What is he best known for?
The fields of study he is best known for:
His primary areas of study are Cell biology, Biochemistry, Phosphorylation, Molecular biology and Mitogen-activated protein kinase kinase.
His Cell biology study combines topics from a wide range of disciplines, such as Tubulin deacetylase activity, Acetylation and HDAC6.
His work on Trypsin and Protease as part of general Biochemistry study is frequently linked to TMPRSS6 and Thrombin, bridging the gap between disciplines.
The various areas that Daniel Hess examines in his Phosphorylation study include Proteomics, Kinase and Arabidopsis, Mutant.
His Molecular biology research is multidisciplinary, relying on both MRNA destabilization, Messenger RNA, Untranslated region and DHX36.
His study in Mitogen-activated protein kinase kinase is interdisciplinary in nature, drawing from both Akt/PKB signaling pathway, MAP2K7, Cyclin-dependent kinase 2 and MAP kinase kinase kinase.
His most cited work include:
- HDAC-6 interacts with and deacetylates tubulin and microtubules in vivo (566 citations)
- Histone Methylation by PRC2 Is Inhibited by Active Chromatin Marks (465 citations)
- Identification of a PKB/Akt Hydrophobic Motif Ser-473 Kinase as DNA-dependent Protein Kinase (410 citations)
What are the main themes of his work throughout his whole career to date?
Daniel Hess mostly deals with Cell biology, Biochemistry, Phosphorylation, Molecular biology and Kinase.
His Cell biology research focuses on Mitogen-activated protein kinase kinase in particular.
The Mitogen-activated protein kinase kinase study combines topics in areas such as Akt/PKB signaling pathway, MAP kinase kinase kinase and Kinase activity.
His study focuses on the intersection of MAP kinase kinase kinase and fields such as Cyclin-dependent kinase 9 with connections in the field of MAP2K7.
His Phosphorylation study incorporates themes from Cancer research, Signal transduction and Mutant.
His Molecular biology study which covers Histone methyltransferase that intersects with Chromatin remodeling and Histone code.
He most often published in these fields:
- Cell biology (42.59%)
- Biochemistry (35.19%)
- Phosphorylation (23.15%)
What were the highlights of his more recent work (between 2017-2021)?
- Cell biology (42.59%)
- Transcription factor (10.19%)
- DNA damage (8.33%)
In recent papers he was focusing on the following fields of study:
His primary areas of investigation include Cell biology, Transcription factor, DNA damage, Gene and DNA.
Particularly relevant to Phosphorylation is his body of work in Cell biology.
He combines subjects such as Cyclin-dependent kinase, MYB and Kinase with his study of Phosphorylation.
Daniel Hess has researched Transcription factor in several fields, including Cytoplasm, GTPase, Lysosome, CRISPR and Signal transduction.
His research investigates the connection between DNA damage and topics such as Homologous recombination that intersect with problems in Interactome, DNA repair, Nuclease, Rad50 and Cell cycle.
His work deals with themes such as Chaperone and Genetic screen, which intersect with DNA.
Between 2017 and 2021, his most popular works were:
- Zc3h13/Flacc is required for adenosine methylation by bridging the mRNA-binding factor Rbm15/Spenito to the m6A machinery component Wtap/Fl(2)d. (146 citations)
- Acetylation of intrinsically disordered regions regulates phase separation. (69 citations)
- Activity-dependent neuroprotective protein recruits HP1 and CHD4 to control lineage-specifying genes. (61 citations)
In his most recent research, the most cited papers focused on:
His scientific interests lie mostly in Cell biology, Transcription factor, Organelle, RNA Helicase A and Stress granule.
His Cell biology study focuses on Phosphorylation in particular.
His Transcription factor study integrates concerns from other disciplines, such as GTPase, Lysosome, CRISPR and PI3K/AKT/mTOR pathway, Signal transduction.
His Organelle research is multidisciplinary, incorporating elements of In vitro, Acetylation, Biophysics, Lysine and HDAC6.
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