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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.

Estrogen receptor 2b

esr2b, zfERbeta1, zfERbeta, ERbeta-A
Top mentioned proteins: esr2a, aromatase, Estrogen Receptor, CAN, ERbeta
Papers on esr2b
Estrogen receptor 2b deficiency impairs the antiviral response of zebrafish.
Mulero et al., Murcia, Spain. In Dev Comp Immunol, Nov 2015
In this study, we used a homozygous line carrying an insertion of 8 amino acids in the ligand-binding domain of the estrogen receptor 2b gene (esr2b) to further understand the role of estrogen signaling on innate immunity.
Differential expression patterns of three aromatase genes and of four estrogen receptors genes in the testes of trout (Oncorhynchus mykiss).
Le Gac et al., France. In Mol Reprod Dev, Sep 2015
We evaluated the expression patterns and regulation of three aromatase isoforms (cyp19a, cyp19b-I, and cyp19b-II) and four estrogen receptors (esr1a, esr1b, esr2a, and esr2b) by quantitative reverse-transcriptase PCR during testicular maturation and in isolated germ cell populations.
Transcript variability and physiological correlates in the fathead minnow ovary: Implications for sample size, and experimental power.
Martyniuk et al., Saint John, Canada. In Comp Biochem Physiol B Biochem Mol Biol, Sep 2015
Estrogen receptor 2b (esr2b) and 5α-reductase a3 (srd5a3) showed high variability in the ovary (CV>1.0)
Gene expression profiling of key genes in hypothalamus-pituitary-gonad axis of rare minnow Gobiocypris rarus in response to EE2.
Wang et al., China. In Gene, 2014
Adult G. rarus was exposed to EE2 at 1, 5, 25 and 125 ng/L for 3 and 6 days and the expression of brain cyp19a1b, fshβ and lhβ, estrogen receptors (esr1, esr2a, and esr2b) and gonadal fshr, lhr and cyp19a1a were assessed.
Developmental toxicity of endocrine disruptors in early life stages of zebrafish, a genetic and embryogenesis study.
Coimbra et al., Vila Real, Portugal. In Neurotoxicol Teratol, 2014
In parallel, the expression patterns of hormone receptors (esr1, esr2a, esr2b and ar) and apoptotic pathways related genes (p53 and c-jun) were determined using quantitative real-time PCR.
Transcriptomics profiling and steroid production in mummichog (Fundulus heteroclitus) testes after treatment with 5α-dihydrotestosterone.
Martyniuk et al., Saint John, Canada. In Gen Comp Endocrinol, 2014
While the gene expression levels of actb, efla, rps12, rps18, star, and hsd11b3 remained unchanged, esr2a (esrba), esr2b (esrbb) and cyp11a1 were significantly lower in incubated tissue compared to flash frozen tissue.
Sexually dimorphic transcription of estrogen receptors in cod gonads throughout a reproductive cycle.
Fernandes et al., Bodø, Norway. In J Mol Endocrinol, 2014
Three nuclear ER partial cDNA sequences (esr1, esr2a, and esr2b) were cloned and all esr transcripts were detected mainly in liver and gonads of fish of both sexes.
Progesterone increases ex vivo testosterone production and decreases the expression of progestin receptors and steroidogenic enzymes in the fathead minnow (Pimephales promelas) ovary.
Martyniuk et al., Saint John, Canada. In Gen Comp Endocrinol, 2014
Androgen receptor (ar) and estrogen receptor 2a (esr2a) mRNA were significantly reduced at 6h with P4 treatment, but there was no change in esr2b mRNA at either time point.
Morpholino-mediated knockdown of ERα, ERβa, and ERβb mRNAs in zebrafish (Danio rerio) embryos reveals differential regulation of estrogen-inducible genes.
Callard et al., Boston, United States. In Endocrinology, 2013
Each MO knocked down its respective normal transcript and increased production of variants with a retained intron III (esr1 MO) or a deleted or mis-spliced exon III (esr2a and esr2b MOs).
Molecular characterization of five steroid receptors from pengze crucian carp and their expression profiles of juveniles in response to 17α-ethinylestradiol and 17α-methyltestosterone.
Wang et al., China. In Gen Comp Endocrinol, 2013
The full-length cDNAs of five steroid receptors (esr1, er alpha2, esr2a, esr2b, ar) and partial cDNA of vtg B were isolated.
