1976 - Fellow of John Simon Guggenheim Memorial Foundation
His primary areas of investigation include Molecular biology, Actin, Gene, Cell biology and Gene expression. The various areas that Larry Kedes examines in his Molecular biology study include Complementary DNA, Messenger RNA, Untranslated region, Regulation of gene expression and Transcription. His work carried out in the field of Complementary DNA brings together such families of science as Nucleic acid sequence and Beta-actin.
His study in Actin is interdisciplinary in nature, drawing from both Myosin and Skeletal muscle. The Hes3 signaling axis, Notch proteins, Notch signaling pathway and MyoD Protein research Larry Kedes does as part of his general Cell biology study is frequently linked to other disciplines of science, such as PITX2, therefore creating a link between diverse domains of science. His biological study spans a wide range of topics, including Xenopus, Histone and Chromosome 7.
Larry Kedes mainly investigates Molecular biology, Gene, Cell biology, Gene expression and Actin. The study incorporates disciplines such as Transcription factor, Complementary DNA, Skeletal muscle, Regulation of gene expression and Transcription in addition to Molecular biology. Gene is a primary field of his research addressed under Genetics.
His work deals with themes such as Internal medicine, Biochemistry and Gene isoform, which intersect with Cell biology. His biological study deals with issues like Messenger RNA, which deal with fields such as Sea urchin. His studies in Actin integrate themes in fields like Myofibril, C2C12 and Cytoskeleton.
His primary areas of study are Cell biology, Molecular biology, Internal medicine, Notch signaling pathway and Transcription factor. The Cell biology study combines topics in areas such as Serum response factor and Receptor. His Molecular biology research includes themes of Retrovirus, Chromatin and Adenoviridae, Genetic enhancement, Gene delivery.
His Internal medicine research is multidisciplinary, incorporating perspectives in Endocrinology, Oncology and Cardiology. His Notch signaling pathway research integrates issues from BMPR2 and SMAD. His Transcription factor research is multidisciplinary, relying on both Regulation of gene expression, DNA binding site and Gene expression.
Larry Kedes focuses on Molecular biology, Notch signaling pathway, Transcription factor, Myocyte and Hes3 signaling axis. His Molecular biology research includes elements of Acetyltransferase, PCAF, Transcription and Transduction. Larry Kedes has researched Transcription factor in several fields, including Carcinogenesis, Regulation of gene expression, Oncogene and Mdm2.
The concepts of his Myocyte study are interwoven with issues in Cellular differentiation, Pathology, Myocardial infarction, Sodium butyrate and Transplantation. His Hes3 signaling axis study introduces a deeper knowledge of Cell biology. His Cell biology research is multidisciplinary, incorporating elements of Chromatin, Histone Acetyltransferases, Transcriptional regulation, N-terminus and Acetyltransferases.
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.
Isolation and characterization of full-length cDNA clones for human alpha-, beta-, and gamma-actin mRNAs: skeletal but not cytoplasmic actins have an amino-terminal cysteine that is subsequently removed.
P Gunning;P Ponte;H Okayama;J Engel.
Molecular and Cellular Biology (1983)
HES and HERP families: multiple effectors of the Notch signaling pathway.
Tatsuya Iso;Larry Kedes;Yasuo Hamamori.
Journal of Cellular Physiology (2003)
Evolutionary conservation in the untranslated regions of actin mRNAs: DNA sequence of a human beta-actin cDNA
Phyllis Ponte;Sun-Yu Ng;Joanne Engel;Peter Gunning.
Nucleic Acids Research (1984)
A human beta-actin expression vector system directs high-level accumulation of antisense transcripts
Peter Gunning;John Leavitt;George Muscat;Sun-Yu Ng.
Proceedings of the National Academy of Sciences of the United States of America (1987)
twist is a potential oncogene that inhibits apoptosis
Roberta Maestro;Angelo P. Dei Tos;Yasuo Hamamori;Svetlana Krasnokutsky.
Genes & Development (1999)
Survival and development of neonatal rat cardiomyocytes transplanted into adult myocardium.
Jochen Müller-Ehmsen;Peter Whittaker;Robert A. Kloner;Joan S. Dow.
Journal of Molecular and Cellular Cardiology (2002)
Upstream regions of the human cardiac actin gene that modulate its transcription in muscle cells: presence of an evolutionarily conserved repeated motif
A Minty;L Kedes.
Molecular and Cellular Biology (1986)
Differential roles of p300 and PCAF acetyltransferases in muscle differentiation
Pier Lorenzo Puri;Pier Lorenzo Puri;Vittorio Sartorelli;Vittorio Sartorelli;Xiang Jiao Yang;Yasuo Hamamori.
Molecular Cell (1997)
Evolution of the functional human beta-actin gene and its multi-pseudogene family: conservation of noncoding regions and chromosomal dispersion of pseudogenes.
Sun-Yu Ng;P. Gunning;R. Eddy;P. Ponte.
Molecular and Cellular Biology (1985)
Transplantation of fetal myocardial tissue into the infarcted myocardium of rat. A potential method for repair of infarcted myocardium
J. Leor;M. Patterson;M. J. Quinones;L. H. Kedes.
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: