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.
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.
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.
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.
SH2 domains recognize specific phosphopeptide sequences
Songyang Zhou;Songyang Zhou;Steven E. Shoelson;Manas Chaudhuri;Gerald Gish.
SH2 and SH3 domains: From structure to function
Tony Pawson;Gerald D. Gish.
The Discoidin Domain Receptor Tyrosine Kinases Are Activated by Collagen
Wolfgang Vogel;Gerald D Gish;Frauke Alves;Tony Pawson;Tony Pawson.
Molecular Cell (1997)
The Nedd4 family of E3 ubiquitin ligases: functional diversity within a common modular architecture
Robert J Ingham;Gerald Gish;Tony Pawson;Tony Pawson.
Bcr-Abl oncoproteins bind directly to activators of the Ras signalling pathway.
Lorri Puil;Jiaxin Liu;Gerald Gish;Geraldine Mbamalu.
The EMBO Journal (1994)
SH2 domains, interaction modules and cellular wiring.
Tony Pawson;Gerald D Gish;Piers Nash.
Trends in Cell Biology (2001)
Enteropathogenic E. coli Tir binds Nck to initiate actin pedestal formation in host cells.
Samantha Gruenheid;Rebekah DeVinney;Rebekah DeVinney;Friedhelm Bladt;Danika Goosney.
Nature Cell Biology (2001)
A Rich1/Amot Complex Regulates the Cdc42 GTPase and Apical-Polarity Proteins in Epithelial Cells
Clark D. Wells;James P. Fawcett;Andreas Traweger;Yojiro Yamanaka.
Transgenic RNA interference in ES cell–derived embryos recapitulates a genetic null phenotype
Tilo Kunath;Tilo Kunath;Gerald Gish;Heiko Lickert;Nina Jones.
Nature Biotechnology (2003)
The Carboxyl Terminus of B Class Ephrins Constitutes a PDZ Domain Binding Motif
Dan Lin;Dan Lin;Gerald D. Gish;Zhou Songyang;Tony Pawson;Tony Pawson.
Journal of Biological Chemistry (1999)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: