Stewart, Colin L.

LBR and lamin A/C sequentially tether peripheral heterochromatin and inversely regulate differentiation

Solovei, I., Wang, A. S., Thanisch, K., Schmidt, C. S., Krebs, S., Zwerger, M., Cohen, T. V., Devys, D., Foisner, R., Peichl, L., et al. (2013) · Cell

Nuclear Structure and FunctionGenomics and Chromatin Dynamics

Cited by 809

Astrocytes promote myelination in response to electrical impulses

Ishibashi, T., Dakin, K. A., Stevens, B., Lee, P. R., Kozlov, S. V., Stewart, C. L., & Fields, R. D. (2006) · Neuron

Neurogenesis and neuroplasticity mechanismsMultiple Sclerosis Research Studies

Cited by 689

Targeted disruption of NMDA receptor 1 gene abolishes NMDA response and results in neonatal death

Forrest, D., Yuzaki, M., Soares, H. D., Ng, L., Luk, D. C., Sheng, M., Stewart, C. L., Morgan, J. I., Connor, J. A., & Curran, T. (1994) · Neuron

Neuroscience and Neuropharmacology ResearchAmino Acid Enzymes and Metabolism

Cited by 491

Accelerated ageing in mice deficient in Zmpste24 protease is linked to p53 signalling activation

Varela, I., Cadiñanos, J., Pendás, A. M., Gutiérrez-Fernández, A., Folgueras, A. R., Sánchez, L. M., Zhou, Z., Rodríguez, F. J., Stewart, C. L., Vega, J. A., et al. (2005) · Nature

Nuclear Structure and FunctionGenetics, Aging, and Longevity in Model Organisms

Cited by 466

Lamin B1 fluctuations have differential effects on cellular proliferation and senescence

Dreesen, O., Chojnowski, A., Ong, P. F., Zhao, T. Y., Common, J. E., Lunny, D., Lane, E. B., Lee, S. J., Vardy, L. A., Stewart, C. L., et al. (2013) · Journal of Cell Biology

Nuclear Structure and FunctionTelomeres, Telomerase, and Senescence

Cited by 250

Normal spatial learning despite regional inhibition of LTP in mice lacking Thy-1

Nosten-Bertrand, M., Errington, M. L., Murphy, K. P. S. J., Tokugawa, Y., Barboni, E., Kozlova, E., Michalovich, D., Morris, R. G. M., Silver, J., Stewart, C. L., et al. (1996) · Nature

Neuroscience and Neuropharmacology ResearchMemory and Neural Mechanisms

Cited by 232

Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader–Willi syndrome genetic region

Jong, M. T. C., Carey, A. H., Caldwell, K. A., Lau, M. H., Handel, M. A., Driscoll, D. J., Stewart, C. L., Rinchik, E. M., & Nicholls, R. D. (1999) · Human Molecular Genetics

Genetic Syndromes and ImprintingGenomics and Chromatin Dynamics

Cited by 112

The Ancient Source of a Distinct Gene Family Encoding Proteins Featuring RING and C3H Zinc-Finger Motifs with Abundant Expression in Developing Brain and Nervous System

Gray, T. A., Hernandez, L., Carey, A. H., Schaldach, M. A., Smithwick, M. J., Rus, K., Marshall Graves, J. A., Stewart, C. L., & Nicholls, R. D. (2000) · Genomics

Genetics and Neurodevelopmental DisordersChromosomal and Genetic Variations

Cited by 108