His main research concerns Cell biology, Cyclin-dependent kinase, Cyclin-dependent kinase 7, Phosphorylation and Cyclin-dependent kinase complex. His work carried out in the field of Cell biology brings together such families of science as Spindle apparatus, Central spindle, Cyclin-dependent kinase 2, Cyclin H and Cyclin A. In his work, he performs multidisciplinary research in Cyclin-dependent kinase and RNA polymerase II.
His Cyclin-dependent kinase 7 research is multidisciplinary, incorporating elements of Cyclin-dependent kinase 1, CDK-activating kinase and Transcription factor. His study in Transcription factor is interdisciplinary in nature, drawing from both Molecular biology and RNA polymerase II holoenzyme. His Cyclin-dependent kinase complex research is multidisciplinary, incorporating perspectives in Cyclin A2, Cyclin binding and Cyclin D.
The scientist’s investigation covers issues in Cell biology, Cyclin-dependent kinase, RNA polymerase II, Transcription and Cyclin-dependent kinase 1. His studies deal with areas such as Chromatin, Cyclin-dependent kinase complex, Cell division and Cyclin A as well as Cell biology. His research in Cyclin A tackles topics such as Cyclin A2 which are related to areas like Cyclin E.
Robert P. Fisher combines subjects such as Kinase and Cyclin-dependent kinase 2, Cyclin-dependent kinase 7 with his study of Cyclin-dependent kinase. Other disciplines of study, such as Cyclin-dependent kinase 9, Molecular biology, P-TEFb, Transcription factor II D and Transcription factor II H, are mixed together with his RNA polymerase II studies. His Transcription study combines topics from a wide range of disciplines, such as Cancer cell and Gene expression.
His primary areas of investigation include Cell biology, Transcription, RNA polymerase II, Cyclin-dependent kinase 9 and Kinase. His work on Phosphorylation as part of general Cell biology study is frequently connected to P-TEFb, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them. The study incorporates disciplines such as Cancer cell and Cyclin-dependent kinase 7 in addition to Transcription.
His study in RNA polymerase II intersects with areas of studies such as Cyclin-dependent kinase, Gene, RNA polymerase II holoenzyme and Transcription factor II D. The concepts of his Cyclin-dependent kinase study are interwoven with issues in Protein phosphatase 2 and Cell signaling. His work focuses on many connections between Cyclin-dependent kinase 9 and other disciplines, such as Kinase activity, that overlap with his field of interest in Schizosaccharomyces pombe.
His primary scientific interests are in Cell biology, Transcription, Cyclin-dependent kinase 7, RNA polymerase II and Gene. Many of his research projects under Cell biology are closely connected to P-TEFb with P-TEFb, tying the diverse disciplines of science together. His biological study spans a wide range of topics, including Cancer research and Kinase.
Robert P. Fisher performs multidisciplinary studies into RNA polymerase II and Cyclin-dependent kinase 9 in his work. His Cyclin-dependent kinase 9 study integrates concerns from other disciplines, such as Polyadenylation and Chromatin. His work on Cyclin-dependent kinase and Schizosaccharomyces pombe as part of general Gene study is frequently connected to Transcription factor II H, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.
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.
A novel cyclin associates with M015/CDK7 to form the CDK-activating kinase
Robert P. Fisher;David O. Morgan.
Cell (1994)
Cdk-activating kinase complex is a component of human transcription factor TFIIH
Ramin Shiekhattar;Fred Mermelstein;Robert P. Fisher;Ronny Drapkin.
Nature (1995)
Secrets of a double agent: CDK7 in cell-cycle control and transcription
Robert P. Fisher.
Journal of Cell Science (2005)
TFIIH-Associated Cdk7 Kinase Functions in Phosphorylation of C-Terminal Domain Ser7 Residues, Promoter-Proximal Pausing, and Termination by RNA Polymerase II
Kira Glover-Cutter;Stéphane Larochelle;Benjamin Erickson;Chao Zhang.
Molecular and Cellular Biology (2009)
Alternative mechanisms of CAK assembly require an assembly factor or an Activating Kinase
Robert P. Fisher;Pei Jin;Holly M. Chamberlin;David O. Morgan.
Cell (1995)
Cyclin-dependent kinase control of the initiation-to-elongation switch of RNA polymerase II
Stéphane Larochelle;Ramon Amat;Kira Glover-Cutter;Miriam Sansó.
Nature Structural & Molecular Biology (2012)
Chemical genetics reveals the requirement for Polo-like kinase 1 activity in positioning RhoA and triggering cytokinesis in human cells
Mark E. Burkard;Catherine L. Randall;Stéphane Larochelle;Chao Zhang.
Proceedings of the National Academy of Sciences of the United States of America (2007)
The Pathogenesis of Esophageal Dysfunction in Scleroderma and Raynaud's Disease
Sidney Cohen;Robert Fisher;William Lipshutz;Robert Turner.
Journal of Clinical Investigation (1972)
Requirements for Cdk7 in the assembly of Cdk1/cyclin B and activation of Cdk2 revealed by chemical genetics in human cells.
Stéphane Larochelle;Karl A. Merrick;Karl A. Merrick;Marie-Emilie Terret;Lara Wohlbold.
Molecular Cell (2007)
Cdk7 is essential for mitosis and for in vivo Cdk-activating kinase activity.
Stéphane Larochelle;Judit Pandur;Robert P. Fisher;Helen K. Salz.
Genes & Development (1998)
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