Tether-free photothermal deep-brain stimulation in freely behaving mice via wide-field illumination in the near-infrared-II window

Statistical Power Analysis for the Behavioral Sciences

Cohen, J. (2013) · doi:10.4324/9780203771587 · Cited by 25,373

Calcium's Role in Mechanotransduction during Muscle Development

Damm, T. B., & Egli, M. (2014) · Cellular Physiology and Biochemistry · doi:10.1159/000356667 · Cited by 14,552

Calcium signalling: dynamics, homeostasis and remodelling

Berridge, M. J., Bootman, M. D., & Roderick, H. L. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1155 · Cited by 5,719

Genome-wide atlas of gene expression in the adult mouse brain

Lein, E. S., Hawrylycz, M. J., Ao, N., Ayres, M., Bensinger, A., Bernard, A., Boe, A. F., Boguski, M. S., Brockway, K. S., Byrnes, E. J., et al. (2007) · Nature · doi:10.1038/nature05453 · Cited by 5,572

Near-infrared fluorophores for biomedical imaging

Hong, G., Antaris, A. L., & Dai, H. (2017) · Nature Biomedical Engineering · doi:10.1038/s41551-016-0010 · Cited by 3,048

Second window for in vivo imaging

Smith, A. M., Mancini, M. C., & Nie, S. (2009) · Nature Nanotechnology · doi:10.1038/nnano.2009.326 · Cited by 2,848

Neurodegenerative Disorders: Parkinson's Disease and Huntington's Disease

Hague, S., Klaffke, S., & Bandmann, O. (2006) · IMPERIAL COLLEGE PRESS eBooks · doi:10.1142/9781860948961_0007 · Cited by 2,767

The development and application of optogenetics

Fenno, L., Yizhar, O., & Deisseroth, K. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113817 · Cited by 1,822

Optical properties of human skin, subcutaneous and mucous tissues in the wavelength range from 400 to 2000 nm

Bashkatov, A. N., Genina, E. A., Kochubey, V. I., & Tuchin, V. V. (2005) · Journal of Physics D: Applied Physics · doi:10.1088/0022-3727/38/15/004 · Cited by 1,720

Engineered AAVs for efficient noninvasive gene delivery to the central and peripheral nervous systems

Chan, K. Y., Jang, M. J., Yoo, B. B., Greenbaum, A., Ravi, N., Wu, W.-L., Sánchez-Guardado, L., Lois, C., Mazmanian, S. K., Deverman, B. E., et al. (2017) · Nature Neuroscience · doi:10.1038/nn.4593 · Cited by 1,578

Optical Deconstruction of Parkinsonian Neural Circuitry

Gradinaru, V., Mogri, M., Thompson, K. R., Henderson, J. M., & Deisseroth, K. A. (2009) · Science · doi:10.1126/science.1167093 · Cited by 1,527

Deep brain stimulation: current challenges and future directions

Lozano, A. M., Lipsman, N., Bergman, H., Brown, P., Chabardès, S., Chang, J. W., Matthews, K., McIntyre, C. C., Schlaepfer, T. E., Schulder, M., et al. (2019) · Nature Reviews Neurology · doi:10.1038/s41582-018-0128-2 · Cited by 1,475

A toolbox of Cre-dependent optogenetic transgenic mice for light-induced activation and silencing

Madisen, L., Mao, T., Koch, H., Zhuo, J.-M., Berenyi, A., Fujisawa, S., Hsu, Y.-W. A., Garcia, A. J., Gu, X., Zanella, S., et al. (2012) · Nature Neuroscience · doi:10.1038/nn.3078 · Cited by 1,398

Phasic Firing in Dopaminergic Neurons Is Sufficient for Behavioral Conditioning

Tsai, H.-C., Zhang, F., Adamantidis, A., Stuber, G. D., Bonci, A., de Lecea, L., & Deisseroth, K. (2009) · Science · doi:10.1126/science.1168878 · Cited by 1,266

Injectable, Cellular-Scale Optoelectronics with Applications for Wireless Optogenetics

Kim, T.-I., McCall, J. G., Jung, Y. H., Huang, X., Siuda, E. R., Li, Y., Song, J., Song, Y. M., Pao, H. A., Kim, R.-H., et al. (2013) · Science · doi:10.1126/science.1232437 · Cited by 1,174

Near-infrared deep brain stimulation via upconversion nanoparticle–mediated optogenetics

Chen, S., Weitemier, A. Z., Zeng, X., He, L., Wang, X., Tao, Y., Huang, A. J. Y., Hashimotodani, Y., Kano, M., Iwasaki, H., et al. (2018) · Science · doi:10.1126/science.aaq1144 · Cited by 1,134

Remote Control of Neuronal Activity in Transgenic Mice Expressing Evolved G Protein-Coupled Receptors

Alexander, G. M., Rogan, S. C., Abbas, A. I., Armbruster, B. N., Pei, Y., Allen, J., Nonneman, R. J., Hartmann, J. F., Moy, S. S., Nicolelis, M. A. L., et al. (2009) · Neuron · doi:10.1016/j.neuron.2009.06.014 · Cited by 1,019

Temperature-feedback upconversion nanocomposite for accurate photothermal therapy at facile temperature

Zhu, X., Feng, W., Chang, J., Tan, Y.-W., Li, J., Chen, M., Sun, Y., & Li, F. (2016) · Nature Communications · doi:10.1038/ncomms10437 · Cited by 1,014

Molecular afterglow imaging with bright, biodegradable polymer nanoparticles

Miao, Q., Xie, C., Xu, Z. J., Lyu, Y., Duan, H., Liu, X., Jokerst, J. V., & Pu, K. (2017) · Nature Biotechnology · doi:10.1038/nbt.3987 · Cited by 980

Deep-tissue anatomical imaging of mice using carbon nanotube fluorophores in the second near-infrared window

Welsher, K., Sherlock, S. P., & Dai, H. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1014501108 · Cited by 958

Lanthanide-doped upconversion nano-bioprobes: electronic structures, optical properties, and biodetection

Zheng, W., Huang, P., Tu, D., Ma, E., Zhu, H., & Chen, X. (2014) · Chemical Society Reviews · doi:10.1039/c4cs00178h · Cited by 894

ReaChR: a red-shifted variant of channelrhodopsin enables deep transcranial optogenetic excitation

Lin, J. Y., Knutsen, P. M., Muller, A., Kleinfeld, D., & Tsien, R. Y. (2013) · Nature Neuroscience · doi:10.1038/nn.3502 · Cited by 821

Trp ion channels and temperature sensation

Dhaka, A., Viswanath, V., & Patapoutian, A. (2006) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.112958 · Cited by 782

Remote control of ion channels and neurons through magnetic-field heating of nanoparticles

Huang, H. S., Delikanli, S., Zeng, H., Ferkey, D. M., & Pralle, A. (2010) · Nature Nanotechnology · doi:10.1038/nnano.2010.125 · Cited by 781

