Saturation in Phosphene Size with Increasing Current Levels Delivered to Human Visual Cortex
Electrically stimulating early visual cortex results in a visual percept known as a phosphene. Although phosphenes can be evoked by a wide range of electrode sizes and current amplitudes, they are invariably described as small. To better understand this observation, we electrically stimulated 93 ele...
Saved in:
Published in | The Journal of neuroscience Vol. 37; no. 30; pp. 7188 - 7197 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Society for Neuroscience
26.07.2017
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Electrically stimulating early visual cortex results in a visual percept known as a phosphene. Although phosphenes can be evoked by a wide range of electrode sizes and current amplitudes, they are invariably described as small. To better understand this observation, we electrically stimulated 93 electrodes implanted in the visual cortex of 13 human subjects who reported phosphene size while stimulation current was varied. Phosphene size increased as the stimulation current was initially raised above threshold, but then rapidly reached saturation. Phosphene size also depended on the location of the stimulated site, with size increasing with distance from the foveal representation. We developed a model relating phosphene size to the amount of activated cortex and its location within the retinotopic map. First, a sigmoidal curve was used to predict the amount of activated cortex at a given current. Second, the amount of active cortex was converted to degrees of visual angle by multiplying by the inverse cortical magnification factor for that retinotopic location. This simple model accurately predicted phosphene size for a broad range of stimulation currents and cortical locations. The unexpected saturation in phosphene sizes suggests that the functional architecture of cerebral cortex may impose fundamental restrictions on the spread of artificially evoked activity and this may be an important consideration in the design of cortical prosthetic devices.
Understanding the neural basis for phosphenes, the visual percepts created by electrical stimulation of visual cortex, is fundamental to the development of a visual cortical prosthetic. Our experiments in human subjects implanted with electrodes over visual cortex show that it is the activity of a large population of cells spread out across several millimeters of tissue that supports the perception of a phosphene. In addition, we describe an important feature of the production of phosphenes by electrical stimulation: phosphene size saturates at a relatively low current level. This finding implies that, with current methods, visual prosthetics will have a limited dynamic range available to control the production of spatial forms and that more advanced stimulation methods may be required. |
---|---|
AbstractList | Electrically stimulating early visual cortex results in a visual percept known as a phosphene. Although phosphenes can be evoked by a wide range of electrode sizes and current amplitudes, they are invariably described as small. To better understand this observation, we electrically stimulated 93 electrodes implanted in the visual cortex of 13 human subjects who reported phosphene size while stimulation current was varied. Phosphene size increased as the stimulation current was initially raised above threshold, but then rapidly reached saturation. Phosphene size also depended on the location of the stimulated site, with size increasing with distance from the foveal representation. We developed a model relating phosphene size to the amount of activated cortex and its location within the retinotopic map. First, a sigmoidal curve was used to predict the amount of activated cortex at a given current. Second, the amount of active cortex was converted to degrees of visual angle by multiplying by the inverse cortical magnification factor for that retinotopic location. This simple model accurately predicted phosphene size for a broad range of stimulation currents and cortical locations. The unexpected saturation in phosphene sizes suggests that the functional architecture of cerebral cortex may impose fundamental restrictions on the spread of artificially evoked activity and this may be an important consideration in the design of cortical prosthetic devices.
