The histone methyltransferase, NSD2, enhances androgen receptor‐mediated transcription
Copyright policy )The histone methyltransferase, NSD2, enhances androgen receptor‐mediated transcription
MINT‐7103733: P53 (uniprotkb:P04637) physically interacts (MI:0915) with alpha AR (uniprotkb:P10275) by two hybrid (MI:0018)
- CHA University Korea (Republic of)
- CHA Advanced Research Institute Korea (Republic of)
- Yonsei University Korea (Republic of)
- University of Suwon Korea (Republic of)
- Yonsei University Health System Korea (Republic of)
Male, Histones/metabolism, Recombinant Proteins/chemistry, Ligands, Histone-Lysine N-Methyltransferase/genetics, Histone-Lysine N-Methyltransferase/metabolism*, Repressor Proteins/chemistry, Histones, Androgen/chemistry, Receptors, Recombinant Proteins/genetics, Recombinant Proteins/metabolism, Tumor, Prostate cancer, Prostatic Neoplasms/genetics, Prostatic Neoplasms/metabolism, Prostate-Specific Antigen/genetics, Androgen/metabolism*, Active Transport, Recombinant Proteins, Androgen receptor, Enhancer Elements, Genetic, Receptors, Androgen, Repressor Proteins/metabolism*, Transcription, Transcriptional Activation, 570, Chromatin Immunoprecipitation, Enhancer Elements, Transcription Factors/genetics, Active Transport, Cell Nucleus, 610, Cell Line, Genetic, Cell Line, Tumor, Homeodomain Proteins/metabolism, Humans, Transcription Factors/metabolism, Protein Interaction Domains and Motifs, Histone-Lysine N-Methyltransferase/chemistry, DNA Primers, Cell Nucleus, Homeodomain Proteins, DNA Primers/genetics, Repressor Proteins/genetics, Nuclear SET domain-containing 2, Base Sequence, Androgen/genetics, Prostatic Neoplasms, Histone-Lysine N-Methyltransferase, Prostate-Specific Antigen, Prostatic Neoplasms/etiology, Repressor Proteins, Prostate-Specific Antigen/metabolism, Histone methyltransferase, Homeodomain Proteins/genetics, Transcription Factors
Male, Histones/metabolism, Recombinant Proteins/chemistry, Ligands, Histone-Lysine N-Methyltransferase/genetics, Histone-Lysine N-Methyltransferase/metabolism*, Repressor Proteins/chemistry, Histones, Androgen/chemistry, Receptors, Recombinant Proteins/genetics, Recombinant Proteins/metabolism, Tumor, Prostate cancer, Prostatic Neoplasms/genetics, Prostatic Neoplasms/metabolism, Prostate-Specific Antigen/genetics, Androgen/metabolism*, Active Transport, Recombinant Proteins, Androgen receptor, Enhancer Elements, Genetic, Receptors, Androgen, Repressor Proteins/metabolism*, Transcription, Transcriptional Activation, 570, Chromatin Immunoprecipitation, Enhancer Elements, Transcription Factors/genetics, Active Transport, Cell Nucleus, 610, Cell Line, Genetic, Cell Line, Tumor, Homeodomain Proteins/metabolism, Humans, Transcription Factors/metabolism, Protein Interaction Domains and Motifs, Histone-Lysine N-Methyltransferase/chemistry, DNA Primers, Cell Nucleus, Homeodomain Proteins, DNA Primers/genetics, Repressor Proteins/genetics, Nuclear SET domain-containing 2, Base Sequence, Androgen/genetics, Prostatic Neoplasms, Histone-Lysine N-Methyltransferase, Prostate-Specific Antigen, Prostatic Neoplasms/etiology, Repressor Proteins, Prostate-Specific Antigen/metabolism, Histone methyltransferase, Homeodomain Proteins/genetics, Transcription Factors
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).55 popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.Top 10% influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).Top 10% impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.Top 10%
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