Optical-Thermal Response of Laser-Irradiated Tissue

Welch, A. J., & van Gemert, M. J. C. (1995) · Springer eBooks · doi:10.1007/978-1-4757-6092-7 · Cited by 705

Novel electrode technologies for neural recordings

Hong, G., & Lieber, C. M. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0140-6 · Cited by 695

Wireless magnetothermal deep brain stimulation

Chen, R., Romero, G., Christiansen, M. G., Mohr, A. C., & Anikeeva, P. (2015) · Science · doi:10.1126/science.1261821 · Cited by 694

Optical properties of selected native and coagulated human brain tissues in vitro in the visible and near infrared spectral range

Yaroslavsky, A. N., Schulze, P. C., Yaroslavsky, I. V., Schober, R., Ulrich, F., & Schwarzmaier, H.-J. (2002) · Physics in Medicine and Biology · doi:10.1088/0031-9155/47/12/305 · Cited by 656

Cortical layer-specific critical dynamics triggering perception

Marshel, J. H., Kim, Y. S., Machado, T. A., Quirin, S., Benson, B., Kadmon, J., Raja, C., Chibukhchyan, A., Ramakrishnan, C., Inoue, M., et al. (2019) · Science · doi:10.1126/science.aaw5202 · Cited by 652

Glial responses to implanted electrodes in the brain

Salatino, J. W., Ludwig, K. A., Kozai, T. D. Y., & Purcell, E. K. (2017) · Nature Biomedical Engineering · doi:10.1038/s41551-017-0154-1 · Cited by 642

Infrared light excites cells by changing their electrical capacitance

Shapiro, M. G., Homma, K., Villarreal, S., Richter, C., & Bezanilla, F. (2012) · Nature Communications · doi:10.1038/ncomms1742 · Cited by 613

Wirelessly powered, fully internal optogenetics for brain, spinal and peripheral circuits in mice

Montgomery, K. L., Yeh, A. J., Ho, J. S., Tsao, V., Mohan Iyer, S., Grosenick, L., Ferenczi, E. A., Tanabe, Y., Deisseroth, K., Delp, S. L., et al. (2015) · Nature Methods · doi:10.1038/nmeth.3536 · Cited by 565

Noninvasive optical inhibition with a red-shifted microbial rhodopsin

Miri, M. L., Busskamp, V., Young, A., Ogawa, M., Ramanlal, S. B., Forest, C. R., Chow, B. Y., Han, X., Lin, Y., Roska, B., et al. (2014) · DSpace@MIT (Massachusetts Institute of Technology) · Cited by 554

Projections from neocortex mediate top-down control of memory retrieval

Rajasethupathy, P., Sankaran, S., Marshel, J. H., Kim, C. K., Ferenczi, E., Lee, S. Y., Berndt, A., Ramakrishnan, C., Jaffe, A., Lo, M., et al. (2015) · Nature · doi:10.1038/nature15389 · Cited by 509

Molecular basis of infrared detection by snakes

Gracheva, E. O., Ingolia, N. T., Kelly, Y. M., Cordero-Morales, J. F., Hollopeter, G., Chesler, A. T., Sanchez, E. E., Pérez, J. C., Weissman, J. S., & Julius, D. J. (2010) · Nature · doi:10.1038/nature08943 · Cited by 490

Targeting and Readout Strategies for Fast Optical Neural ControlIn VitroandIn Vivo

Gradinaru, V., Thompson, K. R., Zhang, F., Mogri, M., Kay, K., Schneider, M. B., & Deisseroth, K. A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3578-07.2007 · Cited by 466

Semiconducting Polymer Nanobioconjugates for Targeted Photothermal Activation of Neurons

Lyu, Y., Xie, C., Chechetka, S. A., Miyako, E., & Pu, K. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b05192 · Cited by 461

Thermal constraints on in vivo optogenetic manipulations

Owen, S. F., Liu, M. H., & Kreitzer, A. C. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0422-3 · Cited by 415

Bioinspired neuron-like electronics

Yang, X., Zhou, T., Zwang, T. J., Hong, G., Zhao, Y., Viveros, R. D., Fu, T.-M., Gao, T., & Lieber, C. M. (2019) · Nature Materials · doi:10.1038/s41563-019-0292-9 · Cited by 384

Sonogenetics is a non-invasive approach to activating neurons in Caenorhabditis elegans

Ibsen, S. D., Tong, A., Schutt, C. E., Esener, S. C., & Chalasani, S. H. (2015) · Nature Communications · doi:10.1038/ncomms9264 · Cited by 377

Enhancing Both Biodegradability and Efficacy of Semiconducting Polymer Nanoparticles for Photoacoustic Imaging and Photothermal Therapy

Lyu, Y., Zeng, J., Jiang, Y., Xu, Z. J., Wang, T., Qiu, S., Lou, X., Gao, M., & Pu, K. (2018) · ACS Nano · doi:10.1021/acsnano.7b08616 · Cited by 359

Photosensitivity of Neurons Enabled by Cell-Targeted Gold Nanoparticles

Carvalho-de-Souza, J. L., Treger, J. S., Dang, B., Kent, S. B. H., Pepperberg, D. R., & Bezanilla, F. (2015) · Neuron · doi:10.1016/j.neuron.2015.02.033 · Cited by 356

Stable long-term chronic brain mapping at the single-neuron level

Tian-ming Fu, B., Hong, G., Zhou, T., Schuhmann, T. G., Viveros, R. D., & Lieber, C. M. (2016) · Nature Methods · doi:10.1038/nmeth.3969 · Cited by 330

Light scattering study of tissues

Tuchin, V. V. (1997) · Physics-Uspekhi · doi:10.1070/pu1997v040n05abeh000236 · Cited by 305

Preferential labeling of inhibitory and excitatory cortical neurons by endogenous tropism of adeno-associated virus and lentivirus vectors

Nathanson, J. L., Yanagawa, Y., Obata, K., & Callaway, E. M. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.03.032 · Cited by 305

Rational design of silicon structures for optically controlled multiscale biointerfaces

Jiang, Y., Li, X., Liu, B., Yi, J., Fang, Y., Shi, F., Gao, X., Sudzilovsky, E., Parameswaran, R., Koehler, K., et al. (2018) · Nature Biomedical Engineering · doi:10.1038/s41551-018-0230-1 · Cited by 258

Monte Carlo Modeling of Light Transport in Tissues

Jacques, S. L., & Wang, L. V. (1995) · Springer eBooks · doi:10.1007/978-1-4757-6092-7_4 · Cited by 253

Light propagation through biological tissue and other diffusive media: Theory, solutions, and software

Martelli, F., Bianco, S. D., Ismaelli, A., & Zaccanti, G. (2009) · Florence Research (University of Florence) · doi:10.1117/3.824746 · Cited by 239

Temperature-induced opening of TRPV1 ion channel is stabilized by the pore domain

Grandl, J. M., Kim, S. E., Uzzell, V., Bursulaya, B. D., Petrus, M. J., Bandell, M., & Patapoutian, A. (2010) · Nature Neuroscience · doi:10.1038/nn.2552 · Cited by 234