Perfluorooctane sulfonate (PFOS) affects hormone receptor activity, steroidogenesis, and expression of endocrine-related genes in vitro and in vivo.
Wang et al., Nanjing, China. In Environ Toxicol Chem, 2013
In addition, PFOS increased early thyroid development gene (hhex and pax8) expression in a concentration-dependent manner, decreased steroidogenic enzyme gene (CYP17, CYP19a, CYP19b) expression, and changed the expression pattern of estrogen receptor production genes (esr1, esr2b) after 500 µg/L PFOS treatment in zebrafish embryos.
The effects of the urea-based herbicide linuron on reproductive endpoints in the fathead minnow (Pimephales promelas).
Martyniuk et al., Canada. In Comp Biochem Physiol C Toxicol Pharmacol, 2013
p450scc, cyp19a, star, tspo, hsd17b and hsd11b) and estrogen-mediated responses (esr1, esr2b, esr2a).
Molecular characterization of estrogen receptor genes in loach Paramisgurnus dabryanus and their expression upon 17α-ethinylestradiol exposure in juveniles.
Wang et al., China. In Gen Comp Endocrinol, 2012
The full-length cDNAs for estrogen receptor 1 (esr1), esr2a and esr2b were isolated and characterized from the loach (Paramisgurnus dabryanus, Cobitidae, cypriniformes).
Identification and transcriptional modulation of the largemouth bass, Micropterus salmoides, vitellogenin receptor during oocyte development by insulin and sex steroids.
Sabo-Attwood et al., Columbia, United States. In Biol Reprod, 2012
Coexposure with insulin and E(2) or of insulin and 11-KT increased ovarian esr2b and ar mRNA levels, respectively, which suggest a role for these nuclear receptors in insulin-mediated signaling pathways.
Selective activation of zebrafish estrogen receptor subtypes by chemicals by using stable reporter gene assay developed in a zebrafish liver cell line.
Aït-Aïssa et al., Verneuil-sur-Seine, France. In Toxicol Sci, 2012
Report stable reporter gene assays based on stable expression of subtypes of zebrafish ER (zfERalpha, zfERbeta1, and zfERbeta2) coupled to estrogen response element-driven luciferase in a zebrafish liver cell line.
Efficacy of pharmacological estrogen receptor antagonists in blocking activation of zebrafish estrogen receptors.
Mayer et al., United States. In Gen Comp Endocrinol, 2011
Full length cDNA of zebrafish estrogen receptor 1 (esr1), estrogen receptor 2a (esr2a) and estrogen receptor 2b (esr2b) were cloned into expression vectors and transfected into cells that do not endogenously express any estrogen receptor along with an estrogen responsive luciferase vector.
Temperature and photoperiod affect the endocrine disruption effects of ethinylestradiol, nonylphenol and their binary mixture in zebrafish (Danio rerio).
Fu et al., Hangzhou, China. In Comp Biochem Physiol C Toxicol Pharmacol, 2010
Data show that temperature and photoperiod significantly influence the transcription of the estrogen-responsive genes, Vtg1, Vtg2, ER alpha and ER beta after a 21-day exposure to endocrine-disrupting chemicals.
Levels of 17beta-estradiol receptors expressed in embryonic and adult zebrafish following in vivo treatment of natural or synthetic ligands.
Andersson Lendahl et al., Stockholm, Sweden. In Plos One, 2009
during embryogenesis two of the three 17beta-estradiol receptor genes, esr1 and esr2b are expressed, and in presence of ligand the mRNA levels of these two genes increase
The phytoestrogen genistein affects zebrafish development through two different pathways.
Laudet et al., Lyon, France. In Plos One, 2008
genistein binds and activates the three zebrafish estrogen receptors ERalpha, ERbeta-A and ERbeta-B and induces apoptosis in an ER-independent manner
Analysis of the estrogen regulation of the zebrafish estrogen receptor (ER) reveals distinct effects of ERalpha, ERbeta1 and ERbeta2.
Pakdel et al., Rennes, France. In J Mol Endocrinol, 2004
Data show that the hepatic expression of estrogen receptor alpha, beta1 and beta2 genes responds differently to estradiol.
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