What is he best known for?
The fields of study he is best known for:
Jinrong Min mostly deals with Biochemistry, Histone, Tudor domain, Genetics and Computational biology.
The study of Histone is intertwined with the study of Chromatin in a number of ways.
His Tudor domain research includes elements of Protein arginine methyltransferase 5 and Messenger RNA.
The Genetics study combines topics in areas such as Plasma protein binding and Cell biology.
The study incorporates disciplines such as MRNA modification, Histone binding and Methyllysine in addition to Computational biology.
His Histone code research integrates issues from Histone H2A, Histone methylation and Histone H1.
His most cited work include:
- Structural basis for specific binding of Polycomb chromodomain to histone H3 methylated at Lys 27 (517 citations)
- Genome-wide Regulation of 5hmC, 5mC, and Gene Expression by Tet1 Hydroxylase in Mouse Embryonic Stem Cells (498 citations)
- Structure and function of WD40 domain proteins. (351 citations)
What are the main themes of his work throughout his whole career to date?
His primary scientific interests are in Cell biology, Biochemistry, Histone, Genetics and Computational biology.
He has included themes like Acetylation, Tudor domain, DNA-binding protein, Regulation of gene expression and Transcription in his Cell biology study.
His Histone methyltransferase, Methyltransferase, Histone H2A, Protein domain and DNA study are his primary interests in Biochemistry.
His work in Histone methyltransferase tackles topics such as Histone code which are related to areas like Histone methylation.
His work deals with themes such as Chromatin and Heterochromatin protein 1, which intersect with Histone.
His Computational biology research incorporates themes from Epigenetics and Protein family.
He most often published in these fields:
- Cell biology (62.64%)
- Biochemistry (53.58%)
- Histone (56.98%)
What were the highlights of his more recent work (between 2018-2021)?
- Cell biology (62.64%)
- Transcription (23.77%)
- Histone (56.98%)
In recent papers he was focusing on the following fields of study:
His scientific interests lie mostly in Cell biology, Transcription, Histone, DNA and Methyltransferase.
His Cell biology research is multidisciplinary, incorporating elements of Chromatin, Antagonist, Tudor domain and Binding selectivity.
His Transcription research includes themes of Protein subunit, Epigenetics, Acetylation and DNA repair.
As part of the same scientific family, he usually focuses on Histone, concentrating on Neural development and intersecting with Histone H3.
His DNA study integrates concerns from other disciplines, such as Binding domain, Computational biology and Gene.
Jinrong Min is interested in Plasma protein binding, which is a branch of Biochemistry.
Between 2018 and 2021, his most popular works were:
- Structural insights into SETD3-mediated histidine methylation on beta-actin. (15 citations)
- Structural insights into SETD3-mediated histidine methylation on beta-actin. (15 citations)
- Structure and function of eTudor domain containing TDRD proteins (13 citations)
In his most recent research, the most cited papers focused on:
The scientist’s investigation covers issues in Cell biology, Methylation, Methyltransferase, Binding selectivity and Structural biology.
His Cell biology research is multidisciplinary, relying on both Degron, Histone, Ubiquitin and Transcription.
He works on Histone which deals in particular with Histone H4.
The various areas that he examines in his Binding selectivity study include Biogenesis, Piwi-interacting RNA and Germ cell.
His Structural biology research incorporates elements of PRC2, Hox gene, Tudor domain, Chromatin and Histone methylation.
His Enhancer study introduces a deeper knowledge of Biochemistry.
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