What is he best known for?
The fields of study he is best known for:
Byron Kemper mainly focuses on Biochemistry, Molecular biology, Gene, Cytochrome P450 and DNA.
In his research, Plasmid, Terminator, Origin of replication and Expression vector is intimately related to Complementary DNA, which falls under the overarching field of Molecular biology.
Gene is a primary field of his research addressed under Genetics.
In general Genetics study, his work on Gene family and Biological evolution often relates to the realm of Roman numerals, thereby connecting several areas of interest.
His research investigates the connection with DNA and areas like Subfamily which intersect with concerns in Escherichia coli, Enzyme, Aryl Hydrocarbon Hydroxylases and Cloning.
Byron Kemper interconnects Cytoplasm and Transmembrane domain in the investigation of issues within Endoplasmic reticulum.
His most cited work include:
- The P450 gene superfamily: recommended nomenclature. (694 citations)
- Single-stranded DNA 'blue' T7 promoter plasmids: a versatile tandem promoter system for cloning and protein engineering. (640 citations)
- The P450 Superfamily: Updated Listing of All Genes and Recommended Nomenclature for the Chromosomal Loci (523 citations)
What are the main themes of his work throughout his whole career to date?
His primary scientific interests are in Biochemistry, Molecular biology, Cell biology, Cytochrome P450 and Gene.
His Molecular biology research is multidisciplinary, incorporating perspectives in Nucleic acid sequence, Complementary DNA, Enhancer, Transcription and Binding site.
As a part of the same scientific study, he usually deals with the Cell biology, concentrating on Nuclear receptor and frequently concerns with Histone and Transactivation.
His work in Cytochrome P450 tackles topics such as Protein–protein interaction which are related to areas like Bimolecular fluorescence complementation.
He has included themes like Plasma protein binding and DNA in his Gene study.
His work in the fields of Genetics, such as Exon, overlaps with other areas such as Arabic numerals.
He most often published in these fields:
- Biochemistry (44.76%)
- Molecular biology (38.10%)
- Cell biology (24.76%)
What were the highlights of his more recent work (between 2014-2021)?
- Small heterodimer partner (10.48%)
- Nuclear receptor (15.24%)
- Cell biology (24.76%)
In recent papers he was focusing on the following fields of study:
Byron Kemper spends much of his time researching Small heterodimer partner, Nuclear receptor, Cell biology, FGF19 and Farnesoid X receptor.
His Small heterodimer partner research incorporates elements of Cancer research and Lipogenesis.
He combines subjects such as DNA methylation, Downregulation and upregulation, Sirtuin 1, Cistrome and Histone with his study of Cell biology.
His Histone research is under the purview of Biochemistry.
He brings together Biochemistry and SUMO protein to produce work in his papers.
His Transcription factor research is multidisciplinary, incorporating elements of Molecular biology, Chromatin immunoprecipitation and Sterol.
Between 2014 and 2021, his most popular works were:
- Obesity and aging diminish sirtuin 1 (SIRT1)-mediated deacetylation of SIRT3, leading to hyperacetylation and decreased activity and stability of SIRT3. (49 citations)
- A postprandial FGF19‐SHP‐LSD1 regulatory axis mediates epigenetic repression of hepatic autophagy (30 citations)
- FXR Primes the Liver for Intestinal FGF15 Signaling by Transient Induction of β-Klotho (29 citations)
In his most recent research, the most cited papers focused on:
Byron Kemper mostly deals with Histone, Small heterodimer partner, Nuclear receptor, Cell biology and Cancer research.
His Histone study contributes to a more complete understanding of Biochemistry.
His Nuclear receptor research focuses on Cholesterol 7 alpha-hydroxylase and how it relates to FGF19.
The concepts of his Cell biology study are interwoven with issues in Beta oxidation, SIRT3, Sirtuin 1 and Acetylation.
His studies in Cancer research integrate themes in fields like Epigenetics, Demethylase, TFEB, Transcriptional regulation and Epigenetic Repression.
His Farnesoid X receptor study incorporates themes from Receptor, Internal medicine, Signal transduction and FGF15.
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