His primary scientific interests are in Biochemistry, Proteome, Molecular biology, Spectrin and Cell biology. David W. Speicher regularly links together related areas like Antibody in his Biochemistry studies. His research integrates issues of Blood proteins, Chromatography, Mass spectrometry and Proteomics in his study of Proteome.
His research in Molecular biology intersects with topics in Amino acid, Cyclophilin, Affinity chromatography and Melanoma-associated antigen. His Spectrin research is multidisciplinary, incorporating perspectives in Protein structure, Cleavage, Peptide and Protein folding. His Cell biology research incorporates themes from Corepressor, Genetics, Cellular differentiation and Zinc finger.
David W. Speicher mainly focuses on Biochemistry, Cell biology, Spectrin, Molecular biology and Chromatography. His research investigates the connection with Cell biology and areas like Autophagy which intersect with concerns in Cancer research. His Spectrin research includes elements of Protein structure, Biophysics and Tetramer.
In his study, which falls under the umbrella issue of Molecular biology, Antigen is strongly linked to Antibody. His Chromatography study integrates concerns from other disciplines, such as Isoelectric focusing, Proteome, Membrane and Proteomics. His Proteome research is multidisciplinary, incorporating elements of Tandem mass spectrometry, Mass spectrometry, Blood proteins, Protein profiling and Computational biology.
His primary areas of study are Cancer research, Cell biology, Cancer, Biochemistry and Melanoma. His study in Cancer research is interdisciplinary in nature, drawing from both Tumor microenvironment, Cancer cell, Immunology, Metastasis and Programmed cell death. His studies deal with areas such as Autophagy and Carcinogenesis as well as Cell biology.
His Cancer research focuses on EZH2 and how it connects with ARID1A. His study in Spectrin, Protein structure, Glutathione, Enzyme and Membrane protein are all subfields of Biochemistry. The Spectrin study combines topics in areas such as Mutation, Biophysics, Mutant, Protein quaternary structure and Heterotetramer.
David W. Speicher focuses on Cancer research, Cell biology, Cancer, Autophagy and Biochemistry. His Cancer research research integrates issues from Tumor microenvironment, Cancer cell, Immunology, Signal transduction and Tumor progression. His research is interdisciplinary, bridging the disciplines of Regulation of gene expression and Cell biology.
David W. Speicher has researched Cancer in several fields, including PI3K/AKT/mTOR pathway and EZH2. His Biochemistry study frequently draws connections between related disciplines such as Antiparallel. His study looks at the relationship between Cytoplasm and topics such as Kinase, which overlap with RNA, RNA editing and Molecular biology.
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.
Cyclophilin: a specific cytosolic binding protein for cyclosporin A.
Robert E. Handschumacher;Matthew W. Harding;Jeffrey Rice;Rhett J. Drugge.
Science (1984)
Nuclear lamin-A Scales With Tissue Stiffness and Enhances Matrix-Directed Differentiation
Joe Swift;Irena L. Ivanovska;Amnon Buxboim;Takamasa Harada.
Science (2013)
Embryonic cardiomyocytes beat best on a matrix with heart-like elasticity: scar-like rigidity inhibits beating
Adam J. Engler;Christine Carag-Krieger;Colin P. Johnson;Matthew Raab.
Journal of Cell Science (2008)
Overview of the HUPO Plasma Proteome Project: results from the pilot phase with 35 collaborating laboratories and multiple analytical groups, generating a core dataset of 3020 proteins and a publicly-available database.
Gilbert S. Omenn;David J. States;Marcin Adamski;Thomas W. Blackwell.
Proteomics (2005)
KAP-1, a novel corepressor for the highly conserved KRAB repression domain.
Josh R. Friedman;William J. Fredericks;David E. Jensen;David W. Speicher.
Genes & Development (1996)
Overcoming Intrinsic Multidrug Resistance in Melanoma by Blocking the Mitochondrial Respiratory Chain of Slow-Cycling JARID1Bhigh Cells
Alexander Roesch;Adina Vultur;Ivan Bogeski;Huan Wang.
Cancer Cell (2013)
Erythrocyte spectrin is comprised of many homologous triple helical segments
David W. Speicher;Vincent T. Marchesi.
Nature (1984)
HUPO Plasma Proteome Project specimen collection and handling : Towards the standardization of parameters for plasma proteome samples
Alex J Rai;Craig A Gelfand;Bruce C Haywood;David J Warunek.
Proteomics (2005)
Synthetic lethality by targeting EZH2 methyltransferase activity in ARID1A -mutated cancers
Benjamin G. Bitler;Katherine M. Aird;Azat Garipov;Hua Li.
Nature Medicine (2015)
Depletion of multiple high-abundance proteins improves protein profiling capacities of human serum and plasma.
Lynn A. Echan;Hsin‐Yao Tang;Nadeem Ali‐Khan;KiBeom Lee.
Proteomics (2005)
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 Pennsylvania
Thomas Jefferson University
Yale University
University of Pennsylvania
The Wistar Institute
Yale University
University of Pennsylvania
The Wistar Institute
University of Pennsylvania
Johns Hopkins University
University of Manchester
National Institutes of Health
University of Connecticut
University of California, Berkeley
The University of Texas at Austin
RWTH Aachen University
MIT
Thermo Fisher Scientific (Norway)
Institute of Cancer Research
Zhengzhou University
University of Erlangen-Nuremberg
Indian Institute of Technology Bombay
University of Limerick
Binghamton University
University of Pittsburgh
Stanford University