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Journal of Molecular Endocrinology

Print ISSN
0952-5041
Electronic ISSN
1479-6813
Impact factor
3.628
Publisher
highwire
URL
http://jme.endocrinology-journals.org
Usage rank
2097
Article count
1755
Free count
1011
Free percentage
0.576068
PDFs via platforms
CSA, Proquest, Ama, Aacr, Endocrine, Csh, Highwire from 1988, Aaas, Rupress, and Nephrology

  1. Editorial.

    Journal of Molecular Endocrinology 40(1):1 (2008) PMID 18096991

    We had previously achieved, because of the way it is calculated. We have also increased the journal's online frequency to monthly, ensuring that the journal is poised ready for the rapid publication of greater numbers of higher quality papers. With this legacy, I am pleased to hand over the reins of...
  2. EPAC2-mediated calreticulin regulates LIF and COX2 expression in human endometrial glandular cells.

    Journal of Molecular Endocrinology 54(1):17 (2015) PMID 25378661

    We have previously reported that exchange protein directly activated by cAMP 2 (EPAC2, RAPGEF4), another cAMP mediator, is involved in the differentiation of endometrial stromal cells through the regulation of the expression of calreticulin (CALR). To address whether EPAC2-CALR signaling is involved...
  3. Molecular evolution of GPCRs: Melanocortin/melanocortin receptors.

    Journal of Molecular Endocrinology 52(3):T29 (2014) PMID 24868105

    The melanocortin receptors (MCRs) are a family of G protein-coupled receptors that are activated by melanocortin ligands derived from the proprotein, proopiomelanocortin (POMC). During the radiation of the gnathostomes, the five receptors have become functionally segregated (i.e. melanocortin 1 rece...
  4. Essential roles of 11β-HSD1 in regulating brown adipocyte function.

    Journal of Molecular Endocrinology 50(1):103 (2013) PMID 23197361

    We investigated the roles of 11β-HSD1 in regulating BAT function. We observed a significant increase in the expression of BAT-specific genes, including UCP1, Cidea, Cox7a1, and Cox8b, in BVT.2733 (a selective inhibitor of 11β-HSD1)-treated and 11β-HSD1-deficient primary brown adipocytes of mice. By...
  5. Role of sex hormones in modulation of brown adipose tissue activity.

    Journal of Molecular Endocrinology 49(1):R1 (2012) PMID 22460126

    The recent demonstration that metabolically active brown adipose tissue (BAT) is present with a high prevalence in humans undoubtedly represents one of the major advancements in the field of metabolic research in the last few years. The increasing interest in BAT is justified by preclinical observat...
  6. GATA transcription factors regulate LHβ gene expression.

    Journal of Molecular Endocrinology 47(1):45 (2011) PMID 21571865

    We demonstrate expression of both GATA2 and GATA4 in primary mouse gonadotropes and the gonadotrope cell line, LβT2. Based on the transient transfection in fibroblast cells, GATA factors increase LH β-subunit gene (LHβ) promoter activity alone and in synergy with the orphan nuclear receptors steroid...
  7. Dietary restriction of mice on a high-fat diet induces substrate efficiency and improves metabolic health.

    Journal of Molecular Endocrinology 47(1):81 (2011) PMID 21830320

    We report that HF-DR improves metabolic health of mice compared with mice receiving the same diet on an ad libitum basis (HF-AL). Already after five weeks of restriction, the serum levels of cholesterol and leptin were significantly decreased in HF-DR mice, whereas their glucose sensitivity and seru...
  8. Crystal structure of the TSH receptor (TSHR) bound to a blocking-type TSHR autoantibody.

    Journal of Molecular Endocrinology 46(2):81 (2011) PMID 21247981

    A complex of the TSH receptor extracellular domain (amino acids 22-260; TSHR260) bound to a blocking-type human monoclonal autoantibody (K1-70) was purified, crystallised and the structure solved at 1.9 Å resolution. K1-70 Fab binds to the concave surface of the TSHR leucine-rich domain (LRD) formin...
  9. Role of reduced expression of SMAD4 in papillary thyroid carcinoma.

    Journal of Molecular Endocrinology 45(4):229 (2010) PMID 20685810

    We examined the TGFβ response in two cell lines, TPC-1 and BCPAP. Our data demonstrated for the first time that these cells showed a strong reduction in the level of SMAD4 protein, which was responsible for an alteration of TGFβ signaling and for some of the TGFβ-mediated biological effects. The ove...
  10. Imaging of persistent cAMP signaling by internalized G protein-coupled receptors.

    Journal of Molecular Endocrinology 45(1):1 (2010) PMID 20378719

    We review these recent data and explain the optical methods used for such studies. Based on these findings, we propose a revision of the current model of the GPCR-cAMP signaling pathway to accommodate receptor signaling at endosomes....