What is she best known for?
The fields of study she is best known for:
Genetics, Cell biology, Proteomics, Histone methyltransferase and Gene are her primary areas of study.
Her work deals with themes such as Protein subunit, Nuclear protein, Mad1, Molecular biology and Spindle pole body, which intersect with Cell biology.
Her research integrates issues of Chromatography, Tandem mass spectrometry, Mass spectrometry and Computational biology in her study of Proteomics.
The various areas that she examines in her Histone methyltransferase study include Histone H2A and Histone H3.
Her RBBP4, MYB, Promoter and Psychological repression study in the realm of Gene connects with subjects such as Plasmodium falciparum.
Her research in Chromatin focuses on subjects like Histone, which are connected to Methylation.
Her most cited work include:
- A proteomic view of the Plasmodium falciparum life cycle (1105 citations)
- Histone H3 methylation by Set2 directs deacetylation of coding regions by Rpd3S to suppress spurious intragenic transcription. (1060 citations)
- Vpx relieves inhibition of HIV-1 infection of macrophages mediated by the SAMHD1 protein (892 citations)
What are the main themes of her work throughout her whole career to date?
Her primary areas of study are Cell biology, Genetics, Molecular biology, Histone and Chromatin.
Her Cell biology research includes elements of Protein subunit, Biochemistry, Transcription factor, RNA polymerase II and Transcription.
Her research on Genetics frequently links to adjacent areas such as Computational biology.
Her Molecular biology research incorporates themes from Coactivator, Histone acetyltransferase and Signal transduction.
Laurence Florens usually deals with Histone and limits it to topics linked to Regulation of gene expression and Gene expression.
In the subject of general Proteomics, her work in Shotgun proteomics is often linked to Abundance, thereby combining diverse domains of study.
She most often published in these fields:
- Cell biology (42.90%)
- Genetics (22.44%)
- Molecular biology (18.15%)
What were the highlights of her more recent work (between 2018-2021)?
- Cell biology (42.90%)
- Histone (16.50%)
- Chromatin (14.19%)
In recent papers she was focusing on the following fields of study:
The scientist’s investigation covers issues in Cell biology, Histone, Chromatin, Computational biology and Biophysics.
The Cell biology study combines topics in areas such as RNA polymerase II, Gene expression and Ubiquitin ligase.
Laurence Florens combines subjects such as Acetylation, Protein subunit, Yeast, Function and Regulation of gene expression with her study of Histone.
Her study on Histone H3 and Establishment of sister chromatid cohesion is often connected to Fusion protein as part of broader study in Chromatin.
Her work carried out in the field of Computational biology brings together such families of science as Interaction network, Proteome, Acetyltransferase and Proteomics.
Laurence Florens mostly deals with Quantitative proteomics in her studies of Proteomics.
Between 2018 and 2021, her most popular works were:
- A Chemoproteomic Portrait of the Oncometabolite Fumarate (35 citations)
- Dynamic RNA acetylation revealed by quantitative cross-evolutionary mapping. (29 citations)
- Topological scoring of protein interaction networks. (19 citations)
In her most recent research, the most cited papers focused on:
Her primary scientific interests are in Cell biology, Computational biology, Histone, Chromatin and Protein subunit.
The concepts of her Cell biology study are interwoven with issues in Myeloid, Suppressor and SPOP.
Laurence Florens has included themes like Proteome, RNA, RNA acetylation, Ribosomal RNA and Conserved sequence in her Computational biology study.
Her studies in Histone integrate themes in fields like Cajal body, Small nuclear RNA, RNA polymerase II, Transcription and MED26.
Her research in Chromatin intersects with topics in SIN3A, Scaffold protein, Transcription factor and Function.
Her study looks at the relationship between Protein subunit and topics such as SAGA complex, which overlap with Actin, WAVE regulatory complex, Actin cytoskeleton and Actin cytoskeleton organization.
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