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6 documents found
1: Title: Genetic Profiles Associated with Chemoresistance in Patient-Derived Xenograft Models of Ovarian Cancer.
Authors: Li, Lan Ying, et.al. .
Journal: Cancer research and treatment : official journal of Korean Cancer Association (Cancer Res Treat), 2018 .
Snippet: Differential expression of SAP25, HLA-DPA1, AKT3, and PIK3R5 genes and mutation of TMEM205 and POLR2A may have important functions in the progression of ovarian cancer chemoresistance.
Affiliation: Department of Obstetrics and Gynecology, Women's Cancer Center, Yonsei Cancer Center, Institute of Women's Life Medical Science, Yonsei University College of Medicine, Seoul, Korea. .
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2: Title: Sin3A recruits Tet1 to the PAH1 domain via a highly conserved Sin3-Interaction Domain.
Authors: Chandru, Aditya, et.al. .
Journal: Scientific reports (Sci Rep), Vol. 8 (1): 14689, 2018 .
Snippet: Using a combination of NMR spectroscopy and homology modelling we present a model of the PAH1/Tet1-SID complex, which binds in a Type-II orientation similar to Sap25.
Affiliation: Department of Molecular and Cell Biology, University of Leicester, Lancaster Road, Leicester, LE1 7RH, United Kingdom. Leicester Institute of Structural and Chemical Biology, Leicester, United Kingdom. Department of Molecular and Cell Biology, University of Leicester, Lancaster Road, Leicester, LE1 7RH, United Kingdom. smc57@le.ac.uk. .
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3: Title: A structured workflow for mapping human Sin3 histone deacetylase complex interactions using Halo-MudPIT AP-MS.
Authors: Banks, Charles A S, et.al. .
Journal: Molecular & cellular proteomics : MCP (Mol Cell Proteomics), 2018 .
Snippet: Intriguingly, we do not detect the Sin3 subunits SAP18 and SAP25 among the 128 high-confidence interactions identified, suggesting that these subunits may not be common to all versions of the Sin3 complex in human cells.
Affiliation: Stowers Institute for Medical Research, United States. Stowers Institute for Medical Research, United States of America. Stowers Institute for Medical Research. Proteomics, Stowers Institute for Medical Research, United States. Stowers Institute for Medical Research, United States of America mpw@stowers.org. .
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4: Title: Redox-dependent disulfide bond formation in SAP30L corepressor protein: Implications for structure and function.
Authors: Laitaoja, Mikko, et.al. .
Journal: Protein science : a publication of the Protein Society (Protein Sci), Vol. 25 (3): 572-86, 2016 .
Snippet: SAP30L, together with a highly homologous SAP30 as well as other SAP proteins (i.e., SAP25, SAP45, SAP130, and SAP180), is an essential component of the Sin3A corepressor complex, although its actual role has remained elusive.
Affiliation: Department of Chemistry, University of Eastern Finland, Joensuu, Finland. Institute of Biotechnology, University of Helsinki, Helsinki, Finland. BioMediTech, University of Tampere, Tampere, Finland. Center for Child Health Research and Tampere University Hospital, University of Tampere, Tampere, Finland. .
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5: Title: Conserved themes in target recognition by the PAH1 and PAH2 domains of the Sin3 transcriptional corepressor.
Authors: Sahu, Sarata C, et.al. .
Journal: Journal of molecular biology (J Mol Biol), Vol. 375 (5): 1444-56, 2008 .
Snippet: Here, we describe the solution structures of the mSin3A PAH1 domain in the apo form and when bound to SAP25, a component of the corepressor complex.
Affiliation: Department of Biochemistry, Molecular Biology, and Cell Biology, Northwestern University, Evanston, IL 60208-3500, USA. .
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6: Title: Identification and characterization of SAP25, a novel component of the mSin3 corepressor complex.
Authors: Shiio, Yuzuru, et.al. .
Journal: Molecular and cellular biology (Mol Cell Biol), Vol. 26 (4): 1386-97, 2006 .
Snippet: A fraction of SAP25 is located in promyelocytic leukemia protein (PML) nuclear bodies, and PML induces a striking nuclear accumulation of SAP25.
Affiliation: Division of Basic Sciences, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, Seattle, WA 98109-1024, USA. .
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