1973 - Fellow of John Simon Guggenheim Memorial Foundation
His primary scientific interests are in Ataxia-telangiectasia, Genetics, Molecular biology, Mutation and Immunology. Richard A. Gatti works in the field of Ataxia-telangiectasia, namely Nijmegen breakage syndrome. He combines subjects such as Ataxia and Radiosensitivity with his study of Nijmegen breakage syndrome.
His Molecular biology study combines topics from a wide range of disciplines, such as DNA ligase, DNA, DNA-binding protein, Complementary DNA and Transcription. As a part of the same scientific study, Richard A. Gatti usually deals with the Mutation, concentrating on Heterozygote advantage and frequently concerns with Missense mutation, Chromosomal region, Thymic hypoplasia and Genetic marker. His Immunology study combines topics in areas such as Disease and Transplantation.
The scientist’s investigation covers issues in Ataxia-telangiectasia, Genetics, Immunology, Molecular biology and Gene. His Ataxia-telangiectasia research focuses on Nijmegen breakage syndrome in particular. His Nijmegen breakage syndrome study integrates concerns from other disciplines, such as Nibrin and Microcephaly.
His work in Molecular biology tackles topics such as DNA repair which are related to areas like Cell biology. His Gene mapping research includes themes of Restriction fragment length polymorphism and Locus. Richard A. Gatti has researched Cancer research in several fields, including Cancer and Radiosensitivity.
Richard A. Gatti focuses on Ataxia-telangiectasia, Genetics, Molecular biology, DNA repair and Mutation. His research integrates issues of Cancer research, Immunology, Ataxia, Cerebellar ataxia and Disease in his study of Ataxia-telangiectasia. His work deals with themes such as Cancer and Cell cycle checkpoint, which intersect with Cancer research.
The study incorporates disciplines such as DNA, Superoxide dismutase, Mutant and Gentamicin protection assay in addition to Molecular biology. His DNA repair research incorporates elements of Cell culture, DNA damage, Homologous recombination and Cell biology. Richard A. Gatti has included themes like Transfection, Messenger RNA, Exon, Oligonucleotide and Intron in his Mutation study.
Richard A. Gatti mainly investigates Ataxia-telangiectasia, Molecular biology, DNA repair, Genetics and DNA damage. The Ataxia-telangiectasia study combines topics in areas such as Dermatology, Mutation, Ataxia, Nonsense mutation and Transcription. His Mutation research is multidisciplinary, incorporating elements of Cerebellum, Cancer research, Exon, Pediatrics and Genetic testing.
His research in Molecular biology intersects with topics in Cancer cell, Gene and Gentamicin protection assay. His study in DNA repair is interdisciplinary in nature, drawing from both Stem cell and Cell biology. His DNA damage research is multidisciplinary, incorporating perspectives in Cellular differentiation, Immunoglobulin class switching, CREB, Promoter and Signal transduction.
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.
A SINGLE ATAXIA TELANGIECTASIA GENE WITH A PRODUCT SIMILAR TO PI-3 KINASE
Kinneret Savitsky;Anat Bar-Shira;Shlomit Gilad;Galit Rotman.
Science (1995)
Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome
Raymonda Varon;Christine Vissinga;Matthias Platzer;Karen M Cerosaletti.
Cell (1998)
Occurrence of malignancy in immunodeficiency diseases. A literature review.
Richard A. Gatti;Robert A. Good.
Cancer (1971)
Localization of an ataxia-telangiectasia gene to chromosome 11q22–23
Richard A. Gatti;Izzet Berkel;Elena Boder;Gary Braedt.
Nature (1988)
ATM-dependent phosphorylation of nibrin in response to radiation exposure
Magtouf Gatei;David Young;Karen M. Cerosaletti;Ami Desai-Mehta.
Nature Genetics (2000)
Functional link between ataxia-telangiectasia and Nijmegen breakage syndrome gene products
Song Zhao;Yi-Chinn Weng;Shyng-Shiou F. Yuan;Shyng-Shiou F. Yuan;Yi-Tzu Lin.
Nature (2000)
DNA Ligase IV Mutations Identified in Patients Exhibiting Developmental Delay and Immunodeficiency
Mark O'Driscoll;Karen M. Cerosaletti;Pierre M. Girard;Yan Dai.
Molecular Cell (2001)
Ataxia–telangiectasia, an evolving phenotype
Helen H Chun;Richard A Gatti.
DNA Repair (2004)
Splicing Defects in the Ataxia-Telangiectasia Gene, ATM: Underlying Mutations and Consequences
Sharon N. Teraoka;Milhan Telatar;Sara Becker-Catania;Teresa Liang.
American Journal of Human Genetics (1999)
Ataxia-telangiectasia: an interdisciplinary approach to pathogenesis.
Richard A. Gatti;Elena Boder;Harry V. Vinters;Robert S. Sparkes.
Medicine (1991)
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:
University of Florida
University of Minnesota
University of Queensland
University of Colorado Anschutz Medical Campus
Oslo University Hospital
University of California, Los Angeles
University of California, Los Angeles
QIMR Berghofer Medical Research Institute
University of Pittsburgh
Vanderbilt University Medical Center
University of Zaragoza
North Carolina State University
University of Southern California
Kyoto University
University of Toronto
University of Strasbourg
Macquarie University
National Institutes of Health
Kiel University
University of New Mexico
University of Bremen
Adolfo Ibáñez University
University of Bergen
Stanford University
Mayo Clinic
Leiden University