Understanding the neural basis for phosphenes, the visual percepts created by electrical stimulation of visual cortex, is fundamental to the development of a visual cortical prosthetic. Our experiments in human subjects implanted with electrodes over visual cortex show that it is the activity of a large population of cells spread out across several millimeters of tissue that supports the perception of a phosphene. In addition, we describe an important feature of the production of phosphenes by electrical stimulation: phosphene size saturates at a relatively low current level. This finding implies that, with current methods, visual prosthetics will have a limited dynamic range available to control the production of spatial forms and that more advanced stimulation methods may be required. Electrically stimulating early visual cortex results in a visual percept known as a phosphene. Although phosphenes can be evoked by a wide range of electrode sizes and current amplitudes, they are invariably described as small. To better understand this observation, we electrically stimulated 93 electrodes implanted in the visual cortex of 13 human subjects who reported phosphene size while stimulation current was varied. Phosphene size increased as the stimulation current was initially raised above threshold, but then rapidly reached saturation. Phosphene size also depended on the location of the stimulated site, with size increasing with distance from the foveal representation. We developed a model relating phosphene size to the amount of activated cortex and its location within the retinotopic map. First, a sigmoidal curve was used to predict the amount of activated cortex at a given current. Second, the amount of active cortex was converted to degrees of visual angle by multiplying by the inverse cortical magnification factor for that retinotopic location. This simple model accurately predicted phosphene size for a broad range of stimulation currents and cortical locations. The unexpected saturation in phosphene sizes suggests that the functional architecture of cerebral cortex may impose fundamental restrictions on the spread of artificially evoked activity and this may be an important consideration in the design of cortical prosthetic devices.SIGNIFICANCE STATEMENT Understanding the neural basis for phosphenes, the visual percepts created by electrical stimulation of visual cortex, is fundamental to the development of a visual cortical prosthetic. Our experiments in human subjects implanted with electrodes over visual cortex show that it is the activity of a large population of cells spread out across several millimeters of tissue that supports the perception of a phosphene. In addition, we describe an important feature of the production of phosphenes by electrical stimulation: phosphene size saturates at a relatively low current level. This finding implies that, with current methods, visual prosthetics will have a limited dynamic range available to control the production of spatial forms and that more advanced stimulation methods may be required.Electrically stimulating early visual cortex results in a visual percept known as a phosphene. Although phosphenes can be evoked by a wide range of electrode sizes and current amplitudes, they are invariably described as small. To better understand this observation, we electrically stimulated 93 electrodes implanted in the visual cortex of 13 human subjects who reported phosphene size while stimulation current was varied. Phosphene size increased as the stimulation current was initially raised above threshold, but then rapidly reached saturation. Phosphene size also depended on the location of the stimulated site, with size increasing with distance from the foveal representation. We developed a model relating phosphene size to the amount of activated cortex and