2015 - Fellow of the American Association for the Advancement of Science (AAAS)
Michelle Craig Barton mainly investigates Molecular biology, Cancer research, Psychological repression, Histone and Chromatin. Her study in Molecular biology is interdisciplinary in nature, drawing from both Transcription, TRIM24 and Promoter, RNA polymerase II, Transcription factor II D. Her studies in Cancer research integrate themes in fields like Cancer cell, Histone methyltransferase and Bladder cancer.
Michelle Craig Barton works mostly in the field of Psychological repression, limiting it down to topics relating to Transcription factor and, in certain cases, Derepression, as a part of the same area of interest. Her Histone research includes themes of Regulation of gene expression, Epigenetics, Pharmacology and Cell biology. Chromatin immunoprecipitation is closely connected to Transcriptional regulation in her research, which is encompassed under the umbrella topic of Chromatin.
Her primary areas of investigation include Cell biology, Chromatin, Cancer research, Molecular biology and Histone. She has included themes like Cell cycle checkpoint, Genetics, Embryonic stem cell, Induced pluripotent stem cell and Xenopus in her Cell biology study. Her Chromatin research includes elements of Chromatin immunoprecipitation, Epigenetics and Cellular differentiation.
Her research in Cancer research intersects with topics in TRIM24, Cancer cell, Transcription factor, Signal transduction and Regulation of gene expression. Her biological study spans a wide range of topics, including Transcription, Psychological repression, Gene expression, General transcription factor and DNA replication. Her work deals with themes such as Gene silencing and Acetylation, which intersect with Histone.
Michelle Craig Barton mainly investigates Cancer research, Cell biology, Chromatin, Histone and Epigenetics. Michelle Craig Barton combines subjects such as TRIM24, Cancer cell, Transcription factor, Breast cancer and Androgen receptor with her study of Cancer research. She has researched Cell biology in several fields, including Embryonic stem cell, Histone H3, Cellular differentiation and Cytosol.
Her Chromatin study combines topics from a wide range of disciplines, such as Molecular biology, Chromatin immunoprecipitation and Mdm2. Her Histone research incorporates themes from Cell cycle and Acetylation. As a part of the same scientific study, Michelle Craig Barton usually deals with the Epigenetics, concentrating on Gene silencing and frequently concerns with Regulator, Endogeny and Death-associated protein 6.
Michelle Craig Barton mainly focuses on Cancer research, Chromatin, Histone, Cellular differentiation and Regulation of gene expression. Her Cancer research research is multidisciplinary, incorporating elements of Carcinogenesis, Epigenomics, Epigenetics and Apoptosis. Her Chromatin study incorporates themes from Transcription, Acetylation and DNA damage.
Her study with Histone involves better knowledge in Genetics. Her research integrates issues of Reprogramming and Cell biology in her study of Cellular differentiation. Her work carried out in the field of Regulation of gene expression brings together such families of science as Transcription factor and Gene expression.
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TRIM24 links a non-canonical histone signature to breast cancer
Wen Wei Tsai;Zhanxin Wang;Teresa T. Yiu;Teresa T. Yiu;Kadir C. Akdemir.
Kaiso/p120-Catenin and TCF/β-Catenin Complexes Coordinately Regulate Canonical Wnt Gene Targets
Jae Il Park;Jae Il Park;Si Wan Kim;Jon P. Lyons;Jon P. Lyons;Hong Ji.
Developmental Cell (2005)
ZMYND11 links histone H3.3K36me3 to transcription elongation and tumour suppression
Hong Wen;Yuanyuan Li;Yuanxin Xi;Shiming Jiang.
Hypoxia induces a novel signature of chromatin modifications and global repression of transcription.
Amber Buescher Johnson;Nicholas Denko;Michelle Craig Barton.
Mutation Research (2008)
Trim24 targets endogenous p53 for degradation
Kendra Allton;Abhinav K. Jain;Hans-Martin Herz;Wen-Wei Tsai;Wen-Wei Tsai.
Proceedings of the National Academy of Sciences of the United States of America (2009)
p53 Regulates Cell Cycle and MicroRNAs to Promote Differentiation of Human Embryonic Stem Cells
Abhinav K. Jain;Kendra Allton;Michelina Iacovino;Elisabeth Mahen.
PLOS Biology (2012)
p53-Mediated repression of alpha-fetoprotein gene expression by specific DNA binding
Kathleen C. Lee;Alison J. Crowe;Michelle Craig Barton.
Molecular and Cellular Biology (1999)
3-Hydroxy-3-methylglutaryl-coenzyme A reductase is present in peroxisomes in normal rat liver cells
Gilbert-A. Keller;Michelle C. Barton;David J. Shapiro;S. J. Singer.
Proceedings of the National Academy of Sciences of the United States of America (1985)
UV-induced inhibition of transcription involves repression of transcription initiation and phosphorylation of RNA polymerase II
Davy A. P. Rockx;Rebecca Mason;Rebecca Mason;Anneke van Hoffen;Michelle Craig Barton.
Proceedings of the National Academy of Sciences of the United States of America (2000)
The p63 Protein Isoform ΔNp63α Inhibits Epithelial-Mesenchymal Transition in Human Bladder Cancer Cells ROLE OF MIR-205
Mai N. Tran;Woonyoung Choi;Matthew F. Wszolek;Neema Navai.
Journal of Biological Chemistry (2013)
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