2002 - Fellow of the American Academy of Arts and Sciences
Ronald C. Conaway focuses on RNA polymerase II, Cell biology, Molecular biology, Protein subunit and Transcription factor. His study in RNA polymerase II is interdisciplinary in nature, drawing from both MED1, General transcription factor, Transcription and Transcription factor II D. In his study, Chromatin remodeling, Transcriptional regulation and Multiprotein complex is strongly linked to Saccharomyces cerevisiae, which falls under the umbrella field of Cell biology.
The study incorporates disciplines such as Von Hippel–Lindau tumor suppressor, HeLa, Histone acetyltransferase and Cullin Proteins in addition to Molecular biology. The various areas that he examines in his Protein subunit study include Plasma protein binding and Ubiquitin. His Transcription factor research includes elements of Peptide sequence, Hypoxia-inducible factors and G alpha subunit.
Ronald C. Conaway mainly investigates RNA polymerase II, Cell biology, Molecular biology, Transcription and Transcription factor II D. His RNA polymerase II research is multidisciplinary, incorporating elements of Protein subunit, Transcription factor, Mediator and General transcription factor. The Cell biology study combines topics in areas such as Chromatin, Nucleosome and Ubiquitin, Ubiquitin ligase.
His research investigates the link between Molecular biology and topics such as Helicase that cross with problems in Transcription factor II H. His studies deal with areas such as RNA and DNA repair as well as Transcription. His Transcription factor II D research integrates issues from Transcription factor II A, Transcription factor II B, Transcription factor II F and RNA polymerase II holoenzyme.
The scientist’s investigation covers issues in Cell biology, RNA polymerase II, Transcription, Mediator and RNA. Ronald C. Conaway combines subjects such as Enhancer, Histone, Nucleosome and Ubiquitin with his study of Cell biology. His RNA polymerase II research is multidisciplinary, relying on both Chromatin and Protein subunit.
His Transcription research also works with subjects such as
Cell biology, RNA polymerase II, Transcription, Histone and Histone acetyltransferase activity are his primary areas of study. His work deals with themes such as Protein domain and Structure–activity relationship, which intersect with Cell biology. The various areas that Ronald C. Conaway examines in his RNA polymerase II study include RNA, Transcriptome, Genome instability, Developmental biology and DNA repair.
His Transcription research includes themes of Ubiquitin, DNA damage, Bioinformatics, Protein subunit and Mediator. His Histone study combines topics from a wide range of disciplines, such as H3K4me3, Chromatin and Methylation. Ronald C. Conaway interconnects NSL complex, Molecular biology and Transferase in the investigation of issues within Histone acetyltransferase activity.
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Activation of HIF1alpha ubiquitination by a reconstituted von Hippel-Lindau (VHL) tumor suppressor complex.
Takumi Kamura;Shigeo Sato;Kazuhiro Iwai;Maria Czyzyk-Krzeska.
Proceedings of the National Academy of Sciences of the United States of America (2000)
The Elongin BC complex interacts with the conserved SOCS-box motif present in members of the SOCS, ras, WD-40 repeat, and ankyrin repeat families
Takumi Kamura;Shigeo Sato;Dewan Haque;Li Liu.
Genes & Development (1998)
Biochemical purification and pharmacological inhibition of a mammalian prolyl hydroxylase acting on hypoxia-inducible factor
Mircea Ivan;Thomas Haberberger;David C. Gervasi;Kristen S. Michelson.
Proceedings of the National Academy of Sciences of the United States of America (2002)
Identification of the von Hippel–Lindau tumor-suppressor protein as part of an active E3 ubiquitin ligase complex
Kazuhiro Iwai;Koji Yamanaka;Takumi Kamura;Nagahiro Minato.
Proceedings of the National Academy of Sciences of the United States of America (1999)
General Initiation Factors for RNA Polymerase II
Ronald C. Conaway;Joan Weliky Conaway.
Annual Review of Biochemistry (1993)
Degradation of p53 by adenovirus E4orf6 and E1B55K proteins occurs via a novel mechanism involving a Cullin-containing complex
Emmanuelle Querido;Paola Blanchette;Qin Yan;Takumi Kamura.
Genes & Development (2001)
Emerging roles of ubiquitin in transcription regulation.
Ronald C. Conaway;Christopher S. Brower;Joan Weliky Conaway;Joan Weliky Conaway;Joan Weliky Conaway.
Reconstitution of G1 cyclin ubiquitination with complexes containing SCFGrr1 and Rbx1.
Dorota Skowyra;Deanna M. Koepp;Takumi Kamura;Michael N. Conrad.
Quantitative proteomic analysis of distinct mammalian Mediator complexes using normalized spectral abundance factors.
Andrew C. Paoletti;Tari J. Parmely;Chieri Tomomori-Sato;Shigeo Sato.
Proceedings of the National Academy of Sciences of the United States of America (2006)
AFF4, a Component of the ELL/P-TEFb Elongation Complex and a Shared Subunit of MLL Chimeras, Can Link Transcription Elongation to Leukemia
Chengqi Lin;Edwin R. Smith;Hidehisa Takahashi;Ka Chun Lai.
Molecular Cell (2010)
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