Deep brain optogenetics without intracranial surgery

Chen, R., Gore, F., Nguyen, Q.-A., Ramakrishnan, C., Patel, S., Kim, S. H., Raffiee, M., Kim, Y. S., Hsueh, B., Krook-Magnuson, E. I., et al. (2020) · Nature Biotechnology · doi:10.1038/s41587-020-0679-9 · Cited by 233

Using the tube test to measure social hierarchy in mice

Fan, Z., Zhu, H. L., Zhou, T., Wang, S., Wu, Y., & Hu, H. (2019) · Nature Protocols · doi:10.1038/s41596-018-0116-4 · Cited by 227

Sono-optogenetics facilitated by a circulation-delivered rechargeable light source for minimally invasive optogenetics

Wu, X., Zhu, X., Chong, P., Liu, J., Andre, L. N., Ong, K. S., Brinson, K., Mahdi, A. I., Li, J., Fenno, L. E., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1914387116 · Cited by 227

Spatiotemporal constraints on optogenetic inactivation in cortical circuits

Li, N., Chen, S., Guo, Z. V., Chen, H., Huo, Y., Inagaki, H., Chen, G., Davis, C., Hansel, D., Guo, C., et al. (2019) · eLife · doi:10.7554/elife.48622 · Cited by 226

Structure of TRPV1 channel revealed by electron cryomicroscopy

Moiseenkova‐Bell, V. Y., Stanciu, L., Serysheva, I. I., Tobe, B. J., & Wensel, T. G. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0711835105 · Cited by 213

Machine learning-guided channelrhodopsin engineering enables minimally invasive optogenetics

Bedbrook, C. N., Yang, K., Robinson, J. E., Mackey, E. D. W., Gradinaru, V., & Arnold, F. H. (2019) · Nature Methods · doi:10.1038/s41592-019-0583-8 · Cited by 203

Novel NanoLuc substrates enable bright two-population bioluminescence imaging in animals

Su, Y., Walker, J. R., Park, Y., Smith, T. P., Liu, L. X., Hall, M. P., Labanieh, L., Hurst, R., Wang, D. C., Encell, L. P., et al. (2020) · Nature Methods · doi:10.1038/s41592-020-0889-6 · Cited by 201

Magnetothermal genetic deep brain stimulation of motor behaviors in awake, freely moving mice

Munshi, R., Qadri, S. M., Zhang, Q. Y., Castellanos-Rubio, I., del Pino, P., & Pralle, A. (2017) · eLife · doi:10.7554/elife.27069 · Cited by 200

Ultrapotent chemogenetics for research and potential clinical applications

Magnus, C. J., Lee, P. H., Bonaventura, J., Zemla, R., Gomez, J. L., Ramirez, M. H., Hu, X., Galván, A., Basu, J., Michaelides, M., et al. (2019) · Science · doi:10.1126/science.aav5282 · Cited by 197

Near-infrared optogenetic engineering of photothermal nanoCRISPR for programmable genome editing

Chen, X., Chen, Y., Xin, H., Wan, T. Y., & Yuan, P. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1912220117 · Cited by 196

An atlas of nano-enabled neural interfaces

Ledesma, H. A., Li, X., Carvalho-de-Souza, J. L., Wei, W., Bezanilla, F., & Tian, B. (2019) · Nature Nanotechnology · doi:10.1038/s41565-019-0487-x · Cited by 187

Theranostic Strategy of Focused Ultrasound Induced Blood-Brain Barrier Opening for CNS Disease Treatment

Chen, K., Wei, K., & Liu, H.-L. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00086 · Cited by 173

Brain refractive index measured in vivo with high-NA defocus-corrected full-field OCT and consequences for two-photon microscopy

Binding, J., Arous, J. B., Léger, J., Gigan, S., Boccara, C., & Bourdieu, L. (2011) · Optics Express · doi:10.1364/oe.19.004833 · Cited by 173

Heterogeneous silicon mesostructures for lipid-supported bioelectric interfaces

Jiang, Y., Carvalho-de-Souza, J. L., Wong, R. C. S., Luo, Z., Isheim, D., Zuo, X., Nicholls, A., Jung, I. W., Yue, J., Liu, D., et al. (2016) · Nature Materials · doi:10.1038/nmat4673 · Cited by 164

Rapid Temperature Jump by Infrared Diode Laser Irradiation for Patch-Clamp Studies

Yao, J., Liu, B., & Qin, F. (2009) · Biophysical Journal · doi:10.1016/j.bpj.2009.02.016 · Cited by 161

The optical properties of mouse skin in the visible and near infrared spectral regions

Sabino, C. P., Deana, A. M., Yoshimura, T. M., da Silva, D. D. F. T., França, C. M., Hamblin, M. R., & Ribeiro, M. S. (2016) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2016.03.047 · Cited by 155

An Ultra-Sensitive Step-Function Opsin for Minimally Invasive Optogenetic Stimulation in Mice and Macaques

Gong, X., Mendoza-Halliday, D., Ting, J. T., Kaiser, T., Sun, X., Bastos, A. M., Wimmer, R. D., Guo, B., Chen, Q., Zhou, Y., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.03.032 · Cited by 152

Restoring light sensitivity using tunable near-infrared sensors

Nelidova, D., Morikawa, R. K., Cowan, C. S., Raics, Z., Goldblum, D., Scholl, H. P. N., Szikra, T., Szabó, A., Hillier, D., & Roska, B. (2020) · Science · doi:10.1126/science.aaz5887 · Cited by 140

REVISION OF GUIDELINES ON LIMITS OF EXPOSURE TO LASER RADIATION OF WAVELENGTHS BETWEEN 400 nm AND 1.4 μm

&NA; (2000) · Health Physics · doi:10.1097/00004032-200010000-00013 · Cited by 140

Thermosensitive Ion Channel Activation in Single Neuronal Cells by Using Surface‐Engineered Plasmonic Nanoparticles

Nakatsuji, H., Numata, T., Morone, N., Kaneko, S., Mori, Y., Imahori, H., & Murakami, T. (2015) · Angewandte Chemie International Edition · doi:10.1002/anie.201505534 · Cited by 120

Neuronal firing modulation by a membrane-targeted photoswitch

DiFrancesco, M. L., Lodola, F., Colombo, E., Maragliano, L., Bramini, M., Paternò, G. M., Baldelli, P., Serra, M. D., Lunelli, L., Marchioretto, M., et al. (2020) · Nature Nanotechnology · doi:10.1038/s41565-019-0632-6 · Cited by 118

Re-evaluation of the near infrared spectra of mitochondrial cytochrome c oxidase: Implications for non invasive in vivo monitoring of tissues

Mason, M. G., Nicholls, P. J., & Cooper, C. E. (2014) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2014.08.005 · Cited by 110

Measurement of bone mineral density via light scattering

Ugryumova, N., Matcher, S. J., & Attenburrow, D. P. (2004) · Physics in Medicine and Biology · doi:10.1088/0031-9155/49/3/009 · Cited by 110

