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Zinc finger protein 131

ZNF131, zinc finger protein 131
Top mentioned proteins: Smt3, SUZ12, GAPDH, Ubiquitin, importin
Papers on ZNF131
BTB-ZF Protein Znf131 Regulates Cell Growth of Developing and Mature T Cells.
Miyatake et al., Tokyo, Japan. In J Immunol, Sep 2015
The role of zinc finger Znf131 (also known as Zbtb35) in T cell lineage was elucidated through the production of mice with floxed allele to disrupt at different stages of development.
UHRF2, a ubiquitin E3 ligase, acts as a small ubiquitin-like modifier E3 ligase for zinc finger protein 131.
Chung et al., Seoul, South Korea. In J Biol Chem, 2013
UHRF2 effectively enhances zinc finger protein 131 (ZNF131) SUMOylation but does not enhance ZNF131 ubiquitination.
Zinc finger protein 131 inhibits estrogen signaling by suppressing estrogen receptor α homo-dimerization.
Chung et al., Seoul, South Korea. In Biochem Biophys Res Commun, 2013
The functional role of zinc finger protein 131 (ZNF131) is poorly understood, but it is assumed to possess transcriptional regulation activity due to the presence of a DNA binding motif.
Identification of optimal housekeeping genes for examination of gene expression in bovine corpus luteum.
Kotwica et al., Olsztyn, Poland. In Reprod Biol, 2012
The mRNA expression of thirteen housekeeping genes: C2orf29, SUZ12, TBP, TUBB2B, ZNF131, HPRT1, 18s RNA, GAPDH, SF3A1, SDHA, MRPL12, B2M and ACTB was measured by Real-time PCR.
Small ubiquitin-like modifier (SUMO) modification of zinc finger protein 131 potentiates its negative effect on estrogen signaling.
Chung et al., Seoul, South Korea. In J Biol Chem, 2012
SUMOylation is a novel regulator of ZNF131 action in estrogen signaling and breast cancer cell proliferation.
Kaiso regulates Znf131-mediated transcriptional activation.
Daniel et al., Hamilton, Canada. In Exp Cell Res, 2010
Znf131 is a transcriptional activator, a less common function of POZ-ZF proteins, that is negatively regulated by its heterodimerization partner Kaiso.
Evaluation of real-time PCR endogenous control genes for analysis of gene expression in bovine endometrium.
Littlejohn et al., Hamilton, New Zealand. In Bmc Mol Biol, 2008
RESULTS: The expression profiles of five commonly used endogenous control genes (GAPDH, PPIA, RPS9, RPS15A, and UXT) and 10 experimentally derived candidate endogenous control genes (SUZ12, C2ORF29, ZNF131, ACTR1A, HDAC1, SLC30A6, CNOT7, DNAJC17, BBS2, and RANBP10) were analysed across 44 samples to determine the most stably expressed gene.
High-throughput cell-based screening reveals a role for ZNF131 as a repressor of ERalpha signaling.
Ma et al., Beijing, China. In Bmc Genomics, 2007
Interaction between ZNF131 and ERalpha interrupts or prevents ERalpha binding to the estrogen response element. ZNF131 also suppresses the expression of TFF1.
Nuclear trafficking of the POZ-ZF protein Znf131.
Daniel et al., Hamilton, Canada. In Biochim Biophys Acta, 2007
The mechanism of Znf131 nuclear localization, is reported.
The murine BTB/POZ zinc finger gene Znf131: predominant expression in the developing central nervous system, in adult brain, testis, and thymus.
Burfeind et al., Göttingen, Germany. In Biochem Biophys Res Commun, 2002
Results suggest that Znf131/ZNF131 plays a role during development and organogenesis as well as in the function of the adult central nervous system.
Isolation and fine mapping of 16 novel human zinc finger-encoding cDNAs identify putative candidate genes for developmental and malignant disorders.
Vissing et al., Glostrup, Denmark. In Genomics, 1995
We have isolated and chromosomally fine-mapped 16 novel genes belonging to the human zinc finger Krüppel family (ZNF131-140, 142, 143, 148, 151, 154, and 155), including 1 of the GLI type (ZNF143) and 3 containing a KRAB (Krüppel-associated box) segment (ZNF133, 136, and 140).
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