Cox, Gregory A.

Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia

Tam, O. H., Rozhkov, N. V., Shaw, R., Kim, D., Hubbard, I., Fennessey, S., Propp, N., Phatnani, H., Kwan, J., Sareen, D., et al. (2019) · Cell Reports

Amyotrophic Lateral Sclerosis ResearchAlzheimer's disease research and treatments

Cited by 327

Gait analysis detects early changes in transgenic SOD1(G93A) mice

Wooley, C. M., Sher, R. B., Kale, A., Frankel, W. N., Cox, G. A., & Seburn, K. L. (2005) · Muscle & Nerve

Amyotrophic Lateral Sclerosis ResearchHereditary Neurological Disorders

Cited by 182

Development-on-chip: in vitro neural tube patterning with a microfluidic device

Demers, C. J., Soundararajan, P., Chennampally, P., Cox, G. A., Briscoe, J., Collins, S. D., & Smith, R. L. (2016) · Development

Developmental Biology and Gene RegulationMicrofluidic and Capillary Electrophoresis Applications

Cited by 149

Identification of the Mouse Neuromuscular Degeneration Gene and Mapping of a Second Site Suppressor Allele

Cox, G. A., Mahaffey, C. L., & Frankel, W. N. (1998) · Neuron

Amyotrophic Lateral Sclerosis ResearchHereditary Neurological Disorders

Cited by 125

Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy

Mitsuhashi, S., Hatakeyama, H., Karahashi, M., Koumura, T., Nonaka, I., Hayashi, Y. K., Noguchi, S., Sher, R. B., Nakagawa, Y., Manfredi, G., et al. (2011) · Human Molecular Genetics

Mitochondrial Function and PathologyMuscle Physiology and Disorders

Cited by 95

Grey, a novel mutation in the murine Lyst gene, causes the beige phenotype by skipping of exon 25

Runkel, F., Büssow, H., Seburn, K. L., Cox, G. A., Ward, D. M., Kaplan, J., & Franz, T. (2006) · Mammalian Genome

melanin and skin pigmentationImmunodeficiency and Autoimmune Disorders

Cited by 61