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

Transglutaminase 4

TGP, prostate transglutaminase, prostate-specific transglutaminase, TGM4
Top mentioned proteins: CAN, Transglutaminase, HAD, ACID, V1a
Papers on TGP
Discovery of transcriptional targets regulated by nuclear receptors using a probabilistic graphical model.
Tong et al., Rockville, United States. In Toxicol Sci, Jan 2016
The Japanese Toxicogenomics Project (TGP), one of the most comprehensive efforts in the field of toxicogenomics, generated large-scale gene expression profiles on the effect of 131 compounds (in its first phase of study) at various doses, and different durations, and their combinations.
Hodgkin lymphoma as a novel presentation of familial DICER1 syndrome.
Troeger et al., Düsseldorf, Germany. In Eur J Pediatr, Dec 2015
Immunohistochemical staining of the Hodgkin and Reed-Sternberg cells revealed CD30, TGP, CD2, CD3, CD15, and IRF4 positivity and weekly positivity of PAX5.
A mutein of human basic fibroblast growth factor TGP-580 accelerates colonic ulcer healing by stimulating angiogenesis in the ulcer bed in rats.
Szabo et al., Tottori, Japan. In J Physiol Pharmacol, Oct 2015
Previously, we reported that TGP-580, a mutein of human basic fibroblast growth factor (bFGF), accelerated the healing of gastric and duodenal ulcers in rats.
Clinical, Histological, and Molecular Markers Associated With Allograft Loss in Transplant Glomerulopathy Patients.
Akalin et al., New York City, United States. In Transplantation, Sep 2015
BACKGROUND: We aimed to investigate the clinical, histopathological, and molecular factors associated with allograft loss in transplant glomerulopathy (TGP) patients.
Gene profiling and circulating tumor cells as biomarker to prognostic of patients with locoregional breast cancer.
Del Giglio et al., Santo André, Brazil. In Tumour Biol, Sep 2015
In this study, our objective was to perform tumor gene profiling (TGP) in combination with CTC characterization in women with nonmetastatic breast cancer.
Total glucosides of peony attenuates experimental autoimmune encephalomyelitis in C57BL/6 mice.
Chen et al., Guangzhou, China. In J Neuroimmunol, Aug 2015
Total glucosides of peony (TGP), an active compound extracted from the roots of Paeonia lactiflora Pall, has wide pharmacological effects on nervous system.
Towards simultaneous individual and tissue identification: A proof-of-principle study on parallel sequencing of STRs, amelogenin, and mRNAs with the Ion Torrent PGM.
Kayser et al., Rotterdam, Netherlands. In Forensic Sci Int Genet, Jul 2015
We demonstrated that 9 autosomal STRs commonly used for individual identification (CSF1PO, D16S539, D3S1358, D5S818, D7S820, D8S1179, TH01, TPOX, and vWA), the AMELX/AMELY system widely applied for sex identification, and 12 mRNA markers previously established for forensic tissue identification (ALAS2 and SPTB for peripheral blood, MMP10 and MMP11 for menstrual blood, HTN3 and STATH for saliva, PRM1 and TGM4 for semen, CYP2B7P1 and MUC4 for vaginal secretion, CCL27 and LCE1C for skin) together with two candidate reference mRNA markers (HPRT1 and SDHA) can all be successfully combined.
Transglutaminase 4 as a prostate autoantigen in male subfertility.
Kämpe et al., Stockholm, Sweden. In Sci Transl Med, Jul 2015
By screening human protein arrays with male and female patient sera and by selecting for gender-imbalanced autoantibody signals, we identified transglutaminase 4 (TGM4) as a male-specific autoantigen.
Effects of total glucosides of peony on AQP-5 and its mRNA expression in submandibular glands of NOD mice with Sjogren's syndrome.
Li et al., Hangzhou, China. In Eur Rev Med Pharmacol Sci, 2015
OBJECTIVE: The aim of this study was to observe the effects of total glucosides of peony (TGP) on pathological change, Aquaporin-5 (AQP-5) and its mRNA expression in submandibular glands of non-obese diabetic (NOD) mice with Sjogren's Syndrome, to investigate its regulation on secretion of salivary glands.
Protective Effects of Total Glucosides of Paeony on N-nitrosodiethylamine-induced Hepatocellular Carcinoma in Rats via Down-regulation of Regulatory B Cells.
Wei et al., Hefei, China. In Immunol Invest, 2014
Total glucoside of paeony (TGP), extracted from the root of Paeonia Lactiflora, has been known to show anti-inflammatory, anti-oxidative, hepato-protective and immuno-regulatory activities.
Gene expression in the chicken caecum in response to infections with non-typhoid Salmonella.
Kyrova et al., Brno, Czech Republic. In Vet Res, 2013
Additional highly inducible genes in the caecum following S. Enteritidis infection include immune responsive gene 1 (IRG1), serum amyloid A (SAA), extracellular fatty acid binding protein (ExFABP), serine protease inhibitor (SERPINB10), trappin 6-like (TRAP6), calprotectin (MRP126), mitochondrial ES1 protein homolog (ES1), interferon-induced protein with tetratricopeptide repeats 5 (IFIT5), avidin (AVD) and transglutaminase 4 (TGM4).
Mechanisms involved in the therapeutic effects of Paeonia lactiflora Pallas in rheumatoid arthritis.
Dai et al., Shanghai, China. In Int Immunopharmacol, 2012
A water/ethanol extract of Radix Paeoniae is known as total glycosides of paeony (TGP), of which paeoniflorin is the major active component.
Retinoic acid and androgen receptors combine to achieve tissue specific control of human prostatic transglutaminase expression: a novel regulatory network with broader significance.
Maitland et al., York, United Kingdom. In Nucleic Acids Res, 2012
Evidence that the retinoic acid receptor gamma plays a major role in the regulation of the hTGP gene and that presence of the androgen receptor, but not its transcriptional transactivation activity, is critical for hTGP transcription.
Vena cava and aortic smooth muscle cells express transglutaminases 1 and 4 in addition to transglutaminase 2.
Watts et al., East Lansing, United States. In Am J Physiol Heart Circ Physiol, 2012
These studies demonstrate that tranglutaminase 2 independent activity exists in the vasculature and that Tgm1 and tgm4 are expressed in vascular tissues
Analysis of laser-microdissected prostate cancer tissues reveals potential tumor markers.
Wernert et al., Bonn, Germany. In Int J Mol Med, 2011
CDKN2A, GATA3, CREBBP, ITGA2, NBL1 and TGM4 were down-regulated in the prostate carcinoma glands compared to the corresponding normal glands
Prostate transglutaminase: a unique transglutaminase and its role in prostate cancer.
Ablin et al., Cardiff, United Kingdom. In Biomark Med, 2011
Prostate transglutaminase-4, also known as TGM4 or transglutaminase P, belongs to the prostate transglutaminase protein family, but is almost uniquely distributed in the prostate gland.
Prostate transglutaminase (TGase-4) antagonizes the anti-tumour action of MDA-7/IL-24 in prostate cancer.
Jiang et al., Tucson, United States. In J Transl Med, 2010
The presence of TGase-4 has a biological impact on a prostate cancer cell's response to MDA-7.
The prostate transglutaminase, TGase-4, coordinates with the HGFL/MSP-RON system in stimulating the migration of prostate cancer cells.
Mason et al., Cardiff, United Kingdom. In Int J Oncol, 2010
TGase-4 expression is intrinsically linked to the activation of RON in prostate cancer cells and that this autoactivation of RON contributes to the increased cell motility in TGase-4 expressing cells.
Slender, older women appear to be more susceptible to nontuberculous mycobacterial lung disease.
Iseman et al., Denver, United States. In Gend Med, 2010
We further speculate that in some patients with features mindful of MPS (slender, scoliosis, pectus excavatum, or mitral valve prolapse), there may be anomalies of fibrillin, similar to MFS, that lead to the expression of the immunosuppressive cytokine TGP-beta further increasing their susceptibility to NTM.
Gene birth, death, and divergence: the different scenarios of reproduction-related gene evolution.
Monget et al., Tours, France. In Biol Reprod, 2009
By finding their "place of death" in genomes, it also demonstrates that ZP genes TGM4 and OVGP1 have been lost in certain species during vertebrate evolution.
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