2013 - Excellence in Science Award, Federation of American Societies for Experimental Biology (FASEB)
2010 - Fellow of the American Association for the Advancement of Science (AAAS)
2006 - Member of the National Academy of Sciences
His primary scientific interests are in Genetics, Cell biology, Gene, Sister chromatids and Cell cycle. His work in Control of chromosome duplication, Origin recognition complex, Saccharomyces cerevisiae, Gene conversion and Meiosis is related to Genetics. In his research, Computational biology is intimately related to RAD52 Gene, which falls under the overarching field of Gene conversion.
He is interested in Mitosis, which is a field of Cell biology. Terry L. Orr-Weaver focuses mostly in the field of Sister chromatids, narrowing it down to matters related to Cohesin and, in some cases, Anaphase. The various areas that Terry L. Orr-Weaver examines in his Cell cycle study include Transcription factor and DNA replication.
The scientist’s investigation covers issues in Genetics, Cell biology, Sister chromatids, DNA replication and Gene. His study in Genetics concentrates on Establishment of sister chromatid cohesion, Meiosis, Centromere, Chromosome segregation and Origin recognition complex. His research in Establishment of sister chromatid cohesion intersects with topics in Meiosis II, Spindle apparatus and Kinetochore.
His Cell biology research is multidisciplinary, incorporating elements of Cell cycle and Drosophila melanogaster. The Cell cycle study combines topics in areas such as Ploidy, Mitosis, Drosophila Protein and Cell fate determination. His work in Sister chromatids addresses issues such as Anaphase, which are connected to fields such as Metaphase.
Terry L. Orr-Weaver spends much of his time researching Cell biology, Genetics, Embryo, DNA replication and Origin recognition complex. His study connects Polyadenylation and Cell biology. All of his Genetics and Genome, Gene, DNA re-replication, Aurora B kinase and Polyploid investigations are sub-components of the entire Genetics study.
His Embryo research also works with subjects such as
Terry L. Orr-Weaver mostly deals with Genetics, Cell biology, Embryo, Anaphase-promoting complex and DNA replication. Polyploid, Eukaryotic DNA replication, Replication factor C, DNA replication factor CDT1 and Control of chromosome duplication are the core of his Genetics study. His studies in Cell biology integrate themes in fields like Molecular biology, Ploidy and Organogenesis.
His Ploidy research is multidisciplinary, incorporating perspectives in Cell cycle, Cell type and Drosophila melanogaster. Within one scientific family, Terry L. Orr-Weaver focuses on topics pertaining to Proteome under Embryo, and may sometimes address concerns connected to Drosophila Protein, Transcription and Protein turnover. His DNA replication research integrates issues from Double Strand Break Repair, Homologous recombination and DNA repair.
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.
Yeast transformation: a model system for the study of recombination
Terry L. Orr-Weaver;Jack W. Szostak;Rodney J. Rothstein.
Proceedings of the National Academy of Sciences of the United States of America (1981)
Identification of Functional Elements and Regulatory Circuits by Drosophila modENCODE
Sushmita Roy;Jason Ernst;Peter V. Kharchenko;Pouya Kheradpour.
Science (2010)
Endoreplication cell cycles: more for less.
Bruce A. Edgar;Terry L. Orr-Weaver.
Cell (2001)
Yeast recombination: the association between double-strand gap repair and crossing-over
Terry L. Orr-Weaver;Jack W. Szostak.
Proceedings of the National Academy of Sciences of the United States of America (1983)
Genetic applications of yeast transformation with linear and gapped plasmids.
Terry L. Orr-Weaver;Jack W. Szostak;Rodney J. Rothstein.
Methods in Enzymology (1983)
Regulation of APC/C Activators in Mitosis and Meiosis
Jillian A. Pesin;Terry L. Orr-Weaver.
Annual Review of Cell and Developmental Biology (2008)
The regulation of the cell cycle during Drosophila embryogenesis: the transition to polyteny.
A.V. Smith;T.L. Orr-Weaver.
Development (1991)
SMAUG Is a Major Regulator of Maternal mRNA Destabilization in Drosophila and Its Translation Is Activated by the PAN GU Kinase
Wael Tadros;Aaron L. Goldman;Tomas Babak;Fiona Menzies.
Developmental Cell (2007)
Mei-S332, a Drosophila protein required for sister-chromatid cohesion, can localize to meiotic centromere regions.
Anne W. Kerrebrock;Daniel P. Moore;Jim S. Wu;Terry L. Orr-Weaver.
Cell (1995)
DNA replication control through interaction of E2F–RB and the origin recognition complex
Giovanni Bosco;Wei Du;Terry L. Orr-Weaver.
Nature Cell Biology (2001)
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