Sulfotransferases
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Subject Areas on Research
- Activation of nuclear receptor CAR ameliorates diabetes and fatty liver disease.
- Allelic heterogeneity of the carbohydrate sulfotransferase-6 gene in patients with macular corneal dystrophy.
- Brominated flame retardants in placental tissues: associations with infant sex and thyroid hormone endpoints.
- CHST1 and CHST2 sulfotransferase expression by vascular endothelial cells regulates shear-resistant leukocyte rolling via L-selectin.
- CHST1 and CHST2 sulfotransferases expressed by human vascular endothelial cells: cDNA cloning, expression, and chromosomal localization.
- CHST6 mutations in North American subjects with macular corneal dystrophy: a comprehensive molecular genetic review.
- Cerebroside sulfotransferase deficiency ameliorates L-selectin-dependent monocyte infiltration in the kidney after ureteral obstruction.
- Characterization of the human B cell RAG-associated gene, hBRAG, as a B cell receptor signal-enhancing glycoprotein dimer that associates with phosphorylated proteins in resting B cells.
- Disruption of thyroid hormone sulfotransferase activity by brominated flame retardant chemicals in the human choriocarcinoma placenta cell line, BeWo.
- Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms.
- Evolution of flux control in the glucosinolate pathway in Arabidopsis thaliana.
- Gpr126/Adgrg6 deletion in cartilage models idiopathic scoliosis and pectus excavatum in mice.
- Human skin and platelet minoxidil sulfotransferase activities: biochemical properties, correlations and contribution of thermolabile phenol sulfotransferase.
- Inhibition of thyroid hormone sulfotransferase activity by brominated flame retardants and halogenated phenolics.
- L-selectin ligands expressed by human leukocytes are HECA-452 antibody-defined carbohydrate epitopes preferentially displayed by P-selectin glycoprotein ligand-1.
- Localization of a site for interaction with hepatic male-specific proteins in two rat estrogen sulfotransferase genes.
- Macular corneal dystrophy types I and II are caused by distinct mutations in the CHST6 gene in Iceland.
- Mutations in corneal carbohydrate sulfotransferase 6 gene (CHST6) cause macular corneal dystrophy in Iceland.
- Neurohormonal signaling via a sulfotransferase antagonizes insulin-like signaling to regulate a Caenorhabditis elegans stress response.
- Novel mutations of the carbohydrate sulfotransferase-6 (CHST6) gene causing macular corneal dystrophy in India.
- Polymorphisms in the SULF1 gene are associated with early age of onset and survival of ovarian cancer.
- Sulfotransferases of two specificities function in the reconstitution of high endothelial cell ligands for L-selectin.
- Targeted downregulation of N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase significantly mitigates chondroitin sulfate proteoglycan-mediated inhibition.
- The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes.
- Visualizing mechanosensory endings of TrkC-expressing neurons in HS3ST-2-hPLAP mice.
- [Localization of matrix-associated elements in the 5'-region of the rat estrogen sulfotransferase gene].
- [PCR amplification and structural analysis of two paralogous rat estrogen sulfotransferase genes].
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Keywords of People
- Gunn, Michael Dee, Professor of Medicine, Immunology