Synaptic Plasticity in the Hippocampus

Haas, H. L., & Buzsáki, G. (1988) · Springer eBooks · doi:10.1007/978-3-642-73202-7 · Cited by 106

Optical properties of human cranial bone in the spectral range from 800 to 2000 nm

Bashkatov, A. N., Genina, E. A., Kochubey, V. I., & Tuchin, V. V. (2006) · Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE · doi:10.1117/12.697305 · Cited by 104

Tetherless near-infrared control of brain activity in behaving animals using fully implantable upconversion microdevices

Wang, Y., Lin, X., Chen, X., Chen, X., Xu, Z. C., Zhang, W., Liao, Q., Duan, X., Wang, X., Liu, M., et al. (2017) · Biomaterials · doi:10.1016/j.biomaterials.2017.07.017 · Cited by 97

A robust and reliable non-invasive test for stress responsivity in mice

Zimprich, A., Garrett, L., Deussing, J. M., Wotjak, C. T., Fuchs, H., Gailus‐Durner, V., de Angelis, M. H., Wurst, W., & Hölter, S. M. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00125 · Cited by 88

Technique for Dissection and Measurement of Refractive Index of Osteones

Ascenzi, A., & Fabry, C. (1959) · The Journal of Cell Biology · doi:10.1083/jcb.6.1.139 · Cited by 88

Near‐Infrared‐Fluorescence‐Enhanced Molecular Imaging of Live Cells on Gold Substrates

Hong, G., Tabakman, S. M., Welsher, K., Chen, Z., Robinson, J. T., Wang, H., Zhang, B., & Dai, H. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201100934 · Cited by 84

Visualization of Intra‐neuronal Motor Protein Transport through Upconversion Microscopy

Zeng, X. C., Chen, S., Weitemier, A. Z., Han, S., Blasiak, A., Prasad, A., Zheng, K., Yi, Z., Luo, B., Yang, I. H., et al. (2019) · Angewandte Chemie International Edition · doi:10.1002/anie.201904208 · Cited by 69

Computational Modeling of the Photon Transport, Tissue Heating, and Cytochrome C Oxidase Absorption during Transcranial Near-Infrared Stimulation

Bhattacharya, M., & Dutta, A. (2019) · Brain Sciences · doi:10.3390/brainsci9080179 · Cited by 57

Nanoscale Heat Transfer from Magnetic Nanoparticles and Ferritin in an Alternating Magnetic Field

Davis, H. C., Kang, S., Lee, J., Shin, T.-H., Putterman, H., Cheon, J., & Shapiro, M. G. (2020) · Biophysical Journal · doi:10.1016/j.bpj.2020.01.028 · Cited by 51

Conjugated polymers mediate effective activation of the Mammalian Ion Channel Transient Receptor Potential Vanilloid 1

Lodola, F., Martino, N., Tullii, G., Lanzani, G., & Antognazza, M. R. (2017) · Scientific Reports · doi:10.1038/s41598-017-08541-6 · Cited by 47

ASSESSMENT OF OPTICAL CLEARING AGENTS USING REFLECTANCE-MODE CONFOCAL SCANNING LASER MICROSCOPY

Samatham, R. V., PHILLIPS, K. G., & Jacques, S. L. (2010) · Journal of Innovative Optical Health Sciences · doi:10.1142/s1793545810001064 · Cited by 45

Noninvasive optical inhibition with a red-shifted microbial rhodopsin

Chuong, A. S., Miri, M. L., Busskamp, V., Matthews, G. A. C., Acker, L. C., Sørensen, A. T., Young, A., Klapoetke, N. C., Henninger, M. A., Kodandaramaiah, S. B., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3752 · Cited by 33

Revision of guidelines on limits of exposure to laser radiation of wavelengths between 400 nm and 1.4 microm. International Commission on Non-Ionizing Radiation Protection.

(2000) · PubMed · Cited by 31

Validation of Interventional Fiber Optic Spectroscopy With MR Spectroscopy, MAS-NMR Spectroscopy, High-Performance Thin-Layer Chromatography, and Histopathology for Accurate Hepatic Fat Quantification

Nachabe, R. A., van der Hoorn, J. W. A., van de Molengraaf, R. A., Lamerichs, R. M. J. N., Pikkemaat, J. A., Sio, C. F., Hendriks, B. H. W., & Sterenborg, H. J. C. M. (2012) · Investigative Radiology · doi:10.1097/rli.0b013e318237527b · Cited by 28

Model for estimating the penetration depth limit of the time-reversed ultrasonically encoded optical focusing technique

Jang, M., Ruan, H., Judkewitz, B., & Yang, C. (2014) · Optics Express · doi:10.1364/oe.22.005787 · Cited by 23

The Neural Basis for Response Latency in a Sensory-Motor Behavior

Lee, J., Darlington, T. R., & Lisberger, S. G. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz294 · Cited by 15

The mazes with minds of their own

Choi, C. Q. (2018) · Nature · doi:10.1038/d41586-018-02403-5 · Cited by 7

The blood–brain barrier: Structure, regulation and drug delivery

Wu, D., Chen, Q., Chen, X., Han, F., Chen, Z., & Wang, Y. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01481-w · Cited by 1,906

Near-infrared II fluorescence imaging

Schmidt, E. L., Ou, Z., Ximendes, E. C., Cui, H., Keck, C. H. C., Jaque, D., & Hong, G. (2024) · Nature Reviews Methods Primers · doi:10.1038/s43586-024-00301-x · Cited by 358

J‐Aggregation Strategy toward Potentiated NIR‐II Fluorescence Bioimaging of Molecular Fluorophores

Hu, X., Zhu, C., Sun, F., Chen, Z., Zou, J., Chen, X. S., & Yáng, Z. (2023) · Advanced Materials · doi:10.1002/adma.202304848 · Cited by 181

Nanocrystals for Deep-Tissue In Vivo Luminescence Imaging in the Near-Infrared Region

Yang, Y., Jiang, Q., & Zhang, F. (2023) · Chemical Reviews · doi:10.1021/acs.chemrev.3c00506 · Cited by 186

In vivo ultrasound-induced luminescence molecular imaging

Wang, Y., Yi, Z., Guo, J., Liao, S., Li, Z., Xu, S., Yin, B., Liu, Y., Feng, Y., Rong, Q., et al. (2024) · Nature Photonics · doi:10.1038/s41566-024-01387-1 · Cited by 165

Bioactive NIR-II gold clusters for three-dimensional imaging and acute inflammation inhibition

Ma, H., Zhang, X., Liu, L., Huang, Y., Sun, S., Chen, K., Qi, X., Liu, P., Yan, Y., Wang, Y., et al. (2023) · Science Advances · doi:10.1126/sciadv.adh7828 · Cited by 151

Activatable Multimodal Probes for In Vivo Imaging and Theranostics

Wang, Y., Hu, Y., & Ye, D. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202209512 · Cited by 142

An Emerging Toolkit of Ho 3+ Sensitized Lanthanide Nanocrystals with NIR-II Excitation and Emission for in Vivo Bioimaging

