reinhard Buettner
Reinhart Kluge
Sandra Dahmen
P2860
P304
P356
10.1097/01.LAB.0000064703.92382.50
P577
2003-04-01T00:00:00Z
P6179
1022867145