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Single-cell q-PCR derived expression profiles of identified sensory neurons

Adelman, P. C., Baumbauer, K. M., Friedman, R. L., Shah, M. A., Wright, M. C., Young, E. E., Jankowski, M. P., Albers, K. M., & Koerber, H. R. (2019) · Molecular Pain · doi:10.1177/1744806919884496 · Cited by 28

A role for the neuropeptide somatostatin in the neurobiology of behaviors associated with substances abuse and affective disorders

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Spinoparabrachial projection neurons form distinct classes in the mouse dorsal horn

Browne, T. J., Smith, K. M., Gradwell, M. A., Iredale, J. A., Dayas, C. V., Callister, R. J., Hughes, D. I., & Graham, B. A. (2021) · Pain · doi:10.1097/j.pain.0000000000002194 · Cited by 29

TRPV1 SUMOylation suppresses itch by inhibiting TRPV1 interaction with H1 receptors

Gao, Y., Ma, R., Weng, W., Zhang, H., Wang, Y., Guo, R., Gu, X., Yang, Y., Yang, F., Zhou, A., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110972 · Cited by 29

Neuron‒Mast Cell Cross-Talk in the Skin

Zhang, S., Sumpter, T. L., & Kaplan, D. H. (2021) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2021.10.006 · Cited by 30

Intrinsic braking role of descending locus coeruleus noradrenergic neurons in acute and chronic itch in mice

Koga, K., Shiraishi, Y., Yamagata, R., Tozaki‐Saitoh, H., Shiratori‐Hayashi, M., & Tsuda, M. (2020) · Molecular Brain · doi:10.1186/s13041-020-00688-0 · Cited by 27

Neuron-specific spinal cord translatomes reveal a neuropeptide code for mouse dorsal horn excitatory neurons

Gupta, R. R. D., Scheurer, L., Pelczar, P., Wildner, H., & Zeilhofer, H. U. (2021) · Scientific Reports · doi:10.1038/s41598-021-84667-y · Cited by 27

An Integrated View on Neuronal Subsets in the Peripheral Nervous System and Their Role in Immunoregulation

Jakob, M. O., Kofoed-Branzk, M., Deshpande, D., Murugan, S., & Klose, C. S. N. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.679055 · Cited by 28

Interventions in the B ‐type natriuretic peptide signalling pathway as a means of controlling chronic itch

Meng, J., Chen, W., & Wang, J. (2019) · British Journal of Pharmacology · doi:10.1111/bph.14952 · Cited by 28

Neural ensembles that encode nocifensive mechanical and heat pain in mouse spinal cord

Zhang, M., Kupari, J., Su, J., Magnusson, K. A., Hu, Y., Calvo-Enrique, L., Usoskin, D., Albisetti, G. W., Ceder, M. M., Henriksson, K., et al. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-01921-6 · Cited by 31

Expression of green fluorescent protein defines a specific population of lamina II excitatory interneurons in the GRP::eGFP mouse

Bell, A. M., Gutierrez-Mecinas, M., Stevenson, A., Casas-Benito, A., Wildner, H., West, S. J., Watanabe, M., & Todd, A. J. (2020) · Scientific Reports · doi:10.1038/s41598-020-69711-7 · Cited by 25

Upconversion Nanoparticles–Based Multiplex Protein Activation to Neuron Ablation for Locomotion Regulation

Zhang, Y., Zhang, W., Zeng, K., Ao, Y., Wang, M., Yu, Z., Qi, F., Yu, W., Mao, H., Tao, L., et al. (2020) · Small · doi:10.1002/smll.201906797 · Cited by 25

Spinal gastrin releasing peptide receptor expressing interneurons are controlled by local phasic and tonic inhibition

Freitag, F. B., Ahemaiti, A., Jakobsson, J. E. T., Weman, H. M., & Lagerström, M. C. (2019) · Scientific Reports · doi:10.1038/s41598-019-52642-3 · Cited by 25

Kappa opioids inhibit spinal output neurons to suppress itch

Sheahan, T. D., Warwick, C. A., Cui, Y., Baranger, D. A. A., Perry, V. J., Smith, K. M., Manalo, A. P., Nguyen, E. K., Koerber, H. R., & Ross, S. E. (2024) · Science Advances · doi:10.1126/sciadv.adp6038 · Cited by 24

GRPR/Extracellular Signal–Regulated Kinase and NPRA/Extracellular Signal–Regulated Kinase Signaling Pathways Play a Critical Role in Spinal Transmission of Chronic Itch

Liu, X., Wang, Y., Tao, T., Zeng, L., De, W., Wen, Y., Li, Y., Zhao, Z., & Tao, A. (2020) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2020.09.008 · Cited by 25

Mechanisms and treatments of neuropathic itch in a mouse model of lymphoma

Ouyang, C., He, Q., Han, Q., Furutani, K., Gu, Y., Olexa, M., & Ji, R. (2022) · Journal of Clinical Investigation · doi:10.1172/jci160807 · Cited by 24

Identification of a Sacral, Visceral Sensory Transcriptome in Embryonic and Adult Mice

Anttila, C. J. A., Mason, E. A., Wells, C. A., Aronow, B. J., Osborne, P. B., & Keast, J. R. (2020) · eNeuro · doi:10.1523/eneuro.0397-19.2019 · Cited by 24

Neonatal Injury Evokes Persistent Deficits in Dynorphin Inhibitory Circuits within the Adult Mouse Superficial Dorsal Horn

Brewer, C. L., Li, J., O'Conor, K., Serafin, E. K., & Baccei, M. L. (2020) · The Journal of Neuroscience · doi:10.1523/jneurosci.0029-20.2020 · Cited by 23

Spinal somatostatin-positive interneurons transmit chemical itch

Fatima, M., Ren, X., Pan, H., Slade, H. F. E., Asmar, A. J., Xiong, C. M., Shi, A., Xiong, A. E., Wang, L., & Duan, B. (2019) · Pain · doi:10.1097/j.pain.0000000000001499 · Cited by 41

Targeting and driving somatosensory neurons

Freitag, F. B. (2020) · Uppsala University Publications (Uppsala University)

Neuropeptide Y in itch regulation

Jakobsson, J. E. T., Ma, H., & Lagerström, M. C. (2019) · Neuropeptides · doi:10.1016/j.npep.2019.101976 · Cited by 20

Transmission of Pruriceptive Signals

Mishra, S. K., & Hoon, M. A. (2015) · Handbook of experimental pharmacology · doi:10.1007/978-3-662-44605-8_8 · Cited by 27

Roles for substance P and gastrin-releasing peptide as neurotransmitters released by primary afferent pruriceptors

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