1955 - Fellow of the American Association for the Advancement of Science (AAAS)
His primary areas of investigation include Cell biology, Transcription factor, Chromatin, Fluorescence recovery after photobleaching and Biophysics. Particularly relevant to Mitosis is his body of work in Cell biology. His Transcription factor study incorporates themes from Molecular biology, Transcription, Nucleosome, Regulation of gene expression and Response element.
His Chromatin research integrates issues from Mouse mammary tumor virus, Histone, Cell cycle and Green fluorescent protein. James G. McNally has included themes like Plasma protein binding, Molecular network, Nucleus, Chromatin binding and Biological system in his Fluorescence recovery after photobleaching study. His Biophysics research incorporates themes from Photobleaching, Fluorescence and Function.
The scientist’s investigation covers issues in Cell biology, Biophysics, Chromatin, Molecular biology and Transcription factor. His Cell biology research is multidisciplinary, incorporating elements of Genetics, Transcription and Actin cytoskeleton, Cytoskeleton. His studies deal with areas such as Photobleaching, Fluorescence recovery after photobleaching, Fluorescence, Analytical chemistry and Binding site as well as Biophysics.
His Chromatin study is concerned with the larger field of DNA. His work is dedicated to discovering how Molecular biology, RNA polymerase II are connected with Transcription factor II D and General transcription factor and other disciplines. His study of DNA-binding protein is a part of Transcription factor.
James G. McNally spends much of his time researching Cell biology, Biophysics, Chromatin, Transcription factor and Fluorescence recovery after photobleaching. His research in Cell biology intersects with topics in Molecular biology, Membrane, General transcription factor and Cytoskeleton. His Biophysics study integrates concerns from other disciplines, such as Ultrastructure, Nanoparticle, Human genetics and Microscopy.
His Chromatin research focuses on In vivo and how it connects with Nuclear protein. James G. McNally combines subjects such as Promoter, Computational biology and Saccharomyces cerevisiae with his study of Transcription factor. His work carried out in the field of Fluorescence recovery after photobleaching brings together such families of science as Live cell imaging and Transcription.
Cell biology, Molecular biology, Fluorescence recovery after photobleaching, Transcription factor and Chromatin binding are his primary areas of study. James G. McNally studies Actin, a branch of Cell biology. James G. McNally has researched Molecular biology in several fields, including Histone H3, Histone methyltransferase, Histone code, Histone H2A and Transcriptional regulation.
His Fluorescence recovery after photobleaching study integrates concerns from other disciplines, such as Live cell imaging, Transcription and Fluorescence microscope. His Transcription factor research is multidisciplinary, incorporating elements of Response element and General transcription factor. His studies deal with areas such as Biophysics and Fluorescence correlation spectroscopy as well as Chromatin binding.
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.
The Glucocorticoid Receptor: Rapid Exchange with Regulatory Sites in Living Cells
James G. McNally;Waltraud G. Müller;Dawn Walker;Ronald Wolford.
Science (2000)
Analysis of Binding Reactions by Fluorescence Recovery after Photobleaching
Brian L. Sprague;Robert L. Pego;Diana A. Stavreva;James G. McNally.
Biophysical Journal (2004)
FRAP analysis of binding: proper and fitting
Brian L. Sprague;James G. McNally.
Trends in Cell Biology (2005)
Three-dimensional imaging by deconvolution microscopy.
James G. McNally;Tatiana Karpova;John Cooper;José Angel Conchello.
Methods (1999)
Changes in chromatin structure and mobility in living cells at sites of DNA double-strand breaks
Michael J. Kruhlak;Arkady Celeste;Graham Dellaire;Oscar Fernandez-Capetillo.
Journal of Cell Biology (2006)
E-cadherin-mediated adhesion inhibits ligand-dependent activation of diverse receptor tyrosine kinases.
Xiaolan Qian;Tatiana Karpova;Allan M Sheppard;James McNally.
The EMBO Journal (2004)
Fluorescence resonance energy transfer from cyan to yellow fluorescent protein detected by acceptor photobleaching using confocal microscopy and a single laser
T. S. Karpova;C. T. Baumann;L. He;X. Wu.
Journal of Microscopy (2003)
SUMO-1 targets RanGAP1 to kinetochores and mitotic spindles
Jomon Joseph;Shyh-Han Tan;Tatiana S. Karpova;James G. McNally.
Journal of Cell Biology (2002)
Three-dimensional cellular ultrastructure resolved by X-ray microscopy
Gerd Schneider;Peter Guttmann;Stefan Heim;Stefan Rehbein.
Nature Methods (2010)
Rapid Glucocorticoid Receptor Exchange at a Promoter Is Coupled to Transcription and Regulated by Chaperones and Proteasomes
Diana A. Stavreva;Waltraud G. Müller;Gordon L. Hager;Carolyn L. Smith.
Molecular and Cellular Biology (2004)
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