The scientist’s investigation covers issues in Cell biology, Biochemistry, Kinase activity, Molecular biology and Signal transduction. His research is interdisciplinary, bridging the disciplines of NODAL and Cell biology. His study in the field of Amino acid and Cellular differentiation also crosses realms of PLCB2.
Malcolm Whitman combines subjects such as Tyrosine kinase and Platelet-derived growth factor receptor with his study of Kinase activity. His Molecular biology study combines topics from a wide range of disciplines, such as Blastula, Xbra, Notochord, Activin type 2 receptors and Phosphatidylinositol. His Signal transduction research is multidisciplinary, incorporating perspectives in In vivo, Autoimmunity, Starvation response and Binding site.
Malcolm Whitman mostly deals with Cell biology, Xenopus, Molecular biology, Transcription factor and Mesoderm. His Cell biology research includes themes of Genetics and NODAL. His Molecular biology research is multidisciplinary, relying on both Rous sarcoma virus, Activin type 2 receptors, Phosphatidylinositol and Kinase activity.
His work carried out in the field of Phosphatidylinositol brings together such families of science as Cell growth and Second messenger system. In the field of Transcription factor, his study on Transcriptional regulation, Enhancer and DNA-binding protein overlaps with subjects such as Mothers against decapentaplegic homolog 2. His Mesoderm research is multidisciplinary, incorporating elements of Gastrulation, Ectoderm, Endoderm and Fibroblast growth factor.
His primary areas of study are Cell biology, Biochemistry, Halofuginone, Pharmacology and Amino acid. The concepts of his Cell biology study are interwoven with issues in Genetics, Tyrosine and Transcription factor. His studies deal with areas such as ROR1, Platelet-derived growth factor receptor, Receptor tyrosine kinase and Proto-oncogene tyrosine-protein kinase Src as well as Tyrosine.
His Halofuginone research incorporates elements of Lung transplantation and Cellular differentiation. The study incorporates disciplines such as Angiogenesis, Transplant rejection, Kinase and Peptide in addition to Pharmacology. Many of his studies on Amino acid apply to Signal transduction as well.
His main research concerns Febrifugine, Halofuginone, Genetics, Biochemistry and Cell biology. You can notice a mix of various disciplines of study, such as Amino acid, Plasmodium berghei, Drug resistance, Pharmacology and Plasmodium falciparum, in his Febrifugine studies. The Halofuginone study combines topics in areas such as Druggability and Malaria.
His research in Genetics intersects with topics in Nucleus and Dependent manner. His work in the fields of Cellular differentiation, Tyrosine and Protein tyrosine phosphatase overlaps with other areas such as Synthetase activity and Prolyl tRNA synthetase. The various areas that he examines in his Cell biology study include MRNA Decay and Platelet-derived growth factor receptor.
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.
Type I phosphatidylinositol kinase makes a novel inositol phospholipid, phosphatidylinositol-3-phosphate.
Malcolm Whitman;Malcolm Whitman;C. Peter Downes;Marilyn Keeler;Tracy Keller.
Nature (1988)
Association of phosphatidylinositol kinase activity with polyoma middle-T competent for transformation.
Malcolm Whitman;David R. Kaplan;Brian Schaffhausen;Lewis Cantley.
Nature (1985)
A transcriptional partner for MAD proteins in TGF-beta signalling.
Xin Chen;Melissa J. Rubock;Malcolm Whitman.
Nature (1996)
Common elements in growth factor stimulation and oncogenic transformation: 85 kd phosphoprotein and phosphatidylinositol kinase activity
David R. Kaplan;Malcolm Whitman;Brian Schaffhausen;David C. Pallas.
Cell (1987)
Smad4 and FAST-1 in the assembly of activin-responsive factor.
Xin Chen;Ellen Weisberg;Valerie Fridmacher;Minoru Watanabe.
Nature (1997)
Activins are expressed early in Xenopus embryogenesis and can induce axial mesoderm and anterior structures.
G. Thomsen;T. Woolf;M. Whitman;S. Sokol.
Cell (1990)
Smads and early developmental signaling by the TGFbeta superfamily.
Malcolm Whitman.
Genes & Development (1998)
Evidence that the Rous sarcoma virus transforming gene product phosphorylates phosphatidylinositol and diacylglycerol
Yoshikazu Sugimoto;Malcolm Whitman;Lewis C. Cantley;R. L. Erikson.
Proceedings of the National Academy of Sciences of the United States of America (1984)
Nodal Signals to Smads through Cripto-Dependent and Cripto-Independent Mechanisms
Chang-Yeol Yeo;Malcolm Whitman.
Molecular Cell (2001)
Halofuginone Inhibits TH17 Cell Differentiation by Activating the Amino Acid Starvation Response
Mark S. Sundrud;Sergei B. Koralov;Markus Feuerer;Dinis Pedro Calado.
Science (2009)
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