Wang, X., Wu, W., Yun, B., Huang, L., Chen, Z., Ming, J., Zhai, F.-H., Zhang, H., & Zhang, F. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.4c16451 · Cited by 110

Mucosa-interfacing electronics

Nan, K., Feig, V. R., Ying, B., Howarth, J. G., Kang, Z., Yang, Y., & Traverso, G. (2022) · Nature Reviews Materials · doi:10.1038/s41578-022-00477-2 · Cited by 105

Lighting up metastasis process before formation of secondary tumor by phosphorescence imaging

Chang, K., Xiao, L., Fan, Y., Gu, J., Wang, Y., Yang, J., Chen, M., Zhang, Y., Li, Q., & Li, Z. (2023) · Science Advances · doi:10.1126/sciadv.adf6757 · Cited by 106

An All‐Rounder for NIR‐II Phototheranostics: Well‐Tailored 1064 nm‐Excitable Molecule for Photothermal Combating of Orthotopic Breast Cancer

Yan, D., Zhang, Z., Zhang, J., Li, X., Wu, Q., Gui, Y., Zhu, J., Kang, M., Chen, X., Tang, B. Z., et al. (2024) · Angewandte Chemie International Edition · doi:10.1002/anie.202401877 · Cited by 103

Sonodynamic therapy combined with phototherapy: Novel synergistic strategy with superior efficacy for antitumor and antiinfection therapy

Hu, H., Zhao, J., Ma, K., Wang, J., Wang, X., Mao, T., Xiang, C., Luo, H., Cheng, Y., Yu, M., et al. (2023) · Journal of Controlled Release · doi:10.1016/j.jconrel.2023.05.041 · Cited by 97

Neural interfaces: Bridging the brain to the world beyond healthcare

Xu, S., Liu, Y., Lee, H., & Li, W. (2024) · Exploration · doi:10.1002/exp.20230146 · Cited by 102

H-bonded organic frameworks as ultrasound-programmable delivery platform

Wang, W., Shi, Y., Chai, W., Tang, K. W. K., Pyatnitskiy, I., Xie, Y., Liu, X., He, W., Jeong, J., Hsieh, J.-C., et al. (2025) · Nature · doi:10.1038/s41586-024-08401-0 · Cited by 111

Neural modulation with photothermally active nanomaterials

Wang, Y., Garg, R., Cohen-Karni, D., & Cohen‐Karni, T. (2023) · Nature Reviews Bioengineering · doi:10.1038/s44222-023-00022-y · Cited by 92

Furan‐modified thiadiazolo quinoxaline as an electron acceptor for constructing second near‐infrared aggregation‐induced emission fluorophores for beyond 1300 nm fluorescence/photoacoustic imaging and photothermal therapy

Liang, M., Liu, L., Sun, Y., Li, J., Zhang, L., Jiang, X., & Wu, W. (2024) · Aggregate · doi:10.1002/agt2.458 · Cited by 90

A Stable Open-Shell Conjugated Diradical Polymer with Ultra-High Photothermal Conversion Efficiency for NIR-II Photo-Immunotherapy of Metastatic Tumor

Gao, Y., Liu, Y., Li, X., Wang, H., Yang, Y., Luo, Y., Wan, Y., Lee, C., Li, S., & Zhang, X. (2023) · Nano-Micro Letters · doi:10.1007/s40820-023-01219-x · Cited by 79

Recent Advances in NIR-II Materials for Biomedical Applications

Zhao, M., & Chen, X. S. (2024) · Accounts of Materials Research · doi:10.1021/accountsmr.4c00025 · Cited by 78

Biomimetic NIR-II fluorescent proteins created from chemogenic protein-seeking dyes for multicolor deep-tissue bioimaging

Xu, J., Zhu, N., Du, Y., Han, T., Zheng, X., Li, J., & Zhu, S. (2024) · Nature Communications · doi:10.1038/s41467-024-47063-4 · Cited by 75

Bimetallic Hyaluronate-Modified Au@Pt Nanoparticles for Noninvasive Photoacoustic Imaging and Photothermal Therapy of Skin Cancer

Han, H. H., Kim, S., Kim, J., Park, W., Kim, C., Kim, H., & Hahn, S. K. (2023) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.3c01858 · Cited by 68

Advances in photobiomodulation for cognitive improvement by near-infrared derived multiple strategies

Pan, W., Liu, P., Ma, D., & Yang, J. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-03988-w · Cited by 67

Illuminating the Brain: Advances and Perspectives in Optoelectronics for Neural Activity Monitoring and Modulation

Xu, S., Momin, M., Ahmed, S., Hossain, A., Veeramuthu, L., Pandiyan, A., Kuo, C., & Zhou, T. (2023) · Advanced Materials · doi:10.1002/adma.202303267 · Cited by 70

Interfacing with the Brain: How Nanotechnology Can Contribute

Ahmed, A. A. A., Alegret, N., Almeida, B., Álvarez‐Puebla, R. A., Andrews, A. M., Ballerini, L., Barrios‐Capuchino, J. J., Becker, C., Blick, R. H., Bonakdar, S., et al. (2025) · ACS Nano · doi:10.1021/acsnano.4c10525 · Cited by 71

Millimeter-scale magnetic implants paired with a fully integrated wearable device for wireless biophysical and biochemical sensing

Wan, J., Nie, Z., Xu, J., Zhang, Z., Yao, S., Xiang, Z., Lin, X., Lu, Y., Xu, C., Zhao, P., et al. (2024) · Science Advances · doi:10.1126/sciadv.adm9314 · Cited by 66

Combination of Efficient Red Fluorescence and High Photothermal Conversion in the Second Near‐Infrared Window from Carbon Dots through Photoinduced Sodium‐Doping Approach

Wang, Q., Zhang, T., Cheng, Q., Wang, B., Liu, Y., Xing, G., Tang, Z., & Qu, S. (2024) · Advanced Functional Materials · doi:10.1002/adfm.202402976 · Cited by 65

Bone disease imaging through the near-infrared-II window

Mi, C., Zhang, X., Yang, C., Wu, J., Chen, X., Ma, C., Wu, S., Yang, Z., Qiao, P., Liu, Y., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-42001-2 · Cited by 66

Giant infrared bulk photovoltaic effect in tellurene for broad-spectrum neuromodulation

Wang, Z., Tan, C., Peng, M., Yu, Y., Zhong, F., Wang, P., He, T., Wang, Y., Zhang, Z., Xie, R., et al. (2024) · Light Science & Applications · doi:10.1038/s41377-024-01640-w · Cited by 60

Principles and applications of sono-optogenetics

Yang, F., Kim, S., Wu, X., Cui, H., Hahn, S. K., & Hong, G. (2023) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2023.114711 · Cited by 61

Plasmonic Nanomaterials in Photothermal Catalysis and Artificial Photosynthesis: Hot Electron Dynamics, Design Challenges, and Future Prospects

Li, S., Yang, J., Ruan, X., Cui, X., & Ravi, S. K. (2025) · Advanced Functional Materials · doi:10.1002/adfm.202503186 · Cited by 57

