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The Structure of the Pro-domain of Mouse proNGF in Contact with the NGF Domain

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Pathogenic tau does not drive activation of the unfolded protein response

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Biologically Enhanced Genome-Wide Association Study Provides Further Evidence for Candidate Loci and Discovers Novel Loci That Influence Risk of Anterior Cruciate Ligament Rupture in a Dog Model

Baker, L. A., Momen, M. M., McNally, R. M., Berres, M. E., Binversie, E. E., Sample, S. J., & Muir, P. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.593515 · Cited by 20

Reversal of Cognitive Impairment in gp120 Transgenic Mice by the Removal of the p75 Neurotrophin Receptor

Speidell, A. P., Asuni, G. P., Avdoshina, V., Scognamiglio, S., Forcelli, P. A., & Mocchetti, I. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00398 · Cited by 19

Disruption of SorCS2 reveals differences in the regulation of stereociliary bundle formation between hair cell types in the inner ear

Forge, A., Taylor, R., Dawson, S. J., Lovett, M., & Jagger, D. J. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1006692 · Cited by 19

Retrograde apoptotic signaling by the p75 neurotrophin receptor

Pathak, A., & Carter, B. D. (2017) · Neuronal Signaling · doi:10.1042/ns20160007 · Cited by 18

Artificial intelligence techniques for retinal prostheses: a comprehensive review and future direction

Wang, C., Fang, C., Zou, Y., Yang, J., & Sawan, M. (2023) · Journal of Neural Engineering · doi:10.1088/1741-2552/acb295 · Cited by 21

Fading memories in aging and neurodegeneration: Is p75 neurotrophin receptor a culprit?

Wong, L., Wang, Z., Ang, S. R. X., & Sajikumar, S. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101567 · Cited by 19

Interrogating Synaptic Architecture: Approaches for Labeling Organelles and Cytoskeleton Components

Reshetniak, S., & Rizzoli, S. O. (2019) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2019.00023 · Cited by 17

Disassembly of bundled F-actin and cellular remodeling via an interplay of Mical, cofilin, and F-actin crosslinkers

Rajan, S., Yoon, J., Wu, H., Srapyan, S., Baskar, R., Ahmed, G., Yang, T., Grintsevich, E. E., Reisler, E., & Terman, J. R. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2309955120 · Cited by 17

Targeting Endogenous Mechanisms of Brain Resilience for the Treatment and Prevention of Alzheimer's Disease

Shanks, H. R. C., Onuska, K. M., Massa, S. M., Schmitz, T. W., & Longo, F. M. (2023) · The Journal of Prevention of Alzheimer s Disease · doi:10.14283/jpad.2023.110 · Cited by 17

SorCS2 binds progranulin to regulate motor neuron development

Thomasen, P. B., Salašová, A., Kjær-Sørensen, K., Woloszczuková, L., Lavický, J., Login, H., Tranberg-Jensen, J., Almeida, S. A. D. O., Beel, S., Kavková, M., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113333 · Cited by 18

Scaled and efficient derivation of loss-of-function alleles in risk genes for neurodevelopmental and psychiatric disorders in human iPSCs

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Highly segregated localization of the functionally related vps10p receptors sortilin and SorCS2 during neurodevelopment

Boggild, S., Mølgaard, S., Glerup, S., & Nyengaard, J. R. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24403 · Cited by 14

Brain-derived neurotrophic factor – a key player in the gastrointestinal system

Singh, A. (2023) · Gastroenterology Review · doi:10.5114/pg.2023.132957 · Cited by 15

p75NTR-dependent Rac1 activation requires receptor cleavage and activation of an NRAGE and NEDD9 signaling cascade

Zeinieh, M. P., Salehi, A. H., Rajkumar, V. S., & Barker, P. A. (2014) · Journal of Cell Science · doi:10.1242/jcs.152173 · Cited by 14

BDNF and its Role in the Alcohol Abuse Initiated During Early Adolescence: Evidence from Preclinical and Clinical Studies

Cutuli, D., & Sampedro-Piquero, P. (2022) · Current Neuropharmacology · doi:10.2174/1570159x20666220624111855 · Cited by 16

Revising the mechanism of p75NTR activation: intrinsically monomeric state of death domains invokes the "helper" hypothesis

Goncharuk, S. A., Artemieva, L. E., Nadezhdin, K. D., Arseniev, A. S., & Mineev, K. S. (2020) · Scientific Reports · doi:10.1038/s41598-020-70721-8 · Cited by 13

RhoGDI phosphorylation by PKC promotes its interaction with death receptor p75NTR to gate axon growth and neuron survival

Ramanujan, A., Li, Z., Ma, Y., Lin, Z., & Ibáñez, C. F. (2024) · EMBO Reports · doi:10.1038/s44319-024-00064-2 · Cited by 12

Cleavage of p75 neurotrophin receptor is linked to Alzheimer’s disease

Chao, M. V. (2016) · Molecular Psychiatry · doi:10.1038/mp.2015.214 · Cited by 12

Long‐distance regressive signaling in neural development and disease

Pathak, A., Clark, S. A., Bronfman, F. C., Deppmann, C. D., & Carter, B. D. (2020) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.382 · Cited by 12

Neuronal Growth Cone Retraction Relies Upon Proneurotrophin Receptor Signaling Through Rac

Mains, R. E., & Eipper, B. A. (2011) · OpenCommons - UConn (University of Connecticut)

Rapid retraction of neurites by sensory neurons in response to increased concentrations of nerve growth factor.

Griffin, C., & Letourneau, P. C. (1980) · The Journal of Cell Biology · doi:10.1083/jcb.86.1.156 · Cited by 57

Neurotrophins Rapidly Modulate Growth Cone Response to the Axon Guidance Molecule, Collapsin-1

Tuttle, R., & O’Leary, D. D. M. (1998) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.1998.0671 · Cited by 104

p75 Neurotrophin Receptor Signaling Regulates Growth Cone Filopodial Dynamics through Modulating RhoA Activity

Gehler, S., Gallo, G., Veien, E. S., & Letourneau, P. C. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.0404-04.2004 · Cited by 131

Regulation of growth cone actin filaments by guidance cues

Gallo, G., & Letourneau, P. C. (2003) · Journal of Neurobiology · doi:10.1002/neu.10282 · Cited by 317