Grinberg, Alexander

Targeted deletion of the gene encoding iron regulatory protein-2 causes misregulation of iron metabolism and neurodegenerative disease in mice

LaVaute, T., Smith, S., Cooperman, S., Iwai, K., Land, W., Meyron-Holtz, E., Drake, S. K., Miller, G., Abu-Asab, M., Tsokos, M., et al. (2001) · Nature Genetics

Iron Metabolism and DisordersNeurological diseases and metabolism

Cited by 509

Mouse models of Tay–Sachs and Sandhoff diseases differ in neurologic phenotype and ganglioside metabolism

Sango, K., Yamanaka, S., Hoffmann, A., Okuda, Y., Grinberg, A., Westphal, H., McDonald, M. P., Crawley, J. N., Sandhoff, K., Suzuki, K., et al. (1995) · Nature Genetics

Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and Myoclonus

Cited by 468

Failure to produce mitochondrial DNA results in embryonic lethality in Rnaseh1 null mice

Cerritelli, S. M., Frolova, E. G., Feng, C., Grinberg, A., Love, P. E., & Crouch, R. J. (2003) · Molecular Cell

Mitochondrial Function and PathologyDNA Repair Mechanisms

Cited by 358

Development and characterization of a hypomorphic Smith-Lemli-Opitz syndrome mouse model and efficacy of simvastatin therapy

Correa-Cerro, L. S., Wassif, C. A., Kratz, L., Miller, G. F., Munasinghe, J. P., Grinberg, A., Fliesler, S. J., & Porter, F. D. (2006) · Human Molecular Genetics

Cholesterol and Lipid MetabolismMetabolism and Genetic Disorders

Cited by 75

Two RNase H2 Mutants with Differential rNMP Processing Activity Reveal a Threshold of Ribonucleotide Tolerance for Embryonic Development

Uehara, R., Cerritelli, S. M., Hasin, N., Sakhuja, K., London, M., Iranzo, J., Chon, H., Grinberg, A., & Crouch, R. J. (2018) · Cell Reports

DNA Repair MechanismsRNA regulation and disease

Cited by 52