2002 - Fellow of the Royal Society of Edinburgh
Member of the European Molecular Biology Organization (EMBO)
Fellow of The Academy of Medical Sciences, United Kingdom
Cell biology, Origin recognition complex, DNA replication, Control of chromosome duplication and Eukaryotic DNA replication are his primary areas of study. His work deals with themes such as Molecular biology, Cell cycle, Semiconservative replication and Cyclin A, which intersect with Cell biology. His research investigates the connection with Origin recognition complex and areas like MCM Protein which intersect with concerns in Computational biology, MCM complex and MCM Protein Complex.
His DNA replication research incorporates themes from Xenopus and Replicon. His Control of chromosome duplication research is within the category of Genetics. His study in Pre-replication complex, DNA replication factor CDT1, Licensing factor and Replication factor C is carried out as part of his Eukaryotic DNA replication studies.
The scientist’s investigation covers issues in Cell biology, DNA replication, Origin recognition complex, Control of chromosome duplication and Eukaryotic DNA replication. His Cell biology research includes themes of G2-M DNA damage checkpoint, Xenopus and Cell cycle, Cyclin-dependent kinase. His DNA replication research incorporates elements of Chromatin, Molecular biology and Cell division.
His study looks at the intersection of Molecular biology and topics like Cyclin A with Cyclin E. J. Julian Blow has researched Origin recognition complex in several fields, including MCM Protein, DNA replication factor CDT1, Minichromosome maintenance, ORC6 and Licensing factor. His Control of chromosome duplication research is included under the broader classification of Genetics.
J. Julian Blow mostly deals with DNA replication, Cell biology, Origin recognition complex, Genetics and Mitosis. Specifically, his work in DNA replication is concerned with the study of Origin of replication. His studies in Cell biology integrate themes in fields like Cell cycle, Mitotic chromosome, Xenopus and Chromosome organisation.
His Origin recognition complex study combines topics from a wide range of disciplines, such as Chromatin and DNA replication factor CDT1, Control of chromosome duplication. His studies deal with areas such as S phase and Eukaryotic DNA replication as well as Control of chromosome duplication. His research on Eukaryotic DNA replication focuses in particular on Licensing factor.
His primary areas of study are DNA replication, Cell biology, Genetics, Origin recognition complex and Genome instability. J. Julian Blow works in the field of DNA replication, namely DNA re-replication. His Cell biology study combines topics in areas such as Cell cycle, Cell cycle progression, Caenorhabditis elegans and Mitotic chromosome.
While the research belongs to areas of Genetics, he spends his time largely on the problem of Computational biology, intersecting his research to questions surrounding Robustness and Phenotypic plasticity. His research investigates the connection between Origin recognition complex and topics such as Control of chromosome duplication that intersect with issues in S phase. As a part of the same scientific family, he mostly works in the field of Genome instability, focusing on Phenotype and, on occasion, Effector, Ubiquitin ligase, Kinase, Downregulation and upregulation and Senescence.
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Biochemical and Cellular Effects of Roscovitine, a Potent and Selective Inhibitor of the Cyclin‐Dependent Kinases cdc2, cdk2 and cdk5
Laurent Meijer;Annie Borgne;Odile Mulner;James P.J. Chong.
FEBS Journal (1997)
Preventing re-replication of chromosomal DNA
J. Julian Blow;Anindya Dutta.
Nature Reviews Molecular Cell Biology (2005)
A role for the nuclear envelope in controlling DNA replication within the cell cycle.
J. Julian Blow;Ronald A. Laskey.
Nature (1988)
Initiation of DNA replication in nuclei and purified DNA by a cell-free extract of Xenopus eggs.
J.Julian Blow;Ronald A. Laskey.
Cell (1986)
Regulatory phosphorylation of the p34cdc2 protein kinase in vertebrates.
C Norbury;J Blow;P Nurse.
The EMBO Journal (1991)
Dormant origins licensed by excess Mcm2–7 are required for human cells to survive replicative stress
Xin Quan Ge;Dean A. Jackson;J. Julian Blow.
Genes & Development (2007)
Repression of origin assembly in metaphase depends on inhibition of RLF-B/Cdt1 by geminin
Shusuke Tada;Anatoliy Li;Domenico Maiorano;Marcel Méchali.
Nature Cell Biology (2001)
Translation of Cyclin mRNA Is Necessary for Extracts of Activated Xenopus Eggs to Enter Mitosis
Jeremy Minshull;J.Julian Blow;Tim Hunt.
Cell (1989)
Purification of an MCM-containing complex as a component of the DNA replication licensing system
James P. J. Chong;Hiro M. Mahbubani;Chong-Yee Khoo;J. Julian Blow.
Nature (1995)
Excess Mcm2–7 license dormant origins of replication that can be used under conditions of replicative stress
Anna M. Woodward;Thomas Göhler;M. Gloria Luciani;Maren Oehlmann.
Journal of Cell Biology (2006)
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