Cleveland, Don W.

ZW10 links mitotic checkpoint signaling to the structural kinetochore

Kops, G. J. P. L., Kim, Y., Weaver, B. A. A., Mao, Y., McLeod, I., Yates, J. R., Tagaya, M., & Cleveland, D. W. (2005) · The Journal of Cell Biology

Microtubule and mitosis dynamicsDNA Repair Mechanisms

Cited by 249

Unattached Kinetochores Catalyze Production of an Anaphase Inhibitor that Requires a Mad2 Template to Prime Cdc20 for BubR1 Binding

Kulukian, A., Han, J. S., & Cleveland, D. W. (2009) · Developmental Cell

Microtubule and mitosis dynamicsDNA Repair Mechanisms

Cited by 246

Blood–spinal cord barrier disruption contributes to early motor-neuron degeneration in ALS-model mice

Winkler, E. A., Sengillo, J. D., Sagare, A. P., Zhao, Z., Ma, Q., Zuniga, E., Wang, Y., Zhong, Z., Sullivan, J. S., Griffin, J. H., et al. (2014) · Proceedings of the National Academy of Sciences

Amyotrophic Lateral Sclerosis ResearchBarrier Structure and Function Studies

Cited by 238

Tubulin requires tau for growth onto microtubule initiating sites.

Witman, G. B., Cleveland, D. W., Weingarten, M. D., & Kirschner, M. W. (1976) · Proceedings of the National Academy of Sciences

Microtubule and mitosis dynamicsAlzheimer's disease research and treatments

Cited by 238

Aurora kinases and protein phosphatase 1 mediate chromosome congression through regulation of CENP-E

Kim, Y., Holland, A. J., Lan, W., & Cleveland, D. W. (2010) · Cell

Microtubule and mitosis dynamicsGenomics and Chromatin Dynamics

Cited by 233

Reduced C9ORF72 function exacerbates gain of toxicity from ALS/FTD-causing repeat expansion in C9orf72

Zhu, Q., Jiang, J., Gendron, T. F., McAlonis-Downes, M., Jiang, L., Taylor, A., Diaz Garcia, S., Ghosh Dastidar, S., Rodriguez, M. J., King, P., et al. (2020) · Nature Neuroscience

Amyotrophic Lateral Sclerosis ResearchGenetic Neurodegenerative Diseases

Cited by 220

Prion-like spread of protein aggregates in neurodegeneration

Polymenidou, M., & Cleveland, D. W. (2012) · Journal of Experimental Medicine

Alzheimer's disease research and treatmentsPrion Diseases and Protein Misfolding

Cited by 184

Activated protein C therapy slows ALS-like disease in mice by transcriptionally inhibiting SOD1 in motor neurons and microglia cells

Zhong, Z., Ilieva, H., Hallagan, L., Bell, R., Singh, I., Paquette, N., Thiyagarajan, M., Deane, R., Fernandez, J. A., Lane, S., et al. (2009) · Journal of Clinical Investigation

Amyotrophic Lateral Sclerosis ResearchAlzheimer's disease research and treatments

Cited by 176

ALS-linked mutant superoxide dismutase 1 (SOD1) alters mitochondrial protein composition and decreases protein import

Li, Q., Vande Velde, C., Israelson, A., Xie, J., Bailey, A. O., Dong, M.-Q., Chun, S.-J., Roy, T., Winer, L., Yates, J. R., et al. (2010) · Proceedings of the National Academy of Sciences

Amyotrophic Lateral Sclerosis ResearchMitochondrial Function and Pathology

Cited by 169

Misregulated RNA processing in amyotrophic lateral sclerosis

Polymenidou, M., Lagier-Tourenne, C., Hutt, K. R., Bennett, C. F., Cleveland, D. W., & Yeo, G. W. (2012) · Brain Research

Amyotrophic Lateral Sclerosis ResearchRNA Research and Splicing

Cited by 169

CRISPR-Cas9 Screens Identify the RNA Helicase DDX3X as a Repressor of C9ORF72 (GGGGCC)n Repeat-Associated Non-AUG Translation

Cheng, W., Wang, S., Zhang, Z., Morgens, D. W., Hayes, L. R., Lee, S., Portz, B., Xie, Y., Nguyen, B. V., Haney, M. S., et al. (2019) · Neuron

Amyotrophic Lateral Sclerosis ResearchGenetic Neurodegenerative Diseases

Cited by 138

Antisense drugs make sense for neurological diseases

Bennett, C. F., Kordasiewicz, H. B., & Cleveland, D. W. (2021) · Annual Review of Pharmacology and Toxicology

RNA Interference and Gene DeliveryAmyotrophic Lateral Sclerosis Research

Cited by 108

Cerebellar c9RAN proteins associate with clinical and neuropathological characteristics of C9ORF72 repeat expansion carriers

Gendron, T. F., van Blitterswijk, M., Bieniek, K. F., Daughrity, L. M., Jiang, J., Rush, B. K., Pedraza, O., Lucas, J. A., Murray, M. E., Desaro, P., et al. (2015) · Acta Neuropathologica

Amyotrophic Lateral Sclerosis ResearchGenetic Neurodegenerative Diseases

Cited by 106

Therapeutically viable generation of neurons with antisense oligonucleotide suppression of PTB

Maimon, R., Chillon-Marinas, C., Snethlage, C. E., Singhal, S. M., McAlonis-Downes, M., Ling, K., Rigo, F., Bennett, C. F., Da Cruz, S., Hnasko, T. S., et al. (2021) · Nature Neuroscience

Neurogenesis and neuroplasticity mechanismsNeuroscience and Neuropharmacology Research

Cited by 62

Gene regulation through messenger RNA stability

Cleveland, D. W. (1989) · Current Opinion in Cell Biology

Immunotherapy and Immune ResponsesRNA Research and Splicing

Cited by 43

A phage nucleus-associated RNA-binding protein is required for jumbo phage infection

Enustun, E., Armbruster, E. G., Lee, J., Zhang, S., Yee, B. A., Malukhina, K., Gu, Y., Deep, A., Naritomi, J. T., Liang, Q., et al. (2024) · Nucleic Acids Research

Bacteriophages and microbial interactionsBacterial Genetics and Biotechnology

Cited by 27

Comment on "A Centrosome-Independent Role for γ-TuRC Proteins in the Spindle Assembly Checkpoint"

Weaver, B. A. A., & Cleveland, D. W. (2007) · Science

Microtubule and mitosis dynamicsDNA Repair Mechanisms

Cited by 21

Aberrant splicing in Huntington’s disease via disrupted TDP-43 activity accompanied by altered m6A RNA modification

Nguyen, T. B., Miramontes, R., Chillon-Marinas, C., Maimon, R., Vazquez-Sanchez, S., Lau, A. L., McClure, N. R., England, W. E., Singha, M., Stocksdale, J. T., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory)

Genetic Neurodegenerative DiseasesRNA Research and Splicing

Cited by 15