Richard A. Gatti
Affiliations: | Biomedical Physics 0119 | University of California, Los Angeles, Los Angeles, CA |
Area:
Cell Biology, General BiophysicsGoogle:
"Richard Gatti"Mean distance: (not calculated yet)
Children
Sign in to add trainee| Sara G. Becker-Catania | grad student | 2000 | UCLA |
| Helen H. Chun | grad student | 2002 | UCLA |
| Chih-Hung Lai | grad student | 2004 | UCLA |
| Shareef A. Nahas | grad student | 2008 | UCLA |
| Julianne M. Pollard | grad student | 2008 | UCLA |
| Nathan T. Martin | grad student | 2014 | UCLA |
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Publications
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| Perez H, Abdallah MF, Chavira JI, et al. (2021) A novel, ataxic mouse model of ataxia telangiectasia caused by a clinically relevant nonsense mutation. Elife. 10 |
| Liu X, Paila UD, Teraoka SN, et al. (2017) Identification of ATIC as a Novel Target for Chemoradiosensitization. International Journal of Radiation Oncology, Biology, Physics |
| Hu H, Nahas S, Gatti RA. (2017) Assaying Radiosensitivity of Ataxia-Telangiectasia. Methods in Molecular Biology (Clifton, N.J.). 1599: 1-11 |
| Pathak A, Seipel K, Pemov A, et al. (2015) Whole-exome sequencing reveals a C-terminal germline variant in CEBPA-associated acute myeloid leukemia: 45-year follow-up of a large family. Haematologica |
| Gómez-Grau M, Garrido E, Cozar M, et al. (2015) Evaluation of Aminoglycoside and Non-Aminoglycoside Compounds for Stop-Codon Readthrough Therapy in Four Lysosomal Storage Diseases. Plos One. 10: e0135873 |
| Patel JP, Puck JM, Srinivasan R, et al. (2015) Nijmegen breakage syndrome detected by newborn screening for T cell receptor excision circles (TRECs). Journal of Clinical Immunology. 35: 227-33 |
| Björkman A, Qvist P, Du L, et al. (2015) Aberrant recombination and repair during immunoglobulin class switching in BRCA1-deficient human B cells. Proceedings of the National Academy of Sciences of the United States of America. 112: 2157-62 |
| Pathak A, Seipel K, Pemov A, et al. (2015) Abstract 2756: Whole-exome sequencing reveals a novel germline variant in CEBPA-associated familial acute myeloid leukemia: 45-year follow-up of a large family Cancer Research. 75: 2756-2756 |
| Nakamura K, Fike F, Haghayegh S, et al. (2014) A-TWinnipeg: Pathogenesis of rare ATM missense mutation c.6200C>A with decreased protein expression and downstream signaling, early-onset dystonia, cancer, and life-threatening radiotoxicity. Molecular Genetics & Genomic Medicine. 2: 332-40 |
| Stewart DR, Pemov A, Johnston JJ, et al. (2014) Dubowitz syndrome is a complex comprised of multiple, genetically distinct and phenotypically overlapping disorders. Plos One. 9: e98686 |