Ultrabright and ultrafast afterglow imaging in vivo via nanoparticles made of trianthracene derivatives

Wang, Y., Guo, J., Chen, M., Liao, S., Xu, L., Chen, Q., Song, G., & Zhang, X. (2024) · Nature Biomedical Engineering · doi:10.1038/s41551-024-01274-8 · Cited by 54

A Through-Intact-Skull (TIS) chronic window technique for cortical structure and function observation in mice

Li, D., Hu, Z., Zhang, H., Yang, Q., Zhu, L. J., Liu, Y., Yu, T., Zhu, J., Wu, J., He, J., et al. (2022) · eLight · doi:10.1186/s43593-022-00022-2 · Cited by 53

Nanotransducer-Enabled Deep-Brain Neuromodulation with NIR-II Light

Wu, X., Yang, F., Cai, S., Pu, K., & Hong, G. (2023) · ACS Nano · doi:10.1021/acsnano.2c12068 · Cited by 54

Activation of mechanoluminescent nanotransducers by focused ultrasound enables light delivery to deep-seated tissue in vivo

Jiang, S., Wu, X., Yang, F., Rommelfanger, N. J., & Hong, G. (2023) · Nature Protocols · doi:10.1038/s41596-023-00895-8 · Cited by 54

Recent Progress of Soft and Bioactive Materials in Flexible Bioelectronics

Wu, X., Ye, Y., Sun, M., Mei, Y., Ji, B., Wang, M., & Song, E. (2025) · Cyborg and Bionic Systems · doi:10.34133/cbsystems.0192 · Cited by 59

Second Near‐Infrared (NIR‐II) Window for Imaging‐Navigated Modulation of Brain Structure and Function

Zhang, K., Chen, F., Wang, L., & Hu, J. (2023) · Small · doi:10.1002/smll.202206044 · Cited by 51

White-light activatable organic NIR-II luminescence nanomaterials for imaging-guided surgery

Li, C., Du, J., Jiang, G., Gong, J., Zhang, Y., Yao, M., Wang, J., Wu, L., & Tang, B. Z. (2024) · Nature Communications · doi:10.1038/s41467-024-50202-6 · Cited by 49

A biomineral-inspired approach of synthesizing colloidal persistent phosphors as a multicolor, intravital light source

Yang, F., Wu, X., Cui, H., Ou, Z., Jiang, S., Cai, S., Zhou, Q., Wong, B. G., Huang, H., & Hong, G. (2022) · Science Advances · doi:10.1126/sciadv.abo6743 · Cited by 47

Photoactive Nanomaterials for Wireless Neural Biomimetics, Stimulation, and Regeneration

Zhao, D. S., Huang, R., Gan, J.-M., & Shen, Q. (2022) · ACS Nano · doi:10.1021/acsnano.2c08543 · Cited by 45

Dual Behavior Regulation: Tether‐Free Deep‐Brain Stimulation by Photothermal and Upconversion Hybrid Nanoparticles

Sun, F., Shen, H., Yang, Q., Yuan, Z., Chen, Y., Guo, W., Wang, Y., Yang, L., Bai, Z., Liu, Q., et al. (2023) · Advanced Materials · doi:10.1002/adma.202210018 · Cited by 43

A local water molecular-heating strategy for near-infrared long-lifetime imaging-guided photothermal therapy of glioblastoma

Kang, D., Kim, H. S., Han, S., Lee, Y., Kim, Y., Lee, D. Y., & Lee, J. (2023) · Nature Communications · doi:10.1038/s41467-023-38451-3 · Cited by 41

Implantable bioelectronic devices for photoelectrochemical and electrochemical modulation of cells and tissues

Shi, J., Li, P., Kim, S., & Tian, B. (2025) · Nature Reviews Bioengineering · doi:10.1038/s44222-025-00285-7 · Cited by 45

AIEgen‐Based Covalent Organic Frameworks for Preventing Malignant Ventricular Arrhythmias Via Local Hyperthermia Therapy

Zhang, L., Guo, F., Xu, S., Deng, Q., Xie, M., Sun, J., Kwok, R. T. K., Lam, J. W. Y., Deng, H., Jiang, H., et al. (2023) · Advanced Materials · doi:10.1002/adma.202304620 · Cited by 40

Ultrasound-Induced Cascade Amplification in a Mechanoluminescent Nanotransducer for Enhanced Sono-Optogenetic Deep Brain Stimulation

Wang, W., Tang, K. W. K., Pyatnitskiy, I., Liu, X., Shi, X., Huo, D., Jeong, J., Wynn, T., Sangani, A., Baker, A., et al. (2023) · ACS Nano · doi:10.1021/acsnano.3c06577 · Cited by 39

Role of opsins and light or heat activated transient receptor potential ion channels in the mechanisms of photobiomodulation and infrared therapy

Sharma, S. K., Sardana, S., & Hamblin, M. R. (2023) · Journal of Photochemistry and Photobiology · doi:10.1016/j.jpap.2023.100160 · Cited by 39

TRPV1-mediated sonogenetic neuromodulation of motor cortex in freely moving mice

Xu, K., Yang, Y., Hu, Z., Yue, Y., Gong, Y., Cui, J., Culver, J. P., Bruchas, M. R., & Chen, H. (2023) · Journal of Neural Engineering · doi:10.1088/1741-2552/acbba0 · Cited by 40

Directed Neural Stem Cells Differentiation via Signal Communication with Ni–Zn Micromotors

Feng, Y., Gao, C., Xie, D., Liu, L., Chen, B., Liu, S., Yang, H., Gao, Z., Wilson, D. A., Tu, Y., et al. (2023) · Advanced Materials · doi:10.1002/adma.202301736 · Cited by 34

Transcranial Nongenetic Neuromodulation via Bioinspired Vesicle‐Enabled Precise NIR‐II Optical Stimulation

Zhang, Y., Yang, D., Nie, J., Dai, J., Wu, H., Zheng, J., Zhang, F., & Fang, Y. (2022) · Advanced Materials · doi:10.1002/adma.202208601 · Cited by 34

Semiconducting Polymer Nanoparticles in the Second Near‐Infrared Region for Biomedical Imaging and Therapy

Zhang, Z., Li, W., Liu, Y., Fang, X., & Wu, C. (2022) · Advanced Optical Materials · doi:10.1002/adom.202202052 · Cited by 32

Targeted Cyclo[8]pyrrole-Based NIR-II Photoacoustic Tomography Probe for Suppression of Orthotopic Pancreatic Tumor Growth and Intra-abdominal Metastases

Chen, J., Chen, R., Chau, C. V., Sedgwick, A. C., Xue, Q., Chen, T., Zeng, S., Chen, N., Wong, K. K. Y., Song, L., et al. (2024) · Journal of the American Chemical Society · doi:10.1021/jacs.3c11666 · Cited by 30

Activatable Multimodal Probes for In Vivo Imaging and Theranostics

Wang, Y., Hu, Y., & Ye, D. (2022) · Angewandte Chemie · doi:10.1002/ange.202209512 · Cited by 30