its location within the retinotopic map. First, a sigmoidal curve was used to predict the amount of activated cortex at a given current. Second, the amount of active cortex was converted to degrees of visual angle by multiplying by the inverse cortical magnification factor for that retinotopic location. This simple model accurately predicted phosphene size for a broad range of stimulation currents and cortical locations. The unexpected saturation in phosphene sizes suggests that the functional architecture of cerebral cortex may impose fundamental restrictions on the spread of artificially evoked activity and this may be an important consideration in the design of cortical prosthetic devices.SIGNIFICANCE STATEMENT Understanding the neural basis for phosphenes, the visual percepts created by electrical stimulation of visual cortex, is fundamental to the development of a visual cortical prosthetic. Our experiments in human subjects implanted with electrodes over visual cortex show that it is the activity of a large population of cells spread out across several millimeters of tissue that supports the perception of a phosphene. In addition, we describe an important feature of the production of phosphenes by electrical stimulation: phosphene size saturates at a relatively low current level. This finding implies that, with current methods, visual prosthetics will have a limited dynamic range available to control the production of spatial forms and that more advanced stimulation methods may be required. Electrically stimulating early visual cortex results in a visual percept known as a phosphene. Although phosphenes can be evoked by a wide range of electrode sizes and current amplitudes, they are invariably described as small. To better understand this observation, we electrically stimulated 93 electrodes implanted in the visual cortex of 13 human subjects who reported phosphene size while stimulation current was varied. Phosphene size increased as the stimulation current was initially raised above threshold, but then rapidly reached saturation. Phosphene size also depended on the location of the stimulated site, with size increasing with distance from the foveal representation. We developed a model relating phosphene size to the amount of activated cortex and its location within the retinotopic map. First, a sigmoidal curve was used to predict the amount of activated cortex at a given current. Second, the amount of active cortex was converted to degrees of visual angle by multiplying by the inverse cortical magnification factor for that retinotopic location. This simple model accurately predicted phosphene size for a broad range of stimulation currents and cortical locations. The unexpected saturation in phosphene sizes suggests that the functional architecture of cerebral cortex may impose fundamental restrictions on the spread of artificially evoked activity and this may be an important consideration in the design of cortical prosthetic devices. Electrically stimulating early visual cortex results in a visual percept known as a phosphene. Although phosphenes can be evoked by a wide range of electrode sizes and current amplitudes, they are invariably described as small. To better understand this observation, we electrically stimulated 93 electrodes implanted in the visual cortex of 13 human subjects who reported phosphene size while stimulation current was varied. Phosphene size increased as the stimulation current was initially raised above threshold, but then rapidly reached saturation. Phosphene size also depended on the location of the stimulated site, with size increasing with distance from the foveal representation. We developed a model relating phosphene size to the amount of activated cortex and its location within the retinotopic map. First, a sigmoidal curve was used to predict the amount