What is he best known for?
The fields of study he is best known for:
- Gene
- Amino acid
- Signal transduction
Cell biology, SH2 domain, SH3 domain, Biochemistry and Proto-oncogene tyrosine-protein kinase Src are his primary areas of study.
Gerald D. Gish has included themes like Transcription and Nedd4 Ubiquitin Protein Ligases in his Cell biology study.
The subject of his SH2 domain research is within the realm of Receptor tyrosine kinase.
He interconnects Interaction network, Structural biology, GRB2 and Protein domain in the investigation of issues within SH3 domain.
His research in Proto-oncogene tyrosine-protein kinase Src intersects with topics in Discoidin domain-containing receptor 2, Discoidin domain, Peptide sequence, Protein structure and Phosphopeptide.
The various areas that Gerald D. Gish examines in his Peptide sequence study include Phosphotyrosine-binding domain, FYN, Phosphotyrosine binding and Adapter molecule crk.
His most cited work include:
- SH2 domains recognize specific phosphopeptide sequences (2506 citations)
- SH2 and SH3 domains: From structure to function (831 citations)
- The Discoidin Domain Receptor Tyrosine Kinases Are Activated by Collagen (795 citations)
What are the main themes of his work throughout his whole career to date?
Gerald D. Gish mainly investigates Cell biology, SH2 domain, Biochemistry, Proto-oncogene tyrosine-protein kinase Src and SH3 domain.
Gerald D. Gish regularly ties together related areas like Protein domain in his Cell biology studies.
His SH2 domain research is multidisciplinary, incorporating elements of ABL, Adapter molecule crk, Kinase activity, GRB2 and Phosphopeptide.
Within one scientific family, Gerald D. Gish focuses on topics pertaining to Biophysics under Biochemistry, and may sometimes address concerns connected to Proto-Oncogene Proteins c-abl.
His Proto-oncogene tyrosine-protein kinase Src study combines topics in areas such as Peptide sequence, Receptor tyrosine kinase, Signal transducing adaptor protein and Homology.
Gerald D. Gish has researched Phosphotyrosine-binding domain in several fields, including Shc Signaling Adaptor Proteins and Phosphotyrosine binding.
He most often published in these fields:
- Cell biology (41.77%)
- SH2 domain (39.24%)
- Biochemistry (37.97%)
What were the highlights of his more recent work (between 2016-2021)?
- Proto-oncogene tyrosine-protein kinase Src (32.91%)
- Cell biology (41.77%)
- Computational biology (12.66%)
In recent papers he was focusing on the following fields of study:
Gerald D. Gish focuses on Proto-oncogene tyrosine-protein kinase Src, Cell biology, Computational biology, Phosphorylation and Homology.
A large part of his Proto-oncogene tyrosine-protein kinase Src studies is devoted to SH3 domain.
His Cell biology research is multidisciplinary, relying on both Ubiquitin ligase and Cyclin.
Gerald D. Gish has included themes like Protein phosphorylation, Phage display and Human proteome project in his Computational biology study.
His research investigates the link between Phosphorylation and topics such as Signal transduction that cross with problems in Proteomics.
His Phosphoproteomics research includes elements of Tyrosine kinase, FYN, SH2 domain, CD19 and breakpoint cluster region.
Between 2016 and 2021, his most popular works were:
- Direct Phosphorylation of SRC Homology 3 Domains by Tyrosine Kinase Receptors Disassembles Ligand-Induced Signaling Networks (10 citations)
- The Shb scaffold binds the Nck adaptor protein, p120 RasGAP, and Chimaerins and thereby facilitates heterotypic cell segregation by the receptor EphB2. (2 citations)
- Dimerization of a ubiquitin variant leads to high affinity interactions with a ubiquitin interacting motif (2 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Amino acid
- Phosphorylation
Gerald D. Gish mainly focuses on Cell biology, Phosphorylation, Signal transduction, Receptor tyrosine kinase and Signal transducing adaptor protein.
His study brings together the fields of Receptor and Cell biology.
Tyrosine phosphorylation and Proto-oncogene tyrosine-protein kinase Src are among the areas of Phosphorylation where the researcher is concentrating his efforts.
This overview was generated by a machine learning system which analysed the scientist’s
body of work. If you have any feedback, you can
contact us
here.
