Christophe Erneux mainly focuses on Biochemistry, Inositol, Cell biology, Phosphatase and Molecular biology. His work in Phosphorylation, Calmodulin, Second messenger system, Kinase and Binding site are all subfields of Biochemistry research. Christophe Erneux has researched Inositol in several fields, including Phosphatidylinositol, Calcium, Pleckstrin homology domain and Phospholipase C.
The Cell biology study combines topics in areas such as Actin cytoskeleton and Cytoskeleton. His Phosphatase research includes elements of Chinese hamster ovary cell, Tensin, PTEN, Molecular mass and Isozyme. His research integrates issues of cDNA library, Western blot, Clone and Transfection in his study of Molecular biology.
His primary scientific interests are in Biochemistry, Inositol, Cell biology, Phosphatase and Molecular biology. His work is connected to Enzyme, Calmodulin, Phosphorylation, Phosphatidylinositol and Phosphodiesterase, as a part of Biochemistry. The study incorporates disciplines such as Endocrinology, Internal medicine and Cyclic nucleotide in addition to Phosphodiesterase.
His Inositol research is multidisciplinary, incorporating perspectives in Kinase, Stereochemistry and Second messenger system. The concepts of his Phosphatase study are interwoven with issues in Pi and Tensin, PTEN. His biological study spans a wide range of topics, including Complementary DNA, cDNA library, Transfection and In situ hybridization.
Christophe Erneux mainly investigates Cell biology, Phosphatase, Signal transduction, Inositol and Phosphorylation. Christophe Erneux combines subjects such as Cell migration and Biochemistry with his study of Cell biology. His Phosphatase research incorporates elements of Pi, Protein kinase B, PTEN and Function.
His MAPK/ERK pathway and Phospholipase C study, which is part of a larger body of work in Signal transduction, is frequently linked to Cyclin D3, bridging the gap between disciplines. His Inositol research focuses on Enzyme and how it relates to Phosphatidylinositol. His Kinase research is multidisciplinary, incorporating elements of Molecular biology and Inositol-trisphosphate 3-kinase.
Cell biology, Signal transduction, Phosphorylation, Inositol and Kinase are his primary areas of study. His Cell biology research is multidisciplinary, relying on both Shigella, Calcium and Cell growth. His Cell growth research entails a greater understanding of Biochemistry.
His Phosphorylation study integrates concerns from other disciplines, such as Scaffold protein, Cell adhesion, Cytoskeleton, Second messenger system and Growth factor receptor. His Inositol study is concerned with the larger field of Receptor. His work on Protein tyrosine phosphatase, Proto-oncogene tyrosine-protein kinase Src and MAPK/ERK pathway as part of his general Kinase study is frequently connected to Fibroblast growth factor receptor, thereby bridging the divide between different branches of science.
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The lipid phosphatase SHIP2 controls insulin sensitivity
Serge Clément;Ulrike Krause;Florence Desmedt;Jean-François Tanti.
Nature (2001)
IDENTIFICATION OF A SECOND SH2-DOMAIN-CONTAINING PROTEIN CLOSELY RELATED TO THE PHOSPHATIDYLINOSITOL POLYPHOSPHATE 5-PHOSPHATASE SHIP
Xavier Pesesse;Sandrine Deleu;Florence De Smedt;Lyndsay Drayer.
Biochemical and Biophysical Research Communications (1997)
Octreotide, a somatostatin analogue, mediates its antiproliferative action in pituitary tumor cells by altering phosphatidylinositol 3-kinase signaling and inducing Zac1 expression.
Marily Theodoropoulou;Jing Zhang;Sandra Laupheimer;Marcelo Paez-Pereda.
Cancer Research (2006)
Involvement of inositol 1,4,5-trisphosphate and calcium in the action of adenine nucleotides on aortic endothelial cells.
Sabine Pirotton;Eric Raspé;Dominique Demolle;Christophe Erneux.
Journal of Biological Chemistry (1987)
The diversity and possible functions of the inositol polyphosphate 5-phosphatases
Christophe Erneux;Cédric Govaerts;David Communi;Xavier Pesesse.
Biochimica et Biophysica Acta (1998)
A small molecule inhibitor for phosphatase and tensin homologue deleted on chromosome 10 (PTEN).
Erika Rosivatz;Jonathan G. Matthews;Neil Q. McDonald;Neil Q. McDonald;Xavier Mulet.
ACS Chemical Biology (2006)
Distribution of the src-homology-2-domain-containing inositol 5-phosphatase SHIP-2 in both non-haemopoietic and haemopoietic cells and possible involvement of SHIP-2 in negative signalling of B-cells.
Eric Muraille;Xavier Pesesse;Céline Kuntz;Christophe Erneux.
Biochemical Journal (1999)
The SH2 domain containing inositol 5-phosphatase SHIP2 displays phosphatidylinositol 3,4,5-trisphosphate and inositol 1,3,4,5-tetrakisphosphate 5-phosphatase activity
Xavier Pesesse;Colette Moreau;A.Lyndsay Drayer;Rüdiger Woscholski;Rüdiger Woscholski.
FEBS Letters (1998)
Xestospongin C is an equally potent inhibitor of the inositol 1,4,5-trisphosphate receptor and the endoplasmic-reticulum Ca(2+) pumps.
P De Smet;Jb Parys;G Callewaert;Af Weidema.
Cell Calcium (1999)
The kinetics of tyrosine phosphorylation by the purified epidermal growth factor receptor kinase of A-431 cells.
Christophe Erneux;S Cohen;D L Garbers.
Journal of Biological Chemistry (1983)
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