Timothy A.J. Haystead mainly investigates Biochemistry, Molecular biology, Phosphorylation, Mitogen-activated protein kinase kinase and Protein kinase A. His Molecular biology research is multidisciplinary, incorporating elements of Proteome, Genome, Affinity chromatography, Purine and Protein sequencing. His Phosphorylation research integrates issues from EIF4E, Eukaryotic Initiation Factor-4E and Kinase.
He combines subjects such as MAP2K7, Cyclin-dependent kinase 2, MAP kinase kinase kinase and Protein tyrosine phosphatase with his study of Mitogen-activated protein kinase kinase. His MAP2K7 research focuses on subjects like Cyclin-dependent kinase 9, which are linked to ASK1. His Protein kinase A research includes themes of Phosphatase and Protein subunit.
His primary scientific interests are in Biochemistry, Phosphorylation, Molecular biology, Kinase and Cell biology. His is involved in several facets of Biochemistry study, as is seen by his studies on Mitogen-activated protein kinase kinase, MAP2K7, Protein phosphorylation, Affinity chromatography and Biotin. The study incorporates disciplines such as Cyclin-dependent kinase 2 and MAP kinase kinase kinase in addition to Mitogen-activated protein kinase kinase.
His Phosphorylation study combines topics in areas such as Endocrinology and Internal medicine. His work deals with themes such as Staurosporine and Proteome, which intersect with Molecular biology. His studies in Phosphatase integrate themes in fields like Protein subunit and Myosin.
Timothy A.J. Haystead focuses on Cancer research, Kinase, Breast cancer, Hsp90 inhibitor and Cancer. Kinase is a subfield of Cell biology that Timothy A.J. Haystead explores. His Breast cancer research is multidisciplinary, incorporating perspectives in Stage, Molecular imaging, In vivo and Hsp90.
His Ubiquitin study also includes fields such as
The scientist’s investigation covers issues in Cancer research, Hsp90, Immunology, Hsp90 inhibitor and In vivo. His Cancer research research incorporates themes from Protein phosphatase 2, Cell signaling, Signal transduction, Extracellular and Idiopathic pulmonary fibrosis. His Hsp90 research is multidisciplinary, relying on both Kinase, Cell biology and Virology.
His work carried out in the field of Immunology brings together such families of science as Malignancy, Cell and Cancer. His Hsp90 inhibitor research incorporates elements of Plasmodium falciparum, Plasmodium, Malaria, Parasite load and Breast cancer. He has included themes like Clinical trial, Tumor cells, Phenotype, Stage and Metabolism in his In vivo study.
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.
Effects of the tumour promoter okadaic acid on intracellular protein phosphorylation and metabolism
T. A. J. Haystead;A. T. R. Sim;D. Carling;R. C. Honnor.
Nature (1989)
Activation of mitogen-activated protein kinase kinase by v-Raf in NIH 3T3 cells and in vitro
Paul Dent;Wayne Haser;Timothy A. J. Haystead;Leigh Ann Vincent.
Science (1992)
The Amino-terminal Domain of Heat Shock Protein 90 (hsp90) That Binds Geldanamycin Is an ATP/ADP Switch Domain That Regulates hsp90 Conformation
James P. Grenert;William P. Sullivan;Patrick Fadden;Timothy A.J. Haystead.
Journal of Biological Chemistry (1997)
PHAS-I as a link between mitogen-activated protein kinase and translation initiation.
Tai-An Lin;Xianming Kong;Timothy A. J. Haystead;Arnim Pause.
Science (1994)
Molecular Biologist's Guide to Proteomics
Paul R. Graves;Timothy A. J. Haystead;Timothy A. J. Haystead.
Microbiology and Molecular Biology Reviews (2002)
Altered blood pressure responses and normal cardiac phenotype in ACE2-null mice
Susan B. Gurley;Alicia Allred;Thu H. Le;Robert Griffiths.
Journal of Clinical Investigation (2006)
Regulatory interactions between the Reg1-Glc7 protein phosphatase and the Snf1 protein kinase.
Pascual Sanz;Geoffrey R. Alms;Timothy A. J. Haystead;Marian Carlson.
Molecular and Cellular Biology (2000)
Discovery of novel targets of quinoline drugs in the human purine binding proteome.
Paul R. Graves;Jesse J. Kwiek;Patrick Fadden;Rupa Ray.
Molecular Pharmacology (2002)
Identification of Phosphorylation Sites in the Translational Regulator, PHAS-I, That Are Controlled by Insulin and Rapamycin in Rat Adipocytes
Patrick Fadden;Timothy A.J. Haystead;John C. Lawrence.
Journal of Biological Chemistry (1997)
Getting More from Less Algorithms for Rapid Protein Identification with Multiple Short Peptide Sequences
Aaron J. Mackey;Timothy A.J. Haystead;William R. Pearson.
Molecular & Cellular Proteomics (2002)
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:
University of Virginia
University of Virginia
University of Virginia
University of Cambridge
National University of Singapore
Temple University
University of Dundee
Duke University
University of Arizona
Vanderbilt University
University of Bologna
California Institute of Technology
Portland State University
Arizona State University
Indian Institute of Technology Bombay
Universidade Federal de Santa Catarina
University of Cambridge
James Hutton Institute
Kent State University
University of Illinois at Urbana-Champaign
University of Bergen
Marine Biological Laboratory
Drexel University
University of Geneva
Max Planck Society
University of Jyväskylä