of activated cortex at a given current. Second, the amount of active cortex was converted to degrees of visual angle by multiplying by the inverse cortical magnification factor for that retinotopic location. This simple model accurately predicted phosphene size for a broad range of stimulation currents and cortical locations. The unexpected saturation in phosphene sizes suggests that the functional architecture of cerebral cortex may impose fundamental restrictions on the spread of artificially evoked activity and this may be an important consideration in the design of cortical prosthetic devices. SIGNIFICANCE STATEMENT Understanding the neural basis for phosphenes, the visual percepts created by electrical stimulation of visual cortex, is fundamental to the development of a visual cortical prosthetic. Our experiments in human subjects implanted with electrodes over visual cortex show that it is the activity of a large population of cells spread out across several millimeters of tissue that supports the perception of a phosphene. In addition, we describe an important feature of the production of phosphenes by electrical stimulation: phosphene size saturates at a relatively low current level. This finding implies that, with current methods, visual prosthetics will have a limited dynamic range available to control the production of spatial forms and that more advanced stimulation methods may be required. |
Author | Ozker, Muge Yoshor, Daniel Beauchamp, Michael S. Bosking, William H. Sun, Ping Pei, Xiaomei Foster, Brett L. |
Author_xml | – sequence: 1 givenname: William H. orcidid: 0000-0002-4999-8946 surname: Bosking fullname: Bosking, William H. – sequence: 2 givenname: Ping surname: Sun fullname: Sun, Ping – sequence: 3 givenname: Muge orcidid: 0000-0001-7472-4528 surname: Ozker fullname: Ozker, Muge – sequence: 4 givenname: Xiaomei surname: Pei fullname: Pei, Xiaomei – sequence: 5 givenname: Brett L. orcidid: 0000-0002-2621-5574 surname: Foster fullname: Foster, Brett L. – sequence: 6 givenname: Michael S. orcidid: 0000-0002-7599-9934 surname: Beauchamp fullname: Beauchamp, Michael S. – sequence: 7 givenname: Daniel surname: Yoshor fullname: Yoshor, Daniel |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28652411$$D View this record in MEDLINE/PubMed |
BookMark | eNqFkUtv1DAUhS1URKeFv1BZYsMmg-3YTiwhJBQKHTSiiCmskCzHuem4ythTOxkevx4PfQi6YXUX9zvnHvscoQMfPCB0QsmcCla-_PDx9Mvn81WzmLNayYLKOSO0eoRmeasKxgk9QDPCKlJIXvFDdJTSFSGkytATdMhqKRindIa-rcw4RTO64LHz-NM6pO0aPOCV-wX4uxvXeOFtBJOcv8TNFCP4ES9hB0PCb2FwO4jQ4THgs2ljPP7q0mQG3IQ4wo-n6HFvhgTPbucxunh3etGcFcvz94vmzbKwnLOxoK0pVcfK3tbEUgCpRAcV62vJeVczSsC2THS87LilVWdaED3prRFA2l715TF6fWO7ndoNdDYnjGbQ2-g2Jv7UwTj978a7tb4MOy0El6Wqs8GLW4MYridIo964ZGEYjIcwJU0V5UwRLkVGnz9Ar8IUfX6dZkSVXCklVaZO_k50H-Xu3zPw6gawMaQUodfWjX9ayAHdoCnR-5r1fc16X7OmUu9rznL5QH534T_C3_xWrvA |
CitedBy_id | crossref_primary_10_1523_JNEUROSCI_1141_20_2020 crossref_primary_10_1016_j_brs_2021_08_024 crossref_primary_10_1016_j_cub_2019_08_004 crossref_primary_10_1155_2018_8525706 crossref_primary_10_1016_j_brs_2022_08_007 crossref_primary_10_1007_s11427_023_2436_x crossref_primary_10_1016_j_cell_2020_04_033 crossref_primary_10_1167_jov_21_13_10 crossref_primary_10_1016_j_brainres_2019_146312 crossref_primary_10_1007_s12264_021_00760_2 crossref_primary_10_1016_j_brs_2021_04_020 crossref_primary_10_1007_s13311_018_0660_1 crossref_primary_10_1080_03091902_2021_1907468 crossref_primary_10_3390_s24082512 crossref_primary_10_1016_j_clinph_2017_10_019 crossref_primary_10_1016_j_cub_2024_10_057 crossref_primary_10_3390_brainsci11020221 crossref_primary_10_1172_JCI154983 crossref_primary_10_1007_s00429_021_02417_2 crossref_primary_10_1172_JCI151331 crossref_primary_10_1016_j_trf_2024_06_014 crossref_primary_10_1038_s41562_020_0910_1 crossref_primary_10_1088_1741_2552_ab7321 crossref_primary_10_1016_j_neuron_2022_09_003 crossref_primary_10_1088_1741_2552_ac77bf crossref_primary_10_1126_science_abd7435 crossref_primary_10_1088_1741_2552_ab021b crossref_primary_10_1016_j_neuron_2019_03_027 crossref_primary_10_1088_1741_2552_aca69d crossref_primary_10_1038_s41598_024_65337_1 crossref_primary_10_3390_prosthesis4040049 crossref_primary_10_1167_iovs_65_5_38 crossref_primary_10_1523_JNEUROSCI_1085_21_2021 crossref_primary_10_1088_1741_2552_ace07e crossref_primary_10_3171_2019_3_JNS182774 crossref_primary_10_1088_1741_2552_ab0b80 crossref_primary_10_1088_1741_2552_aceca2 crossref_primary_10_1088_1741_2552_ab9d11 crossref_primary_10_1016_j_jneumeth_2024_110169 crossref_primary_10_1016_j_celrep_2022_110617 crossref_primary_10_3389_fnins_2022_918767 crossref_primary_10_1093_scan_nsz015 crossref_primary_10_1016_j_pbiomolbio_2020_08_002 crossref_primary_10_1146_annurev_vision_111815_114525 |
ContentType | Journal Article |
Copyright | Copyright © 2017 the authors 0270-6474/17/377188-10$15.00/0. Copyright Society for Neuroscience Jul 26, 2017 Copyright © 2017 the authors 0270-6474/17/377188-10$15.00/0 2017 |
Copyright_xml | – notice: Copyright © 2017 the authors 0270-6474/17/377188-10$15.00/0. – notice: Copyright Society for Neuroscience Jul 26, 2017 – notice: Copyright © 2017 the authors 0270-6474/17/377188-10$15.00/0 2017 |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7QG 7QR 7TK 7U7 7U9 8FD C1K FR3 H94 P64 7X8 5PM |
DOI | 10.1523/JNEUROSCI.2896-16.2017 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Animal Behavior Abstracts Chemoreception Abstracts Neurosciences Abstracts Toxicology Abstracts Virology and AIDS Abstracts Technology Research Database Environmental Sciences and Pollution Management Engineering Research Database AIDS and Cancer Research Abstracts Biotechnology and BioEngineering Abstracts MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Virology and AIDS Abstracts Technology Research Database Toxicology Abstracts Animal Behavior Abstracts AIDS and Cancer Research Abstracts Chemoreception Abstracts Engineering Research Database Neurosciences Abstracts Biotechnology and BioEngineering Abstracts Environmental Sciences and Pollution Management MEDLINE - Academic |
DatabaseTitleList | MEDLINE MEDLINE - Academic Virology and AIDS Abstracts |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Anatomy & Physiology |
EISSN | 1529-2401 |
EndPage | 7197 |
ExternalDocumentID | PMC5546398 28652411 10_1523_JNEUROSCI_2896_16_2017 |
Genre | Journal Article Research Support, N.I.H., Extramural |
GrantInformation_xml | – fundername: NIMH NIH HHS grantid: R00 MH103479 – fundername: NEI NIH HHS grantid: R01 EY023336 |
GroupedDBID | --- -DZ -~X .55 18M 2WC 34G 39C 53G 5GY 5RE 5VS AAFWJ AAJMC AAYXX ABBAR ABIVO ACGUR ACNCT ADBBV ADCOW ADHGD AENEX AFCFT AFOSN AFSQR AHWXS ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL BTFSW CITATION CS3 DIK DU5 E3Z EBS EJD F5P GX1 H13 HYE H~9 KQ8 L7B OK1 P0W P2P QZG R.V RHI RPM TFN TR2 W8F WH7 WOQ X7M YBU YHG YKV YNH YSK AFHIN AIZTS CGR CUY CVF ECM EIF NPM RHF 7QG 7QR 7TK 7U7 7U9 8FD C1K FR3 H94 P64 7X8 5PM |
ID | FETCH-LOGICAL-c442t-1ba39d23fc80c1ee695de72f8644d8210ecb25d43d4c17dabe5f0fca5e0bf9f3 |
ISSN | 0270-6474 1529-2401 |
IngestDate | Thu Aug 21 17:50:06 EDT 2025 Fri Jul 11 10:11:04 EDT 2025 Mon Jun 30 16:44:37 EDT 2025 Wed Feb 19 02:35:52 EST 2025 Tue Jul 01 03:47:39 EDT 2025 Thu Apr 24 22:57:16 EDT 2025 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 30 |
Keywords | direct cortical stimulation electrical stimulation visual cortex phosphene electrical brain stimulation magnification factor |
Language | English |
License | Copyright © 2017 the authors 0270-6474/17/377188-10$15.00/0. |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c442t-1ba39d23fc80c1ee695de72f8644d8210ecb25d43d4c17dabe5f0fca5e0bf9f3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Author contributions: W.H.B., X.P., M.S.B., and D.Y. designed research; W.H.B., P.S., M.O., X.P., M.S.B., and D.Y. performed research; W.H.B., P.S., M.O., X.P., and B.L.F. analyzed data; W.H.B., B.L.F., M.S.B., and D.Y. wrote the paper. |
ORCID | 0000-0001-7472-4528 0000-0002-7599-9934 0000-0002-4999-8946 0000-0002-2621-5574 |
OpenAccessLink | https://www.jneurosci.org/content/jneuro/37/30/7188.full.pdf |
PMID | 28652411 |
PQID | 2093499969 |
PQPubID | 2049535 |
PageCount | 10 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_5546398 proquest_miscellaneous_1914290465 proquest_journals_2093499969 pubmed_primary_28652411 crossref_citationtrail_10_1523_JNEUROSCI_2896_16_2017 crossref_primary_10_1523_JNEUROSCI_2896_16_2017 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2017-07-26 20170726 |
PublicationDateYYYYMMDD | 2017-07-26 |
PublicationDate_xml | – month: 07 year: 2017 text: 2017-07-26 day: 26 |
PublicationDecade | 2010 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States – name: Baltimore |
PublicationTitle | The Journal of neuroscience |
PublicationTitleAlternate | J Neurosci |
PublicationYear | 2017 |
Publisher | Society for Neuroscience |
Publisher_xml | – name: Society for Neuroscience |
SSID | ssj0007017 |
Score | 2.4470816 |
Snippet | Electrically stimulating early visual cortex results in a visual percept known as a phosphene. Although phosphenes can be evoked by a wide range of electrode... |
SourceID | pubmedcentral proquest pubmed crossref |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | 7188 |
SubjectTerms | Adult Cerebral cortex Electric Stimulation Electrodes Evoked Potentials, Visual - physiology Female Humans Male Mathematical models Middle Aged Nerve Net - physiology Neural prostheses Phosphene Phosphenes Phosphenes - physiology Retina Saturation Stimulation Visual cortex Visual Cortex - physiology Visual Fields - physiology Visual observation |
Title | Saturation in Phosphene Size with Increasing Current Levels Delivered to Human Visual Cortex |
URI | https://www.ncbi.nlm.nih.gov/pubmed/28652411 https://www.proquest.com/docview/2093499969 https://www.proquest.com/docview/1914290465 https://pubmed.ncbi.nlm.nih.gov/PMC5546398 |
Volume | 37 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLZgvPCCYONSGMhIiBeULXbsXB6nCbQNNg21oD4gRU7ibBFrMi2pBP31nOM4l0IRl5eoqhtH6vfl5Pj4O18IeeWHoWY5E04QRqkjUs2dBKjiyDTgPAs0UAjrHadn_tEncTKX86Ggb7pLmmQvXW3sK_kfVOE7wBW7ZP8B2X5S-AI-A75wBITh-FcYT9GVU3VyxfPLqkbFln4zLVa6rbDC7Y-qc7O5b52YPqBMqIZAc4WSDMg3IftsS_mfi3ppagk3jf42zlqH_jGTuY48MIc9-ar-al-PYks4Q9vDdGlC23n3lMSa7sqqOU6XF3oIz0ZaMC9UtdDFuB7BTKGTWzdrG0O52bRh4yDbOrtYMtmdmDZkwsMx3BjLpfGUODlDSeP08HgPloa-w1BW0nZ7jgC-XhiEscsWMhI2PNt6xWE3dJvc4bCgwIj4_uPgKx_AnLZ_HC67v_miaBxtp1nPYn5ZmvyssB2lLLP75J5FjB60xHlAbulym-wclKqpFt_pa2rUv2ZbZYd8GbhEi5L2XKLIJYpcogOXqOUSbblEey7RpqKGS7TlEm259JDM3r2dHR459s0bTioEbxyWKC_KuJenoZsyrf1IZjrgeQjZcxZy5uo04TITXiZSFmQq0TJ381RJ7SZ5lHuPyFZZlfoJoUKJnCU5JNkqE74WkA1LKZWSrgiCyA8nRHZ_ZJxaV3p8OcpVjKtTwCLusYgRi5j5MWIxIfv9edetL8sfz9jtcIrtPVzDQOSZNX80IS_7YYiwuG2mSl0t6xgdEHnkCl9OyOMW1v6SHR8mJFgDvP8Burevj5TFpXFxR3moF4VPfzvnM3J3uL92yVZzs9TPIQNukheGvD8ABpewfw |
linkProvider | Colorado Alliance of Research Libraries |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Saturation+in+Phosphene+Size+with+Increasing+Current+Levels+Delivered+to+Human+Visual+Cortex&rft.jtitle=The+Journal+of+neuroscience&rft.au=Bosking%2C+William+H&rft.au=Sun%2C+Ping&rft.au=Ozker%2C+Muge&rft.au=Pei%2C+Xiaomei&rft.date=2017-07-26&rft.eissn=1529-2401&rft.volume=37&rft.issue=30&rft.spage=7188&rft_id=info:doi/10.1523%2FJNEUROSCI.2896-16.2017&rft_id=info%3Apmid%2F28652411&rft.externalDocID=28652411 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0270-6474&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0270-6474&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0270-6474&client=summon |