Atomic‐Thin 2D Copper Sulfide Nanocrystals with over 94% Photothermal Conversion Efficiency as Superior NIR‐II Photoacoustic Agents

Su, M., Wu, Z., Yan, T., Li, N., Li, X., Hou, T., Liu, J., Zhang, C., Zhu, C., Wang, Z., et al. (2024) · Advanced Functional Materials · doi:10.1002/adfm.202409580 · Cited by 29

Modulation of Near‐Infrared Afterglow Luminescence in Inorganic Nanomaterials for Biological Applications

Gao, L., Liu, Y., Su, J., Liu, K., & Zhang, H. (2025) · Advanced Materials · doi:10.1002/adma.202419349 · Cited by 29

Photo‐Activated Oxidative Stress Amplifier: A Strategy for Targeting Glutathione Metabolism and Enhancing ROS‐Mediated Therapy in Triple‐Negative Breast Cancer Treatment

Zhao, L., Tong, Y., Yin, J., Li, H., Du, L., Li, J., & Jiang, Y. (2024) · Small · doi:10.1002/smll.202403861 · Cited by 27

High temporal resolution transparent thermoelectric temperature sensors for photothermal effect sensing

Lee, J., Hwang, S., Hong, N., Kwak, J., Jang, J. E., Chung, S., & Kang, H. (2022) · Materials Horizons · doi:10.1039/d2mh00813k · Cited by 27

Ion-Selective Micropipette Sensor for In Vivo Monitoring of Sodium Ion with Crown Ether-Encapsulated Metal–Organic Framework Subnanopores

Liu, J., Lu, J., Ji, W., Guang-wen, L., Wang, J., Ye, T., Jiang, Y., Zheng, J., Yu, P., Liu, N., et al. (2024) · Analytical Chemistry · doi:10.1021/acs.analchem.3c05366 · Cited by 26

Graphdiyne as a Highly Efficient and Neuron-Targeted Photothermal Transducer for in Vivo Neuromodulation

Shao, L., Wei, H., Liu, J., Ma, W., Yu, P., Wang, M., & Mao, L. (2024) · ACS Nano · doi:10.1021/acsnano.4c01037 · Cited by 28

Beyond 25 years of biomedical innovation in nano-bioelectronics

Li, P., Kim, S., & Tian, B. (2024) · Device · doi:10.1016/j.device.2024.100401 · Cited by 28

Bioprinted optoelectronically active cardiac tissues

Ershad, F., Rao, Z., Maharjan, S., Mesquita, F., Ha, J., Gonzalez, L., Haideri, T., da Costa, E. C., Moctezuma-Ramirez, A., Wang, Y., et al. (2025) · Science Advances · doi:10.1126/sciadv.adt7210 · Cited by 26

Furan Donor for NIR-II Molecular Fluorophores with Enhanced Bioimaging Performance

Liu, C., Li, M., Ma, H., Hu, Z., Wang, X., Ma, R., Jiang, Y., Sun, H., Zhu, S., & Liang, Y. (2023) · Research · doi:10.34133/research.0039 · Cited by 26

Unrestricted molecular motions enable mild photothermy for recurrence-resistant FLASH antitumor radiotherapy

Shen, H., Wang, H., Mo, J., Zhang, J., Xu, C., Sun, F., Ou, X., Zhu, X., Du, L., Ju, H., et al. (2024) · Bioactive Materials · doi:10.1016/j.bioactmat.2024.03.024 · Cited by 26

Recent advances in stimuli-responsive controlled release systems for neuromodulation

Shi, J., Tan, C., Ge, X., Qin, Z., & Xiong, H. (2024) · Journal of Materials Chemistry B · doi:10.1039/d4tb00720d · Cited by 25

Optothermal‐Stimulated Persistent Luminescence Imaging and Therapy (OSPLIT)

Pei, P., Chen, Y., Chen, X. S., Zhang, F., Liu, X., & Wang, J. (2025) · Advanced Materials · doi:10.1002/adma.202500769 · Cited by 23

Enhanced Proliferation of Visualizable Mesenchymal Stem Cell–Platelet Hybrid Cell for Versatile Intracerebral Hemorrhage Treatment

Wu, G., Liu, Z., Mu, C., Song, D. F., Wang, J., Meng, X., Li, Z., Qing, H., Dong, Y., Xie, H., et al. (2023) · ACS Nano · doi:10.1021/acsnano.2c11329 · Cited by 24

Mechanoluminescent Light Sources Based on Nanostructured Systems for Biomedical Applications: A Review

Yang, M., Ge, X., Zheng, L., Huang, Y. S., Zhong, J., Tu, D., Hong, G., & Yang, F. (2024) · ACS Applied Nano Materials · doi:10.1021/acsanm.4c00675 · Cited by 24

Cobalt-Catalyzed Cascade C–H Activation/Annulation Polymerizations toward Diversified and Multifunctional Sulfur-Containing Fused Heterocyclic Polymers

Fan, D., Wang, D., Zhang, J., Fu, X., Yan, X., Wang, D., Qin, A., Han, T., & Tang, B. Z. (2024) · Journal of the American Chemical Society · doi:10.1021/jacs.4c03889 · Cited by 23

Rational Molecular Engineering of Organic Semiconducting Nanoplatforms for Advancing NIR‐II Fluorescence Theranostics

Hu, X., Chen, Z., Ao, H., Fan, Q., Yáng, Z., & Huang, W. (2022) · Advanced Optical Materials · doi:10.1002/adom.202201067 · Cited by 23

Black Phosphorus Flake-Enabled Wireless Neuromodulation for Epilepsy Treatment

Yang, D., Ren, Q., Nie, J., Zhang, Y., Wu, H., Chang, Z., Wang, B., Dai, J., & Fang, Y. (2023) · Nano Letters · doi:10.1021/acs.nanolett.3c03472 · Cited by 23

Nanoparticles Encapsulated in Red Blood Cell Membranes for Near-Infrared Second Window Imaging-Guided Photothermal-Enhanced Immunotherapy on Tumors

Ye, J., Yu, Y., Li, Y., Yao, B., Gu, M., Yang, L., & Yin, S. (2024) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.4c05334 · Cited by 23

Quinoidal π-Bridges for a Fused-Ring Acceptor with Enhanced Near-Infrared-II Photothermal Therapy and Fluorescent Emission beyond 1500 nm

Cao, W., Zhang, X., Yang, X., Sun, H., Chen, Z., & Liang, Y. (2024) · ACS Materials Letters · doi:10.1021/acsmaterialslett.4c00759 · Cited by 22

Minocycline nanoplatform penetrates the BBB and enables the targeted treatment of Parkinson's disease with cognitive impairment

Cheng, G., Liu, Z., Yan, Z., Wu, J., Li, Z., Gao, S., Zheng, C., Guo, S., Pan, Y., Chen, X., et al. (2024) · Journal of Controlled Release · doi:10.1016/j.jconrel.2024.11.066 · Cited by 22

Terahertz photons promote neuron growth and synapse formation through cAMP signaling pathway

