What is he best known for?
The fields of study he is best known for:
His primary scientific interests are in Cell biology, Rab, Biochemistry, GTPase and Lipid bilayer fusion.
His Cell biology study combines topics in areas such as Vesicular transport protein and Cell membrane.
His biological study spans a wide range of topics, including EEA1, Signal transduction, Proto-oncogene tyrosine-protein kinase Src and Syntaxin.
His research in the fields of Proteome, Cytoplasm, Protein aggregation and Protein degradation overlaps with other disciplines such as HDAC6.
In his work, Protein structure, RHO protein GDP dissociation inhibitor and Effector is strongly intertwined with Small GTPase, which is a subfield of GTPase.
His work in Lipid bilayer fusion addresses subjects such as GTP', which are connected to disciplines such as Membrane docking.
His most cited work include:
- Functional organization of the yeast proteome by systematic analysis of protein complexes (4283 citations)
- A Novel Rab5 GDP/GTP Exchange Factor Complexed to Rabaptin-5 Links Nucleotide Exchange to Effector Recruitment and Function (503 citations)
- Oligomeric Complexes Link Rab5 Effectors with NSF and Drive Membrane Fusion via Interactions between EEA1 and Syntaxin 13 (445 citations)
What are the main themes of his work throughout his whole career to date?
His scientific interests lie mostly in Cell biology, Biochemistry, Actin, Molecular biology and Plasma protein binding.
In his study, which falls under the umbrella issue of Cell biology, Small GTPase is strongly linked to Endocytic cycle.
His works in Phosphatase, Amino acid, Protein structure, Isothermal titration calorimetry and Proteome are all subjects of inquiry into Biochemistry.
His Plasma protein binding research includes elements of Cooperativity and Pleckstrin homology domain.
His Rab research incorporates themes from Lipid bilayer fusion and GTP'.
His studies examine the connections between GTP' and genetics, as well as such issues in RHO protein GDP dissociation inhibitor, with regards to GTPase.
He most often published in these fields:
- Cell biology (38.96%)
- Biochemistry (35.06%)
- Actin (12.99%)
What were the highlights of his more recent work (between 2012-2018)?
- Cell biology (38.96%)
- Biochemistry (35.06%)
- Chromatin (9.09%)
In recent papers he was focusing on the following fields of study:
Vladimir Rybin mainly focuses on Cell biology, Biochemistry, Chromatin, Genetics and Phosphatase.
His Cell biology research incorporates elements of Exocytosis and Clathrin adaptor proteins.
His work on Amino acid as part of general Biochemistry research is frequently linked to Phosphoserine, thereby connecting diverse disciplines of science.
His research in Chromatin focuses on subjects like Histone, which are connected to DNA replication.
His Germ plasm study in the realm of Genetics connects with subjects such as Germline.
His work carried out in the field of Phosphatase brings together such families of science as Enzyme structure, RNA polymerase, Transcriptional regulation and Histidine.
Between 2012 and 2018, his most popular works were:
- A family of macrodomain proteins reverses cellular mono-ADP-ribosylation (197 citations)
- Structural basis of histone H2A–H2B recognition by the essential chaperone FACT (134 citations)
- Crystal structures of the phosphorylated BRI1 kinase domain and implications for brassinosteroid signal initiation. (105 citations)
In his most recent research, the most cited papers focused on:
Vladimir Rybin mainly investigates Cell biology, Chromatin, Plasma protein binding, Biochemistry and Histone.
As part of his studies on Cell biology, Vladimir Rybin often connects relevant areas like Genetics.
Vladimir Rybin has researched Genetics in several fields, including Condensin and Condensin complex.
His research integrates issues of Amino acid, DNA damage, Bromodomain, BRD4 and Nucleosome binding in his study of Plasma protein binding.
His study deals with a combination of Biochemistry and PARP1.
The various areas that Vladimir Rybin examines in his Histone study include Chaperone and DNA replication.
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