Gideon Rechavi
Affiliations: | BCH Biological Chemistry | Weizmann Institute of Science, Rehovot, Israel |
Area:
Biochemistry, Cell Biology, Oncology, GeneticsGoogle:
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Publications
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| Vardi I, Chermesh I, Werner L, et al. (2020) Monogenic Inflammatory Bowel Disease: It's Never Too Late to Make a Diagnosis. Frontiers in Immunology. 11: 1775 |
| Goldberg L, Simon AJ, Lev A, et al. (2020) Atypical immune phenotype in severe combined immunodeficiency patients with novel mutations in IL2RG and JAK3. Genes and Immunity |
| Goldberg L, Simon AJ, Rechavi G, et al. (2020) Congenital neutropenia with variable clinical presentation in novel mutation of the SRP54 gene. Pediatric Blood & Cancer. e28237 |
| Livneh I, Moshitch-Moshkovitz S, Amariglio N, et al. (2019) The mA epitranscriptome: transcriptome plasticity in brain development and function. Nature Reviews. Neuroscience |
| Heimer G, van Woerden GM, Barel O, et al. (2019) Netrin-G2 dysfunction causes a Rett-like phenotype with areflexia. Human Mutation |
| Manevitz-Mendelson E, Leichner GS, Barel O, et al. (2018) Somatic NRAS mutation in patient with generalized lymphatic anomaly. Angiogenesis |
| Somech R, Lev A, Lee YN, et al. (2017) Disruption of Thrombocyte and T Lymphocyte Development by a Mutation in ARPC1B. Journal of Immunology (Baltimore, Md. : 1950) |
| Campbell BB, Light N, Fabrizio D, et al. (2017) Comprehensive Analysis of Hypermutation in Human Cancer. Cell |
| Marcu-Malina V, Goldberg S, Vax E, et al. (2016) ADAR1 is vital for B cell lineage development in the mouse bone marrow. Oncotarget |
| Simon AJ, Lev A, Zhang Y, et al. (2016) Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects. The Journal of Experimental Medicine |