Zhong, Y., Yu, Y., Li, Y., Yin, J., Sun, Y., Jiang, R., & Chang, C. (2025) · PhotoniX · doi:10.1186/s43074-025-00165-8 · Cited by 23

Atomically Precise Metal Nanoclusters for Near-Infrared-II Photonics

Liu, Z., Sardar, A., Chen, S., Wang, Y., & Jin, R. M. (2026) · Accounts of Chemical Research · doi:10.1021/acs.accounts.5c00782 · Cited by 22

Optical control of neuronal activities with photoswitchable nanovesicles

Xiong, H., Alberto, K. A., Youn, J., Taura, J. J., Morstein, J., Li, X., Wang, Y., Trauner, D. H., Slesinger, P. A., Nielsen, S. O., et al. (2022) · Nano Research · doi:10.1007/s12274-022-4853-x · Cited by 21

Recent advances in 2D material-based phototherapy

Tan, Y. L., Khan, H. M., Sheikh, B. A., Sun, H., Zhang, H., Chen, J., Huang, D., Chen, X., Zhou, C., & Sun, J. (2023) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2023.1141631 · Cited by 21

Advancing Neuroscience and Therapy: Insights into Genetic and Non-Genetic Neuromodulation Approaches

Zhi, W., Li, Y., Wang, L., & Hu, X. (2025) · Cells · doi:10.3390/cells14020122 · Cited by 25

Rotor-based image-guided therapy of glioblastoma

Pan, Z., Zeng, Y., Ye, Z., Li, Y., Wang, Y., Feng, Z., Bao, Y., Yuan, J., Cao, G., Dong, J., et al. (2024) · Journal of Controlled Release · doi:10.1016/j.jconrel.2024.03.020 · Cited by 20

Physical mechanisms of emerging neuromodulation modalities

Karatum, O., Han, M., Erdoğan, E. T., Karamürsel, S., & Nizamoğlu, S. (2023) · Journal of Neural Engineering · doi:10.1088/1741-2552/acd870 · Cited by 20

Applications of nanotheranostics in the second near-infrared window in bioimaging and cancer treatment

Li, H., Li, P., Zhang, J., Lin, Z., Bai, L., & Shen, H. (2024) · Nanoscale · doi:10.1039/d4nr03058c · Cited by 22

Tailoring Physicochemical Properties of Photothermal Hydrogels Toward Intrinsically Regenerative Therapies

Xiao, T., Dai, H., Wu, Y., Liu, Z., Yeow, J., Xing, X., & Geng, H. (2024) · Advanced Functional Materials · doi:10.1002/adfm.202414419 · Cited by 20

Instant noninvasive near-infrared deep brain stimulation using optoelectronic nanoparticles without genetic modification

Jin, S., Li, J., Jiang, L., Ye, Y., Ma, C., Yang, Y., Su, H., Gao, L., Ni, M., Zhao, Y., et al. (2025) · Science Advances · doi:10.1126/sciadv.adt4771 · Cited by 23

Cascade Energy Transformation in Hybrid Nanosensitizer Enables Ultrasound-Activated Luminescence Imaging and Enhanced Sonodynamic Therapy

Li, X., Tan, Y., Li, Z., Wang, Y., Lu, C., Liao, S., Yin, B., Chen, B., Liu, H., Wei, H., et al. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.5c06434 · Cited by 20

Dual Activation of Calcium Channels Using Near-Infrared Responsive Conjugated Oligomer Nanoparticles for Precise Regulation of Blood Glucose Homeostasis

Li, N., Li, C., Li, B., Li, C., Zhao, Q., Huang, Z., Shu, Y., Qu, X., Wang, B., Li, S., et al. (2023) · Nano Letters · doi:10.1021/acs.nanolett.3c03701 · Cited by 19

A FRET-Based Ratiometric H 2 S Sensor for Sensitive Optical Molecular Imaging in Second Near-Infrared Window

Lei, S., Jiang, K., Zhang, C., Sun, W., Pan, Y., Wang, D., Huang, P., & Lin, J. (2023) · Research · doi:10.34133/research.0286 · Cited by 19

Highly Branched Au Superparticles as Efficient Photothermal Transducers for Optical Neuromodulation

Cheng, X., Li, W., Wang, Y., Weng, K., Xing, Y., Huang, Y., Sheng, X., Yao, J., Zhang, H., & Li, J. (2024) · ACS Nano · doi:10.1021/acsnano.4c07163 · Cited by 21

In Situ Synthesis and Assembly of Functional Materials and Devices in Living Systems

Wang, W., Sessler, C. D., Wang, X., & Jia Liu, B. (2024) · Accounts of Chemical Research · doi:10.1021/acs.accounts.4c00049 · Cited by 18

Skin Thermal Management for Subcutaneous Photoelectric Conversion Reaching 500 mW

Lyu, S., He, Y., Li, X., Wang, H., Yao, Y., Peng, Z., Ding, Y., & Wang, Y. (2023) · Advanced Materials · doi:10.1002/adma.202306903 · Cited by 20

Wireless deep-brain neuromodulation using photovoltaics in the second near-infrared spectrum

Cui, H., Zhao, S., & Hong, G. (2023) · Device · doi:10.1016/j.device.2023.100113 · Cited by 18

A microneedle patch realizes weight loss through photothermal induction of fat browning

Gao, Z., Liu, Y., Lin, W., Lian, H., & Meng, Z. (2024) · Biomaterials Science · doi:10.1039/d3bm01767b · Cited by 18

Nanotechnology for vision restoration

Lanzani, G., Chiaravalli, G., Colombo, E., Manfredi, G., Marco, S. D., Vurro, V., & Benfenati, F. (2024) · Nature Reviews Bioengineering · doi:10.1038/s44222-024-00210-4 · Cited by 18

Distributed Optical Fiber Vibration Sensors Using Light Interference Technology: Fundamental Principles and Major Advancements

Sun, Z., Sun, D., Yang, H., & Zhao, C. (2025) · IEEE Transactions on Instrumentation and Measurement · doi:10.1109/tim.2025.3538088 · Cited by 17

Highly Efficient Charge Transfer between Water and Two-Dimensional Materials with Polar Bonds

Cao, Y., Zhou, C., Zhou, W., Shen, C. L., Jin, B., Ma, T., Qiu, H., & Guo, W. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.5c00480 · Cited by 18

Intravitreally Injected Plasmonic Nanorods Activate Bipolar Cells with Patterned Near-Infrared Laser Projection

Nie, J., Eom, K., AlGhosain, H. M., Neifert, A. R., Cherian, A., Gerbaka, G. M., Ma, K. Y., Liu, T., & Lee, J. (2025) · ACS Nano · doi:10.1021/acsnano.4c14061 · Cited by 16

Size-dependent penetration depth of colloidal nanoparticles into cell spheroids

Zhu, D., Brückner, D., Sosniok, M., Skiba, M., Feliu, N., Gallego, M., Liu, Y., Schulz, F., Falkenberg, G., Parak, W. J., et al. (2025) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2025.115593 · Cited by 16

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