His primary scientific interests are in Cell biology, Endocytosis, Dynamin, Phosphorylation and Biochemistry. His work deals with themes such as Exocytosis and Receptor-mediated endocytosis, which intersect with Cell biology. As part of one scientific family, Phillip J. Robinson deals mainly with the area of Endocytosis, narrowing it down to issues related to the Dephosphorylation, and often Depolarization.
His Dynamin research is multidisciplinary, relying on both Synaptic vesicle, Bulk endocytosis, Synaptic vesicle recycling and GTPase. His Synaptic vesicle recycling research incorporates themes from Endocytosis Inhibition, Clathrin coat and Clathrin adaptor proteins. His Phosphorylation research includes elements of Chromatography and Neuroscience.
Phillip J. Robinson mostly deals with Cell biology, Dynamin, Biochemistry, Endocytosis and Phosphorylation. The study incorporates disciplines such as Exocytosis and Endocytic cycle, Synaptic vesicle endocytosis, Synaptic vesicle, Bulk endocytosis in addition to Cell biology. His study in Dynamin is interdisciplinary in nature, drawing from both Dephosphorylation, GTPase, Stereochemistry and Cytokinesis.
His Biochemistry research is multidisciplinary, incorporating perspectives in Molecular biology and Biophysics. The various areas that Phillip J. Robinson examines in his Endocytosis study include Internalization and Endosome. Phillip J. Robinson interconnects Calcium and Kinase in the investigation of issues within Phosphorylation.
The scientist’s investigation covers issues in Cell biology, Dynamin, Endocytosis, GTPase and Clathrin. His Cell biology study integrates concerns from other disciplines, such as Endocytic cycle, Synaptic vesicle endocytosis and Bulk endocytosis. The Dynamin study combines topics in areas such as Exocytosis, Stem cell, Cytokinesis and Stereochemistry.
His work in Endocytosis addresses subjects such as Internalization, which are connected to disciplines such as Function. His research on GTPase concerns the broader Biochemistry. The concepts of his Clathrin study are interwoven with issues in Combinatorial chemistry, Pharmacology and Synaptic vesicle recycling.
Phillip J. Robinson spends much of his time researching Dynamin, Cell biology, Endocytosis, Bulk endocytosis and Synaptic vesicle endocytosis. His studies deal with areas such as GTPase, Cytokinesis, Mutation, IC50 and Stereochemistry as well as Dynamin. His Cell biology study combines topics from a wide range of disciplines, such as Endocytic cycle, Dynamin II and Exocytosis.
His Endocytosis study is concerned with the larger field of Biochemistry. His Bulk endocytosis research integrates issues from Plasma protein binding and Phosphorylation. His Synaptic vesicle endocytosis research is multidisciplinary, incorporating elements of Synaptic plasticity and Neurotransmission.
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.
Protein composition of catalytically active human telomerase from immortal cells.
Scott B. Cohen;Mark E. Graham;George O. Lovrecz;Nicolai Bache.
Science (2007)
Role of the Clathrin Terminal Domain in Regulating Coated Pit Dynamics Revealed by Small Molecule Inhibition.
Lisa von Kleist;Wiebke Stahlschmidt;Haydar Bulut;Kira Gromova.
Cell (2011)
SIMAC (Sequential Elution from IMAC), a Phosphoproteomics Strategy for the Rapid Separation of Monophosphorylated from Multiply Phosphorylated Peptides
Tine E. Thingholm;Ole N. Jensen;Phillip J. Robinson;Martin R. Larsen.
Molecular & Cellular Proteomics (2008)
Involvement of novel autophosphorylation sites in ATM activation
Sergei V Kozlov;Mark E Graham;Cheng Peng;Philip Chen.
The EMBO Journal (2006)
Bronchiectasis in Infants and Preschool Children Diagnosed with Cystic Fibrosis after Newborn Screening
Stephen M. Stick;Stephen M. Stick;Siobhain Brennan;Conor Murray;Tonia Douglas;Tonia Douglas.
The Journal of Pediatrics (2009)
Cyclic GMP-dependent protein kinase and cellular signaling in the nervous system.
Xin Wang;Phillip J. Robinson.
Journal of Neurochemistry (2002)
The dephosphins: dephosphorylation by calcineurin triggers synaptic vesicle endocytosis.
Michael A Cousin;Phillip J Robinson.
Trends in Neurosciences (2001)
Cdk5 is essential for synaptic vesicle endocytosis
Timothy C Tan;Valentina A Valova;Chandra S Malladi;Mark E Graham.
Nature Cell Biology (2003)
A rapid Percoll gradient procedure for preparation of synaptosomes
Peter R Dunkley;Paula E Jarvie;Phillip J Robinson.
Nature Protocols (2008)
Cdk1/Erk2- and Plk1-dependent phosphorylation of a centrosome protein, Cep55, is required for its recruitment to midbody and cytokinesis
Megan Fabbro;Bin-Bing Zhou;Mikiko Takahashi;Boris Sarcevic.
Developmental Cell (2005)
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